Cobalt-nitrogen-doped ordered macro-/mesoporous carbon for highly efficient oxygen reduction reaction

被引:159
|
作者
Sun, Tingting [1 ]
Xu, Lianbin [1 ]
Li, Shengyu [1 ]
Chai, Wenxia [1 ]
Huang, Yan [1 ]
Yan, Yushan [2 ]
Chen, Jianfeng [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[2] Univ Delaware, Dept Chem & Biomol Engn, Newark, DE 19716 USA
基金
中国国家自然科学基金;
关键词
Co-N-doping; Ordered macro-/mesoporous carbon; Dual-templating synthesis; Electrocatalyst; Oxygen reduction reaction; Durability; POROUS CARBON; ELECTROCATALYTIC ACTIVITY; ALKALINE MEDIA; FUEL-CELLS; COMPOSITE ELECTROCATALYST; MESOPOROUS POLYMERS; ENERGY-CONVERSION; GRAPHENE OXIDE; FREE CATALYSTS; PERFORMANCE;
D O I
10.1016/j.apcatb.2016.04.006
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
Cobalt-nitrogen-doped three-dimensionally (3D) ordered macro-/mesoporous carbons (Co-N-OMMCs) have been fabricated through a dual-templating synthesis approach in a one-pot controllable procedure by the use of silica colloidal crystal (opal) as a macroporous mold and triblock copolymer Pluronic F127 as a mesoporous template. The optimal catalyst (Co-N-OMMC-0.6) exhibits comparable catalytic activity but much higher durability and tolerance of methanol in comparison with the commercial 20 wt% Pt/C catalyst for oxygen reduction reaction (ORR) in an alkaline medium. The remarkable ORR electrocatalytic performance of the Co-N-OMMC-0.6 is ascribed to the homogeneous distribution of abundant Co-N-x active sites, as well as the large surface area and efficient mass/charge transport from the unique structure combining well-ordered bicontinuous mesopores with 3D interconnected periodic macropores. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 8
页数:8
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