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Self-supported spinel nanosphere as bifunctional electrocatalysts for energy-saving hydrogen production via urea-water electrolysis.
Jiang, Li-Hua; Cheng, Xue-Feng; Zhang, Hao-Yu; Cao, Qiang; Song, Kai; He, Jing-Hui.
Afiliação
  • Jiang LH; College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China.
  • Cheng XF; College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China.
  • Zhang HY; College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China.
  • Cao Q; College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China.
  • Song K; Department of Nephrology, Second Affiliated Hospital of Soochow University, Suzhou, PR China. Electronic address: songkaift3@live.cn.
  • He JH; College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, PR China. Electronic address: jinghhe@suda.edu.cn.
J Colloid Interface Sci ; 643: 403-408, 2023 Aug.
Article em En | MEDLINE | ID: mdl-37084620
ABSTRACT
Electrochemical oxidation of urea is of great importance in the removal and energy exchange and storage of urea from wastewater as well as of potential applications in potable dialysis of end-stage renal disease. However, the lack of economical electrocatalysts hinders its widespread application. In this study, we successfully fabricated ZnCo2O4 nanospheres with bifunctional catalysis on nickel foam (NF). The catalytic system has high catalytic activity and durability for urea overall electrolysis. The urea oxidation and hydrogen evolution reactions required only 1.32 V and -80.91 mV to obtain ± 10 mA cm-2. Only 1.39 V was needed to obtain 10 mA cm-2 for 40 h without noticeably declining activity. The excellent performance could be attributed to the fact that the material can provide multiple redox couplings and a three-dimensional porous structure to facilitate the release of gases from the surface.
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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: J Colloid Interface Sci Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: J Colloid Interface Sci Ano de publicação: 2023 Tipo de documento: Article