The Enhanced Performance of NiCuOOH/NiCu(OH)2 Electrode Using Pre-Conversion Treatment for the Electrochemical Oxidation of Ammonia

Author:

Yin Xuejiao1,Wen Jiaxin1,Zhao Jujiao2ORCID,An Ran2,Zhang Ruolan2,Xiong Yin3,Tao Yanzong3,Wang Lingxin4,Liu Yuhang4,Zhou Huanyu5,Huang Yuanyuan67

Affiliation:

1. School of Architecture and Engineering, Chongqing Industry Polytechnic College, Chongqing 401120, China

2. College of Environment and Resources, Chongqing Technology and Business University, Chongqing 400067, China

3. Chongqing Baihan Wastewater Treatment Co., Ltd., Chongqing 400000, China

4. School of Civil Engineering and Architecture, Chongqing University of Science and Technology, Chongqing 401331, China

5. Green Intelligence Environmental School, Yangtze Normal University, Chongqing 408100, China

6. Key Laboratory of Hydraulic and Waterway Engineering of the Ministry of Education, School of River and Ocean Engineering, Chongqing Jiaotong University, Chongqing 400074, China

7. Chongqing Academy of Science and Technology, Chongqing 401120, China

Abstract

Electrochemical oxidation of ammonia is an attractive process for wastewater treatment, hydrogen production, and ammonia fuel cells. However, the sluggish kinetics of the anode reaction has limited its applications, leading to a high demand for novel electrocatalysts. Herein, the electrode with the in situ growth of NiCu(OH)2 was partially transformed into the NiCuOOH phase by a pre-treatment using highly oxidative solutions. As revealed by SEM, XPS, and electrochemical analysis, such a strategy maintained the 3D structure, while inducing more active sites before the in situ generation of oxyhydroxide sites during the electrochemical reaction. The optimized NiCuOOH-1 sample exhibited the current density of 6.06 mA cm−2 at 0.5 V, which is 1.67 times higher than that of NiCu(OH)2 (3.63 mA cm−2). Moreover, the sample with a higher crystalline degree of the NiCuOOH phase exhibited lower performance, demonstrating the importance of a moderate treatment condition. In addition, the NiCuOOH-1 sample presented low selectivity (<20%) towards NO2− and stable activity during the long-term operation. The findings of this study would provide valuable insights into the development of transition metal electrocatalysts for ammonia oxidation.

Funder

National Natural Science Foundation of China

Chongqing Municipal Education Commission

Doctor’s foundation of Chongqing Industry Polytechnic College

Natural Science Foundation of Chongqing

Publisher

MDPI AG

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