Iron and nitrogen anchored hierarchical hollow porous carbon microtubes for an electrocatalytic oxygen evolution reaction

被引:12
|
作者
Li, Na [1 ,2 ,3 ]
Qu, Shijie [1 ]
Ma, Jingjing [4 ]
Shen, Wenzhong [1 ]
机构
[1] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Peoples R China
[2] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
[3] Shanxi Coll Technol, Sch Energy Ind, Shuozhou 036000, Peoples R China
[4] Ningxia Univ, State Key Lab High Efficiency Utilizat Coal & Gree, Yinchuan 750021, Peoples R China
基金
中国国家自然科学基金;
关键词
Fe/N-doping; Asphaltene; Cotton; Oxygen evolution reaction; Electrocatalyst; NANOROD ARRAY; EFFICIENT; HYDROGEN; NANOPARTICLES; PERFORMANCE; FE; OXIDATION; CATALYST; SELENIDE;
D O I
10.1016/j.jallcom.2022.166746
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
The development of active nonprecious-metal and heteroatom-doped materials is critical for the oxygen evolution reaction (OER). Herein, asphaltene-derived carbon-coated Fe-and N-doped hierarchical hollow porous carbon microtubes were prepared through feasible freeze-drying and carbonization/activation strategies. Cotton with a fibrous morphology acted as a soft template and carbon precursor, while asphaltene with easy graphitization properties was utilized to stabilize the structure of microtubes and accelerate the charge conductivity. Meanwhile, Fe-and N-doping changed the electronic structure of carbon and increased the number of active sites. In particular, the optimum sample displayed excellent OER activity with a lower overpotential of 261.4 mV at 10 mA/cm(2) and Tafel slope of 94.60 mV/dec under alkaline conditions. Moreover, the catalyst demonstrated excellent long-term durability with a 10% attenuation rate after continuous operation for 50 h by the chronoamperometry method at a constant potential of 1.5 V. This work provides a strategy for the effective resource utilization of biomass and asphaltene to prepare highly efficient OER electrocatalysts. (C) 2022 Elsevier B.V. All rights reserved.
引用
收藏
页数:15
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