4.7 Review

A review on plasmonic nanoparticle-semiconductor photocatalysts for water splitting

Journal

JOURNAL OF CLEANER PRODUCTION
Volume 294, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jclepro.2021.126200

Keywords

Plasmonic photocatalyst; Water splitting; Surface plasmon resonance; Light trapping mechanism; Hot electron injection; Plasmon induced resonance energy transfer

Funding

  1. Egyptian cultural affairs and Missions' sector, Ministry of Higher Education, Egypt
  2. JSPS [18H03841, 18K04701]
  3. Grants-in-Aid for Scientific Research [18K04701, 18H03841] Funding Source: KAKEN

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This review examines the use of plasmonic metal nanoparticles decorated on semiconductors to enhance photocatalytic activity, focusing on the main features, energy transfer mechanisms, and recent advancements in plasmonic photocatalysts widely studied for water splitting applications.
Transforming solar energy into chemicals through the photoelectrochemical or photocatalytic water splitting process is considered a powerful technique for implementing an effective, clean, and affordable energy source. The main issues are charge carriers recombination, the large bandgap of the photocatalysts, and the occurrence of the back (water-forming) reaction. The decoration of plasmonic metal nanoparticles onto semiconductors has recently been reported as an auspicious technique to overcome these limitations and promote photocatalytic activity through the transfer of plasmonic energy from the plasmonic metal nanoparticles to the semiconductor. This review focuses on three main objectives: surveying the main features of the plasmonic metal nanostructure that influence its photocatalytic activity; providing a brief explanation of the four main mechanisms of the plasmonic energy transfer, and summarizing some noteworthy recent plasmonic photocatalysts which widely investigated for photo catalytic or photoelectrochemical water splitting with emphasis on their influence on the behavior of charge carriers. (c) 2021 Elsevier Ltd. All rights reserved.

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