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Article

Surface Coverage- and Excitation Laser Wavelength-Dependent Luminescence Properties of U(VI) Species Adsorbed on Amorphous SiO2

1
Nuclear Chemistry Research Team, Korea Atomic Energy Research Institute, Daejeon 34057, Korea
2
Department of Nuclear and Quantum Engineering, KAIST, Daejeon 34141, Korea
3
Disposal Safety Evaluation Research Division, Korea Atomic Energy Research Institute, Daejeon 34057, Korea
*
Author to whom correspondence should be addressed.
Present Address: Institute for Nuclear Waste Disposal (INE), Karlsruhe Institute of Technology (KIT), 76344 Karlsruhe, Germany.
Minerals 2022, 12(2), 230; https://doi.org/10.3390/min12020230
Submission received: 16 November 2021 / Revised: 7 February 2022 / Accepted: 8 February 2022 / Published: 10 February 2022

Abstract

:
Time-resolved luminescence spectroscopy is usefully used to identify U(VI) surface species adsorbed on SiO2. However, the cause of the inconsistent luminescence lifetimes and spectral shapes reported previously remains undetermined. In this study, the U(VI) surface coverage (Γ) and excitation laser wavelength (λex) were examined as the predominant factors governing the luminescence properties of U(VI) surface species. At neutral pH, the luminescence lifetimes of U(VI) surface species increased with decreasing Γ. In the low-Γ region, where a relatively large number of adjacent surface sites are involved in the formation of multidentate surface complexes, the displacement of more number of coordinated water molecules in the equatorial plane of U(VI) results in a longer lifetime. The pH-dependent luminescence lifetimes of U(VI) surface species at the same U(VI) to SiO2 concentration ratio in the pH range of 4.5–7.5 also explain the effect of the surface binding sites on the luminescence lifetime. The time-resolved luminescence properties of the U(VI) surface species were also investigated at different excitation wavelengths. Continued irradiation of the SiO2 surface with a UV laser beam at λex = 266 nm considerably reduced the luminescence intensities of the U(VI) surface species. The higher the laser pulse energy, the greater the decrease in luminescence intensity. Laser-induced thermal desorption (LITD) of U(VI) surface species is suggested to be the origin of the decrease in luminescence intensity. LITD effects were not observed at λex = 355 and 422 nm, even at high laser pulse energies.

1. Introduction

Environmentally mobile uranium exists in the hexavalent oxidation state (U(VI)) under oxic conditions. Silicon dioxide (SiO2) is an abundant component of geological media and clay minerals. The adsorption of U(VI) onto SiO2 surfaces has been extensively studied to understand its transport behavior under geochemical conditions [1,2,3,4]. Recent reviews have described related studies of several mineral surfaces [5,6,7]. The adsorption characteristics of U(VI) onto SiO2 surfaces have been investigated at the molecular scale using spectroscopic techniques, such as extended X-ray absorption fine structure (EXAFS) spectroscopy [8,9,10,11,12], X-ray photoelectron spectroscopy [13,14], and time-resolved laser-induced fluorescence spectroscopy (TRLFS) [13,14,15,16,17,18,19,20,21,22,23,24]. Among these techniques, TRLFS has received considerable attention because of its high sensitivity. Information about the number of distinct U(VI) surface species at very low concentrations can be obtained by measuring the luminescence properties: intensity, lifetime, peak position, and spectral shape.
In previous TRLFS studies of U(VI)-adsorbed SiO2 suspensions, at least two pH-dependent luminescent U(VI) species have been distinguished. These species are prominent under acidic and near-neutral pH conditions [13,17]. The surface complexation of UO22+ results in the formation of ≡SiO2UO2 under acidic pH conditions. The formation of this surface complex has been unquestionably confirmed by EXAFS studies, indicating the inner-sphere bidentate bonding structure, at approximately pH 4 in the U(VI) concentration ([U(VI)]) range of 5 × 10−2 −2 × 10−5 M [9,10]. Under the near-neutral pH condition, a red-shift of approximately a few nanometres in the luminescence peak positions in comparison to those of ≡SiO2UO2 represents the surface complexation of U(VI)-hydroxo species. Two different complexes, ≡SiO2(UO2)OH and ≡SiO2(UO2)3(OH)5, have been proposed [13,17]. However, the spectroscopic differences between these U(VI)-hydroxo surface complexes remain a subject of discussion. Following EXAFS studies, Sylwester et al. [11] reported the formation of polynuclear surface complexes including surface precipitates by observing the U–U interatomic distance at approximately pH 6.5 and [U(VI)] = 4.15 × 10−5 M, whereas Reich et al. [9,10] reported a contradictory result. Among TRLFS researchers, Gabriel et al. proposed ≡SiO2(UO2)OH as the U(VI)-hydroxo surface complex in the low [U(VI)] range of 0.1–1 μM onto SiO2 above pH 6.7 [17]. In contrast, Kowal-Fouchard et al. reported that the U(VI) surface species were dominated by the U(VI) aqueous species; thus, ≡SiO2(UO2)3(OH)5 was suggested to be the U(VI)-hydroxo surface complex at high [U(VI)] of 0.1 mM above pH 5.9 [13]. Similar luminescence lifetimes of 360 ± 50 μs and 400 ± 30 μs were observed for ≡SiO2(UO2)OH and ≡SiO2(UO2)3(OH)5, respectively, in these works [13,17]. However, the luminescence spectral shapes of these U(VI)-hydroxo surface species have not yet been compared in detail. It is also of interest to note that the luminescence spectral shapes observed in other studies differ markedly for U(VI) surface species under near-neutral pH conditions [18,23,24]. Moreover, a wide range of luminescence lifetimes has been reported. For instance, lifetimes of 192–258 μs [23], 308 μs [18], 361.8 ± 206.4 μs [20], longer than 450 μs [21], and 599 ± 60 μs [24] have been reported for U(VI) surface species at pH 7–8. Until now, the reasons for these inconsistent lifetimes have not been clarified. The main results of previously reported U(VI) surface species, thermodynamic surface complexation constants, and luminescence characteristics are summarized in Table S1 of the Supplementary Materials.
The ambiguous luminescence properties are presumably due to the application of various experimental factors related to both the sample preparation and TRLFS instrumentation. Solution and surface parameters, such as pH and U(VI) surface coverage (Γ), are representative factors for sample preparation. Γ is determined by the specific surface area (SSA), adsorbed [U(VI)], and mass-to-volume ratio (m/v) of SiO2 and plays a significant role in the formation of surface complexes. It is known that polynuclear surface complexes are formed under high Γ conditions for montmorillonite, quartz, and Al hydroxide [25,26,27]. On the other hand, the excitation laser wavelength (λex) and laser pulse energy can be chosen as experimental factors for TRLFS instrumentation. In most TRLFS measurements, luminescence spectra have been obtained at λex = 266, 355 nm and 415–430 nm. Despite the fact that the first electronic absorption band of U(VI) is in the wavelength range of 415–430 nm [28,29], 266 nm UV laser beams are widely adopted owing to their high luminescence quantum yields [30,31]. The luminescence intensities measured by using different excitation wavelengths have been compared for aqueous U(VI) complexes and solid-state U(VI) compounds [32,33], but relatively little attention has been paid to the λex-dependent luminescence properties of the U(VI) surface species. The λex-dependent luminescence intensity change during laser irradiation has only been demonstrated for the U(VI) adsorbed titanium dioxide (TiO2) surface [34,35]. The decreases in the luminescence intensities of U(VI) surface species on TiO2 have been explained by the photoreduction of U(VI) to the tetravalent oxidation state (U(IV)) [34,35]. As the band gap energy of TiO2 is slightly above 3.0 eV, irradiation of laser light shorter than approximately λex = 413 nm provides photoelectrons from TiO2 to U(VI) [36]. In contrast, photoelectron generation is difficult at the SiO2–water interface because amorphous SiO2 has a bandgap energy of approximately 9.0 eV, approximately three times greater than that of TiO2 [37]. Accordingly, the λex-dependent luminescence intensity change of U(VI) surface species on SiO2 observed in this study has rarely been considered so far.
The objective of the present study was to elucidate the origin of the ambiguous luminescence properties measured using TRLFS. First, the Γ-dependent luminescence properties of U(VI) surface species were examined at λex = 266 nm for the three different SiO2 samples (two high SSA samples and one low SSA sample) at pH 7.5. The luminescence spectra were analyzed according to the decomposition processes via both parallel factor (PARAFAC) analysis [38,39,40] and manual subtraction method [22,41,42] using Origin 9.5. The results obtained from the latter method, in particular, were discussed in detail to understand the origin of the ambiguous luminescence lifetimes. Comparisons of the luminescence spectra and lifetimes between samples at various Γ provided new insights that resolve the confusion reported previously. The effects of the U(VI)-SiO2 reaction time (called the ‘ageing’ effect) on the luminescence properties were also inspected. Second, the λex-dependent luminescence properties were examined in the laser pulse energy range of 0.1–2.4 mJ at λex = 266, 355, and 422 nm for the aforementioned SiO2 samples at pH 7.5. Under the assumption that the photoreduction of U(VI) to U(IV) is not the major cause of the decrease in the luminescence intensities observed for the U(VI)-SiO2 system, another mechanism referred to as laser-induced thermal desorption (LITD) was studied for the first time to the best of the knowledge of the authors. Quantitative analysis of the desorbed U(VI) was performed to verify that LITD occurred during UV laser irradiation. The changes in the luminescence spectra resulting from the UV laser irradiation were examined. The luminescence characteristics of desorbed U(VI) species in the filtrates prepared after UV laser irradiation were also studied.

