电催化剂
析氧
电解
电化学
阳极
制氢
化学
环境友好型
无机化学
电流密度
化学工程
吉布斯自由能
分解水
煅烧
材料科学
催化作用
电极
物理化学
电解质
热力学
有机化学
生态学
生物
物理
量子力学
工程类
光催化
作者
Ping Li,Yanhong Wang,Xiaoqiang Du,Xiaoshuang Zhang
出处
期刊:Dalton Transactions
[The Royal Society of Chemistry]
日期:2023-01-01
卷期号:52 (30): 10499-10506
被引量:66
摘要
Water electrolysis is relatively an environmentally friendly hydrogen production technology, but due to the slow transfer of four electrons in the anodic oxidation reaction, it needs a theoretical voltage of up to 1.23 V. Therefore, in this experiment, a series of transition metal oxides, ACo2O4 (A = Fe, Cu, Zn, Ni), was synthesized on Ni foam current collectors by a hydrothermal and calcination method, and the material was applied in urea electrolysis to produce hydrogen. What is noteworthy is that the CuCo2O4 electrode has a unique flower-like nanoneedle structure, and has a larger electrochemical active area, more reactive active sites, and a faster charge transfer rate. In 1.0 M KOH and 0.5 M urea solution, CuCo2O4 provides a potential of only 1.268 V at a current density of 10 mA cm-2 during the urea oxidation reaction (UOR), while in 1.0 M KOH solution, with the same current density, the oxygen evolution reaction (OER) is required to provide a potential of 1.53 V, indicating that the UOR can effectively replace the OER. Density functional theory calculations show that the CuCo2O4 material exhibits Gibbs free energy of the hydrogen closest to zero, thus promoting the electrochemistry performance of the electrode. In a cell composed of CuCo2O4//CuCo2O4, the current density of 10 mA cm-2 can be achieved by providing a potential of only 1.509 V. This work offers a novel scheme for reducing energy consumption of the OER and improving catalytic performance of the UOR.
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