Design and Synthesis of Hollow Nanostructures for Electrochemical Water Splitting

被引:222
作者
Yang, Min [1 ]
Zhang, Cai Hong [1 ]
Li, Nian Wu [1 ]
Luan, Deyan [2 ]
Yu, Le [1 ]
Lou, Xiong Wen [2 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[2] Nanyang Technol Univ, Sch Chem & Biomed Engn, 62 Nanyang Dr, Singapore 637459, Singapore
基金
中国国家自然科学基金;
关键词
architecture optimization; compositional manipulation; hollow nanostructures; water electrolysis; ENHANCED ELECTROCATALYTIC ACTIVITY; SINGLE-ATOM CATALYSTS; HYDROGEN; EVOLUTION; EFFICIENT; OXYGEN; NI; CONVERSION; NANOFRAMES; HYDROXIDE;
D O I
10.1002/advs.202105135
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrocatalytic water splitting using renewable energy is widely considered as a clean and sustainable way to produce hydrogen as an ideal energy fuel for the future. Electrocatalysts are indispensable elements for large-scale water electrolysis, which can efficiently accelerate electrochemical reactions occurring at both ends. Benefitting from high specific surface area, well-defined void space, and tunable chemical compositions, hollow nanostructures can be applied as promising candidates of direct electrocatalysts or supports for loading internal or external electrocatalysts. Herein, some recent progress in the structural design of micro-/nanostructured hollow materials as advanced electrocatalysts for water splitting is summarized. First, the design principles and corresponding strategies toward highly effective hollow electrocatalysts for oxygen/hydrogen evolution reactions are highlighted. Afterward, an overview of current reports about hollow electrocatalysts with diverse architectural designs and functionalities is given, including direct hollow electrocatalysts with single-shelled, multi-shelled, or open features and heterostructured electrocatalysts based on hollow hosts. Finally, some future research directions of hollow electrocatalysts for water splitting are discussed based on personal perspectives.
引用
收藏
页数:17
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