2. Materials and Methods

2.1. Materials

Table 1 lists the three different SiO2 powders used in this study. The first is hydrophilic fumed SiO2 with a diameter of a few tens of nanometers (Evonik, Essen, Germany, Aerosil 200; this SiO2 is referred to as ‘sample No. 1’). It is a nonporous, amorphous material composed of spherical particles with an SSA of approximately 156 m2/g. The second is a high-purity grade SiO2 gel with a particle size of 40–63 μm (Sigma–Aldrich, Saint Louis, MO, USA, 227196; this SiO2 is referred to as ‘sample No. 2’). The pore size of this SiO2 gel is approximately 6 nm (0.8 cm3/g pore volume) with an SSA of approximately 477 m2/g. The third is a spherical SiO2 powder with a particle size of 1.5 μm and an SSA of approximately 2 m2/g (Alfa Aesar, Ward Hill, MA, USA, L16987; this SiO2 is referred to as ‘sample No. 3’). For each sample, the SSA was determined using the N2 Brunauer–Emmett–Teller method. The SiO2 sample No. 2 was washed with 1 M HNO3 and Millipore water and dried at 383 K. The other two samples were used as they were received from the manufacturer. Powder XRD analyses (Bruker Corporation, Billerica, MA, USA, D8 Advance) were performed using a diffractometer with CuKα radiation over the range 10–80° (2θ), step size of 0.01°, and scan rate of 0.3 s/step. X-ray patterns show that all SiO2 samples used were essentially amorphous (data not shown).
For the Γ-dependent TRLFS measurements, these samples were employed to prepare a suspension with m/v values of 0.01, 0.1, and 1.0 g/L. U(VI) adsorption reactions were performed in 50 mL of mixed solution (0.034, 0.34, and 3.4 μM UO22+ and 0.1 M NaClO4) at pH 7.5. Samples were prepared by adding known amounts of SiO2 to Millipore water, and reagents were added in the following order: 5.77 M NaClO4, 1.5 mM UO22+ in 1.02 M HClO4, which resulted in a pH of approximately 4.3. For the pH-dependent TRLFS measurements, the samples at [U(VI)] = 3.4 μM and m/v = 1.0 g/L were prepared with pH values in the range of approximately 3.4–7.6. The desired pH conditions were achieved by slowly adding known amounts of 0.1 M NaOH (CO2 free) or HClO4 determined from pre-titration processes. All sample preparations were carried out in an Ar-conditioned glove box with continuous stirring. Samples were further equilibrated in a rotary shaker for two or more days, after which the pH of the samples was measured using a glass combination electrode (OrionTM Ross UltraTM, Thermo Scientific, Waltham, MA, USA). As a representative example, the amount of U(VI) adsorbed to SiO2 sample No. 2 is shown in Figure S1a as a function of pH. The adsorption edge was observed near pH 3.7 in the [U(VI)] range of 1–30 μM. The quantitative analysis of dissolved U(VI) was performed using inductively coupled plasma-atomic emission spectrometry (ICP-AES, Agilent Technologies, Inc., Santa Clara, CA, USA, 5100 ICP-OES) or inductively coupled plasma-mass spectrometry (ICP-MS, Varian, Inc., Palo Alto, CA, USA, Redtop) to determine the adsorbed U(VI) amount.
The Γ is calculated by dividing the adsorbed U(VI) amount by the surface area (SSA multiplied by m/v), and the unit is μmol U/m2 [25,26,27]. High SSA SiO2 samples with Γ of approximately 0.0007–1.526 μmol U/m2 were prepared by adjusting m/v to 0.01–1.0 g/L at initial [U(VI)] values of 0.34–3.4 μM. Low SSA SiO2 samples with Γ of approximately 0.017–1.7 μmol U/m2 were prepared by adjusting [U(VI)] to 0.034–3.4 μM at m/v = 1.0 g/L. The U(VI) adsorbed SiO2 sample (3 mL aliquot) was withdrawn from 50 mL of suspended solution and transferred to a quartz cell (Hellma Analytics QS 111–10–40) for the TRLFS experiment. The remaining samples were stored in a glove box for a long time and then used again when necessary to investigate the ageing effect as the reaction time of U(VI) and SiO2 elapsed. In order to observe the change in the distribution of U(VI) surface species, the luminescence spectral shapes were monitored as a function of reaction time for up to 16 months, and were compared to those of fresh samples.
Nearly 100% adsorption of U(VI) was confirmed before UV laser irradiation to examine the λex-dependent luminescence properties. As soon as the laser irradiation was complete, each SiO2 sample was centrifuged for 30 min at 18,000 rpm (relative centrifugal force value of around 22,100× g). The supernatants were then filtered using 0.45 μm syringe filters for quantitative analysis of the dissolved U(VI) in the filtrates.

2.2. Laser Spectroscopic Apparatus

Three different laser systems were used in the TRLFS study. Pulsed Nd:YAG lasers (Continuum, Milpitas, CA, USA, Minilite) at 266 nm and 355 nm (Continuum, Milpitas, CA, USA, Surelite) and an optical parametric oscillator at 422 nm (OPOTEK, Inc., Carlsbad, CA, USA, Vibrant B) were used as the excitation light sources. The laser pulse energy and laser beam profile were measured using an energy meter (Coherent, EPM 2000 with J25LP-MB detector) and a laser beam profiler (Newport, LBP-1), respectively. All lasers were operated at a repetition rate of 10 Hz, and the laser beam diameters (1/e2) were approximately 2.5 mm. The pulse energy fluctuations for 5000 laser pulses were within about 3% (266 nm, 355 nm) and 8% (422 nm), and laser pulse energy was monitored before and after measurement. The laser beam passed through the quartz cell, which was located inside the temperature-controlled cuvette holder (Quantum Northwest Turret 4). The sample cell temperature remained constant at 296 K (room temperature), and the SiO2 suspension was stirred with a stirring bar during measurements. The luminescence perpendicular to the direction of propagation of the laser beam was guided using an optical fiber bundle (cross-section of 2 × 8   mm2, 345 fibers). The output of the optical fiber bundle was connected to a spectrograph (Andor Technology, Belfast, Northern Ireland, SR-303i). TRLFS signals of U(VI) species were recorded by accumulating 100 laser pulses using a gated intensified charge-coupled device (ICCD, Andor Technology, Belfast, Northern Ireland, DH-720/18U-03 iStar 720D). All spectra were measured using a constant gate width (tw) of 1000 μs and varying gate delay time (td). The quantum efficiency of the ICCD, which varied for different wavelengths, was corrected in the luminescence spectra. Figure S1b of the Supplementary Materials shows the schematic diagram of the experimental setup for TRLFS. Photos of the cuvette holder and sample suspension are also included in Figure S1b.

