Highly active cobalt oxide-palladium nanohybrid catalyst enables selective electrocatalytic synthesis of glycolic acid

被引:0
|
作者
Jiang, Xiaoli [1 ]
Wang, Penglei [1 ]
Zhang, Yagang [1 ]
Zhao, Lin [1 ]
Yang, Yuanteng [1 ]
Liu, Yang [1 ]
机构
[1] Univ Elect Sci & Technol China, Sch Mat & Energy, Chengdu 611731, Peoples R China
基金
中国国家自然科学基金;
关键词
Glycolic acid; Electrocatalyst; Ethylene glycol oxidation reaction; D -band center; Electro-reforming; INITIO MOLECULAR-DYNAMICS; OXIDATION; CARBON; NANOPARTICLES; PLASTICS; WASTE; SITES;
D O I
10.1016/j.cej.2024.157962
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Glycolic acid is a unique value-added chemical, while its large-scale production is limited by harsh synthesis conditions and poor selectivity. Herein, we have ingeniously constructed a highly active cobalt oxide-supported palladium electrocatalyst on nickel foam (Pd-Co3O4/NF) for ethylene glycol oxidation to glycolic acid with a high Faradaic efficiency (93.1 %) at ultra-low potential (0.9 V vs. RHE). In situ Fourier transform infrared spectroscopy revealed the pathway of ethylene glycol oxidation reaction (EGOR). The theoretical results reveal that Co3O4/NF can effectively promote the formation of *OH and weaken the adsorption of toxic *CO intermediates on Pd-Co3O4/NF. And the downshifted d-band center of Pd-Co3O4/NF is inducive to facilitate the desorption of GA from the Pd surface, prevents the excessive oxidation thus improving the selectivity. Moreover, Pd-Co3O4/NF exhibits considerable anode current density with respect to electro-reforming polyethylene terephthalate (PET)-derived EG oxidation, accompanied by the generation of green hydrogen at the cathode. This work puts forward an innovative approach for catalyst construction toward EGOR and highlights the strategy of electro-upcycling of PET.
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页数:9
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