钴
贵金属
催化作用
锌
氢氧化物
电解质
阳极
无机化学
金属
电化学
层状双氢氧化物
化学
材料科学
化学工程
电极
冶金
有机化学
物理化学
工程类
作者
Hui Yang,Tingting Guo,Qin Kang,Qingyun Liu
标识
DOI:10.1021/acs.jpcc.1c06449
摘要
Layered double hydroxides (LDHs) have been known as highly desired anode materials in the alkaline electrolyte. With regard to non-noble metal electrocatalysts, the interlayer spacing of LDHs has important influences on the electrocatalytic activity toward ethanol oxidation. Herein, ZnCo-LDHs with different interlayer spacing controlled by different interlayer anions (NO3–, Cl–, and CH3COO–) are used as effective non-noble metal electrocatalysts for the ethanol oxidation reaction (EOR). The interlayer spacing of three non-noble metal electrocatalysts follows the order: ZnCo-LDH-CH3COO– (0.763 nm) > ZnCo-LDH-Cl– (0.733 nm) > ZnCo-LDH-NO3– (0.719 nm). ZnCo-LDH-CH3COO– exhibits the highest mass activity (345.4 mA mg–1) for the EOR, which is 1.22 and 1.37 times higher than that of ZnCo-LDH-Cl– (283.8 mA mg–1) and ZnCo-LDH-NO3– (252.8 mA mg–1), respectively, attributed to the enlarged interlayer space. This work proposes a potential mechanism of the catalytic process toward the EOR, which may provide a new idea to design non-noble metal electrocatalysts with high catalytic activity in direct ethanol fuel cells (DEFCs).
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