TY - JOUR
T1 - Controllable Electron Distribution Reconstruction of Spinel NiCo2O4 Boosting Glycerol Oxidation at Elevated Current Density
AU - Luo, Wenshu
AU - Tian, Han
AU - Li, Qin
AU - Meng, Ge
AU - Chang, Ziwei
AU - Chen, Chang
AU - Shen, Ruxiang
AU - Yu, Xu
AU - Zhu, Libo
AU - Kong, Fantao
AU - Cui, Xiangzhi
AU - Shi, Jianlin
N1 - Publisher Copyright:
© 2023 Wiley-VCH GmbH.
PY - 2024/1/15
Y1 - 2024/1/15
N2 - 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 (E300 = 1.42 V, E600 = 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 NiIII-OOH and CoIII-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 ≈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.
AB - 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 (E300 = 1.42 V, E600 = 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 NiIII-OOH and CoIII-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 ≈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.
KW - bimetallic spinel oxide
KW - coupling electrolysis
KW - glycerol oxidation reaction
KW - oxygen vacancies
KW - structural evolution
UR - https://www.scopus.com/pages/publications/85173468391
U2 - 10.1002/adfm.202306995
DO - 10.1002/adfm.202306995
M3 - 文章
AN - SCOPUS:85173468391
SN - 1616-301X
VL - 34
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 3
M1 - 2306995
ER -