Authors

Wenjing Lv, Faculty of Chemical Engineering, Yunnan Provincial Key Laboratory of Energy Saving in Phosphorus Chemical, Engineering and New Phosphorus Materials, Kunming University of Science and Technology, Kunming 650500, Yunnan, China.
Xiaoman Tang, Faculty of Chemical Engineering, Yunnan Provincial Key Laboratory of Energy Saving in Phosphorus Chemical, Engineering and New Phosphorus Materials, Kunming University of Science and Technology, Kunming 650500, Yunnan, China.
Xuetong Wang, Faculty of Chemical Engineering, Yunnan Provincial Key Laboratory of Energy Saving in Phosphorus Chemical, Engineering and New Phosphorus Materials, Kunming University of Science and Technology, Kunming 650500, Yunnan, China.
Wencai Liu, Faculty of Chemical Engineering, Yunnan Provincial Key Laboratory of Energy Saving in Phosphorus Chemical, Engineering and New Phosphorus Materials, Kunming University of Science and Technology, Kunming 650500, Yunnan, China.
Jianwen Zhu, Faculty of Chemical Engineering, Yunnan Provincial Key Laboratory of Energy Saving in Phosphorus Chemical, Engineering and New Phosphorus Materials, Kunming University of Science and Technology, Kunming 650500, Yunnan, China.
Guojing Wang, Faculty of Chemical Engineering, Yunnan Provincial Key Laboratory of Energy Saving in Phosphorus Chemical, Engineering and New Phosphorus Materials, Kunming University of Science and Technology, Kunming 650500, Yunnan, China.
Yuanzhi Zhu, Faculty of Chemical Engineering, Yunnan Provincial Key Laboratory of Energy Saving in Phosphorus Chemical, Engineering and New Phosphorus Materials, Kunming University of Science and Technology, Kunming 650500, Yunnan, China.

Document Type

Article

Corresponding Author(s)

Guojing Wang(gjwang@kust.edu.cn);
Yuanzhi Zhu(yuanzhi_zhu@kust.edu.cn)

Abstract

The conversion of urea-containing wastewater into clean hydrogen energy has gained increasing attention. However, challenges remain, particularly with sluggish catalytic kinetics and limited long-term stability of urea oxidation reaction (UOR). Herein, we report loosely porous CoOOH nano-architecture (CoOOH LPNAs) with hydrophilic surface and abundant oxygen vacancies (Ov) on carbon fiber paper (CFP) by electrochemical reconstruction of the CoP nanoneedles precursor. The resulting three-dimensional electrode exhibits an impressively low potential of 1.38 V at 1000 mA cm−2 and excellent durability for UOR. Furthermore, in an anion exchange membrane (AEM) electrolyzer, it requires only 1.53 V at 1000 mA cm−2 for industrial urea-assisted water splitting and operates stably for 100 h without degradation. Experimental and theoretical investigations reveal that rich oxygen vacancies effectively modulate the electronic structure of the CoOOH while creating unique Co3-triangle sites with Co atoms close together. As a result, the adsorption and desorption processes of reactants and intermediates in UOR are finely tuned, thereby significantly reducing thermodynamic barriers. Additionally, the superhydrophilic self-supported nanoarray structure facilitates rapid gas bubble release, improving the overall efficiency of the reaction and preventing potential catalyst detachment caused by bubble accumulation, thereby improving both catalytic activity and stability at high current densities.

Graphical Abstract

Keywords

CoOOH, electrochemical reconstruction, oxygen vacancies, superhydrophilic surface, urea electrooxidation

Online Date

5-21-2025

2503231-SI.pdf (3969 kB)

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