4.8 Article

Enhanced Electrochemistry of Single Plasmonic Nanoparticles

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 61, Issue 8, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202115819

Keywords

Cobalt metal-organic framework nanosheets (Co-MOFNs); Hot carriers; Hydrogen evolution reaction; Nanoparticle impact electrochemistry; Plasmonic silver; gold nanoparticles

Funding

  1. National Natural Science Foundation of China [21804036, 21972039]
  2. Science and Technology Project of Hunan Province [2020SK2014, 2020RC3021, 2020JJ3005]

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The structure-function relationship of plasmon-enhanced electrochemistry (PEEC) is investigated at the single nanoparticle level using nanoparticle impact electrochemistry. It is found that plasmon-excited hot carrier injection can lower the reaction activation energy and promote the reaction probability and integral charge generated from individual collisions. Additionally, a plasmonic nanoparticle filtering method is established to effectively distinguish different types of plasmonic nanoparticles.
The structure-function relationship of plasmon-enhanced electrochemistry (PEEC) is of great importance for the design of efficient PEEC catalysts, but is rarely investigated at single nanoparticle level for the lack of an efficient nanoscale methodology. Herein, we report the utilization of nanoparticle impact electrochemistry to allow single nanoparticle PEEC, where the effect of incident light on the plasmonic Ag/Au nanoparticles for accelerating cobalt metal-organic framework nanosheets (Co-MOFNs) catalyzed hydrogen evolution reaction (HER) is systematically explored. It is found that the plasmon-excited hot carrier injection can lower the reaction activation energy, resulting in a much promoted reaction probability and the integral charge generated from individual collisions. Besides, a plasmonic nanoparticle filtering method is established to effectively distinguish different plasmonic nanoparticles. This work provides a unique view in understanding the intrinsic physicochemical properties for PEEC at the nano-confined domains.

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