双功能
聚丙烯腈
析氧
电催化剂
材料科学
碳纤维
纳米纤维
化学工程
碳纳米纤维
静电纺丝
纤维素
过电位
纳米技术
化学
催化作用
电极
电化学
碳纳米管
复合材料
聚合物
有机化学
复合数
物理化学
工程类
作者
Kun Gao,Mengxia Shen,Chao Duan,Chuanyin Xiong,Lei Dai,Wei Zhao,Wanli Lu,Shujiang Ding,Yonghao Ni
标识
DOI:10.1021/acssuschemeng.1c06040
摘要
A reasonable design of the pore structure of carbon nanofiber-based electrocatalysts can effectively accelerate the slow kinetics of the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). In this study, we report an electrospinning method by adding supramolecular coordination polymers to selected polyacrylonitrile (PAN) and cellulose acetate (CA) spinning systems. Benefiting from the difference in the thermal decomposition temperature of each component during the pyrolysis process, CA was applied as a sacrificial template to prepare a high-efficiency ORR/OER bifunctional electrocatalyst (Co-N@PCNFs-0.2) with directional hollow channels and a hierarchical pore structure. This unique multichannel carbon nanofiber morphology and hierarchical pore structure led to abundant active sites while also boosting the electron transfer rates. Notably, applying Co-N@PCNFs-0.2 as an air electrode to Zn–air batteries results in a large specific discharge capacity of 884 W h kgZn–1 and a maximum power density of 151 mW cm–2.
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