Journal
JOURNAL OF PHYSICAL CHEMISTRY C
Volume 123, Issue 10, Pages 6010-6017Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.8b11716
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Funding
- National Natural Science Foundation of China [21403147]
- Natural Science Research Programme of Higher Education of Jiangsu Province [18KJB150026]
- Soochow University-Western University Center for Synchrotron Radiation Research
- Collaborative Innovation Center of Suzhou Nano Science and Technology (NANO-CIC), Soochow University
- NSERC
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Luminescent Au(I)-thiolate complexes (Au-(I)-SR) are synthesized at room temperature using glutathione as both a reducing agent and capping ligand. The photoluminescence (PL) intensity and emission wave-length are found to be strongly affected by the pH environment during and post synthesis. Although there is no Au(0) core present in these complexes, Au(I)-SR exhibit PL which can be further enhanced through an aggregation-induced emission mechanism. The structures of these Au(I)-SR at each pH stage are carefully characterized. Using X-ray absorption fine structure, we further establish a relationship between the PL intensity and degree of aurophilic interactions. We find that the luminescence of Au(I)-SR is tunable over a wide pH range with good reversibility.
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