4.8 Article

Photocatalyst for High-Performance H2 Production: Ga-Doped Polymeric Carbon Nitride

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 60, Issue 11, Pages 6124-6129

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202015779

Keywords

carbon nitride; hydrogen; gallium; photocatalysis; structure elucidation

Funding

  1. Beijing Municipal High-Level Innovative Team Building Program [IDHT20180504]
  2. Beijing Outstanding Young Scientists Program [BJJWZYJH0201910005017]
  3. National Natural Science Foundation of China [21805004, 21671011, 21872001, 51801006]
  4. Beijing Natural Science Foundation [2192005]
  5. Beijing Municipal Science and Natural Science Fund Project [KM201910005016]
  6. Beijing Postdoctoral Research Foundation [2020-ZZ-041]

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This study integrates the active GaN4 site into a polymeric carbon nitride photocatalyst, achieving excellent H-2 production rate and investigating the reactions and storage processes of electrons and protons on the catalyst under light irradiation.
A photocatalyst system is generally comprises a catalyst and cocatalyst to achieve light absorption, electron-hole separation, and surface reaction. It is a challenge to develop a single photocatalyst having all functions so as to lower the efficiency loss. Herein, the active GaN4 site is integrated into a polymeric carbon nitride (CN) photocatalyst (GCN), which displays an excellent H-2 production rate of 9904 mu mol h(-1) g(-1). It is 162 and 3.3 times higher than that of CN with the absence (61 mu mol h(-1) g(-1)) and presence (2981 mu mol h(-1) g(-1)), respectively, of 1.0 wt % Pt. Under light irradiation the electron is injected and stored at the GaN4 site, where the LUMO locates. The HOMO distributes on the aromatic ring resulting in spatial charge separation. Transient photovoltage discloses the electron-storage capability of GCN. The negative GaN4 promotes proton adsorption in the excited state. The positive adsorption energy drives H-2 desorption from GaN4 after passing the electron to the proton. This work opens up opportunities for exploring a novel catalyst for H-2 production.

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