4.6 Article

Dopant-Induced Edge and Basal Plane Catalytic Sites on Ultrathin C3N4 Nanosheets for Photocatalytic Water Reduction

Journal

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
Volume 8, Issue 19, Pages 7497-7502

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.0c02122

Keywords

dual-doping; catalytic sites; C3N4; hydrogen evolution; photocatalysis

Funding

  1. National Natural Science Foundation of China [5171101651, 21822603, 21811540394, 21677048, 21773062, 21577036]
  2. State Key Research Development Program of China [2016YFA0204200]
  3. Shanghai Municipal Science and Technology Major Project [2018SHZDZX03, 17520711500]
  4. Program of Introducing Talents of Discipline to Universities [B16017, B20031]
  5. Fundamental Research Funds for the Central Universities [22A201514021]

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The emerging carbon nitride (C3N4) offers a serious possibility for realizing a highly effective hydrogen evolution reaction (HER). However, their insufficient catalytic sites and poor conductivity hamper the HER performance. Herein, an oxygen, phosphorus dual-doped ultrathin C3N4 nanosheet (O, P-CNS) is synthesized through a two-step method without a liquid solution, including calcination under air and subsequent chemical vapor deposition (CVD) with sodium hypophosphite (NaH2PO2) in N-2 atmosphere. The first thermal treatment in the air atmosphere results in the introduction of O dopant on the edge of C3N4 and the exfoliation of bulk C3N4 into ultrathin nanosheets. The following P incorporation contributes to the activation of the basal plane of C3N4 and the improvement of the intrinsic electronic conductivity, thus giving rise to the facilitated H-2 generation rate. Particularly, a superior H-2 generation rate of 8.7 mmol g(-1) h(-1) under visible light and an apparent quantum yield of 23.65% with 420 nm could be realized after the two-step dual-doping-induced calcination, further confirming the enhanced charge separation with the full activation of the edge and basal plane catalytic sites of C3N4. Our work on dual-doping-induced catalytic site activation on the edge and basal plane of C3N4 will provide more guidance in the field of designing C3N4-based photocatalysts.

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