S, N Dual-Doped Graphene-like Carbon Nanosheets as Efficient Oxygen Reduction Reaction Electrocatalysts

被引:191
作者
Li, Jiajie [1 ]
Zhang, Yumin [1 ]
Zhang, Xinhong [1 ]
Huang, Jinzhen [1 ]
Han, Jiecai [1 ]
Zhang, Zhihua [2 ]
Han, Xijiang [3 ]
Xu, Ping [3 ]
Song, Bo [1 ,4 ,5 ]
机构
[1] Harbin Inst Technol, Ctr Composite Mat & Struct, Harbin 150080, Peoples R China
[2] Dalian Jiaotong Univ, Sch Mat Sci & Engn, Liaoning Key Mat Lab Railway, Dalian 116028, Peoples R China
[3] Harbin Inst Technol, Sch Chem & Chem Engn, Harbin 150080, Peoples R China
[4] Harbin Inst Technol, Acad Fundamental & Interdisciplinary Sci, Harbin 150080, Peoples R China
[5] Harbin Inst Technol, Dept Phys, Harbin 150080, Peoples R China
基金
中国国家自然科学基金; 对外科技合作项目(国际科技项目);
关键词
S; N-doped carbon; graphene-like; oxygen reduction reaction; electrocatalysis; metal-free; METAL-FREE ELECTROCATALYSTS; MESOPOROUS CARBONS; RAMAN-SPECTRA; ACTIVE-SITES; NITROGEN; SULFUR; CATALYST; OXIDE; NANOPARTICLES; FRAMEWORKS;
D O I
10.1021/acsami.6b12547
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Replacement of rare and precious metal catalysts with low-cost and earth-abundant ones is currently among the major goals of sustainable chemistry. Herein, we report the synthesis of S, N dual-doped graphene-like carbon nanosheets via a simple pyrolysis of a mixture of melamine and dibenzyl sulfide as efficient metal free electrocatalysts for oxygen reduction reaction (ORR). The S, N dual-doped graphene-like carbon nanosheets show enhanced activity toward ORR as compared with mono-doped counterparts, and excellent durability in contrast to the conventional Pt/C electrocatalyst in both alkaline and acidic media. A high content of graphitic-N and pyridinic-N is necessary for ORR electrocatalysis in the graphenelike carbon nanosheets, but an appropriate amount of S atoms further contributes to the improvement of ORR activity. Superior ORR performance from the as-prepared S, N dual-doped graphene-like carbon nanosheets implies great promises in practical applications in energy devices.
引用
收藏
页码:398 / 405
页数:8
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