0D CoP cocatalyst/ 2D g‐C 3 N 4 nanosheets: An efficient photocatalyst for promoting photocatalytic hydrogen evolution

Abstract In this work, cobalt phosphide (CoP) nanoparticles were successfully decorated on an ultrathin g‐C 3 N 4 nanosheet photocatalysts by in situ chemical deposition. The built‐in electric field formed by heterojunction interface of the CoP/g‐C 3 N 4 composite semiconductor can accelerate the tr...

Full description

Saved in:
Bibliographic Details
Published inJournal of the American Ceramic Society Vol. 102; no. 9; pp. 5484 - 5493
Main Authors Han, Changcun, Zhang, Tong, Cai, Qijun, Ma, Chonghao, Tong, Zhengfu, Liu, Zhifeng
Format Journal Article
LanguageEnglish
Published 01.09.2019
Online AccessGet full text

Cover

Loading…
More Information
Summary:Abstract In this work, cobalt phosphide (CoP) nanoparticles were successfully decorated on an ultrathin g‐C 3 N 4 nanosheet photocatalysts by in situ chemical deposition. The built‐in electric field formed by heterojunction interface of the CoP/g‐C 3 N 4 composite semiconductor can accelerate the transmission and separation of photogenerated charge‐hole pairs and effectively improve the photocatalytic performance. TEM, HRTEM, XPS, and SPV analysis showed that CoP/g‐C 3 N 4 formed a stable heterogeneous interface and effectively enhanced photogenerated electron‐hole separation. UV‐vis DRS analysis showed that the composite had enhanced visible light absorption than pure g‐C 3 N 4 and was a visible light driven photocatalyst. In this process, NaH 2 PO 2 and CoCl 2 are used as the source of P and Co, and typical preparation of CoP can be completed within 3 hours. Under visible light irradiation, the optimal H 2 evolution rate of 3.0 mol% CoP/g‐C 3 N 4 is about 15.1 μmol h −1 . The photocatalytic activity and stability of the CoP/g‐C 3 N 4 materials were evaluated by photocatalytic decomposition of water. The intrinsic relationship between the microstructure of the composite catalyst and the photocatalytic performance was analyzed to reveal the photocatalytic reaction mechanism.
ISSN:0002-7820
1551-2916
DOI:10.1111/jace.16443