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Highly luminescent near-infrared (NIR)-emitting gold nanoclusters (Au NCs) protected by glutathione with ultra-small size were prepared at high temperature following with a further natural etching at room temperature. The optical and surface properties of Au NCs were monitored by ultraviolet–visible and photoluminescence (PL) spectra, high-resolution transmission electron microscopy, and electrospray ionization mass spectrometry. The diameter of the etched Au NCs was reduced to approximately 1.35nm with 30% PL quantum yield. Interestingly, the PL of Au NCs was decreased obviously by the addition of Hg2+ and increased by the addition of Pb2+ at certain concentration. Our preliminary results illustrated that the highly luminescent NIR-emitting Au NCs would be an alternative probe for the detection of heavy metal ions in water and environmental monitoring.
Gold nanoclusters (Au NCs) have received extensive attention because of their interesting optical properties [1-3], fluorescence [4,5], magnetism , and redox properties , as well as their potential applications in many fields such as optics [8-10] and catalysis [11,12]. To synthesize these highly fluorescent Au NCs, several methods have been developed. A method of synthesizing Au NCs is based on the reducing Au3+ ions in the presence of thiol ligands. For example, Dyer et al. exemplified the application of this approach by synthesizing Au NCs encapsulated by polyamidoamine dendrimers . Ying and coworkers developed a new method of Au NC synthesis using protein bovine serum albumin (BSA) as sole reduction agent at high pH . The other method of synthesizing Au NCs is based on the etching process using polymers. For example, Duan and Nie report a ligand-induced etching process for preparing highly fluorescent and water-soluble Au NCs . Jin et al. found that gold nanoparticles could be etched to produce ultrasmall clusters under reflux at high temperature . Inspired by this discovery, we wonder whether the etching method can be applied to using thiol ligands other than polymers.
Glutathione (GSH), the most abundant low-molecular weight thiol with naturally defined chemical components and structures, has been extensively used as ligands to induce the nucleation and growth of nanocrystals based on biomineralization or as templates to synthesize nanocrystals with well-defined morphologies . Au NCs, protected with GSH, have been well studied [17,18]. Recently, Shichibu et al. discovered that some GSH-protected clusters could be etched by GSH, which generated GSH-protected Au25 as the main product [3,19]. However, the quantum yield of these reported gold nanoclusters is relatively low. Hence, a method of creating Au NCs with monodispersed, ultra-small size, high quantum yield and near-infrared (NIR) emission would be extremely valuable for extending their fundamental properties and investigation of a wider range of applications.
In this work, we reported a novel synthetic method, based on the capability of a common commercially available thiol ligands, GSH, for the preparation of ultra-small size highly luminescent Au NCs at high temperature following with a further natural etching at RT with NIR emission (λem max=650nm, quantum yield (QY)≈30%). Our process is similar to the biomineralization behavior of organisms in nature: sequestering and interacting with organisms, followed by providing scaffolds for the minerals formed. The optical and structural properties of the etched Au NCs were performed by ultraviolet–visible (UV–vis) and photoluminescence (PL) spectroscopies, high-resolution transmission electron microscopy (HRTEM), and electrospray ionization mass spectrometry. The PL of the etched Au NCs was decreased obviously by the addition of Hg2+ and increased by the addition Pb2+ at certain concentration. Such etched Au NCs have great potential application in heavy metal ion detection in water and environmental monitoring.
Chloroauric acid trihydrate (HAuCl4·3H2O, 99.99%) was purchased from Alfa Aesar (Ward Hill, MA, USA). Sodium tetrahydroborate (NaBH4, 99%) and GSH in the reduced (GSH, 98%) form were obtained from ACROS ORGANICS (NJ, USA). All other chemicals used in this study were of analytical reagent grade and used without further purification. A JL RO100 Millipore-Q Plus water purifier (Millipore Co., Billerica, MA, USA) supplied deionized water with a resisitivity of 18.25 MΩ·cm.
Au NCs were synthesized using the reported protocol, with a few modifications . To a 50mL methanol solution (0.5mM) of HAuCl4·3H2O, 1.0 mM GSH (1:2 molar ratio, the total volume of methanol was 50mL) was added. The mixture was cooled to 0°C in an ice bath for 30min. An aqueous solution of NaBH4 (0.2M, 12.5mL), cooled to 0°C, was injected rapidly into the above mixture under vigorous stirring. The mixture was allowed to react for another hour. The resulting precipitate was collected and washed repeatedly with methanol through centrifugal precipitation. Finally, the Au NCs precipitate was dried and collected as a dark brown powder.
The above clusters (1mg) were dissolved in 1mL of deionized water that contained 0.0125mol of GSH. The mixture reacted at 65°C±5°C for 24h at 500rpm in the reaction container then the supernatant was put in the dark at room temperature for 5 to 8days. The products were precipitated by added methanol (volume ratio 1:1), then the precipitate was collected and washed repeatedly with methanol through centrifugation. Finally, the products were dried by a vacuum drier and can be dissolved in water easily.
