Nanoporous gold particles modified titanium electrode for hydrazine oxidation

被引:130
作者
Yi, Qingfeng [1 ]
Yu, Wenqiang [1 ]
机构
[1] Hunan Univ Sci & Technol, Sch Chem & Chem Engn, Xiangtan 411201, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Gold nanoparticle; Hydrazine oxidation; Hydrothermal method; Electrocatalytic oxidation; GLASSY-CARBON ELECTRODE; SELF-ASSEMBLED MONOLAYER; SULFURIC-ACID-SOLUTIONS; ELECTROCATALYTIC OXIDATION; ELECTROCHEMICAL SYNTHESIS; PLATINUM-ELECTRODES; ALKALINE-SOLUTIONS; GLUCOSE-OXIDATION; FUEL-CELL; NANOPARTICLES;
D O I
10.1016/j.jelechem.2009.05.008
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A nanoporous gold particles modified titanium electrode (Au/Ti) was prepared by using a hydrothermal method. Gold nanoparticles were stably immobilized on the Ti surface from a mixture of aqueous HAuCl4/polyethylene glycol (PEG) to form a nanoporous network texture. Electrocatalytic activity of the Au/Ti towards hydrazine oxidation in I M NaOH solution was assessed utilizing cyclic voltammetry (CV), linear scanning voltammetry (LSV) and electrochemical impedance spectroscopy (EIS). At the Au/Ti electrode, hydrazine oxidation in 1 M NaOH took place at a potential of -0.55 V (vs. Ag, AgCl) which was 0.53 V less than polycrystalline Au electrode. The Au/Ti electrode also presented much larger current density of hydrazine oxidation than Au electrode. Cyclic voltammetric responses of the Au/Ti electrode showed an irreversible electro-oxidation process of hydrazine. Linear plots of the reduction peak current density from the CVs of the Au/Ti vs. hydrazine concentration provided a potential detection of low concentration hydrazine. The kinetic parameters such as the number of electrons transferred in rate-determining step and total numbers of electrons involved in the hydrazine oxidation were determined using CVs and LSVs. CVs at the Au/Ti electrode also illustrated (relatively) weak interactions of hydrazine with electrode surface at all stages of the hydrazine oxidation process. Further. EIS data showed significantly high electrocatalytic activity of the Au/Ti electrode for hydrazine oxidation in alkaline solutions. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:159 / 164
页数:6
相关论文
共 42 条
[1]   Role of the metal and surface structure in the electro-oxidation of hydrazine in acidic media [J].
Alvarez-Ruiz, B ;
Gómez, R ;
Orts, JM ;
Feliu, JM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2002, 149 (03) :D35-D45
[2]  
[Anonymous], 2007, ELECTROCHIM ACTA, DOI DOI 10.1016/J.ELECTACTA.2007.03.065
[3]   New innovative gold catalysts prepared by an improved incipient wetness method [J].
Baatz, C. ;
Decker, N. ;
Pruesse, U. .
JOURNAL OF CATALYSIS, 2008, 258 (01) :165-169
[4]  
Bard A.J., 2001, ELECTROCHEMICAL METH
[5]   The electroanalytical detection of hydrazine: A comparison of the use of palladium nanoparticles supported on boron-doped diamond and palladium plated BDD microdisc array [J].
Batchelor-McAuley, C ;
Banks, CE ;
Simm, AO ;
Jones, TGJ ;
Compton, RG .
ANALYST, 2006, 131 (01) :106-110
[6]   Electrochemical synthesis of Pd particles on poly(vinylferrocenium) [J].
Celebi, Mutlu Soenmez ;
Pekmez, Kadir ;
Ozyoruk, Haluk ;
Yildiz, Attila .
CATALYSIS COMMUNICATIONS, 2008, 9 (13) :2175-2178
[7]   High dispersion and electrocatalytic activity of Pd/titanium dioxide nanotubes catalysts for hydrazine oxidation [J].
Dong, Bin ;
He, Ben-Lin ;
Huang, Jier ;
Gao, Guo-Yu ;
Yang, Zhi ;
Li, Hu-Lin .
JOURNAL OF POWER SOURCES, 2008, 175 (01) :266-271
[8]   Electrocatalytic oxidation of hydrazine with pyrogallol red as a mediator on glassy carbon electrode [J].
Ensafi, AA ;
Mirmomtaz, E .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2005, 583 (02) :176-183
[9]   Electrocrystallized Ag nanoparticle on functional multi-walled carbon nanotube surfaces for hydrazine oxidation [J].
Gao, Guoyu ;
Guo, Daojun ;
Wang, Ce ;
Li, Hulin .
ELECTROCHEMISTRY COMMUNICATIONS, 2007, 9 (07) :1582-1586
[10]   On the mechanism of electrooxidation of hydrazine on platinum electrodes in acidic solutions [J].
Garcia, MD ;
Marcos, ML ;
Velasco, JG .
ELECTROANALYSIS, 1996, 8 (03) :267-273