Doped fullerene as a metal-free electrocatalyst for oxygen reduction reaction: A first-principles study

被引:87
|
作者
Wang, Ying [1 ]
Jiao, Menggai [1 ,3 ]
Song, Wei [2 ]
Wu, Zhijian [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China
[2] Xinxiang Univ, Phys & Elect Engn Dept, Xinxiang 453003, Peoples R China
[3] Nankai Univ, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Computat Ctr Mol Sci,Natl Inst Adv Mat,Inst New E, Sch Mat Sci & Engn,Tianjin Key Lab Met & Mol Base, Tianjin 300350, Peoples R China
基金
中国国家自然科学基金;
关键词
EVOLUTION REACTIONS; CARBON NANOTUBES; GRAPHENE; BORON; CATALYSTS;
D O I
10.1016/j.carbon.2016.12.028
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 heteroatom-doped fullerene is systematically studied as an electrocatalyst for oxygen reduction reaction (ORR) on the cathode of fuel cells under the alkaline and acid conditions. Nitrogen-doped Co, i.e. C59N, can facilitate the ORR process and it is a promising candidate for efficient ORR electrocatalysts. The intrinsic Cat also possesses a high catalytic activity, which is different from graphene and is probably attributed to the curvature or pentagon defect of fullerene. We deduce that the curvature and pentagon defect are important factors to tune the catalytic ability. The fitted activity volcano diagram shows that the best achievable ORR activity of the heteroatom-doped fullerene, in the thermodynamic viewpoint, appears at Delta G(*OH) = 0.25 eV, which could be realized by dual or three-element-doping of C-60 cage. The estimated standard equilibrium potential values are -0.52 and 0.25 V in alkaline and acid medium, respectively. Since the catalytic activity of the doped fullerenes depends on their IP and E-gap, here we provide a simple and easy method, by measuring the IP and Egap, to roughly evaluate the catalytic ability of designed catalysts. This is vital to guide the design of new ORR catalysts with high catalytic activity and durability. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:393 / 401
页数:9
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