Metal-free carbon semi-tubes for oxygen reduction electrocatalysis

被引:28
作者
Chen, Menghui [1 ]
Chen, Junxiang [2 ]
Jia, Chunguang [3 ]
Luo, Jin [4 ]
Yang, Zhili [1 ]
Jung, Joey Chung -Yen [1 ]
Zhang, Jiujun [1 ]
Chen, Shengli [4 ]
Zhang, Shiming [1 ]
机构
[1] Shanghai Univ, Inst Sustainable Energy, Coll Sci, Shanghai 200444, Peoples R China
[2] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, CAS Key Lab Design & Assembly Funct Nanostruct, Fuzhou 350002, Fujian, Peoples R China
[3] Nanchang Hangkong Univ, Key Lab Jiangxi Prov Persistent Pollutants Control, Nanchang 330063, Peoples R China
[4] Wuhan Univ, Coll Chem & Mol Sci, Hubei Key Lab Electrochem Power Sources, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
ACTIVE-SITES; POLYANILINE; DEFECT; CATALYSTS;
D O I
10.1016/j.xcrp.2022.101204
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
New carbon morphologies are desirable in the development of high-performance carbon-based electrocatalysts for cathodic oxygen reduction reaction (ORR) of polymer electrolyte membrane fuel cells. In this work, a carbon semi-tube (CST) is successfully constructed by polymerizing m-phenylenediamine (mPDA) using surfactant -assem-bled micelles as a soft template. After pyrolysis, the CST morphology is retained in the formed N-doped CST (N-CST) catalyst. This mPDA-induced catalyst can provide rich micropores, high N-content, and good conductivity, imbuing it with superior catalytic ORR activity, sta-bility, and methanol tolerance to the commercial Pt/C catalyst. By us-ing such a metal-free N-CST as a cathode catalyst, an alkaline polymer electrolyte fuel cell exhibits a maximum power density of about 200 mW cm -2. Furthermore, density functional theory (DFT) calculations suggest that high curvature can be greatly conducive to the excellent catalytic ORR activity by the induced strong OOH* adsorption on active sites through a strong dipole-electric field interaction.
引用
收藏
页数:15
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