3. Results and Discussion

3.1. Surface Coverage-Dependent Luminescence Properties

All data presented in this subsection were measured at λex = 266 nm and a laser pulse energy of 0.1 mJ. Before measuring the Γ-dependent luminescence properties, pH-dependent luminescence spectra were measured from the high SSA sample No. 1 at [U(VI)] = 3.4 μM and m/v = 1.0 g/L as a function of pH. Nearly 100% adsorption of U(VI) was observed above pH 5.0, as shown in Figure S1a. The adsorbed quantity of U(VI) was approximately 70% at pH 4.0, and the rest existed in the form of aqueous species. For the luminescence measurement of U(VI) surface species at pH 4.0, the aqueous U(VI) species were removed by centrifugation, after which the separated SiO2 particles were resuspended in a fresh background NaClO4 solution with a pH and an ionic strength identical to the original ones but without U(VI). The data in Figure 1 show the luminescence spectra, which were normalized by the intensity of the strongest peak.
The peak wavelength values are expressed in Arabic numerals in Figure 1. Two U(VI) surface species, ≡SiO2UO2 and ≡SiO2(UO2)OH, were distinguished based on the representative results obtained from the SiO2 samples at similar conditions of [U(VI)] = 1.0 μM and m/v = 1.0 g/L [17]. In the upper panel, the spectrum acquired at pH 4.0 is completely controlled by ≡SiO2UO2 and the luminescence peaks are located at approximately 500, 521, and 542 nm. The peak maxima are shifted to 506, 527, and 551 nm at pH 7.3. The shift of peak maxima represents the existence of the U(VI)-hydroxo surface species [13,17,18,21,22,23]. The spectra measured under different pH values (pH 5.0 and 5.6) in the upper panel demonstrate the transition of the dominant species from acidic to near-neutral pH conditions.
In the lower panel of Figure 1, the spectra acquired at td = 2501 μs can be considered the luminescence of the U(VI)-hydroxo surface species alone because the spectral overlap between these species is eliminated because of the much shorter luminescence lifetime of ≡SiO2UO2, as discussed later in association with spectral decomposition using the luminescence lifetime. To compare the luminescence spectral shapes in more detail, we defined the valley-to-peak (V/P) intensity ratio as the luminescence intensity of the first valley versus the intensity of the strongest peak, designated by an arrow in Figure 1. In the lower panel, there are no significant differences between the V/P intensity ratios measured at various pH values. In addition, the peak wavelengths and spectral shapes remain unchanged for td in the range of 2001–3001 μs. Thus, the spectra measured under the long-td condition were generated by a unique U(VI)-hydroxo surface species. The change in the V/P intensity ratio at various pH values results from the overlap of the luminescence spectra generated by multiple U(VI) species, as shown in the upper panel of Figure 1. An increase in pH leads to a lower V/P intensity ratio. This result is ascribed to the increase in the relative quantity of U(VI)-hydroxo surface species with pH, which shows a highly resolved spectrum at neutral pH values. In Figure S2 of the Supplementary Materials, the luminescence spectra measured for the other high SSA SiO2 (sample No. 2, [U(VI)] = 3.4 μM, m/v = 1.0 g/L) at various pH values show very similar shapes to those displayed in Figure 1.
The spectral shape with a V/P intensity ratio close to 0.6 at the near-neutral pH in Figure 1 is significantly different from those observed in other studies [18,23]. For example, Chisholm-Brause et al. [18] reported a V/P intensity ratio of approximately 0.9 (judging by Figure 1 in Chisholm-Brause et al.; the V/P intensity ratio was not given specifically) in the luminescence spectrum under the conditions of pH 8 and Γ = 3.846 μmol U/m2 (initial [U(VI)] = 9 μM, m/v = 0.013 g/L, and SSA = 180 m2/g) for the same SiO2 sample (Aerosil 200) used in this study. They predicted that the overall distribution consisted of about 20% ≡SiO2UO2 and 80% ≡SiO2(UO2)3(OH)5 based on the thermodynamic model predictions depicted in Figure 3 of McKinley et al. [1]. On the other hand, Gabriel et al. [17] observed a V/P intensity ratio of approximately 0.7 (judging by Figure 5 in Gabriel et al.; the V/P intensity ratio was not given specifically) under the conditions of pH 7.7 and Γ = 0.006 μmol U/m2 (initial [U(VI)] = 1 μM, m/v = 1.0 g/L, and SSA = 169 m2/g) for the same SiO2 sample. They observed that the overall distribution consisted entirely of ≡SiO2(UO2)OH under the high m/v condition. Considering the [U(VI)] and m/v values used in these studies [17,18], it seems plausible that an increase in Γ leads to a higher V/P intensity ratio under near-neutral pH conditions.
The Γ-dependent luminescence spectra were measured from the high SSA sample No. 1 at pH 7.5. Six samples with different [U(VI)] and m/v conditions were prepared, as shown in the legends of Figure 2. Among these samples, the adsorbed U(VI) amount of the sample with the highest Γ ([U(VI)] = 3.4 μM, m/v = 0.01 g/L) was about 70%, and all other samples showed an adsorbed U(VI) amount of 98% or more. The data in Figure 2 represent the normalized luminescence spectra measured at pH 7.5, and all spectra were acquired at td = 1 μs. The upper and lower panels in Figure 2 were measured at [U(VI)] = 0.34 and 3.4 μM, respectively. The normalized luminescence spectra obviously change in shape as m/v changes, even when [U(VI)] remains the same. An increase in m/v leads to a lower V/P intensity ratio in Figure 2, as expected based on comparison with previous studies [17,18]. The change in the V/P intensity ratio becomes more pronounced at higher [U(VI)], as shown in the lower panel of Figure 2.
Figure S3 in the Supplementary Materials presents the normalized luminescence spectra derived from the data in Figure 2. Lower V/P intensity ratios with narrower spectral widths are observed as [U(VI)] decreases from 3.4 to 0.34 μM under the same m/v value in Figure S3a,b. In the case of a sufficiently high m/v condition in Figure S3c, the normalized luminescence spectra show identical spectral shapes with the same V/P intensity ratio when [U(VI)] = 0.34 and 3.4 μM. Similarly, Gabriel et al. observed identical spectral shapes with [U(VI)] = 0.1 and 1.0 μM at m/v = 1.0 g/L [17]. The data in Figure 2 and Figure S3 indicate that the existence of different U(VI) surface species at pH 7.5, and their respective proportions depend on Γ.
The luminescence lifetimes were also used to obtain information about the adsorbed U(VI) species on SiO2. Assuming that two U(VI) surface species contribute to the luminescence spectra, the following double exponential decay equation was used [31]:
ln { I ( t ) } = ln { a × exp ( t τ 1 ) + ( 1 a ) × exp ( t τ 2 ) }
where I ( t ) is the normalized luminescence intensity integrated from 475 to 600 nm, and a and 1 a are the relative quantities of short- and long-lived components (called ‘species 1’ and ‘species 2’) with luminescence lifetimes of τ1 and τ2, respectively. Figure 3 shows the fitting results measured from the samples at pH 7.5 used in Figure 2. td varies from 1 to 3001 μs with a gate delay step of 50 μs. The symbols and lines in Figure 3 represent the normalized luminescence intensities on the natural logarithmic scale and the results of fitting the data to Equation (1) using Origin 9.5, respectively.
Table 2 summarises the luminescence lifetimes and relative quantities of species 1 and 2. The coefficients of determination (R2) and the residual sum of squares (RSS) are also listed for all fits. τ2 was provided as a ‘known’ value and was determined as shown in Figure S4 in the Supplementary Materials. The normalized luminescence spectra remain unchanged for td in the range of 2001–3001 μs, as shown in Figure S4a. This result means that τ2 can be determined by fitting the luminescence intensities measured at td = 2001–3001 μs to the linear regression, depicted as the solid line in Figure S4b.
The data listed in Table 2 are plotted as a function of Γ in Figure 4. Interestingly, a change in luminescence lifetime is observed as Γ changes, as shown in the upper panel of Figure 4. τ1 and τ2 change from approximately 170 and 400 μs, respectively, and converge at approximately 310 and 670 μs in the Γ region below 0.01 μmol U/m2. The lower panel of Figure 4 shows the relative quantities of species 1 and 2. The quantity of species 1 ( a in Equation (1)) increases with increasing Γ, and vice versa for species 2 ( ( 1 a ) in Equation (1)).
The decomposition results from the three spectra in the lower panel of Figure 2 are presented in Figure 5. The luminescence spectra of species 1 were resolved by subtracting the corrected spectra of species 2 from the corresponding luminescence spectra taken at td = 1 μs [22,41,42]. The corrected spectra of species 2 at td = 1 μs were obtained from the luminescence spectra acquired at td = 2501 μs by compensating for the exponential decay of the luminescence intensity with a lifetime τ2, as listed in Table 2. Different luminescence peak positions in the luminescence spectra of species 1 are observed with changing Γ, depicted as solid lines in the upper panel of Figure 5. The peak positions of species 1 measured at Γ ≈ 1.526 μmol U/m2 are blue-shifted compared to those measured at lower Γ values (Γ ≈ 0.217 and 0.021 μmol U/m2).
