等离子体子
化学
纳米结构
表面增强拉曼光谱
拉曼光谱
氧气
表面等离子体子
激发态
电子
光化学
纳米颗粒
化学物理
氧化物
载流子
胶体金
热电子
硅
纳米技术
光电子学
原子物理学
拉曼散射
材料科学
光学
物理
有机化学
量子力学
作者
Chao Zhan,Ziyuan Wang,Xia‐Guang Zhang,Xue‐Jiao Chen,Yifan Huang,Shu Hu,Jianfeng Li,De‐Yin Wu,Martin Moskovits,Zhong‐Qun Tian
摘要
Surface plasmons (SPs) are able to promote chemical reactions through the participation of the energetic charge carriers produced following plasmons decay. Using p-aminothiophenol (PATP) as a probe molecule, we used surface-enhanced Raman spectroscopy to follow the progress of its transformation, in situ, to investigate systematically the role of hot electrons and holes. The energetic carrier mediated PATP oxidation was found to occur even in the absence of oxygen, and was greatly influenced by the interface region near the gold surface. The observed reaction, which occurred efficiently on Au@TiO2 nanostructures, did not happen on bare gold nanoparticles (NPs) or core-shell nanostructures when a silicon oxide layer blocked access to the gold. Moreover, the product of the PATP oxidation with oxygen on Au@TiO2 nanostructures differed from what was obtained without oxygen, suggesting that the mechanism through which "hot holes" mediated the oxidation reaction was different from that operating with oxygen activated by hot electrons.
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