电催化剂
双功能
催化作用
电化学
分解水
尿素
镍
化学工程
电解质
材料科学
化学
无机化学
电极
物理化学
冶金
有机化学
工程类
光催化
作者
Xinyu Li,Yanhong Wang,Xiaoqiang Du,Xiaoshuang Zhang
标识
DOI:10.1016/j.ijhydene.2022.11.202
摘要
Developing highly efficient bifunctional urea oxidation reaction (UOR) and hydrogen evolution reaction (HER) catalysts for urea splitting to hydrogen are one of the strategies to cope with the energy crisis. Here, a series of CrxPy-a/ComPn-b composites were synthesized on Ni foam through hydrothermal and low-temperature phosphorization process for the first time. It is worth noting that CrxPy-1/ComPn[email protected] exhibited excellent UOR performance (1.331 V at 100 mA cm−2) and HER performance (0.299 V at 100 mA cm−2) in an electrolyte of 1 M KOH and 0.5 M urea due to the synergistic effect of Cr–Co. The CrxPy-1/ComPn[email protected]||CrxPy-1/ComPn[email protected] two-electrode system call for only 1.52 V to provide current density of 10 mA cm−2, which is one of the best electrochemistry performances reported up to now. Experimental analysis show that the promoted electrochemistry performances is assigned to faster charge transfer rate, the exposure of more reaction site and better properties of metals. Density Functional theory (DFT) results demonstrate that the presence of the ComPn material accelerates the kinetics of hydrogen production and the CrxPy material improves the properties of metals for the electrode. The work provides a new idea to develop the environmentally friendly and low cost overall urea splitting catalyst with transition metals instead of noble metals.
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