Shining Light on Anion-Mixed Nanocatalysts for Efficient Water Electrolysis: Fundamentals,Progress, and Perspectives

被引:13
|
作者
Yaoda Liu [1 ]
Paranthaman Vijayakumar [1 ]
Qianyi Liu [1 ]
Thangavel Sakthivel [1 ]
Fuyi Chen [2 ]
Zhengfei Dai [1 ]
机构
[1] State Key Laboratory for Mechanical Behavior of Materials, Xi'an Jiaotong University
[2] State Key Laboratory of Solidification Processing, Northwestern Polytechnical University
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
D O I
暂无
中图分类号
TQ116.2 [氢气]; TQ426 [催化剂(触媒)];
学科分类号
080502 ; 0817 ; 081705 ;
摘要
Hydrogen with high energy density and zero carbon emission is widely acknowledged as the most promising candidate toward world’s carbon neutrality and future sustainable eco-society. Water-splitting is a constructive technology for unpolluted and high-purity H2 production, and a series of non-precious electrocatalysts have been developed over the past decade. To further improve the catalytic activities, metal doping is always adopted to modulate the 3 d-electronic configuration and electron-donating/accepting(e-DA) properties, while for anion doping, the electronegativity variations among different non-metal elements would also bring some potential in the modulations of e-DA and metal valence for tuning the performances. In this review, we summarize the recent developments of the many different anion-mixed transition metal compounds(e.g., nitrides, halides,phosphides, chalcogenides, oxyhydroxides, and borides/borates) for efficient water electrolysis applications. First, we have introduced the general information of water-splitting and the description of anion-mixed electrocatalysts and highlighted their complementary functions of mixed anions. Furthermore, some latest advances of anion-mixed compounds are also categorized for hydrogen and oxygen evolution electrocatalysis. The rationales behind their enhanced electrochemical performances are discussed. Last but not least, the challenges and future perspectives are briefly proposed for the anion-mixed water dissociation catalysts.
引用
收藏
页码:85 / 125
页数:41
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