乙二醇
双金属片
试剂
催化作用
溴化铵
电化学
电催化剂
化学
甘油
化学工程
酒精氧化
无机化学
材料科学
有机化学
电极
肺表面活性物质
工程类
物理化学
生物化学
作者
Luyao Jiang,Fang-Min Tian,Xiaohong Chen,Xinxin Ren,Jiu‐Ju Feng,Youqiang Yao,Lu Zhang,Ai‐Jun Wang
标识
DOI:10.1016/j.jcis.2023.06.044
摘要
The fabrication of effective and stable electrocatalysts is crucial for practical applications of direct alcohol fuel cells (DAFCs). In this study, bimetallic PdCu nanostars (PdCu NSs) were fabricated by a Cu2+-modulated one-pot wet-chemical method, where cetyltrimethyl ammonium bromide (CTAB) worked as a structure-regulating reagent. The morphology, compositions, crystal structures and formation mechanism of the as-prepared PdCu NSs were investigated by a series of techniques. The unique architectures created abundant active sites, which resulted in a large electrochemical active surface area (9.5 m2 g-1). The PdCu NSs showed negative shifts in the onset potentials and large forward peak current densities by contrast with those of commercial Pd black for the catalytic ethylene glycol oxidation reaction (EGOR) and glycerol oxidation reaction (GOR). It revealed that the PdCu NSs outperformed Pd black in the similar surroundings. This work provides a constructive strategy for fabrication of high-efficiency electrocatalysts for alcohol fuel cells.
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