等离子体子
光催化
光化学
催化作用
热电子
等离子纳米粒子
材料科学
化学物理
电子
纳米颗粒
分子
表面等离子体子
纳米技术
化学
光电子学
物理
有机化学
量子力学
作者
Ying Wang,Yonglong Li,Xian Yang,Teng Wang,Xiaomeng Du,Aonan Zhu,Weiwei Xie,Wei Xie
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-01-15
卷期号:63 (10): e202318817-e202318817
被引量:8
标识
DOI:10.1002/anie.202318817
摘要
Abstract Plasmonic catalysis has emerged as a promising approach to solar‐chemical energy conversion. Notably, hot carriers play a decisive role in plasmonic catalysis since only when their energy matches with the LUMO or HOMO energy of the reactant molecule, can the reaction be activated. However, the hot carrier energy depends on the intrinsic physicochemical properties of the plasmonic metal substrate and the interaction with incident light. Tuning the hot carrier energy is of great significance for plasmonic catalysis but remains challenging. Here, we demonstrate that the energy of hot electrons can be significantly elevated to an unprecedented level through the coordination of amines on Ag surface. The bonding of amines and Ag reduces the work function of nanoparticles, leading to the increase of hot electron energy by 0.4 eV. This enhancement of energy promotes the cleavage of C−X (X=Cl, F) bonds upon excitation by visible light. This study provides new insights for promoting plasmonic charge transfer and enhancing the photocatalytic performance of plasmon‐mediated systems.
科研通智能强力驱动
Strongly Powered by AbleSci AI