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...
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Published in | Journal of the American Ceramic Society Vol. 102; no. 9; pp. 5484 - 5493 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
01.09.2019
|
Online Access | Get full text |
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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. |
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ISSN: | 0002-7820 1551-2916 |
DOI: | 10.1111/jace.16443 |