双金属银铜三聚氰胺配合物的CO2电还原C2产物

Munzir H. Suliman , Muhammad Usman , Husain Al Naji , Maryam Abdinejad , Naimat Ullah , Aasif Helal , Mahmoud M. Abdelnaby , Guillermo Díaz-Sainz , Gabriele Centi
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引用次数: 0

摘要

双金属ag - cu -三聚氰胺分子配合物的纳米立方晶体最初被开发为有效的电催化剂,用于二氧化碳选择性还原成多碳产品,特别是乙烯和乙醇。含有10 wt.% Ag的双金属配合物在h型和流动电池中均表现出最高的电还原CO2性能。C2产品的法拉第效率为70%,其中40%为乙醇,其余为乙烯。这些结果是在阴极电位为-1.0 V vs可逆氢电极(RHE)时获得的,流动电池中的总电流密度为-50 mA·cm-2,比h电池中的电流密度高5倍。配合物中没有Ag,只检测到C1产物(CO和甲酸)。流动电池的使用,除了更高的电流密度外,还增强了C2的形成,特别是乙烯,这在h型电池实验中是不存在的。这些新型电催化剂也表现出稳定的性能,并提供了Ag和Cu串联协同作用的机理指示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

CO2 electroreduction to C2 products on bimetallic silver copper melamine complexes

CO2 electroreduction to C2 products on bimetallic silver copper melamine complexes
Nanocube crystals of bimetallic Ag-Cu-Melamine molecular complexes have been originally developed as effective electrocatalysts for the CO2 selective reduction to multicarbon products, particularly ethylene and ethanol. The bimetallic complex, containing 10 wt.% Ag demonstrates the highest performance in electro-reduction of CO2 in both H-type and flow cells. It achieves a Faradaic efficiency of 70 % for C2 products, with 40 % attributed to ethanol and the remaining to ethylene. These results are obtained at a cathode potential of -1.0 V vs reversible hydrogen electrode (RHE) with a total current density of -50 mA·cm-2 in the flow cell, five times higher current densities than the current densities in the H-Cell. Without Ag in the complex, only C1 products (CO and formic acid) are detected. The use of the flow cell, in addition to higher current densities, enhances C2 formation, especially ethylene, which is absent in H-type cell experiments. These novel electrocatalysts also exhibit stable performances and provide mechanistic indications of the roles of Ag and tandem cooperation with Cu.
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