The spectral shapes of species 2 taken at td = 2501 μs in the lower panel of Figure 5 are almost identical for all samples with different Γ values. Thus, species 2 may have a similar nature for all samples. The peak positions of species 2 in the lower panel imply that species 2 is the U(VI)-hydroxo surface species. Considering the [U(VI)] level of 0.34–3.4 μM used in this study, species 2 likely represents ≡SiO2(UO2)OH [17].
The question is whether the short-lived species 1 represents ≡SiO2UO2, which is known to be the predominant species in the acidic pH range, or another species existing in the near-neutral pH range. The upper panel of Figure 5 compares the spectra of species 1 with the spectrum of ≡SiO2UO2 (dashed line) measured from the SiO2 sample at pH 4.0 (the same spectrum shown in Figure 1). It is clearly observed that the luminescence peak positions of species 1 measured at pH 7.5 do not exactly coincide with those of ≡SiO2UO2 measured at pH 4.0.
PARAFAC analysis was also applied to decompose the spectra in Figure 2. The decomposition with two spectral components converges well with high core-consistency value of 99.8%. However, analysis using the three spectral components resulted in a lack of core-consistency. Figure S5 shows the results of PARAFAC analysis obtained from the six spectra in Figure 2. Similar to the results in Figure 5, species 1 shows the peak maxima shifted in the longer wavelength direction compared to those of ≡SiO2UO2. In the lower panel of Figure S5, the luminescence lifetimes of the decomposed spectra were determined to be τ1 = 219 and τ2 = 617 μs, respectively. However, these values obtained from the five datasets, excluding the highest Γ, changed to τ1 = 306 and τ2 = 641 μs, respectively (data not shown). This result also suggests that the luminescence characteristics of the U(VI) surface species depend on the Γ values, as described in Table 2 and Figure 4. In order to directly present Γ-dependent luminescence characteristics, it is preferred to explain the decomposition results extracted by the manual subtraction method rather than the PARAFAC analysis.
In addition, species 1 shows unstable complexation properties. For example, the luminescence spectrum measured at td = 1 μs in Figure S6a reveals a V/P intensity ratio of approximately 0.64 immediately after sample preparation (in the so-called ‘fresh sample’). After 16 months of reaction time, the V/P intensity ratio changes to approximately 0.55, as shown by the dotted line in Figure S6a, because species 1 (relative quantity of approximately 41% in the fresh sample, as shown in the first row of Table 2) almost disappears for the aged sample, which was stored in an Ar-filled glove box. In contrast, the quantity of species 2 (relative quantity of approximately 59% in the fresh sample, as shown in the first row of Table 2) increases with increasing ageing time at the expense of species 1. Consequently, the luminescence lifetime of the aged sample was determined using a single exponential decay equation (τ2 only) instead of Equation (1), as shown in Figure S6b. These results imply that species 2 is more strongly bonded to the surface than species 1. A very similar ageing effect was observed in the previous TRLFS study on the U(VI) surface species adsorbed on the low SSA quartz powders (US Silica, Katy, TX, USA, Min-U-Sil 30, SSA of 1.63 ± 0.02 m2/g) by Ilton et al. [22]. They reported that the long-term contact of U(VI) with SiO2 under neutral pH conditions resulted in a change in the species distribution and proposed a monodentate U(VI) surface complex as unstable species 1 because of the weak bonding nature to the surface. The increase in the relative quantity of species 2 was attributed to the formation of multidentate U(VI) surface complexes [22] based on the molecular dynamic modelling of hydroxylated-U(VI) adsorption to low-index quartz surfaces [43].
At present, the TRLFS results alone do not provide sufficient information for the chemical speciation of species 1 observed at pH 7.5. A more in-depth study is needed to elucidate whether different peak positions of species 1 compared with those of ≡SiO2UO2 indicate another different U(VI) surface species existing in the near-neutral pH range or a Γ-dependent drift of the luminescence properties of ≡SiO2UO2.
The identical spectral shapes in the lower panel of Figure 5 with the Γ-dependent luminescence lifetimes of the species 2 listed in Table 2 indicate that the luminescence properties are significantly influenced by the surface parameters of SiO2. Multidentate U(VI)-SiO2 surface complexes are most likely formed under low Γ conditions due to the presence of high affinity sites, which are significant when smaller ratios of U(VI) loading to surface sites are involved. Similarly, a bridging bidentate configuration with U(VI) binding to the two surface sites was suggested as the surface species under low U(VI) loading conditions [9,10,44].
In this regard, it is of interest to examine the pH-dependent luminescence lifetimes of U(VI) surface species with a fixed [U(VI)]/(m/v] ratio because the probability of having two or more deprotonated adjacent sites increases with increasing pH [22]. Figure 6 summarizes the luminescence lifetimes determined from 34 fresh samples (sample No. 1, [m/v] = 1.0 g/L, [U(VI)] = 3.4 μM) under various pH conditions in the range of 3.4–7.6. The luminescence lifetime was determined to be τs = 233 ± 16 μs for the samples in the pH range of 3.4–4.1, where only the luminescence spectra of the ≡SiO2UO2 species appear. The lifetimes of species 1 and 2 were determined to be τ1 = 296 ± 17 μs and τ2 = 653 ± 12 μs, respectively, in the pH range of 7.0–7.6. Although the spectral shapes of species 2 are almost identical, as shown in the lower panel of Figure 1, the luminescence lifetimes vary in the pH range of 4.5–7.6, as depicted by the dashed line in Figure 6, which can be seen even with the naked eye. The lifetime increases from approximately 500 μs near pH 4.5 and converges to a constant value at near-neutral pH. The pH-dependent luminescence lifetimes of U(VI) surface species at a fixed [U]/[m/v] ratio in Figure 6 are in accordance with the Γ-dependent luminescence lifetimes at fixed pH in Figure 4. These observations are major experimental results that can explain the cause of the inconsistent luminescence lifetimes reported in previous studies, irrespective of whether species 2 represents ≡SiO2(UO2)OH or ≡SiO2(UO2)3(OH)5. The luminescence lifetimes determined in this study are listed in the last row of Table S1.
The Γ-dependent luminescence properties were examined for the other high SSA SiO2 samples (sample No. 2, pH 7.5), and the results are shown in Figures S7–S9 and Table S2. Although there was a large difference in particle size between SiO2 samples No. 1 and No. 2 (Table 1), very similar trends in the luminescence properties were identified. These results demonstrate that the luminescence properties of the U(VI) surface species on amorphous SiO2 are independent of the particle size. Figures S10 and S11 and Table S3 show the luminescence characteristics measured from the low SSA SiO2 samples (sample No. 3, pH 7.5). The Γ-dependent luminescence properties are also clearly observed.
The upper panel in Figure 7 compares the luminescence spectral shapes measured from the high- and low-SSA samples listed in Table 1. Despite the significantly different m/v values (0.01 g/L for sample No. 1 and 1.0 g/L for sample No. 3), the luminescence spectra resemble each other in a similar Γ range (approximately Γ = 1.5 μmol U/m2 for fresh sample No. 1 and Γ = 1.7 μmol U/m2 for fresh sample No. 3 at [U(VI)] = 3.4 μM). The luminescence spectrum measured from fresh sample No. 3 shows a V/P intensity ratio of approximately 0.8. This ratio changes to approximately 0.65 after one year of reaction time, as indicated by the dashed line because the relative quantity of species 2 increases with time. It is observed that the ageing effect changes the luminescence lifetime as well as the spectral shape. As shown in the lower panel of Figure 7, the luminescence lifetimes of both species 1 and 2 increase with increasing ageing time. As a year passed, the relative amount of species 1 decreased from 93% to 49%, and that of species 2 increased from 7% to 51%. In a previous study on the ageing effect, Ilton et al. performed TRLFS experiments at liquid He temperature and did not report the lifetime information of the U(VI) surface species; thus, direct comparison of their results with those obtained in this study is not possible [22]. Nevertheless, the data displayed in Figure 7 suggest that the ageing time-dependent luminescence properties result from surface complexes, which evolved toward higher coordination with surface sites.

