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Strategies and Perspectives to Catch the Missing Pieces in Energy‐Efficient Hydrogen Evolution Reaction in Alkaline Media

氢氧化物 碱性水电解 氧化物 磷化物 金属氢氧化物 无机化学 硫系化合物 金属 碱金属 电解 化学 材料科学 有机化学 冶金 物理化学 电极 电解质
作者
Sengeni Anantharaj,Suguru Noda,Vasanth Rajendiran Jothi,Sung Chul Yi,Matthias Drieß,Prashanth W. Menezes
出处
期刊:Angewandte Chemie [Wiley]
卷期号:60 (35): 18981-19006 被引量:228
标识
DOI:10.1002/anie.202015738
摘要

Transition metal hydroxides (M-OH) and their heterostructures (X|M-OH, where X can be a metal, metal oxide, metal chalcogenide, metal phosphide, etc.) have recently emerged as highly active electrocatalysts for hydrogen evolution reaction (HER) of alkaline water electrolysis. Lattice hydroxide anions in metal hydroxides are primarily responsible for observing such an enhanced HER activity in alkali that facilitate water dissociation and assist the first step, the hydrogen adsorption. Unfortunately, their poor electronic conductivity had been an issue of concern that significantly lowered its activity. Interesting advancements were made when heterostructured hydroxide materials with a metallic and or a semiconducting phase were found to overcome this pitfall. However, in the midst of recently evolving metal chalcogenide and phosphide based HER catalysts, significant developments made in the field of metal hydroxides and their heterostructures catalysed alkaline HER and their superiority have unfortunately been given negligible attention. This review, unlike others, begins with the question of why alkaline HER is difficult and will take the reader through evaluation perspectives, trends in metals hydroxides and their heterostructures catalysed HER, an understanding of how alkaline HER works on different interfaces, what must be the research directions of this field in near future, and eventually summarizes why metal hydroxides and their heterostructures are inevitable for energy-efficient alkaline HER.
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