Au NCs dissolved in deionized water were used directly. HRTEM specimens were prepared by drop costing one or two drops of the solutions onto an ultra-thin carbon-coated film supported on a copper grid. Bright field HRTEM images were acquired with an electron microscope operated at 200kV (JEM-2100HR, JEOL, Japan). Typical magnifications of the images were×200,000 and×400,000. Moreover, energy-dispersive X-ray spectroscopy (EDS) was taken three points a sample at the same time using the affix of JEM-2100HR IET250.
UV–vis absorption of the Au NCs was recorded in aqueous solution at ambient temperature using a PerkinElmer Lambda 25 spectrophotometer (PerkinElmer, Waltham, MA, USA). The PL spectra were obtained by a spectrofluorometer (F900, Edinburgh Instruments Ltd., West Livingston, UK). The sample solutions were not deaerated prior to the measurement. The cluster concentrations for the PL measurement were typically <10μM, where the intensities increase linearly with the cluster concentrations. The PL quantum yield was determined according to .
Mass spectrometric studies were conducted using an electro spray (electrospray ionization mass spectrometry (ESI-MS)) system (LC-6A, Japan). Samples with a concentration lower than 10ppm, taken in deionized water, were electrosprayed at a low rate of 10 μL/min and an ion spray voltage of 5kV.
A series concentration of aqueous Hg2+ was added to cluster solutions one by one and equilibrated at room temperature for 10min prior to measurement of the PL with an excitation wavelength at 470nm. All other ions (Pb2+, Cu2+, Ca2+, Mg2+, K+, and Na+) tested in interference studies using the same method.
As Hg2+ and Pb2+ are highly toxic and have adverse effects on human health, all experiments involving heavy metal ions should be performed with protective eyeglasses, chemical safety gloves, and protective clothing to prevent skin exposure. The waste solutions containing heavy metal ions should be collectively reclaimed to avoid polluting the environment.
The well-defined GSH-protected Au NCs were further etched by GSH in different mass ratio of Au NCs and GSH in aqueous solution at various temperatures. The as-prepared and etched Au NCs were detected by UV–vis absorbance and PL spectroscopies. As shown in Figure Figure1a,1a, the absorption spectrum of Au NCs exhibited a strong and broad absorption band at approximately 500nm, which indicated that the particle size of Au NCs was smaller than 2.5nm . As shown in Figure Figure1b,1b, the absorption spectrum of the etched Au NCs has no absorption band after natural etching at RT. The spectral behavior of the Au NCs is in sharp contrast to that of the etched Au NCs. The reaction of etching leads to a remarkable depression of the UV–vis absorption, which suggests that a transformation of the original clusters into extremely small clusters has occurred . Au NCs show no emission (Figure (Figure1d),1d), and the strong emission peak of the etched Au NCs was observed at approximately 650nm after natural etching at RT (Figure (Figure1c).1c). The etched Au NC solution was clear under visible light and an intense red PL under UV light (365nm). The maximum PLQY of the as-prepared etched Au NCs was 30%, which was higher than PL BSA-Au NCs reported by Ying's group . The PL intensity can be stable for more than half a year at room temperature when the clusters were freeze dried.
The optical properties of the etched Au NCs were monitored by UV–vis and PL spectra at different time scales at room temperature. As shown in Figure Figure2A,2A, the absorption spectrum of the etched Au NCs exhibited a strong and broad absorption band at approximately 670nm after natural etching at RT for 1day, and the absorption spectrum of the etched Au NCs has no absorption band after natural etching at RT for 2 to 10days. There is no feature at the spectrum of the etched Au NCs with relatively lower absorbance compared to the un-eched Au NCs. The result suggests that the Au NC has transformed into smaller etched Au NCs [17,22]. As shown in Figure Figure2B,2B, the maximum emission peak of the etched Au NCs was observed at approximately 720nm after natural etching at RT for 1day, and the maximum emission peak of the etched Au NCs was blueshifted to approximately 650nm with an obvious change of PL spectrum profiles after natural etching at RT for 2 to 10days.
HRTEM images of the as-prepared and etched Au NCs for 5days, as shown in Figure Figure3,3, indicate that the particles are well-dispersed. The diameter of the dispersed as-prepared Au NCs is approximately 2 to 4nm, with a mean diameter of 3.24nm, and the diameter of the etched Au NCs is approximately 1.0 to 2.5nm, with a mean diameter of 1.89nm.
EDS analysis was employed to determine the chemical identities of the etched Au NCs (Table 1). EDS measurements were conducted to confirm the presence of the GSH at the surface of the etched Au NCs. The element analysis of the etched Au NCs with EDS indicates the presence of Au from the etched Au NCs and also C, N, O, and S from the GSH molecules. The high sulfur percentage confirms an existence of a significant amount of GSH molecule at the surface of the etched Au NCs; the ratio of S/Au was determined to be approximately 1.4.