3.2. Excitation Wavelength- and Pulse Energy-Dependent Luminescence Properties

In this subsection, the term ‘laser-induced reaction’ refers to changes in the luminescence intensity and/or spectral shape that occur during laser irradiation. Figure 8 depicts the laser-induced reaction effect generated by irradiating a laser beam with a pulse energy of 2.4 mJ at λex = 266 nm on the luminescence intensity of U(VI) surface species measured from the low SSA sample (sample No. 3, [U(VI)] = 3.4 μM, and m/v = 1.0 g/L) at pH 7.5. The luminescence spectra were measured at td = 1 μs as a function of the laser irradiation time. The normalized luminescence spectra maintain their shapes as the irradiation time increases, as shown in Figure 8a. The luminescence intensities in Figure 8b were obtained by integrating the signal from 475 to 600 nm in the luminescence spectrum and were normalized by the strongest value measured at an irradiation time of 0.2 min. Figure 8b reveals that the luminescence intensity decreases by approximately 38% after approximately 50 min of laser irradiation. This result can be understood in terms of the LITD of U(VI) surface species by the following processes: (1) when a portion of the laser pulse energy is absorbed into the surface, the localised surface heating induces thermal desorption of adsorbed species; and (2) the desorption of adsorbed U(VI) surface species results in an immediate decrease in the luminescence intensity [45,46,47,48].
The suitability of LITD as a cause of the laser-induced reaction was demonstrated by monitoring the desorbed U(VI) from the surface. Figure 8c represents the quantities of desorbed U(VI) in the filtrates obtained from the same SiO2 samples used in Figure 8a,b at pH values of 6.2–7.2 irradiated under the same laser conditions. The X-axis in Figure 8c denotes the change in the luminescence intensity resulting from the laser-induced reaction, which was controlled by varying the irradiation time of the laser beam. Consequently, the luminescence intensities decreased by approximately 15–45%. As soon as the laser-induced reaction was complete after laser irradiation, the samples were centrifuged and filtered for quantitative analysis of the desorbed U(VI). The Y-axis in Figure 8c denotes the quantities of desorbed U(VI) in the filtrates determined using ICP-AES. A large amount of U(VI) (up to nearly 30% of the adsorbed U(VI)) was desorbed in the filtrates. The solid line in Figure 8c was obtained by fitting the data to a linear regression. The quantity of desorbed U(VI) is linearly dependent on the change in the luminescence intensity. This result provides direct evidence of LITD as the origin of the laser-induced reaction of the U(VI) surface species. Although the quantities of desorbed U(VI) correlate well with the changes in the luminescence intensities, the solid line with a slope of approximately 0.78 and an intercept of approximately −8.3 in Figure 8c indicates that the quantities of desorbed U(VI) are smaller than the changes in the luminescence intensities. The reason for this phenomenon is presumed to be that a small amount of U(VI) desorbed from the SiO2 surface is adsorbed on a quartz cell, and this was not used for quantitative analysis. Under the same measurement conditions, the luminescence intensity of the desorbed U(VI) species in the filtrate (approximately 20% desorbed U(VI) sample) was about 680 times weaker than that of the adsorbed U(VI) species. Therefore, it does not significantly affect the luminescence spectral shapes of adsorbed U(VI) species, as shown in Figure 8a.
Because the absorbed laser energy is a prerequisite for localised surface heating, the dependence of the incident pulse energy on the laser-induced reaction extent was examined at λex = 266 nm. Figure 9 shows the effect of the incident laser pulse energy on the luminescence intensity of the U(VI) surface species measured from the high SSA sample (sample No. 2) at pH 7.5, [U(VI)] = 0.34 μM, and m/v = 1.0 g/L. The spectra were measured at td = 1 μs as a function of the laser irradiation time. The luminescence intensities shown in the graphs were obtained by integrating the signal from 475 to 600 nm in the luminescence spectrum. The luminescence intensity decreases more rapidly as the laser pulse energy increases. The luminescence intensities in the upper panel of Figure 9 are reduced by approximately 34%, 15%, and 7% after approximately 50 min of irradiation by incident laser pulse energies of 2.4, 1.2, and 0.6 mJ, respectively. There are no considerable changes in the luminescence intensities measured at the laser pulse energy of 0.1 mJ. Under the same measurement conditions at the laser pulse energy of 0.1 mJ, the luminescence intensity generated from pure SiO2 suspension without U(VI) was about 0.1–0.3% of the luminescence intensity measured in adsorbed U(VI) species. Accordingly, the offset value generated from the background signal in Figure 9 may be ignored. The lower panel of Figure 9 shows the replotted luminescence intensities of the upper panel of Figure 9 as a function of the incident laser pulse energy. Nonlinear growth of the luminescence intensities is observed with increasing laser pulse energy. The laser pulse energy-dependent nonlinear property becomes more severe as the irradiation time passes, as indicated by the dashed line in Figure 9.
The luminescence spectra of the U(VI) surface species used to derive the data presented in Figure 9 were normalized to the maximum intensity in Figure 10. The initial luminescence spectra, which were measured immediately at 0.2 min after laser irradiation, show almost identical shapes as the same V/P intensity ratio under different laser pulse energies of 0.1–2.4 mJ in Figure 10. The spectral shapes of the U(VI) surface species measured at a laser pulse energy of 0.1 mJ in the left upper panel of Figure 10 do not change with increasing laser irradiation time. Because the measurements were performed for SiO2 samples, which were stored in a globe box for nearly four months, species 2 seems to exist predominantly due to the ageing effect as explained in the previous subsection. Interestingly, the normalized luminescence spectra measured under laser pulse energies of 0.6–2.4 mJ change shapes during laser irradiation. An increase in the laser pulse energy leads to a higher V/P intensity ratio as the irradiation time passes, with the appearance of a shoulder at approximately 497 nm, designated by an ellipse in the right lower panel of Figure 10. The fraction of the shoulder also increases with increasing laser pulse energy. The changes in the luminescence spectral shapes resulting from the laser-induced reaction under laser pulse energies of 0.6–2.4 mJ were ascribed to the appearance of the additional U(VI) species (called ‘species 3’) showing luminescence peaks located at shorter wavelengths. The change in the luminescence intensities of the U(VI) surface species displayed in the upper panel of Figure 9 is very similar to the results observed for the U(VI)-TiO2 system, wherein the photoreduction of U(VI) dominates the laser-induced reaction [34,35]. The formation of non-luminescent U(IV) results in immediate decreases in the luminescence intensities of the U(VI)-TiO2 system. However, the changes in the spectral shapes illustrated in Figure 10 constitute a newly observed phenomenon that has not been reported for the U(VI)-TiO2 system in previous studies [34,35]. This observation indicates that the photoreduction of U(VI) to U(IV) is not the major mechanism of the laser-induced reaction observed for this U(VI)-SiO2 system.
The upper panel of Figure 11 shows the luminescence spectra of the same SiO2 sample used to obtain Figure 9 and Figure 10, measured at λex = 355 nm. The luminescence intensities of these spectra were not normalized. There are no significant changes in either the luminescence intensities or spectral shapes during the laser irradiation even at a laser pulse energy of 2.4 mJ. The lower panel of Figure 11 presents the luminescence intensities as a function of the incident laser pulse energy. Unlike the intensities in Figure 9 measured at λex = 266 nm, the luminescence intensities at λex = 355 nm increase linearly with increasing laser pulse energy. The solid line represents the results of fitting the data to a linear equation.
