Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center, Russian Academy of Sciences, 420088 Kazan, Russia.
Department of Nanotechnology in Electronics, Kazan National Research Technical University Named after A.N. Tupolev-KAI, 420111 Kazan, Russia.
Molecules. 2021 Sep 11;26(18):5524. doi: 10.3390/molecules26185524.
A selective noble-metal-free molecular catalyst has emerged as a fruitful approach in the quest for designing efficient and stable catalytic materials for CO reduction. In this work, we report that a sodium pectate complex of copper (PG-NaCu) proved to be highly active in the electrocatalytic conversion of CO to CH in water. Stability and selectivity of conversion of CO to CH as a product at a glassy carbon electrode were discovered. The copper complex PG-NaCu was synthesized and characterized by physicochemical methods. The electrochemical CO reduction reaction (CORR) proceeds at -1.5 V vs. Ag/AgCl at ~10 mA/cm current densities in the presence of the catalyst. The current density decreases by less than 20% within 12 h of electrolysis (the main decrease occurs in the first 3 h of electrolysis in the presence of CO). This copper pectate complex (PG-NaCu) combines the advantages of heterogeneous and homogeneous catalysts, the stability of heterogeneous solid materials and the performance (high activity and selectivity) of molecular catalysts.
一种选择性的无贵金属分子催化剂在设计高效稳定的 CO 还原催化材料的研究中成为一种很有前途的方法。在这项工作中,我们报告了一种铜的果胶酸钠配合物(PG-NaCu)在水中电催化 CO 转化为 CH 时表现出很高的活性。我们发现了在玻碳电极上 CO 转化为 CH 作为产物的稳定性和选择性。通过物理化学方法合成并表征了铜配合物 PG-NaCu。在催化剂存在的情况下,电化学 CO 还原反应(CORR)在-1.5 V 相对于 Ag/AgCl 进行,在~10 mA/cm 的电流密度下进行。在 12 小时的电解过程中,电流密度下降不到 20%(主要的下降发生在有 CO 存在的前 3 小时的电解过程中)。这种铜果胶酸盐配合物(PG-NaCu)结合了多相和均相催化剂的优点、多相固体材料的稳定性以及分子催化剂的性能(高活性和选择性)。