材料科学
催化作用
X射线光电子能谱
物理吸附
纳米棒
化学工程
复合数
纳米颗粒
电子转移
电化学
吸附
解吸
透射电子显微镜
纳米技术
光化学
物理化学
复合材料
电极
化学
有机化学
工程类
作者
Meiling Wang,Dong Li,Yuzhu Tian,Jin Zhao,Zhizhu Yue,Xiaoxia Wang,Xiaofang Ma,Jinjin Wang,Tianjun Hu,Jianfeng Jia,Hai‐Shun Wu
标识
DOI:10.1021/acsami.1c14320
摘要
The interfacial interaction including chemical bonding or electron transfer and even physisorption in composite electrocatalysts has a considerable effect on electrocatalytic oxidation reaction. Herein, we report a tremendously enhanced catalytic activity and excellent durability for the ethanol electro-oxidation reaction in NiMoO4-C-supported Pd composites (Pd/NiMoO4-C) compared to the commercial Pd/C (10%) catalyst. The X-ray powder diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy measurements disclose that the strong electron transfer between NiMoO4 nanorods and Pd nanoparticles likely induces the formation of more electrochemical active centers and improves the adsorption-desorption capacity of reactants and corresponding intermediates. In addition, the Pd/NiMoO4-C composite exhibits superior specific activity for ethanol oxidation compared to the Pd/NiMoO4 catalyst with physically incorporated carbon black, which further reveals that the stronger anchoring effect between Pd and C and higher electrical conductivity in Pd/NiMoO4-C composites are also conducive to promote the ethanol oxidation reaction. These discoveries provide an effective and simple method for the design of advanced electrocatalysts and provide more insights into optimizing the electronic interaction between the catalyst and support in general.
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