键裂
催化作用
甲醇
材料科学
吸附
阳极
乙醇
动力学
劈理(地质)
选择性
化学工程
纳米线
直接乙醇燃料电池
开路电压
无机化学
电极
纳米技术
化学
物理化学
有机化学
电压
复合材料
量子力学
工程类
断裂(地质)
物理
作者
Hongcheng Peng,Jun Ren,Yuchao Wang,Yu Xiong,Qichen Wang,Qian Li,Xin Zhao,Longsheng Zhan,Lirong Zheng,Yougen Tang,Yongpeng Lei
出处
期刊:Nano Energy
[Elsevier]
日期:2021-07-01
卷期号:88: 106307-106307
被引量:117
标识
DOI:10.1016/j.nanoen.2021.106307
摘要
The high-efficient C-C bond cleavage is the key for ethanol electrooxidation. In this work, PtCu/Cu2−xSe nanowires (NWs) with abundant surface defects were constructed and exhibited remarkable activity of 5.03 A mg−1Pt as well as 5.29 A mg−1Pt for ethanol oxidation and methanol oxidation, respectively, which are 5.0 and 5.3 fold of commercial Pt/C. ex situ, in situ experiments and calculation results reveal that the formation of PtCu alloys lowered the d-band level to promote the adsorption of hydroxyl species. The abundant defects created high density of low-coordinated atoms to boost the reaction kinetics. Thus, PtCu/Cu2−xSe NWs displayed enhanced C-C bond cleavage ability and high selectivity for C1 products (CO2). The assembled direct ethanol fuel cells (DEFCs) with PtCu/Cu2−xSe NWs as anode provided an open-circuit voltage (OCV) of 0.773 V and a peak power density of 7.8 mW cm−2. This work not only give us a potential catalyst for C-C bond cleavage, but also provides an effective strategy to enhance the electrocatalytic activity of ethanol/methanol oxidation.
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