N-doped hard carbon nanotubes derived from conjugated microporous polymer for electrocatalytic oxygen reduction reaction

被引:45
|
作者
Zhang, Wanli [1 ]
Sun, Hanxue [1 ]
Zhu, Zhaoqi [1 ]
Jiao, Rui [1 ]
Mu, Peng [1 ]
Liang, Weidong [1 ]
Li, An [1 ]
机构
[1] Lanzhou Univ Technol, Dept Chem Engn, Coll Petrochem Engn, Lanzhou 730050, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
Conjugated microporous polymer; Oxygen reduction reaction; Graphitic carbon nitride; Nanotube; Hard carbon; METAL-FREE ELECTROCATALYSTS; POROUS CARBONS; FREE CATALYST; MASS ACTIVITY; COBALT ATOMS; FUEL-CELLS; NITROGEN; GRAPHENE; ALKALINE; STRATEGY;
D O I
10.1016/j.renene.2019.08.071
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The development of efficient non-metal catalysts (NMC) towards oxygen reduction reaction (ORR) in both acidic and alkaline electrolyte is of great importance for construction of new generation fuel cell. Herein, we demonstrate the fabrication of N-doped hard carbon nanotubes prepared by carbonization of melamine-incorporated nanotube-like conjugated microporous polymers (CMPs), as novel electrocatalysts for efficient ORR. As a kind of metal-free electrocatalyst, the as-prepared carbon nanotubes exhibit superior ORR activity not only in alkaline electrolyte but also in acidic condition. Interestingly, obvious enhancement on the diffusion-limited current density (increased by 1.8 mA cm(-2)) for the N-doped products in acid solution is observed by comparison with that of carbonized CMPs nanotubes without N-doping. Furthermore the catalysts also show better methanol immunity than that of commercial 20 wt% Pt/C. And only a slight decrease (14 mV negative shift) in half-wave potential is detected after 5000 cycles in 0.1 M KOH, indicating an ideal electrochemical stability which makes the N-doped hard carbon nanotubes promising candidate as an efficient electrocatalyst for ORR, by combination with their desirable electrocatalytic ORR activity, methanol tolerance and stability. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2270 / 2280
页数:11
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