双金属片
纳米材料基催化剂
石墨烯
材料科学
阳极
催化作用
纳米材料
纳米结构
纳米技术
甲酸
电催化剂
氧化物
化学工程
电极
电化学
纳米颗粒
金属
化学
有机化学
物理化学
冶金
工程类
作者
Hui Xu,Bo Yan,Shumin Li,Jin Wang,Caiqin Wang,Jun Guo,Yukou Du
标识
DOI:10.1021/acssuschemeng.7b02935
摘要
The lack of cost-efficient catalysts for the electrooxidation of fuel in the anodic electrode has been a major barrier for the practical large-scale commercial application and hence needs to be optimized. Tuning the morphologies and structures of Pt-based bimetallic nanostructure plays a key role in controlling its interaction with reactants, and thus affects its electrocatalytic efficiency. In this regard, endowing the nanocatalysts with both of high surface active areas and controlled facets through modifying their surface compositions and morphologies can significantly enhance their electrocatalytic performances. To this end, we herein demonstrate a facile wet-chemical method to successfully construct the N-doped graphene supported hollow PtAg nanodendrites under the assistance of ultrasonic treatment. More importantly, the resulting N-doped graphene supported hollow PtAg nanodendrites show high performance for the electrooxidation of formic acid with the mass and specific activities of 1258.5 mA mg–1 and 6.14 mA cm–2, 3.77 and 1.57-fold enhancements than those of commercial Pt/C, respectively. It is believed that the as-prepared nanomaterials can be well-applied to serve as the highly efficient anode electrocatalysts for the commercial application of fuel cells and beyond.
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