材料科学
电化学
纳米复合材料
电解质
电池(电)
催化作用
可逆氢电极
铜
阴极
碳纤维
化学工程
选择性
电催化剂
无机化学
电极
纳米技术
工作电极
冶金
物理化学
化学
复合材料
复合数
有机化学
工程类
物理
功率(物理)
量子力学
作者
Mingyue Peng,Suqin Ci,Ping Shao,Pingwei Cai,Zhenhai Wen
标识
DOI:10.1166/jnn.2019.16589
摘要
Exploiting effective electrocatalysts toward electrochemical conversion of CO 2 into valued-added chemicals is highly desirable for achieving the global carbon cycle. In this work, we report the synthesis of Cu 3 P/C nanocomposites by phosphatizing the copper-based metal organic framework precursor. Systematic electrochemical characterizations demonstrate the Cu 3 P/C nanocomposites hold high activity and favorable selectivity towards CO 2 reduction reaction (CO 2 RR) into CO, as manifested by an onset potential is about −0.25 V versus reversible hydrogen electrode (RHE) and a faradic efficiency (FE) of 47% for CO production at a relatively low potential (−0.3 V). The attractive catalytic properties might be attributed to the synergistic effect of cooper and phosphorus elements, as well as the unique structure of Cu 3 P. Furthermore, we propose an asymmetrical-electrolyte Zn–CO 2 battery with the Cu 3 P/C as cathode catalyst, demonstrating a decent performance with an open-circuit voltage of 1.5 V and a power density of 2.6 mW cm −2 (at 10 mA cm −2 ).
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