A comparison of the results in Figure 11 with those in Figure 9 and Figure 10 suggests that the laser-induced reaction does not occur at λex = 355 nm. The luminescence spectra of the same SiO2 sample shown in Figure 9 and Figure 10 measured at λex = 422 nm, corresponding to the absorption band of the surface U(VI) species [31], suggest that the laser-induced reaction also does not occur at λex = 422 nm with a laser pulse energy of 2.4 mJ, as shown in Figure S12a. In a previous study, the excitation spectrum measured at λex = 266 nm showed a much higher intensity than those measured at λex = 355 and 422 nm [31]. This finding means that a much larger laser energy is absorbed by the surface at 266 nm than at other wavelengths. Consequently, the luminescence intensity at λex = 266 nm is approximately 40 times stronger than the intensities measured at λex = 355 and 422 nm at the same laser pulse energy of 2.4 mJ, as shown in Figure S12b.
PARAFAC analysis was applied for decomposition of the luminescence spectra displayed in Figure 10, Figure 11 and Figure S12. For those in the process of the laser-induced reaction, the decomposition with two spectral components (species 2 and 3) converges well with high core-consistency values (99.7–100%). As representative PARAFAC analysis results, the results of decomposition from the spectra in the right lower panel of Figure 10 are presented in Figure 12. When the laser-induced reaction does not occur, such as in the spectra in Figure 10 (left upper panel), Figure 11, and Figure S12, a unique component corresponding to species 2 exists. The average luminescence lifetimes at three different wavelengths were determined to be τ2 = 649 ± 28 μs, as listed in Table 3. This value corresponds to the value determined in Figure 62 = 653 ± 12 μs). The luminescence spectral shape of species 3 in Figure 12 and its lifetime in Table 3 resemble those of species 1 (τ1 = 296 ± 17 μs), as explained in the previous subsection.
Under the conditions wherein the laser-induced reaction occurs at λex = 266 nm, the lifetimes of species 2 listed in Table 3 decrease gradually to approximately 575 μs with increasing laser pulse energy. Considering the nonlinear increase in the luminescence intensity as a function of the incident laser pulse energy observed in Figure 9, the transfer of a portion of the absorbed laser energy into the thermal heating of the surface presumably promotes the nonradiative decay process. Thus, the excited-state lifetimes determined with high laser energy absorption at λex = 266 nm become shorter owing to the increases in the relevant processes (radiative and nonradiative) that relax the electronic excited states back to the ground state. The lower panel of Figure 12 shows the change in the species distribution determined using PARAFAC analysis. The luminescence intensities of species 3 gradually increase with increasing irradiation time, whereas those of species 2 decrease.
As soon as the laser-induced reaction was complete after 1 h of laser irradiation at λex = 266 nm, sample No. 2 ([U(VI)] = 0.34 μM, m/v = 1.0 g/L, and pH 7.5) was irradiated at λex = 422 nm with a laser pulse energy of 1.7 mJ to monitor the evolution of the luminescence spectrum with time. The luminescence spectral shapes measured at td = 1 μs recover over a long period of time, as shown in the upper panel of Figure 13. The luminescence intensity of species 3 gradually decreases with time; thus, the V/P intensity ratio and the fraction of the shoulder decrease, as indicated by the arrow in Figure 13. These observations demonstrate that the newly appeared species, species 3, resulting from the laser-induced reaction for the high SSA sample, continuously disappears with time. Meanwhile, the luminescence intensity of species 2 increases with time. The lower panel of Figure 13 shows the change in the species distribution as a function of the signal recovery time. PARAFAC analysis was applied for decomposition of the luminescence spectra displayed in the upper panel of Figure 13. The decomposition with two spectral components converges well with a high core-consistency value of 99.8%. The origin of the X-coordinate in the lower panel denotes the time at which the UV laser irradiation ends. The luminescence intensities of species 2 are recovered fast over the first two days with decreasing luminescence intensity of species 3.
As described in the previous subsection, the increase in species 2 at the expense of species 3 with time suggests that species 3 is unstable. Thus, a reasonable hypothesis is that species 3, which appears during the laser-induced reaction, is analogous to species 1 under near-neutral pH conditions. The appearance and disappearance of species 3 shown in Figure 12 and Figure 13, respectively, were easily observed in SiO2 samples with high SSA, but difficult to observe in samples with low SSA. If these phenomena are due to a result of a change in the equilibrium of U(VI)-hydroxo species by the thermal heating of the surface, these phenomena should be observed even in SiO2 samples with low SSA. From the photoreduction perspective, U reoxidation cannot contribute to the luminescence signal recovery because of the formation of a non-luminescent end product, such as an oxide with a structure intermediate between UO2 and UO3, possibly U3O8 [34,49].
Figure 14 shows the luminescence properties measured for the dissolved U(VI) species by laser irradiation. As soon as the laser-induced reaction was complete with a net decrease of approximately 28% in the luminescence intensity after 1 h of laser irradiation at λex = 266 nm with a laser pulse energy of 2.4 mJ, the suspension (high SSA sample No. 2 at pH 7.5, [U(VI)] = 3.4 μM, and m/v = 1.0 g/L) was centrifuged and filtered for quantitative analysis of the dissolved U(VI). The luminescence spectrum of the dissolved U(VI) species in the filtrate illustrated as a solid line in the upper panel of Figure 14 shows peak positions at approximately 500, 520, 544, and 572 nm. The dotted line represents the background luminescence spectrum of the species existing in the filtrate of the same batch of the SiO2 sample, but without laser irradiation. The observation of much stronger luminescence after 1 h of laser irradiation than that of the background spectrum indicates that the increase in the dissolved U(VI) species results from the desorption of U(VI) from the SiO2 surface.
The lower panel of Figure 14 shows the luminescence lifetime measured from the dissolved U(VI) species in the upper panel of Figure 14. The luminescence intensities depicted as symbols were obtained from a series of luminescence spectra measured using the kinetic mode of the ICCD with tw = 10 μs and a td between 1 μs and 151 μs (step size of 5 μs). The symbols and solid lines in the lower panel denote the normalized luminescence intensities on the natural logarithmic scale and the results of fitting the data to a linear regression, respectively. For several filtrates, the luminescence lifetime of the dissolved U(VI) species was determined to be τ = 52 ± 17 μs. The peak wavelengths and luminescence lifetime of the U(VI) species in Figure 14 are comparable to previously reported values (peak wavelengths of 500, 521, 544, and 570 nm and a lifetime of 19 ± 4 μs) at pH 3.9 for the complex in the U(VI)-silicate system, such as the UO2OSi(OH)3+ species [16].
In Figure 14, the quantity of desorbed U(VI) in the filtrate determined using ICP-MS is 0.1 μM, which corresponds to approximately 3% of the adsorbed quantity of 3.4 μM. The quantity of background U(VI) species before laser irradiation was smaller than the detection limit of the analytical instrument. The amount of desorbed U(VI) in the filtrate is quite small compared to the desorbed quantities of approximately 30% for the low SSA samples, as shown in Figure 8c. This phenomenon is attributed to the readsorption of the dissolved U(VI) species, which is responsible for the newly appearing species, species 3, as illustrated in the right lower panel of Figure 10. Considering that the lower adsorption sites of the low SSA samples prevent the desorbed U(VI) from readsorption during the laser irradiation, a large quantity of desorbed U(VI) is expected in filtrates obtained from the low SSA samples. A comparison of the spectra in Figure 8 with those in the right lower panel of Figure 10 reveals that there are no additional U(VI) species in the low SSA sample.

