碳纳米纤维
催化作用
甲醇
材料科学
氧还原反应
氧还原
碳纳米管
碳纤维
合金
燃料电池
甲醇燃料
氧气
纳米纤维
纳米技术
化学工程
电化学
化学
有机化学
电极
冶金
复合材料
物理化学
复合数
工程类
作者
Le Wang,Shiquan Guo,Shuyan Yu,Tianjiao Shi,Fei Chen,Man Guo,Chong Zhang,Congju Li
标识
DOI:10.1002/ente.202301702
摘要
The slow oxygen reduction kinetics of direct methanol fuel cell (DMFCs) are one of the limiting factors affecting its application. Therefore, exploring nonprecious catalysts with high activity and methanol resistance is urgently needed. Herein, zeolitic imidazolate framework‐8 particles are first blended with different proportions of metal salts (Ni as well as Co) and further electrospun to obtain a nanofiber precursor. After pyrolysis treatment, a composite catalyst (CoNi@N‐CNFs) with a highly dispersed CoNi alloy phase supported by porous N‐doped carbon nanofiber and carbon nanotube is prepared. The surface electronic structure can be reasonably adjusted by optimizing the doping ratio of Ni and Co. The CoNi@N‐CNFs shows high oxygen reduction activity and methanol resistance. Half‐wave potential and the onset potential of Co 1 Ni 1 @N‐CNFs (Co: Ni mole ratio = 1:1) are 0.79 and 0.87 V. Additionally, Co 1 Ni 1 @N‐CNF‐modified DMFC endows a high power density (24.07 mW cm −2 ), which is close to Pt/C‐based DMFC (27.59 mW cm −2 ). Rich active sites, large specific surface area, and synergy between CoNi alloy and N configuration of CoNi@N‐CNFs effectively accelerate electron transfer, resulting in the superior catalytic activity. This work provides a new strategy to design effective 1D oxygen reduction reaction catalysts in fuel cells.
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