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用于硝酸盐和甘油电催化转化的铜-银-钌异质结构的理性工程

Rational Engineering on Copper-Silver-Ruthenium Heterostructures for the Electrocatalytic Conversion of Nitrate and Glycerol.

作者信息

Wang Qi, Shen Yi

机构信息

School of Food Science and Engineering, South China University of Technology, Guangzhou, 510640, China.

China-Singapore International Joint Research Institute, Guangzhou Knowledge City, Guangzhou, 510663, China.

出版信息

Small. 2025 Aug;21(34):e2505948. doi: 10.1002/smll.202505948. Epub 2025 Jul 1.

DOI:10.1002/smll.202505948
PMID:40590175
Abstract

Coupling nitrate reduction reaction (NORR) with glycerol oxidation reaction (GOR) establishes a sustainable "C─N co-conversion" electrolysis system to generate ammonium formate. Unfortunately, the rational design of high-performance bifunctional electrocatalysts remains challenging. Herein, we developed a 3D Ag/Ru-decorated CuO/Cu(OH) heterostructures supported by copper foams via interface engineering. The optimal catalyst exhibited outstanding NORR and GOR performance, achieving Faradaic efficiency (FE) of 97.3% and yield of 9.85 mg h cm at -0.5 V vs. RHE for NH synthesis, and FE of 82.6% and yield of 90.31 mg h cm at 1.55 V vs. RHE for formate production. Mechanistic studies revealed that the decoration of Ag and Ru atoms led to electron redistribution around the copper sites, promoting proton-coupled electron transfer and optimizing the adsorption of the reactants/intermediates. Notably, on the basis of the as-prepared bifunctional electrode, a "NORR || GOR" electrolyzer was constructed, which achieved simultaneous output of NH and formate with a current density of 100 mA cm at only 1.48 V. The performance of the electrolyzer was further demonstrated using simulated nitrate pollutants and crude glycerol as feedstock, yielding 20.9 g of ammonium formate via a 4-h electrolysis. This work demonstrates a sustainable pathway for the synthesis of high-value-added ammonium formate by constructing an efficient bifunctional electrocatalyst through rational interfacial engineering.

摘要

将硝酸盐还原反应(NORR)与甘油氧化反应(GOR)耦合,建立了一个可持续的“C─N共转化”电解系统以生成甲酸铵。不幸的是,高性能双功能电催化剂的合理设计仍然具有挑战性。在此,我们通过界面工程开发了一种由泡沫铜支撑的3D Ag/Ru修饰的CuO/Cu(OH)异质结构。最佳催化剂表现出出色的NORR和GOR性能,在相对于可逆氢电极(RHE)为-0.5 V时,NH合成的法拉第效率(FE)为97.3%,产率为9.85 mg h cm,在相对于RHE为1.55 V时,甲酸生产的FE为82.6%,产率为90.31 mg h cm。机理研究表明,Ag和Ru原子的修饰导致铜位点周围的电子重新分布,促进质子耦合电子转移并优化反应物/中间体的吸附。值得注意的是,基于所制备的双功能电极,构建了一个“NORR || GOR”电解槽,其在仅1.48 V的电压下实现了NH和甲酸的同时输出,电流密度为100 mA cm。使用模拟硝酸盐污染物和粗甘油作为原料进一步证明了该电解槽的性能,通过4小时的电解产生了20.9 g甲酸铵。这项工作通过合理的界面工程构建高效双功能电催化剂,展示了一条合成高附加值甲酸铵的可持续途径。

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