The Nature of Plasmonically Assisted Hot -Electron Transfer in a Donor-Bridge-Acceptor Complex

被引:54
|
作者
Kim, Youngsoo [1 ]
Wilson, Andrew J. [1 ]
Jain, Prashant K. [1 ,2 ]
机构
[1] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
[2] Univ Illinois, Mat Res Lab, Urbana, IL 61801 USA
来源
ACS CATALYSIS | 2017年 / 7卷 / 07期
基金
美国国家科学基金会;
关键词
nanoparticle; LSPR; plasmon resonance; photocatalysis; artificial photosynthesis; Marcus theory; self-assembled monolayer; plasmonic catalysis; SELF-ASSEMBLED MONOLAYERS; CROSS-COUPLING REACTIONS; CHARGE-TRANSFER; DISTANCE DEPENDENCE; GOLD NANOPARTICLES; INDUCED DISSOCIATION; TRANSFER RATES; CYTOCHROME-C; MECHANISM; ENERGY;
D O I
10.1021/acscatal.7b01318
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This work provides a mechanistic understanding of hot-electron-based catalysis on Au nanoparticles (NPs) induced under plasmonic excitation. Plasmon excitation-induced hot-electron transfer from an Au NP (donor) to a ferricyanide anion (acceptor) was studied as a function of the donor acceptor distance set by a thiolate-based self-assembled monolayer (SAM). Hot-electron-transfer rates and activation barrier heights were measured as a function of the donor acceptor distance, up to 20 A. Hot-electron transfer was found to be longer range than anticipated. The distance-dependent kinetics reveal that the hot-electron transfer takes place via multistep hopping in a "wire-like" manner across the insulating ligands, quite unlike the tunneling-dominated electron transfer known to take place across SAMs in the absence of plasmonic excitation. Field-assisted electron hopping may play a crucial role in hot-electron extraction and catalysis involving plasmon-excited NPs.
引用
收藏
页码:4360 / 4365
页数:6
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