Controllable Electron Distribution Reconstruction of Spinel NiCo2O4 Boosting Glycerol Oxidation at Elevated Current Density

被引:35
|
作者
Luo, Wenshu [1 ,2 ]
Tian, Han [1 ]
Li, Qin [1 ,3 ]
Meng, Ge [1 ,2 ]
Chang, Ziwei [1 ,3 ]
Chen, Chang [1 ,2 ]
Shen, Ruxiang [1 ,2 ]
Yu, Xu [1 ,2 ]
Zhu, Libo [1 ,2 ]
Kong, Fantao [1 ]
Cui, Xiangzhi [1 ,2 ,4 ]
Shi, Jianlin [1 ,2 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, Shanghai 200050, Peoples R China
[2] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
[3] Shanghai Tech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
[4] Univ Chinese Acad Sci, Hangzhou Inst Adv Study, Sch Chem & Mat Sci, Hangzhou 310024, Peoples R China
基金
中国国家自然科学基金;
关键词
bimetallic spinel oxide; coupling electrolysis; glycerol oxidation reaction; oxygen vacancies; structural evolution; HYDROGEN; DIHYDROXYACETONE; ELECTROOXIDATION; RAMAN; ACID; CO2;
D O I
10.1002/adfm.202306995
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrocatalytic glycerol oxidation reaction (GOR) is an effective way to convert biomass byproduct to high value-added chemicals, which; however, suffers from the low oxidation activity and conversion ratio of the presently available catalysts. Herein, the NiCo2O4/NF bimetallic oxide nanoarray is controllably fabricated by Ni substituting for octahedral Co3+ in Co3O4, which exhibits excellent GOR catalytic activity at elevated current densities (E-300 = 1.42 V, E-600 = 1.62 V) and overall Faradaic efficiency of 97.5% at 1.42 V (FEformic acid = 89.9% and FEglycolic acid = 7.62%). The high performance is attributed to the structure evolution including the rapid generation of Ni-III-OOH and Co-III-OOH active species, the optimized intermediates adsorption, and the accelerated electron transfer owing to the Ni introduction, which are evidenced by the operando spectroscopy measurements and density functional theory calculations, respectively. The GOR/hydrogen evolution coupled two-electrode electrolytic cell voltage is approximate to 299 mV lower than that of the water splitting at 50 mA cm(-2). More importantly, compared to conventional water splitting, this electrolyzer is stable for over 200 h at 1.75 V, reducing energy consumption by 16.9% and obtaining high value-added products at the anode concurrently.
引用
收藏
页数:13
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