材料科学
催化作用
化学工程
纳米颗粒
碳纤维
碳纳米纤维
电化学
合金
可逆氢电极
静电纺丝
多孔性
电催化剂
纳米技术
无机化学
电极
化学
碳纳米管
复合材料
工作电极
有机化学
工程类
物理化学
复合数
聚合物
作者
Lei Zhao,Jinxia Jiang,Shuhao Xiao,Zhao Li,Junjie Wang,Xinxin Wei,Qingquan Kong,Jun Song Chen,Rui Wu
标识
DOI:10.1016/j.nanoms.2022.04.001
摘要
The oxygen reduction reaction (ORR) electrocatalytic activity of Pt-based catalysts can be significantly improved by supporting Pt and its alloy nanoparticles (NPs) on a porous carbon support with large surface area. However, such catalysts are often obtained by constructing porous carbon support followed by depositing Pt and its alloy NPs inside the pores, in which the migration and agglomeration of Pt NPs are inevitable under harsh operating conditions owing to the relatively weak interaction between NPs and carbon support. Here we develop a facile electrospinning strategy to in-situ prepare small-sized PtZn NPs supported on porous nitrogen-doped carbon nanofibers. Electrochemical results demonstrate that the as-prepared PtZn alloy catalyst exhibits excellent initial ORR activity with a half-wave potential (E1/2) of 0.911 V versus reversible hydrogen electrode (vs. RHE) and enhanced durability with only decreasing 11 mV after 30,000 potential cycles, compared to a more significant drop of 24 mV in E1/2 of Pt/C catalysts (after 10,000 potential cycling). Such a desirable performance is ascribed to the created triple-phase reaction boundary assisted by the evaporation of Zn and strengthened interaction between nanoparticles and the carbon support, inhibiting the migration and aggregation of NPs during the ORR.
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