Figure Figure44 shows the negative-ion ESI-MS spectra of the etched Au NCs in detail. The mass range available is not enough to see the singly charged cluster. Besides, orthogonal ESI-MS does not give intact cluster species. Hence, we could not see the intact Au core. However, we see the presence of -SG, and small fragments of the Au NCs. The peaks at m/z 1094.31, 1223.48, 1465.94, 1708.35, and 1835.45 are assigned to [Au8SG3-H+]−, [Au14SG3-3H+]3−, [Au19SG7-4H+]4−, [Au12SG9-3H+]3−, and [Au14SG9-3H+]3−, respectively. The result shows that Au14 is the major core. Although the data shows a few impurities, it did not influence the application.
The effect of Hg2+ on the PL spectra was investigated. As shown in Figure Figure5,5, with the increasing concentration of Hg2+, the PL intensity of the etched Au NCs (etching for 2days) was decreased obviously. Meanwhile, the spectral wavelength maximum was blueshifted 5 to 10nm, which indicates the change of surface states of the clusters since Hg2+ ions bind onto the particle surface . These values implied that the etched Au NCs have high sensitivity and reproducibility for Hg2+ assay. It may be used to detect trace toxicity metal ions in water due to the high PLQY.
PL quenching of the etched Au NCs was studied with the addition of the same concentration of different ion solvents (Pb2+, Ca2+, Cu2+, Mg2+, K+, and Na+) (0.2mM). As shown in Figure Figure6,6, Pb2+ led to decreases in the value, whereas the other ions exhibited no significant effects under identical conditions. These features contributed to the excellent selectivity toward Hg2+ and Pb2+, rendering the etched Au NCs suitable for the heavy metal ions detection in water and environmental monitoring.
A PL quenching was observed in the presence of Hg2+, which could be explained in terms of electron transfer between the excited etched Au NCs to the Hg2+. The mechanism can be explained using a photoinduced electron transfer process. First, the etched Au NCs and Hg2+ ion form a complex. Second, the electrons within the etched Au NCs are firstly excited to the excited state under photo-irradiation. Third, Hg2+ can directly intercept one of the charge carriers and is reduced to Hg+, which can disrupt the radiative recombination of the holes and the excited electrons and quench the PL of the etched Au NCs. This assumption is supported by the following facts: In this test, GSH was used in competition with Au NCs for Hg2+. The PL of Au NCs was not quenched after the addition of the intermixture (1mM Hg2+, 0.1 mM GSH). In a control experiment, GSH showed no influence on the PL of Au NCs in the absence of Hg2+, which confirmed that the complex formation occurred between GSH and Hg2+. Based on the finding, we concluded that the complex of Au NCs and Hg2+ and a photoinduced electron transfer process were the primary mechanism for PL quenching.
The reason of enhanced fluorescence in the presence of Pb2+ was very complicated. The spatial confinement of free electrons in the etched Au NCs results in discrete and size-tunable electronic transitions, leading to molecular-like properties. Therefore, the luminescent mechanism for the etched Au NCs would involve relaxed luminescence across the HOMO-LUMO gap . When the Pb2+ was added into the etched Au NCs, HOMO-LUMO gap would be decreased . Therefore, the enhanced luminescence of the etched Au NCs was observed. Due to the complicated reaction process, the precise luminescence enhancement mechanism remains unclear, and the detail reaction mechanism was under the way.
We report herein a further etching and characterization of well-defined Au NCs protected by GSH ligands. The spectroscopic measurement of these clusters revealed that a new method of etching Au NCs was developed, and high PLQY clusters were obtained. After etching, the diameter of the Au NCs decreased to approximately 1.35nm with 30% PLQY. These features contributed to the excellent selectivity toward Hg2+ and Pb2+, rendering the GSH-Au NCs highly suitable for the analysis of environmental samples containing other metal ions.
The authors declare that they have no competing interests.
ShL and PZ carried out the preparation of Au NCs and drafted the manuscript. DH carried out the assay of ion experiments and modified the manuscript. CZ carried out the HRTEM experiments. SoL took part in the ESI-MS and HRTEM experiments. LC conceived of all the study and participated in its design and coordination. All authors read and approved the final manuscript.
The study was conducted by the research team of the Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences. Prof. LC is the head of the team, and the team carries out the world's leading research on a range of problems of biomedical nanotechnology (nanotechnology, functional materials, surface analytical chemistry, optoelectronics, polymer science, and electrochemistry). Our aim is dedicated to studying multifunctional and nanostructured composite materials, providing highly sensitive and selective detection methods through molecular probes for medical imaging and molecular diagnosis in nanoscale and single molecular level, and exploring new device concepts and self-assembly techniques for the development of biomedical nanodevices and sensors for biosensing, environmental monitoring, information processing, energy utility, and other applications.
The authors gratefully acknowledge the support for this research from the National Basic Research Program of China (973 program #2011CB933600), the ‘Hundred Talents Program’ of Chinese Academy of Sciences, the National Natural Science Foundation of China (grant numbers 81071249, 20875062, and 20905050), Science and Technology Key Project of Guangdong (2009A030301010), and Guangdong Innovation Team of Low-cost Healthcare.