4.6 Article

Plasmonic Hot Hole-Driven Water Splitting on Au Nanoprisms/P-Type GaN

期刊

ACS ENERGY LETTERS
卷 6, 期 4, 页码 1333-1339

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.1c00366

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资金

  1. Institute for Basic Science [IBS-R004]
  2. National Research Foundation of Korea (KRF) - Korea government (MSIT) [2021R1C1C1004794]
  3. Ministry of Science & ICT (MSIT), Republic of Korea [IBS-R004-D1-2021-A00] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  4. National Research Foundation of Korea [2021R1C1C1004794] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Research indicates that the size of metallic nanostructures is crucial for the injection of plasmonic hot holes, with smaller Au nanoprisms showing higher quantum efficiencies and significant enhancement of photoelectrocatalytic reactions.
While hot carrier generation from surface plasmon decay at the surface of a nanostructured metal offers a distinctive concept for boosting photoelectrocatalytic reactions, the nature of the plasmonic hot hole transfer based on the sizes of metallic nanomaterials has not been investigated in depth experimentally. Here, we report direct photoelectrochemical (PEC) experimental proof that the injection of plasmonic hot holes depends on the size of the metallic nanostructures. PEC results clearly indicate that a plasmonic template with smaller Au nanoprisms exhibits higher external and internal quantum efficiencies, leading to a significant enhancement of both oxygen evolution and hydrogen evolution reactions. We verified that these outcomes stemmed from the enhanced hot hole generation with higher energy and transfer efficiency driven by enhanced field confinement. These findings provide a facile strategy by which futuristic photocatalysis and solar energy conversion applications based on plasmonic hot holes can be expedited.

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