Electrocatalytic ammonia oxidation over a nickel foam electrode: Role of Ni(OH)2(s)-NiOOH(s) nanocatalysts

被引:148
作者
Shih, Yu-Jen [1 ]
Huang, Yao-Hui [2 ]
Huang, C. P. [3 ]
机构
[1] Natl Sun Yat Sen Univ, Inst Environm Engn, Kaohsiung 804, Taiwan
[2] Natl Cheng Kung Univ, Dept Chem Engn, Tainan 701, Taiwan
[3] Univ Delaware, Dept Civil & Environm Engn, Newark, DE 19716 USA
基金
美国国家科学基金会;
关键词
Electrode kinetics; Nano-NiOOH(s)-Ni(OH)(2(s)); Nitrogen selectivity; Ammonia oxidation; SELECTIVE CATALYTIC-OXIDATION; ALUMINA-SUPPORTED CATALYSTS; OXIDE CATALYSTS; NH3; OXIDATION; NITROGEN; METAL; REDUCTION; WATER; ELECTROOXIDATION; PERFORMANCE;
D O I
10.1016/j.electacta.2018.01.045
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Direct electrocatalytic oxidation of ammonia was carried out using an open-pore structured nickel foam electrode via electrochemical formation of Ni(OH)(2)/NiOOH nano-flowers (theophrastite phase) on the nickel substrate at specific overpotentials. The electrode surface was analyzed by X-ray diffraction (XRD), scanning electron microscope (SEM), Raman spectrometer (RS), and X-ray photoelectron spectroscopy (XPS). Cyclic voltammograms gave information on the nature of electron transfer between nitrogen species and nickel foam electrode and revealed the potential dependence nature of ammonia oxidation over the potential window of +0.7 V to +0.85 V (vs. Hg/HgO). Batch controlled potential experiments using nickel foam as the working anode in a three-electrode system were conducted to study the oxidation of ammonia in solution containing 0.1 M of Na2SO4 electrolyte, at pH 11 and temperature of 25 degrees C. Based on the current efficiency and reaction kinetics, it was possible to establish the mechanism of selective ammonia conversion to gaseous nitrogen and nitrate. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:261 / 271
页数:11
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