NiXPd1-x (x=0.98, 0.93, and 0.58) nanostructured catalysts for ammonia electrooxidation in alkaline media

被引:44
作者
Allagui, Anis [1 ]
Sarfraz, Saad [1 ]
Baranova, Elena A. [1 ]
机构
[1] Univ Ottawa, Dept Chem & Biol Engn, Ottawa, ON K1N 6N5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Ammonia; Electrooxidation; Nickel-palladium electrocatalyst; pH effect; Electrochemical treatment; ELECTROCHEMICAL OXIDATION; BINARY-ALLOYS; NICKEL ELECTRODE; FUEL-CELL; PD; IR; BEHAVIOR; NITRATE; ELECTROCATALYSTS; NANOPARTICLES;
D O I
10.1016/j.electacta.2013.06.148
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The effect of Pd atomic content in NixPd1-x (x = 0.98, 0.93 and 0.58) nanometer-sized catalysts synthesized with modified polyol method is investigated for the electrooxidation of ammonia in alkaline media. Physicochemical characterization by transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), inductively coupled plasma atomic emission spectroscopy (ICP-AES), and Xray diffraction (XRD) are carried out to identify the sizes, shapes, chemical and structural features of the catalysts. Both synthesized Ni98Pd2 and Ni93Pd2 are composed of large 50-100 nm Ni particles coated with finer Pd ones in the 5-20 nm range. The Ni58Pd42 catalyst has smaller and narrower size distribution in the 20 nm size range, indicating that Pd stabilizes the particle size of Ni. According to XRD, Ni and Pd form two separate face-centred cubic phases with traces of beta-Ni(OH)(2). Before ammonia electrooxidation reaction, the catalysts were subjected to an electrochemical treatment that consisted of 200 potential cycles in NaNO3 at pH 10.5 to build a layer of Ni(OH)(2). Ammonia electrooxidation proceeds on NiOOH phase and follows the direct pathway at low concentrations and indirect pathway at higher concentrations where NiOOH is reducing and NH3 is oxidizing. It was found that the Ni-rich compositions have higher activity towards the degradation of ammonia. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:253 / 259
页数:7
相关论文
共 40 条
[1]  
Allagui A., 2013, ECS Transactions, V50, P1897
[2]   Ammonia electro-oxidation on alloyed PtIr nanoparticles of well-defined size [J].
Allagui, Anis ;
Oudah, Mohamed ;
Tuaev, Xenia ;
Ntais, Spyridon ;
Almomani, Fares ;
Baranova, Elena A. .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2013, 38 (05) :2455-2463
[3]   Nickel particles with increased catalytic activity towards hydrogen evolution reaction [J].
Baranova, Elena A. ;
Cally, Audrey ;
Allagui, Anis ;
Ntais, Spyridon ;
Wuethrich, Rolf .
COMPTES RENDUS CHIMIE, 2013, 16 (01) :28-33
[4]   Electrochemical reductions of Hg(II), ruthenium-nitrosyl complex, chromate, and nitrate in a strong alkaline solution [J].
Bockris, JO ;
Kim, J .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1996, 143 (12) :3801-3808
[5]  
Bode H., 1966, ELECTROCHIM ACTA, V11, P1079
[6]   Electrochemical reduction of nitrate in weakly alkaline solutions [J].
Bouzek, K ;
Paidar, M ;
Sadílková, A ;
Bergmann, H .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 2001, 31 (11) :1185-1193
[7]   INFLUENCE OF PH ON THE REDOX BEHAVIOR OF HYDROUS NICKEL-OXIDE [J].
BURKE, LD ;
TWOMEY, TAM .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1982, 134 (02) :353-362
[8]   VOLTAMMETRIC BEHAVIOR OF NICKEL IN BASE WITH PARTICULAR REFERENCE TO THICK OXIDE-GROWTH [J].
BURKE, LD ;
TWOMEY, TAM .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1984, 162 (1-2) :101-119
[9]   Studies on the chemical synthesis of nanosized nickel powder and its stability [J].
Chou, KS ;
Huang, KC .
JOURNAL OF NANOPARTICLE RESEARCH, 2001, 3 (2-3) :127-132
[10]   The role of adsorbates in the electrochemical oxidation of ammonia on noble and transition metal electrodes [J].
de Vooys, ACA ;
Koper, MTM ;
van Santen, RA ;
van Veen, JAR .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2001, 506 (02) :127-137