Yu Yanhui, Chen Qingrong, Li Jing, Rao Peng, Li Ruisong, Du Yanlian, Jia Chunman, Huang Wei, Luo Junming, Deng Peilin, Shen Yijun, Tian Xinlong
State Key Laboratory of Marine Resource Utilization in South China Sea, Hainan Provincial Key Lab of Fine Chemistry, School of Chemical Engineering and Technology, Hainan University, Haikou 570228, China.
State Key Laboratory of Marine Resource Utilization in South China Sea, Hainan Provincial Key Lab of Fine Chemistry, School of Chemical Engineering and Technology, Hainan University, Haikou 570228, China.
J Colloid Interface Sci. 2022 Feb;607(Pt 2):1091-1102. doi: 10.1016/j.jcis.2021.09.032. Epub 2021 Sep 16.
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, NiP 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 NiP are still inferior to those of noble metal-based catalysts. Heteroatom doping is a universal strategy for enhancing the performance of NiP 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 NiP based electrocatalysts are proposed and discussed.
氢能有望在未来取代化石燃料成为主流能源。目前,通过水电解制氢可获得高纯度氢气,操作简便且不产生污染性副产物。当前,铂族金属及其氧化物是最有效的水分解催化剂;然而,它们的低丰度和高成本阻碍了大规模制氢,尤其是在碱性和中性介质中。因此,开发高效、耐用且低成本的电催化剂对于降低过电位和电能消耗至关重要。作为一种解决方案,NiP因其理想的导电性、高耐腐蚀性以及对整体水分解具有显著的催化活性而备受关注,因此是铂族催化剂的一种有前途的替代品。然而,原始NiP的催化性能和耐久性仍不如贵金属基催化剂。杂原子掺杂是一种在广泛pH范围内提高NiP用于水电解性能的通用策略,因为通过掺杂可以调节催化剂的电子结构和晶体结构,并调整反应中间体的吸附能,从而优化反应性能。在本综述中,首先简要介绍了水电解的反应机制,包括阴极析氢反应和阳极析氧反应。然后,评估了近年来杂原子掺杂磷化镍的研究进展,并对每项代表性工作进行了讨论。最后,提出并讨论了开发先进的基于NiP的电催化剂所面临的机遇和挑战。