4. Conclusions

The comprehensive study presented in this manuscript clarifies the experimental factors that affect the luminescence properties of the U(VI)-SiO2 system, resulting in inconsistent luminescence lifetimes and spectral shapes in previous studies. The key findings described in ‘3.1. Surface Coverage-Dependent Luminescence Properties’ subsection show that the luminescence properties of the U(VI) surface species depend on Γ. For the three considered SiO2 samples, the luminescence lifetimes increased as Γ decreased. Simultaneously, the V/P intensity ratios of the luminescence spectral shapes decreased as Γ decreased. The longest luminescence lifetime of U(VI)-hydroxo surface species, denoted as species 2 in this report, was approximately 650 μs in the Γ region below 0.01 μmol U/m2. The U(VI)-hydroxo surface species are likely highly coordinated by SiO2 in the low Γ region, where a relatively large number of adjacent surface sites are involved in surface complexation. The possible displacement of coordinated water molecules in the equatorial plane of U(VI) results in a longer luminescence lifetime. The importance of the adjacent surface sites was further verified by observing the pH-dependent luminescence lifetimes. The ageing time-dependent luminescence properties revealed the stability of the U(VI)-hydroxo surface species. Further work should focus on the chemical speciation of unstable U(VI) surface species, denoted as species 1 in this study, in the near-neutral pH range. In ‘3.2. Excitation Wavelength- and Pulse Energy-Dependent Luminescence Properties’ subsection, the laser-induced reaction in the U(VI)-SiO2 system by LITD was observed. For both the low and high SSA SiO2 samples, the higher the UV laser pulse energy, the greater the decrease in luminescence intensity. This effect can lead to misinterpretation of the luminescence characteristics of U(VI) surface species. For example, when LITD occurs during luminescence lifetime measurement, the lifetime is determined inaccurately because of the excessive decrease in the luminescence intensity caused by the U(VI) desorbed from the surface. It was also confirmed that irradiation of the SiO2 surface by a UV laser beam at a high pulse energy changed both the luminescence lifetime and spectral shape. The results obtained in the present study provide detailed information for the reliable measurements of the luminescence characteristics of U(VI) surface species in oxide and mineral systems.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/min12020230/s1, Table S1: Previously reported U(VI) surface species, thermodynamic surface complexation constants, and luminescence lifetimes. All measurements were conducted at room temperature. Table S2: Luminescence lifetimes and relative quantities of species 1 and 2 measured from the high SSA SiO2 (sample No. 2, pH 7.5). Table S3: Luminescence lifetimes and relative quantities of species 1 and 2 measured from the low SSA SiO2 (sample No. 3, pH 7.5). Figure S1: (a) Adsorption edge of U(VI)/SiO2 system (b) The Schematic diagram of the experimental setup for TRLFS. Figure S2: Normalized luminescence spectra of U(VI) adsorbed onto high SSA SiO2 (sample No. 2) under various pH conditions. Figure S3: Normalized luminescence spectra derived from the data in Figure 2. Figure S4: The luminescence lifetime of the species 2 can be determined by fitting the luminescence intensities measured at various gate delay times in the range of 2001–3001 μs. Figure S5: PARAFAC analysis obtained from the six spectra displayed in Figure 2. Figure S6: Ageing time effect on the luminescence properties. Figure S7: Γ-dependent luminescence spectral shapes measured from the high SSA SiO2 (sample No. 2, pH 7.5) under various [U(VI)]/(m/v) ratios. Figure S8: Luminescence lifetimes of U(VI) surface species measured from the samples used to obtain Figure S7. Figure S9: (a) Luminescence lifetimes in Table S2 as a function of Γ. (b) The relative contents of species 1 and 2. Figure S10: Γ-dependent luminescence properties measured from the low SSA SiO2 (sample No. 3, pH 7.5) under various [U(VI)]/(m/v) ratios. Figure S11: Luminescence lifetimes in Table S3 as a function of Γ. (b) The relative contents of species 1 and 2. Figure S12: (a) The luminescence intensities measured at λex = 422 nm for the same SiO2 sample used in Figure. 9. (b) Comparison of luminescence intensity measured at λex = 266 nm with the intensities measured at λex = 355 and 422 nm.

