Issue 32, 2021

NiCo LDH in situ derived NiCoP 3D nanoflowers coupled with a Cu3P p–n heterojunction for efficient hydrogen evolution

Abstract

With the extensive consumption of non-renewable energy sources, storing solar energy as chemical energy has aroused people's wide concern. In this study, we successfully developed a novel Cu3P@NiCoP composite photocatalyst to produce hydrogen by splitting water under visible light irradiation. Both the building of a p–n heterojunction between Cu3P and NiCoP and the three-dimensional nanoflower structure of NiCoP play a vital role in improving the performance of the catalyst. On the one hand, the coupling of Cu3P and NiCoP built a p–n heterojunction at the photocatalyst interface, and the heterojunction could promote the separation efficiency of photogenerated carriers and prolong the life span of charges, therefore enhancing the photocatalytic hydrogen production activity. On the other hand, the excellent catalytic performance of the photocatalyst was benefited by the flower-like microsphere structure of NiCoP, which could provide abundant active sites and a large specific surface area, and promote the adsorption of protons by the photocatalyst. Besides, the phosphating degree of the precursors and the ratio of Cu3P and NiCoP were adjusted to get the best photocatalyst for hydrogen production, and the H2 production of the optimal catalyst could reach 8897.44 μmol h−1 g−1. This work provides a new understanding for the rational design of heterojunction photocatalysts for outstanding hydrogen production performance.

Graphical abstract: NiCo LDH in situ derived NiCoP 3D nanoflowers coupled with a Cu3P p–n heterojunction for efficient hydrogen evolution

Article information

Article type
Paper
Submitted
03 May 2021
Accepted
21 Jul 2021
First published
22 Jul 2021

Nanoscale, 2021,13, 13858-13872

NiCo LDH in situ derived NiCoP 3D nanoflowers coupled with a Cu3P p–n heterojunction for efficient hydrogen evolution

M. Yang, Y. Li, T. Yan and Z. Jin, Nanoscale, 2021, 13, 13858 DOI: 10.1039/D1NR02798K

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