Preparation of nitrogen and sulfur co-doped ultrathin graphitic carbon via annealing bagasse lignin as potential electrocatalyst towards oxygen reduction reaction in alkaline and acid media

被引:52
|
作者
Shen, Yixing [1 ]
Peng, Feng [2 ]
Cao, Yonghai [1 ]
Zuo, Jianhang [2 ]
Wang, Hongjuan [1 ]
Yu, Hao [1 ]
机构
[1] South China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Guangdong, Peoples R China
[2] Guangzhou Univ, Sch Chem & Chem Engn, Guangzhou Key Lab New Energy & Green Catalysis, Guangzhou 510006, Guangdong, Peoples R China
来源
JOURNAL OF ENERGY CHEMISTRY | 2019年 / 34卷
基金
中国国家自然科学基金;
关键词
Electrocatalyst; Biocarbon; Lignin; Nitrogen and sulfur co-doped carbon; Oxygen reduction reaction; POROUS CARBON; ELECTRODE MATERIAL; HOLEY GRAPHENE; EFFICIENT; PERFORMANCE; SUPERCAPACITOR; TRANSFORMATION; NANOTUBES; CATALYST; POLYMER;
D O I
10.1016/j.jechem.2018.09.021
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Renewable lignin used for synthesizing materials has been proven to be highly potential in specific electrochemistry. Here, we report a simple method to synthesize nitrogen and sulfur co-doped carbon nanosheets by using bagasse lignin, denoted as lignin-derived carbon (LC). By adjusting the ratio of nitrogen source and annealing temperature, we obtained the ultrathin graphitic lignin carbon (LC-4-1000) with abundant wrinkles with high surface area of 1208 m(2)g(-1) and large pore volume of 1.40 cm(2)g(-1). In alkaline medium, LC-4-1000 has more positive half-wave potential and nearly current density compared to commercial Pt/C for oxygen reduction reaction (ORR). More importantly, LC-4-1000 also exhibits comparable activity and superior stability for ORR in acid medium due to its high graphitic N ratio and a direct four electron pathway for ORR. This study develops a cost-effective and highly efficient method to prepare biocarbon catalyst for ORR in fuel cells. (C) 2018 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.
引用
收藏
页码:33 / 42
页数:10
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