Phase reconstruction of Co3O4 with enriched oxygen vacancies induced by cold plasma for boosting methanol-to-formate electro-oxidation

被引:18
作者
Zhang, Jingsen [1 ]
Hua, Yue [2 ]
Li, Hong [2 ]
Zhang, Xiuling [2 ]
Shi, Chuan [1 ]
Li, Yuxiang [3 ]
Di, Lanbo [2 ,4 ,5 ]
Wang, Zongyuan [3 ]
机构
[1] Dalian Univ Technol, Sch Chem, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] Dalian Univ, Coll Phys Sci & Technol, Dalian 116622, Peoples R China
[3] Shihezi Univ, Sch Chem & Chem Engn, Key Lab Green Proc Chem Engn Xinjiang Bingtuan, Shihezi 832003, Peoples R China
[4] Dalian Univ Technol, State Key Lab Struct Anal Ind Equipment, Dalian 116024, Peoples R China
[5] Dalian Univ Technol, Key Lab Adv Technol Aerosp Vehicles Liaoning Prov, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
Selective methanol oxidation; Oxygen vacancies; Methanol-assisted water electrolysis; Cold plasma; EFFICIENT; HYDROGEN; ELECTROCATALYSTS; CATALYSTS;
D O I
10.1016/j.cej.2023.147288
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Developing high-performance Pt-free electrocatalysts for the electro-oxidation of methanol (MeOH) into highvalue-added formate in alkaline media offers a sustainable avenue for synchronous biomass valorization and MeOH oxidation-assisted hydrogen production. Herein, electrodeposited Co(OH)(2) on Ni foam (NF) was treated by an O-2 cold plasma to obtain oxygen vacancies enriched Co3O4-x/NF-P. The resultant Co3O4-x/NF-P only requires a potential of 1.318 V vs. RHE to upgrade MeOH into formate at 10 mA center dot cm(-2). Characterization and calculation results reveal that oxygen vacancy induced irreversible phase transformation of Co3O4-x/NF-P, facilitating the deprotonation of MeOH, and suppressing further oxidation of HCOO* for selective and efficient formate electrosynthesis. Impressively, a Co3O4-x/NF-P||Co3O4-x/NF-P pair was built to couple the MeOH electrooxidation with H-2 evolution, where it only supplies a cell voltage of 1.540 V at 10 mA center dot cm(-2) and the anodic Faraday efficiency exceeds 95 %. This work clarifies in-depth insight the underlying mechanism of MeOH selective oxidation into formate.
引用
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页数:9
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