Yang Jing-Liang, Wang Hong-Jia, Zhu Zhenwei, Yue Mu-Fei, Yang Wei-Min, Zhang Xia-Guang, Ruan Xiangyu, Guan Zhiqiang, Yang Zhi-Lin, Cai Weiwei, Wu Yuan-Fei, Fan Feng-Ru, Dong Jin-Chao, Zhang Hua, Xu Hongxing, Tian Zhong-Qun, Li Jian-Feng
College of Physical Science and Technology, College of Energy, State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, College of Materials, Fujian Key Laboratory of Advanced Materials, Xiamen University, Xiamen, 361005, China.
Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, 453007, China.
Angew Chem Int Ed Engl. 2022 Jan 26;61(5):e202112749. doi: 10.1002/anie.202112749. Epub 2021 Dec 15.
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.
光激发下的等离子体金属可产生高能热电子以直接引发化学反应。然而,这些热电子在等离子体金属与二维材料界面处的传输能力及基本原理仍不清楚。在此,利用具有原子层精度的表面增强拉曼光谱(SERS)对金 - 石墨烯界面处的热电子转移进行了原位研究。将原位SERS研究与密度泛函理论计算相结合,证明热电子可从等离子体金纳米颗粒注入到石墨烯中,并直接穿透石墨烯以触发光催化反应。随着石墨烯层数的增加,热电子的传输迅速衰减,在五层石墨烯之后将完全受阻。此外,通过施加外部电场可调制热电子的转移,在单层石墨烯存在的情况下,电化学条件下的热电子转移效率提高了三倍以上。