光催化
等离子体子
化学
纳米颗粒
二氧化钛
胶体金
表面等离子体子
可见光谱
还原(数学)
电子转移
异质结
纳米技术
光化学
表面等离子共振
光电子学
化学工程
催化作用
材料科学
工程类
生物化学
数学
几何学
作者
Kun Qian,Brendan C. Sweeny,Aaron C. Johnston‐Peck,Wenxin Niu,Jeremy O. Graham,Joseph S. DuChene,Jingjing Qiu,Yi‐Chung Wang,Mark Engelhard,Dong Su,Eric A. Stach,Wei David Wei
摘要
Water reduction under two different visible-light ranges (λ > 400 nm and λ > 435 nm) was investigated in gold-loaded titanium dioxide (Au-TiO2) heterostructures with different sizes of Au nanoparticles (NPs). Our study clearly demonstrates the essential role played by Au NP size in plasmon-driven H2O reduction and reveals two distinct mechanisms to clarify visible-light photocatalytic activity under different excitation conditions. The size of the Au NP governs the efficiency of plasmon-mediated electron transfer and plays a critical role in determining the reduction potentials of the electrons transferred to the TiO2 conduction band. Our discovery provides a facile method of manipulating photocatalytic activity simply by varying the Au NP size and is expected to greatly facilitate the design of suitable plasmonic photocatalysts for solar-to-fuel energy conversion.
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