Tianci Xiang, Ting Liu, Ting Ouyang, Shenlong Zhao, Zhao-Qing Liu
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引用次数: 0
摘要
开发稳定高效的低成本电催化剂有利于实现二氧化碳的工业化。金属/氧化物异质界面之间的协同效应可以促进 CO2 的转化。本研究合成了在锌板中具有部分还原金属/氧化物异质界面的 Cu2O/ZnO 异质结构(CZZ),用于不同阳离子溶液(K+ 和 Cs+)中的 CO2 电还原。物理表征用于证明 Cu2O/ZnO 的异质结和金属/氧化物的异质界面;电化学测试用于说明在不同阳离子溶液中 CO2 对 CO 的选择性的提高。在 K+ 溶液中,以 CZZ 为催化剂的一氧化碳法拉第效率达到 70.9%(一氧化碳的电流密度为 -3.77 mA cm-2,稳定性为 24 小时);在 Cs+ 溶液中,一氧化碳的法拉第效率为 55.2%(-2.47 mA cm-2,稳定性为 21 小时)。此外,还利用原位技术阐明了在 K+ 和 Cs+ 溶液中将 CO2 转化为 CO 的可能反应机制。
Tuning the selectivity of CO2 conversion to CO on partially reduced Cu2O/ZnO heterogeneous interface
The development of stable and efficient low-cost electrocatalysts is conducive to the industrialization of CO2. The synergy effect between the heterogeneous interface of metal/oxide can promote the conversion of CO2. In this work, Cu2O/ZnO heterostructures with partially reduced metal/oxide heterointerfaces in Zn plates (CZZ) have been synthesized for CO2 electroreduction in different cationic solutions (K+ and Cs+). Physical characterizations were used to demonstrate the heterojunction of Cu2O/ZnO and the heterointerfaces of metal/oxide; electrochemical tests were used to illustrate the enhancement of the selectivity of CO2 to CO in different cationic solutions. Faraday efficiency for CO with CZZ as catalyst reaches 70.9% in K+ solution (current density for CO −3.77 mA cm−2 and stability 24 h), and the Faraday efficiency for CO is 55.2% in Cs+ solution (−2.47 mA cm−2 and 21 h). In addition, in situ techniques are used to elucidate possible reaction mechanisms for the conversion of CO2 to CO in K+ and Cs+ solutions.