4.7 Article

Photo-inactive ZIF-8 is applied to significantly enhance the photocatalytic water reduction by forming a built-in electric field with g-C3N4 and the mechanism analysis

Journal

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jece.2022.107998

Keywords

ZIF-8; g-C3N4; Built-in electric field; Photocatalysis; H-2 evolution

Funding

  1. National Natural Science Foundation of China [51978323, 42077162]
  2. Academic and technical leaders of major disciplines in Jiangxi Province - leading talents [20213BCJ22018]
  3. Key Research and Development Project of Jiangxi Province [20203BBGL73229]

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The combination of ZIF-8 and g-C3N4 is found to convert the photo-inactive ZIF-8 into active and enhance the photocatalytic performance for H-2 production. Experimental results and theoretical calculations suggest a built-in electric field at the interface of g-C3N4 and ZIF-8, which promotes the directional transfer of photo-induced electrons and boosts the catalytic ability. Hence, the construction of a built-in electric field is considered an effective strategy to synthesize robust photocatalysts.
It has been found in this study that the combination of ZIF-8 and g-C3N4 turns the photo-inactive ZIF-8 into active and significantly enhances the photocatalytic performance for H-2 production. The experimental results such as contact potential difference (CPD) and photodeposition analysis suggest that a built-in electric field exists at the interface of g-C3N4 and ZIF-8, and the direction is from ZIF-8 to g-C3N4. Furthermore, the theoretical calculation of charge density difference and work functions uncover the potential forming mechanism of the built-in electric field. The mechanism analysis exhibits that the built-in electric field is conducive to promote the directional transfer of photo-induced electrons from g-C3N4 to ZIF-8, which significantly boosts the catalytic ability. Hence, the construction of a built-in electric field is considered to be an effective strategy to synthesize robust photocatalysts, and the strategy can be extended to prepare a range of advanced catalysts needing directional charge transfer.

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