等离子体子
热电子
激发
异质结
光化学
氧化剂
氧化物
光催化
材料科学
金属
化学物理
表面等离子体子
分子
光电子学
电子
化学
催化作用
物理
生物化学
有机化学
量子力学
冶金
作者
Jiawei Huang,Wenxiao Guo,Shuai He,Justin R. Mulcahy,Alvaro Montoya,Justin L. Goodsell,Namodhi Wijerathne,Alexander Angerhofer,Wei David Wei
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-04-13
卷期号:17 (8): 7813-7820
被引量:6
标识
DOI:10.1021/acsnano.3c00758
摘要
Plasmon-generated hot electrons in metal/oxide heterostructures have been used extensively for driving photochemistry. However, little is known about the origin of plasmon-generated hot holes in promoting photochemical reactions. Herein, we discover that, during the nonradiative plasmon decay, the interband excitation rather than the intraband excitation generates energetic hot holes that enable to drive the water oxidation at the Au/TiO2 interface. Distinct from lukewarm holes via the intraband excitation that only remain on Au, hot holes from the interband excitation are found to be transferred from Au into TiO2 and stabilized by surface oxygen atoms on TiO2, making them available to oxidize adsorbed water molecules. Taken together, our studies provide spectroscopic evidence to clarify the photophysical process for exciting plasmon-generated hot holes, unravel their atomic-level accumulation sites to maintain the strong oxidizing power in metal/oxide heterostructures, and affirm their crucial functions in governing photocatalytic oxidation reactions.
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