Salt-assisted construction of hydrophilic carbon nitride photocatalysts with abundant water molecular adsorption sites for efficient hydrogen production

Chong Wang (Co-first Author), Yichun Lu (Co-first Author), Zequn Wang, Hongwu Liao, Weiming Zhou*, Yuhe He, Sameh M. Osman, Meng An*, Yusuke Asakura*, Yusuke Yamauchi, Liwei Wang*, Zhanhui Yuan*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

40 Citations (Scopus)
33 Downloads (CityUHK Scholars)

Abstract

Polymer carbon nitride (PCN), as an affordable and easily prepared photocatalyst, has acquired extensive attention for hydrogen production. However, bulk carbon nitride material exhibits poor dispersibility in water due to the relatively inert surface which limits its quantum efficiency in photocatalytic hydrogen production. In this study, a hydrophilic carbon nitride (HCN) is successfully synthesized by a novel salt-assisted heating process. The heightened water adsorption capacity may contribute additional active sites conducive to the photocatalytic hydrogen production reaction. Meanwhile, potassium ion doping and material size reduction greatly enhance the charge transfer and separation ability of HCN. Consequently, HCN exhibits highly efficient photocatalytic activity for hydrogen production, achieving a rate of 392 μmol·h−1, which is 16 times greater than that of pristine PCN. The simply developed synthetic strategy adopted here provides a novel concept for functionalizing carbon nitride and opening a distinct pathway for the construction of exceptionally efficient photocatalytic systems. © 2024 The Authors.
Original languageEnglish
Article number123902
JournalApplied Catalysis B: Environmental
Volume350
Online published2 Mar 2024
DOIs
Publication statusPublished - 5 Aug 2024

Research Keywords

  • Carbon nitride
  • Photocatalysis
  • Hydrogen production
  • Hydrophilic
  • Salt-assisted synthesis

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

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