4.8 Article

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

期刊

ACS CATALYSIS
卷 7, 期 7, 页码 4360-4365

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.7b01318

关键词

nanoparticle; LSPR; plasmon resonance; photocatalysis; artificial photosynthesis; Marcus theory; self-assembled monolayer; plasmonic catalysis

资金

  1. National Science Foundation [NSF CHE-1455011]
  2. Springborn postdoctoral fellowship
  3. Division Of Chemistry
  4. Direct For Mathematical & Physical Scien [1455011] Funding Source: National Science Foundation

向作者/读者索取更多资源

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.

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