纳米团簇
等离子体子
纳米材料
共价键
纳米技术
纳米颗粒
再分配(选举)
材料科学
化学物理
等离子纳米粒子
寡肽
纳米结构
碱度
过渡金属
催化作用
化学
光电子学
物理化学
肽
有机化学
政治
法学
生物化学
政治学
作者
Zhiren Zheng,Yanyan Hu,Ying Lv,Lu Liu,Daoqing Fan,Lichao Zhang,Ling Chen,Haizhu Yu,Manzhou Zhu
出处
期刊:ChemNanoMat
[Wiley]
日期:2022-01-04
卷期号:8 (2)
被引量:1
标识
DOI:10.1002/cnma.202100449
摘要
Abstract The stimuli response of nanomaterials represents a highly appealing characteristic, whereas the practical applications (in catalysis, biosensing etc.) are largely restricted by the limited understanding on the recognition mechanism. Herein, we report a pH‐regulated size evolution from atomically precise Au nanoclusters (NCs) to plasmonic nanoparticles (NPs). The spectral monitoring demonstrates a three‐stage aggregative growth pathway. First, the non‐covalent interactions among the exterior oligopeptide ligands are gradually enhanced with the increased alkalinity, and then the Au−S bonding is partially disrupted, with the exposed Au atoms aggregating to form relatively larger, polydisperse clusters under weak alkaline conditions. Finally, size‐redistribution occurs slowly under strong alkaline conditions to form the plasmonic particles. The controllable transition sheds light on the transition characteristics from molecular state to metallic state of Au nanomaterials.
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