3D Carbon Materials for Efficient Oxygen and Hydrogen Electrocatalysis

被引:182
|
作者
Jorge, Ana Belen [1 ]
Jervis, Rhodri [2 ]
Periasamy, Arun Prakash [1 ]
Qiao, Mo [3 ]
Feng, Jingyu [3 ]
Tran, Linh Ngoc [1 ]
Titirici, Maria-Magdalena [3 ]
机构
[1] Queen Mary Univ London, Mat Res Inst, Sch Engn & Mat Sci, Mile End Rd, London E1 4NS, England
[2] UCL, Dept Chem Engn, Electrochem Innovat Lab, Torrington Pl, London WC1 0AJ, England
[3] Imperial Coll London, Dept Chem Engn, South Kensington Campus, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会;
关键词
3D porous carbons; electrocatalysis; hydrogen evolution; oxygen evolution; oxygen reduction; METAL-FREE ELECTROCATALYSTS; NITROGEN-DOPED GRAPHENE; HIERARCHICALLY POROUS CARBON; REDUCTION REACTION CATALYSTS; ELECTROCHEMICAL ENERGY-STORAGE; FUEL-CELL ELECTROCATALYSTS; BOTTOM-UP SYNTHESIS; ACTIVE-SITES; MESOPOROUS CARBON; EVOLUTION REACTION;
D O I
10.1002/aenm.201902494
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
Sustainable energy production at an acceptable cost is key for its widespread application. At present, noble metals and metal oxides are the most widely used for electrocatalysis, but they suffer from low selectivity, poor durability, and scarcity. Because of this, metal-free carbons have become the subject of great interest as promising alternative electrocatalysts for energy conversion and storage devices, and remarkable progress has been accomplished in the advance of metal-free carbons as electrocatalysts for renewable energy technologies. Particularly interesting are 3D porous carbon architectures, which exhibit outstanding features for electrocatalysis applications, including broad range of active sites, interconnected porosity, high conductivity, and mechanical stability. This review summarizes the latest advances in 3D porous carbon structures for oxygen and hydrogen electrocatalysis. The structure-performance relationship of these materials is consequently rationalized and perspectives on creating more efficient 3D carbon electrocatalysts are suggested.
引用
收藏
页数:35
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