纳米片
双功能
催化作用
阳极
燃料电池
材料科学
甲醇
电催化剂
氧化还原
阴极
氧还原反应
化学工程
纳米技术
化学
电化学
冶金
物理化学
电极
工程类
有机化学
作者
Lingzheng Bu,Chongyang Tang,Qi Shao,Xing Zhu,Xiaoqing Huang
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2018-04-17
卷期号:8 (5): 4569-4575
被引量:119
标识
DOI:10.1021/acscatal.8b00455
摘要
Even though extensive efforts have been devoted to pursue promising electrocatalysts, the design of high-efficiency and low-cost electrocatalysts continues to be a formidable challenge for commercializing electrochemical energy technologies. Herein, we report the successful creation of a class of three-dimensional ordered Pd3Pb nanosheet assemblies (NSAs) via a wet-chemical approach. Such controlled nanostructures with ordered phase and highly open structure exhibit enhanced electrochemical activity and durability for both the anodic methanol oxidation reaction (MOR) and cathodic oxygen reduction reaction (ORR). In particular, the ordered Pd3Pb NSAs show ORR mass and specific activities of 0.697 A mgPd–1 and 0.989 mA cm–2 at 0.90 V versusthe reversible hydrogen electrode (RHE), which are 8.3 (10.9) and 7.5 (6.4) times higher than those of the commercial Pt/C (Pd/C), respectively, making them among the most efficient catalysts ever achieved for Pd-based ORR catalysts to date. In addition, the ordered Pd3Pb NSAs can even sustain at least 20000 potential cycles with limited activity decay and structure change.
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