Heteroatom-doped carbon dots based catalysts for oxygen reduction reactions

被引:73
|
作者
Zhang, Peng [1 ,2 ]
Wei, Ji-Shi [1 ,2 ]
Chen, Xiao-Bo [3 ]
Xiong, Huan-Ming [1 ,2 ]
机构
[1] Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China
[2] Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
[3] RMIT Univ, Sch Engn, Carlton, Vic 3053, Australia
基金
中国国家自然科学基金;
关键词
Carbon dots; Doping; Electrocatalysis; Graphene; Oxygen reduction reaction; GRAPHENE QUANTUM DOTS; EFFICIENT ELECTROCATALYST; ACTIVE-SITES; ONE-POT; NITROGEN; OXIDE; NANOPLATELETS; FLUORESCENCE; PERFORMANCE; PLATINUM;
D O I
10.1016/j.jcis.2018.11.024
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
Carbon materials doped with heteroatoms are a class of cost-effective and stable electrocatalysts for oxygen reduction reactions (ORR), whose activities are mainly based on the heteroatom-related active sites. Besides the widely reported one-dimensional carbon nanotubes and two-dimensional graphene materials, carbon dots (CDs), as a new kind of zero-dimensional carbon materials, exhibit a range of unique structures and promising catalytic activities for ORR. In order to optimize the complex conditions of carbon-based catalysts, composites consisting of doped CDs and reduced graphene oxide (rGO) (designated as CD/rGO) are prepared hydrothermally, in comparison with directly doped rGO. All produced composites outperform their corresponding directly doped rGO counterparts in ORR measurements. It is noted that nitrogen and sulfur co-doped samples perform better than those doped by individual N or S. Mechanistic relationships between the ORR catalytic activities and the catalyst features are proposed, including type, location, bonding, fraction and synergistic effects of dopants, as well as the composition and structure of the carbon substrates. It is apparent that doping heteroatoms and constructing carbon substrates play a synergistic role in yielding high-performance carbon based catalysts. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:716 / 724
页数:9
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