过电位
格式化
电解
电化学
制氢
无机化学
本体电解
阳极
电催化剂
氢
傅里叶变换红外光谱
材料科学
化学
化学工程
循环伏安法
电极
催化作用
有机化学
电解质
物理化学
工程类
作者
Dong Lin,Guanru Chang,Yi Feng,Xian-Zhi Yao,Xin‐Yao Yu
出处
期刊:Rare Metals
[Springer Nature]
日期:2022-01-17
卷期号:41 (5): 1583-1594
被引量:47
标识
DOI:10.1007/s12598-021-01881-3
摘要
Energy-saving glycerol electrolysis with lower potential than water spitting endows a promising way for the concurrent production of value-added formate and high-purity hydrogen. However, there is still lack of efficient electrocatalysts at both anode and cathode for glycerol electrolysis. Herein, we report the activation of Ni site in NiV layered double hydroxide (LDH) by electrochemical and N2/H2 plasma regulations for boosting the activity of glycerol oxidation reaction (GOR) and hydrogen evolution reaction (HER), respectively. Specifically, boosted GOR performance with a low overpotential (1.23 V at 10 mA·cm−2) and a high Faradic efficiency (94%) is demonstrated by electrochemically regulated NiV LDH (E-NiV LDH) with elevated valence state of Ni site. In situ Raman spectrum reveals the generation of Ni(III) species by electrochemical regulation, and the highly active Ni(III) can be regenerated with the process of electrochemical oxidation. Additionally, the possible reaction pathway is speculated based on the in situ Fourier transform infrared spectroscopy (FTIR) and high-performance liquid chromatography results. The plasma-regulated NiV LDH (P-NiV LDH) with lower valence state of Ni site exhibits outstanding HER activity, displaying a low overpotential of 45 mV to deliver 10 mA·cm−2. When employing E-NiV LDH and P-NiV LDH as anode and cathode electrocatalyst, respectively, the assembled electrolyzer merely needs 1.25 V to achieve 10 mA·cm−2 for simultaneous production of formate and hydrogen, demonstrating remarkable 320 mV of lower potential than water electrolysis.Graphic abstract
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