Published November 2018 | Version v1
Journal article

Highly dispersed and noble metal-free MPX (M = Ni, Co, Fe) coupled with g-C3N4 nanosheets as 0D/2D photocatalysts for hydrogen evolution

  • 1. School of Physics and Technology, University of Jinan, Jinan, 250022, Shandong Province (China)

Description

Highlights: • Highly dispersed MPX were applied to construct MPX/CNNS system. • The H2 evolution rate of NiPX/CNNS-900 boosts to 4068.84 μmol·g−1·h−1. • Earth-abundant MPX as co-catalyst played an effective role in this system. Developing high-efficiency and low-cost photocatalysts by avoiding expensive noble metals is a great challenge. Here, highly dispersed metal (M = Ni, Co, Fe) phosphides modified g-C3N4 nanosheets (CNNS) were prepared through in situ precipitation and solid/gas-phase phosphorization. The results confirmed that metal phosphides (MPX) nanoparticles with high dispersion were well loaded on CNNS surface. The property well reveals the transfer path of photogenerated charges and the origin of high charge separation efficiency in photocatalytic reaction, thus yielding a remarkable catalytic activity. The apparent quantum efficiency (AQY) based on the NiPX/CNNS-900 is up to 6.61% at 400 nm while the H2 evolution rate boosts to 4068.84 μmol·g−1·h−1, which is 50 times higher than that of pristine CNNS. The mechanism could be attributed to the highly dispersed MPX nanoparticles on the surface of CNNS, which acted as effective active sites to promote the separation and migration of photogenerated charges, leading to greatly increase in H2 production. This study is beneficial to further develop the high-efficient, low cost and environmentally-friendly CNNS-based photocatalytic materials for H2 production.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.apsusc.2018.07.149

Additional details

Identifiers

DOI
10.1016/j.apsusc.2018.07.149;
PII
S0169433218320464;

Publishing Information

Journal Title
Applied Surface Science
Journal Volume
458
Journal Page Range
p. 893-902
ISSN
0169-4332
CODEN
ASUSEE

Optional Information

Copyright
Copyright (c) 2018 Elsevier B.V. All rights reserved.