Heterostructured V-Doped Ni2P/Ni12P5 Electrocatalysts for Hydrogen Evolution in Anion Exchange Membrane Water Electrolyzers

55Citations
Citations of this article
25Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Regulating the electronic structure and intrinsic activity of catalysts’ active sites with optimal hydrogen intermediates adsorption is crucial to enhancing the hydrogen evolution reaction (HER) in alkaline media. Herein, a heterostructured V-doped Ni2P/Ni12P5 (V–Ni2P/Ni12P5) electrocatalyst is fabricated through a hydrothermal treatment and controllable phosphidation process. In comparison with pure-phase V–Ni2P, in/ex situ characterizations and theoretical calculations reveal a redistribution of electrons and active sites in V–Ni2P/Ni12P5 due to the V doping and heterointerfaces effect. The strong coupling between Ni2P and Ni12P5 at the interface leads to an increased electron density at interfacial Ni sites while depleting at P sites, with V-doping further promoting the electron accumulation at Ni sites. This is accompanied by the change of active sites from the anionic P sites to the interfacial Ni–V bridge sites in V–Ni2P/Ni12P5. Benefiting from the interface electronic structure, increased number of active sites, and optimized H-adsorption energy, the V-Ni2P/Ni12P5 exhibits an overpotential of 62 mV to deliver 10 mA cm–2 and excellent long-term stability for HER. The V–Ni2P/Ni12P5 catalyst is applied for anion exchange membrane water electrolysis to deliver superior performance with a current density of 500 mA cm–2 at a cell voltage of 1.79 V and excellent durability.

Cite

CITATION STYLE

APA

Zhao, T., Wang, S., Li, Y., Jia, C., Su, Z., Hao, D., … Zhao, C. (2022). Heterostructured V-Doped Ni2P/Ni12P5 Electrocatalysts for Hydrogen Evolution in Anion Exchange Membrane Water Electrolyzers. Small, 18(40). https://doi.org/10.1002/smll.202204758

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free