Nanostructured Ni2P‐C as an Efficient Catalyst for Urea Electrooxidation. Issue 4 (16th January 2018)

• Record Type: Journal Article
• Authors: Yang, Dawen; Gu, Ying; Yu, Xu; Lin, Zixia; Xue, Huaiguo; Feng, Ligang
• Is Part Of: ChemElectroChem. Volume 5:Issue 4(2018)
• Page Start: 659
• Page End: 664
• Publication Date: 2018-01-16
• Subjects: electrochemical impedance spectroscopy -- electrooxidation -- nickel phosphide -- urea -- voltammetry; Electrochemistry -- Periodicals; 541.37
• DOI: 10.1002/celc.201701304
• Languages: English
• ISSNs: 2196-0216

Abstract

Abstract: Nickel‐based materials are a type of cost‐effective catalyst for urea oxidation. Herein, we first reported nanostructured Ni2 P−C as an efficient catalyst for urea electrooxidation. The Ni2 P−C catalyst was prepared by a facile hydrothermal method and the structure and morphology were further characterized by X‐ray diffraction (XRD) and transmission electron microscope (TEM). The hexagonal crystal structure for Ni2 P was indicated by the characteristic peaks in the XRD patterns, and lattice fringes of Ni2 P were clearly observed in the high‐resolution TEM images. The catalytic ability for urea electrooxidation was studied by cyclic voltammetry and chronoamperometry techniques. It was found that the current density at 0.5 V was ca. 70.4 mA cm −2, about 2.7 times higher than that of the referenced commercial nickel oxide catalyst. A good catalytic stability for urea oxidation was also obtained. A diffusion‐controlled process was observed for urea oxidation on Ni2 P catalyst while the active sites arising from Ni(II) ion oxidation was following a surface‐redox‐reaction‐controlled process. Kinetics studies by impedance spectroscopy and Tafel slope analysis displayed improved charge‐transfer kinetics towards urea electrooxidation. The results demonstrated that Ni2 P would have potential applications for catalytic urea oxidation. Abstract : Cheap and cheerful : Nanostructured Ni2 P−C was demonstrated as an efficient catalyst for urea electrooxidation. The material exhibited an excellent catalytic ability and was found to display improved charge‐transfer kinetics towards urea electrooxidation.