In situ self-template synthesis of cobalt/nitrogen-doped nanocarbons with controllable shapes for oxygen reduction reaction and supercapacitors

被引:14
作者
Liu, Yujing [1 ]
Yu, Liangmin [1 ,2 ]
Jiang, Xiaohui [1 ]
Li, Xia [1 ]
Yan, Xuefeng [1 ]
机构
[1] Ocean Univ China, Minist Educ, Key Lab Marine Chem Theory & Technol, Qingdao 266100, Shandong, Peoples R China
[2] Pilot Natl Lab Marine Sci & Technol, Open Studio Marine Corros & Protect, Qingdao, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon materials; Co; N-doped nanocarbon; in situ self-template method; oxygen reduction reaction; supercapacitors; LITHIUM-ION BATTERIES; CARBON NANOTUBES; POROUS CARBON; DISPERSED COO; ACTIVE-SITES; EVOLUTION; ELECTROCATALYST; NANOSHEETS; PERFORMANCE; ULTRATHIN;
D O I
10.1002/er.4546
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Shape-controlled Co/N-doped nanocarbons derived from polyacrylonitrile (PAN) were synthesized by a one-step in situ self-template method followed by a pyrolysis procedure. This is the first study to tune the nanostructure of Co/N-doped carbon materials by providing a metal salt as the template and additive. The moderate surface area (699.47 m(2) g(-1)), highly developed pore structure, homogenous Co and N doping and designed "egg-box" structure impart Co/N-doped cross-linked porous carbon (Co/N-CLPC) with excellent electrocatalytic activity and capacitive performance. This material displayed an onset potential of 0.805 V (vs RHE), a current density of -5.102 mA cm(-2), excellent long-term durability, and good resistance to methanol crossover, which are comparable with the characteristics of a commercial 20-wt% Pt/C catalyst. In addition, Co/N-CLPC demonstrated a high specific capacitance of 313 F g(-1) at 0.5 A g(-1), notable rate performance of 63% at 50 A g(-1), and good cycling stability of 104.8% retention after 5000 cycles when used as a supercapacitor electrode. This method enables new routes to obtaining Co/N-doped nanocarbons with shape-controlled structures for energy conversion and storage applications.
引用
收藏
页码:4217 / 4228
页数:12
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