石墨烯
拉曼光谱
等离子体子
材料科学
电子
电子转移
光激发
化学物理
纳米技术
石墨烯纳米带
光电子学
化学
原子物理学
光化学
激发态
光学
物理
量子力学
作者
Jingliang Yang,Hong‐Jia Wang,Zhenwei Zhu,Mufei Yue,Weimin Yang,Xia‐Guang Zhang,Xiangyu Ruan,Zhiqiang Guan,Zhilin Yang,Weiwei Cai,Yuanfei Wu,Feng Ru Fan,Jin‐Chao Dong,Hua Zhang,Hongxing Xu,Zhong‐Qun Tian,Jianfeng Li
标识
DOI:10.1002/anie.202112749
摘要
Plasmonic metals under photoexcitation can generate energetic hot electrons to directly induce chemical reactions. However, the capability and fundamental insights of the transportation of these hot electrons at plasmonic metal-2D material interfaces remain unclear. Herein, hot-electron transfer at Au-graphene interfaces has been in situ studied using surface-enhanced Raman spectroscopy (SERS) with atomic layer accuracy. Combining in situ SERS studies with density functional theory calculations, it is proved that hot electrons can be injected from plasmonic Au nanoparticles to graphene and directly penetrate graphene to trigger photocatalytic reactions. With increasing graphene layers, the transportation of hot electrons decays rapidly and would be completely blocked after five layers of graphene. Moreover, the transfer of hot electrons can be modulated by applying an external electric field, and the hot-electron transfer efficiency under electrochemical conditions is improved by over three times in the presence of a monolayer of graphene.
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