Recent advances in layered double hydroxide electrocatalysts for the oxygen evolution reaction

被引:437
|
作者
Cai, Zhengyang [1 ]
Bu, Xiuming [2 ]
Wang, Ping [1 ,3 ]
Ho, Johnny C. [2 ]
Yang, Junhe [1 ,3 ]
Wang, Xianying [1 ,3 ]
机构
[1] Univ Shanghai Sci & Technol, Sch Mat Sci & Technol, Jungong Rd 516, Shanghai 200093, Peoples R China
[2] City Univ Hong Kong, Dept Mat Sci & Engn, Kowloon, 83 Tat Chee Ave, Hong Kong, Peoples R China
[3] Shanghai Innovat Inst Mat, Shanghai 200444, Peoples R China
基金
中国国家自然科学基金;
关键词
HIGH-PERFORMANCE ELECTROCATALYSTS; HIGHLY EFFICIENT ELECTROCATALYST; WATER OXIDATION; BIFUNCTIONAL ELECTROCATALYST; ENERGY-CONVERSION; NICKEL NITRIDE; ACTIVE-SITES; DOPED CARBON; OXIDE-FILMS; THIN-FILM;
D O I
10.1039/c8ta11273h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The energy consumption of hydrogen production from electrolytic water splitting originates from the oxygen evolution reaction (OER). Development of efficient and cost-effective OER electrocatalysts has become a high-priority research task. In this regard, layered double hydroxides (LDHs) as one of the promising OER electrocatalysts have been intensely researched due to their unique 2D layered structure and excellent physicochemical properties. Herein, this review aims to summarize recent strategies to design LDHs, including nanostructuring, hybrid LDHs with conductive materials, partial substitution of cations, interlayer anion replacement, vacancy creation, and combination of computational methods and operando techniques. Specifically, a thorough literature overview in the developments of LDHs to improve OER performance is appraised in detail, based on the compositional difference of transition metal components. Challenges and future directions in designing LDHs as OER electrocatalysts are discussed. The provided discussion will be favorable to explore and develop better catalysts and device units for practical applications and will offer a basic understanding of the OER process along with key issues to evaluate the performance.
引用
收藏
页码:5069 / 5089
页数:21
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