Progress in the development of heteroatom-doped nickel phosphates for electrocatalytic water splitting.

Abstract Hydrogen energy is expected to replace fossil fuels as a mainstream energy source in the future. Currently, hydrogen production via water electrolysis yields high hydrogen purity with easy operation and without producing polluting side products. Presently, platinum group metals and their oxides are the most effective catalysts for water splitting; however, their low abundance and high cost hinder large-scale hydrogen production, especially in alkaline and neutral media. Therefore, the development of high-efficiency, durable, and low-cost electrocatalysts is crucial to improving the overpotential and lowering the electrical energy consumption. As a solution, Ni2P has attracted particular attention, owing to its desirable electrical conductivity, high corrosion resistance, and remarkable catalytic activity for overall water splitting, and thus, is a promising substitute for platinum-group catalysts. However, the catalytic performance and durability of raw Ni2P are still inferior to those of noble metal-based catalysts. Heteroatom doping is a universal strategy for enhancing the performance of Ni2P for water electrolysis over a wide pH range, because the electronic structure and crystal structure of the catalyst can be modulated, and the adsorption energy of the reaction intermediates can be adjusted via doping, thus optimizing the reaction performance. In this review, first, the reaction mechanisms of water electrolysis, including the cathodic hydrogen evolution reaction and anodic oxygen evolution reaction, are briefly introduced. Then, progress into heteroatom-doped nickel phosphide research in recent years is assessed, and a discussion of each representative work is given. Finally, the opportunities and challenges for developing advanced Ni2P based electrocatalysts are proposed and discussed.