光致发光
纳米颗粒
荧光
发光
吸收(声学)
表面电荷
胶体金
圆二色性
材料科学
光化学
配体(生物化学)
光谱学
化学
分析化学(期刊)
纳米技术
结晶学
物理化学
光电子学
光学
有机化学
物理
量子力学
生物化学
复合材料
受体
作者
Jinbin Liu,Paul N. Duchesne,Mengxiao Yu,Xingya Jiang,Xuhui Ning,Rodrigo D. Vinluan,Peng Zhang,Jie Zheng
标识
DOI:10.1002/anie.201602795
摘要
Abstract Size‐independent emission has been widely observed for ultrasmall thiolated gold nanoparticles (AuNPs) but our understanding of the photoluminescence mechanisms of noble metals on the nanoscale has remained limited. Herein, we report how the emission wavelength of a AuNP and the local binding geometry of a thiolate ligand (glutathione) on the AuNP are correlated, as these AuNPs emit at different wavelengths in spite of their identical size (ca. 2.5 nm). By using circular dichroism, X‐ray absorption, and fluorescence spectroscopy, we found that a high Au−S coordination number (CN) and a high surface coverage resulted in strong Au I –ligand charge transfer, a chiral conformation, and 600 nm emission, whereas a low Au−S CN and a low surface coverage led to weak charge transfer, an achiral conformation, and 810 nm emission. These two size‐independent emissions can be integrated into one single 2.5 nm AuNP by fine‐tuning of the surface coverage; a ratiometric pH response was then observed owing to strong energy transfer between two emission centers, opening up new possibilities for the design of ultrasmall ratiometric pH nanoindicators.
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