Physicochemical and electrochemical investigations of an electrodeposited CeNi2@NiO nanomaterial as a novel anode electrocatalyst material for urea oxidation in alkaline media

被引:16
作者
Abd El-Lateef, Hany M. [1 ,2 ]
Almulhim, Norah F. [1 ]
Mohamed, Ibrahim M. A. [2 ]
机构
[1] King Faisal Univ, Coll Sci, Dept Chem, Al Hufuf 31982, Al Ahsa, Saudi Arabia
[2] Sohag Univ, Fac Sci, Dept Chem, Sohag 82524, Egypt
关键词
Urea; Electrodeposition; Fuel cells; Nanocomposites; DOPED CARBON NANOFIBERS; REDUCED GRAPHENE OXIDE; HYDROGEN-PRODUCTION; CATALYTIC-ACTIVITY; ELECTRO-CATALYST; NICKEL; NI; NANOPARTICLES; ELECTROOXIDATION; ETHANOL;
D O I
10.1016/j.molliq.2019.111737
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Energy and water treatment can be considered to be major challenges in socioeconomic growth. The urea fuel cell (UFC) is a system that uses urea-containing waste water to generate power; this system satisfies two aims: treating water that contains urea and providing electricity from waste water. In this work, an electrodeposited material, CeNi2@NiO, was introduced to enhance the anodic behavior of UFC. The as-fabricated CeNi2@NiO nanoparticles (NPs) were studied using field emission-scanning electron microscope (FE-SEM), Energy-dispersive Xray spectroscopy (EDX) and X-ray diffraction (XRD) techniques. These analyses indicated that the presented NPs possessed CeNi2@NiO NPs that have a low CeNi2 content and have NiO as their primary form. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) measurements were conducted in a 3-electrode system to investigate the performance of CeNi2@NiO for urea electrooxidation and/or as an anode material for UFC. The synthesized NPs showed an improved electrocatalytic behavior at high pH (KOH media) in different urea concentrations, up to 1.0 mol/l. The superior electroactivity can be attributed to the assembly of Ce with Ni during the electrodeposition step, which enhances roughness, charge transfer and structural defects of Ni sites. (C) 2019 Elsevier B.V. All rights reserved.
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页数:6
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