材料科学
静电纺丝
双金属片
沸石咪唑盐骨架
纳米颗粒
催化作用
碳化
多孔性
咪唑酯
金属有机骨架
纳米纤维
比表面积
碳纤维
热解
化学工程
纳米技术
电化学
金属
电极
复合材料
聚合物
冶金
有机化学
化学
吸附
物理化学
工程类
扫描电子显微镜
复合数
作者
Chuan‐Ling Zhang,Bing-Rong Lu,Fu‐Hu Cao,Zhenyu Wu,Wang Zhang,Huai‐Ping Cong,Shu‐Hong Yu
出处
期刊:Nano Energy
[Elsevier]
日期:2018-10-30
卷期号:55: 226-233
被引量:167
标识
DOI:10.1016/j.nanoen.2018.10.029
摘要
The rational design of assembled metal-organic frameworks (MOFs) derived carbon materials with rapid mass transport properties and stable porous structure is highly desirable yet a great challenge to date. In this work, MOFs-derived Co/N-doped porous carbon fibers with high electrochemical performance can be prepared simply by carbonizing MOFs nanofibers, which were fabricated by the electrospinning-assisted assembly of bimetallic zeolitic imidazolate framework nanoparticles (BMZIFs) based on ZIF-8 and ZIF-67. The effects of assembly and Zn/Co ratios on the oxygen reduction reaction (ORR) performances of the electrospun fibers derivatives were systematically studied. As expected, compared to the non-electrospun samples, such doped porous carbon nanofibers exhibited excellent electrocatalytic performances without any etching or other activating processes, and the sample with the molar ratio of Zn: Co= 5:1 even showed comparable ORR performance with the commercial Pt/C catalyst under the same conditions. The high catalytic performances root in the dense assembly of MOFs within the electrospun fibers, which was beneficial to endow the derivatives with the high surface area as well as uniform N and Co doping. Besides, the one-dimensional porous structure significantly promoted the mass transfer and exposure of active sites.
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