Author Contributions

Formal analysis, T.-H.K., H.-K.K. and H.-R.C.; investigation, E.C.J., Y.J.; writing, E.C.J.; review and editing, J.-I.Y., H.-K.K., M.H.B. and W.C. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Nuclear Research and Development Program of the National Research Foundation of Korea, grant number 2017M2A8A5014719, and by the Institute for Korea Spent Nuclear Fuel and the National Research Foundation of Korea, grant number 2021M2E1A1085202.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Normalized luminescence spectra of U(VI) adsorbed onto the high SSA SiO2 (sample No. 1, [U(VI)] = 3.4 μM, m/v = 1.0 g/L) under various pH conditions. The (upper) and (lower) panels were measured at td = 1 μs and 2501 μs, respectively.
Figure 1. Normalized luminescence spectra of U(VI) adsorbed onto the high SSA SiO2 (sample No. 1, [U(VI)] = 3.4 μM, m/v = 1.0 g/L) under various pH conditions. The (upper) and (lower) panels were measured at td = 1 μs and 2501 μs, respectively.
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Figure 2. Normalized luminescence spectra of U(VI) adsorbed onto the high SSA sample (sample No. 1, pH 7.5) under various [U(VI)]/(m/v) ratios. The spectra were measured at td = 1 μs. The (upper) and (lower) panels were measured at [U(VI)] = 0.34 and 3.4 μM, respectively.
Figure 2. Normalized luminescence spectra of U(VI) adsorbed onto the high SSA sample (sample No. 1, pH 7.5) under various [U(VI)]/(m/v) ratios. The spectra were measured at td = 1 μs. The (upper) and (lower) panels were measured at [U(VI)] = 0.34 and 3.4 μM, respectively.
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Figure 3. Luminescence lifetimes of U(VI) surface species measured from the samples used to obtain Figure 2. The kinetic mode of the ICCD was utilized with td = 1–3001 μs and a gate delay step of 50 μs. The symbols represent the normalized luminescence intensity on the natural logarithmic scale for U(VI) surface species. The solid lines represent the fitting data calculated using Equation (1).
Figure 3. Luminescence lifetimes of U(VI) surface species measured from the samples used to obtain Figure 2. The kinetic mode of the ICCD was utilized with td = 1–3001 μs and a gate delay step of 50 μs. The symbols represent the normalized luminescence intensity on the natural logarithmic scale for U(VI) surface species. The solid lines represent the fitting data calculated using Equation (1).
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Figure 4. Luminescence lifetimes and relative quantities in Table 2 as a function of Γ. Blue rectangle and red circle represent the characteristics of species 1 and species 2, respectively. The dashed lines represent the results of fitting the data to the polynomial equation ( y = B 1 · x + B 2 · x 2 + i n t e r c e p t ) for easy observation of the increasing and decreasing behaviours of the data.
Figure 4. Luminescence lifetimes and relative quantities in Table 2 as a function of Γ. Blue rectangle and red circle represent the characteristics of species 1 and species 2, respectively. The dashed lines represent the results of fitting the data to the polynomial equation ( y = B 1 · x + B 2 · x 2 + i n t e r c e p t ) for easy observation of the increasing and decreasing behaviours of the data.
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Figure 5. The upper panel represents the normalized luminescence spectra of species 1 (solid lines, pH 7.5) obtained by decomposition of the luminescence spectra displayed in the lower panel of Figure 2. Decomposition was performed using the manual subtraction method. The dashed line measured at pH 4.0 represents the normalized luminescence spectrum of ≡SiO2UO2. Normalized luminescence spectra of species 2 measured at td = 2501 μs are displayed in the lower panel.
Figure 5. The upper panel represents the normalized luminescence spectra of species 1 (solid lines, pH 7.5) obtained by decomposition of the luminescence spectra displayed in the lower panel of Figure 2. Decomposition was performed using the manual subtraction method. The dashed line measured at pH 4.0 represents the normalized luminescence spectrum of ≡SiO2UO2. Normalized luminescence spectra of species 2 measured at td = 2501 μs are displayed in the lower panel.
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Figure 6. pH-dependent luminescence lifetimes of the U(VI) surface species determined from 34 samples in the pH range of 3.4–7.6 at the constant Γ = 0.021 μmol U/m2 (sample No. 1, m/v = 1.0 g/L, [U(VI)] = 3.4 μM).
Figure 6. pH-dependent luminescence lifetimes of the U(VI) surface species determined from 34 samples in the pH range of 3.4–7.6 at the constant Γ = 0.021 μmol U/m2 (sample No. 1, m/v = 1.0 g/L, [U(VI)] = 3.4 μM).
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Figure 7. The luminescence spectra measured from the low and high SSA samples are compared in the upper panel. In the lower panel, the luminescence lifetimes of both species 1 and 2 increase with increasing ageing time. The y-axis is in a natural logarithmic scale.
Figure 7. The luminescence spectra measured from the low and high SSA samples are compared in the upper panel. In the lower panel, the luminescence lifetimes of both species 1 and 2 increase with increasing ageing time. The y-axis is in a natural logarithmic scale.
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Figure 8. (a) Normalized luminescence spectra of U(VI) surface species for the low SSA sample (sample No. 3, [U(VI)] = 3.4 μM, m/v = 1.0 g/L, pH 7.5). (b) These data show the decrease in the luminescence intensity resulting from the laser-induced reaction at λex = 266 nm. (c) Comparison of the desorbed U(VI) quantity with the decrease in the luminescence intensity for the low SSA samples.
Figure 8. (a) Normalized luminescence spectra of U(VI) surface species for the low SSA sample (sample No. 3, [U(VI)] = 3.4 μM, m/v = 1.0 g/L, pH 7.5). (b) These data show the decrease in the luminescence intensity resulting from the laser-induced reaction at λex = 266 nm. (c) Comparison of the desorbed U(VI) quantity with the decrease in the luminescence intensity for the low SSA samples.
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Figure 9. The upper panel shows the laser-induced reaction effect on the luminescence intensity at λex = 266 nm for the high SSA sample (sample No. 2, [U(VI)] = 0.34 μM, m/v = 1.0 g/L, pH 7.5). The lower panel represents the luminescence intensities in the upper panel as a function of incident laser pulse energy. The solid and dashed lines show the results of fitting the data to the polynomial equation (n = 2).
Figure 9. The upper panel shows the laser-induced reaction effect on the luminescence intensity at λex = 266 nm for the high SSA sample (sample No. 2, [U(VI)] = 0.34 μM, m/v = 1.0 g/L, pH 7.5). The lower panel represents the luminescence intensities in the upper panel as a function of incident laser pulse energy. The solid and dashed lines show the results of fitting the data to the polynomial equation (n = 2).
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Figure 10. Normalized luminescence spectra of the U(VI) surface species used to derive the data presented in Figure 9. An increase in the laser pulse energy leads to a higher V/P intensity ratio with the appearance of a shoulder at approximately 497 nm, designated as an ellipse in the right lower panel.
Figure 10. Normalized luminescence spectra of the U(VI) surface species used to derive the data presented in Figure 9. An increase in the laser pulse energy leads to a higher V/P intensity ratio with the appearance of a shoulder at approximately 497 nm, designated as an ellipse in the right lower panel.
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Figure 11. The upper panel shows lluminescence spectra for the same SiO2 sample used to obtain Figure 9 and Figure 10, but with λex = 355 nm (laser pulse energy of 2.4 mJ). The lower panel shows the luminescence intensity plotted as a function of laser pulse energy at 355 nm.
Figure 11. The upper panel shows lluminescence spectra for the same SiO2 sample used to obtain Figure 9 and Figure 10, but with λex = 355 nm (laser pulse energy of 2.4 mJ). The lower panel shows the luminescence intensity plotted as a function of laser pulse energy at 355 nm.
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Figure 12. The upper panel shows PARAFAC analysis results for decomposition of the luminescence (LM) spectra displayed in the right lower panel of Figure 10. In the lower panel, the luminescence intensities of species 3 gradually increase as the irradiation time passes with decreasing luminescence intensity of species 2.
Figure 12. The upper panel shows PARAFAC analysis results for decomposition of the luminescence (LM) spectra displayed in the right lower panel of Figure 10. In the lower panel, the luminescence intensities of species 3 gradually increase as the irradiation time passes with decreasing luminescence intensity of species 2.
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Figure 13. As soon as the laser irradiation at 266 nm was complete (high SSA sample No. 2, [U(VI)] = 0.34 μM, m/v = 1.0 g/L, and pH 7.5), the luminescence spectra were measured at 422 nm to monitor the evolution of the luminescence spectrum. In the upper panel, the spectral shapes measured at td = 1 μs are recovered over a long period of time. In the lower panel, PARAFAC analysis shows that the luminescence intensities of species 2 gradually increase as the recovery time passes with decreasing luminescence intensity of species 3.
Figure 13. As soon as the laser irradiation at 266 nm was complete (high SSA sample No. 2, [U(VI)] = 0.34 μM, m/v = 1.0 g/L, and pH 7.5), the luminescence spectra were measured at 422 nm to monitor the evolution of the luminescence spectrum. In the upper panel, the spectral shapes measured at td = 1 μs are recovered over a long period of time. In the lower panel, PARAFAC analysis shows that the luminescence intensities of species 2 gradually increase as the recovery time passes with decreasing luminescence intensity of species 3.
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Figure 14. Comparison of the luminescence spectrum of the desorbed U(VI) species in the filtrate with the background luminescence spectrum of the species existing in the filtrate obtained from the same high SSA sample (sample No. 2, [U(VI)] = 3.4 μM, m/v = 1.0 g/L, and pH 7.5) before laser irradiation. The lower panel shows the luminescence intensity on the natural logarithmic scale corresponding to gate delay times of 1–151 μs. The slope of the solid line was used to determine the luminescence lifetime of 52 ± 17 μs.
Figure 14. Comparison of the luminescence spectrum of the desorbed U(VI) species in the filtrate with the background luminescence spectrum of the species existing in the filtrate obtained from the same high SSA sample (sample No. 2, [U(VI)] = 3.4 μM, m/v = 1.0 g/L, and pH 7.5) before laser irradiation. The lower panel shows the luminescence intensity on the natural logarithmic scale corresponding to gate delay times of 1–151 μs. The slope of the solid line was used to determine the luminescence lifetime of 52 ± 17 μs.
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Table 1. SiO2 samples used in this study. Symbols * and ** indicate the value in the specification sheet provided by the manufacturer and the value measured in this study, respectively.
Table 1. SiO2 samples used in this study. Symbols * and ** indicate the value in the specification sheet provided by the manufacturer and the value measured in this study, respectively.
SiO2BrandParticle Size SSA (m2/g)Description
Sample No. 1Evonik Aerosil 200* 5–50 nm* 200** 156Fumed SiO2
Sample No. 2Sigma–Aldrich 227196* 40–63 μm* 550** 477SiO2 gel
Sample No. 3Alfa Aesar L16987* 1.5 μm ** 2Spherical SiO2
Table 2. Luminescence lifetimes and relative quantities of species 1 and 2 measured from the high SSA SiO2 (sample No. 1, pH 7.5). These values were determined using the data shown in Figure 2 and Figure 3. R2 and RSS values are listed in the last column.
Table 2. Luminescence lifetimes and relative quantities of species 1 and 2 measured from the high SSA SiO2 (sample No. 1, pH 7.5). These values were determined using the data shown in Figure 2 and Figure 3. R2 and RSS values are listed in the last column.
SamplesΓ (μmol U/m2)Species 1Species 2R2 (RSS)
[U(VI)] (μM)m/v (g/L) a τ1 (μs) 1 a τ2 (μs)
0.341.00.0020.4123110.5886580.99995
(0.00648)
3.41.00.0210.4063050.5946710.99998
(0.00292)
0.340.10.0210.4672980.5336710.99995
(0.00614)
3.40.10.2170.6372750.3636100.99993
(0.01177)
0.340.010.2170.6642770.3366290.99986
(0.02347)
3.40.011.5260.8931680.1074150.99891
(0.44745)
Table 3. Luminescence lifetimes of U(VI) in SiO2, shown in Figure 10, Figure 11 and Figure S12, determined using PARAFAC analysis.
Table 3. Luminescence lifetimes of U(VI) in SiO2, shown in Figure 10, Figure 11 and Figure S12, determined using PARAFAC analysis.
Laser Pulse Energy (Excitation Wavelength)Species 2 (μs) Species 3 (μs)
2.4 mJ (355 nm)649 ± 28-
2.4 mJ (422 nm)
0.1 mJ (266 nm)
0.6 mJ (266 nm)621313
1.2 mJ (266 nm)610292
2.4 mJ (266 nm)575287
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Jung, E.C.; Jo, Y.; Kim, T.-H.; Kim, H.-K.; Cho, H.-R.; Cha, W.; Baik, M.H.; Yun, J.-I. Surface Coverage- and Excitation Laser Wavelength-Dependent Luminescence Properties of U(VI) Species Adsorbed on Amorphous SiO2. Minerals 2022, 12, 230. https://doi.org/10.3390/min12020230

AMA Style

Jung EC, Jo Y, Kim T-H, Kim H-K, Cho H-R, Cha W, Baik MH, Yun J-I. Surface Coverage- and Excitation Laser Wavelength-Dependent Luminescence Properties of U(VI) Species Adsorbed on Amorphous SiO2. Minerals. 2022; 12(2):230. https://doi.org/10.3390/min12020230

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Jung, Euo Chang, Yongheum Jo, Tae-Hyeong Kim, Hee-Kyung Kim, Hye-Ryun Cho, Wansik Cha, Min Hoon Baik, and Jong-Il Yun. 2022. "Surface Coverage- and Excitation Laser Wavelength-Dependent Luminescence Properties of U(VI) Species Adsorbed on Amorphous SiO2" Minerals 12, no. 2: 230. https://doi.org/10.3390/min12020230

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