材料科学
法拉第效率
催化作用
甲酸
阳极
双金属片
电解质
分解水
电解
尖晶石
化学工程
电流密度
电子转移
氧化物
无机化学
电极
物理化学
化学
冶金
光催化
有机化学
金属
物理
量子力学
工程类
作者
Wenshu Luo,Han Tian,Qin Li,Ge Meng,Ziwei Chang,Chang Chen,Ruxiang Shen,Xu Yu,Libo Zhu,Fantao Kong,Xiangzhi Cui,Jianlin Shi
标识
DOI:10.1002/adfm.202306995
摘要
Abstract 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 NiCo 2 O 4 /NF bimetallic oxide nanoarray is controllably fabricated by Ni substituting for octahedral Co 3+ in Co 3 O 4 , 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 (FE formic acid = 89.9% and FE glycolic 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 ≈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.
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