Synthesis of Ni(OH)2 nanoplates on Cu rod and its applications for electrochemical sensors

被引:6
作者
Ji, Rong [1 ,2 ]
Huang, Yan [1 ,2 ]
Wang, Lingling [1 ,2 ]
Yu, Liutao [1 ,2 ]
Wang, Jie [1 ]
Wang, Guangfeng [1 ,3 ]
Zhang, Xiaojun [1 ,2 ]
机构
[1] Anhui Normal Univ, Coll Chem & Mat Sci, Wuhu 241000, Peoples R China
[2] Educ Minist China, Key Lab Funct Mol Solids, Wuhu 241000, Peoples R China
[3] Anhui Normal Univ, Anhui Key Lab Chem Biosensing, Wuhu 241000, Peoples R China
关键词
Composites; Layered compounds; Nanostructures; Electrochemical properties; GLASSY-CARBON ELECTRODE; HYDROGEN-PEROXIDE; NICKEL-HYDROXIDE; ELECTROCATALYTIC OXIDATION; AMPEROMETRIC DETERMINATION; ACTIVE MATERIAL; HYDRAZINE; MORPHOLOGY; BIOSENSOR;
D O I
10.1016/j.materresbull.2013.05.115
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
beta-Nickel hydroxide nanoplates were synthesized on Cu rods by a simple hydrothermal method without the use of surfactants. A novel Ni(OH)(2) nanoplates/Cu rod electrode for hydrazine and non-enzymatic hydrogen peroxide was then fabricated and designated as beta-Ni(OH)(2) nanoplates/Cu rod electrode (beta-Ni(OH)(2) NPS/CRE). This electrode was evaluated by cyclic voltammetry (CV) and the typical amperometric response (I-t) method. beta-Ni(OH)(2) NPS/CRE has a wide linear range for the detection of hydrazine, from 1 to 15,931 mu M, with a low detection limit of 0.3 mu M (S/N = 3) and a response time of less than 3 s. Its detection of hydrogen peroxide, has two linear ranges (5-7612.5 mu M for I; 8862.5-17,612.5 mu M for II) with an optimized detection limit of 1.68 mu M (S/N = 3) and a response time of less than 3 s. The results revealed that beta-Ni(OH)(2) NPS/CRE had favorable electrochemical responses toward those environmental pollutants. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3729 / 3734
页数:6
相关论文
共 35 条
[1]  
[Anonymous], 2007, ELECTROCHIM ACTA, DOI DOI 10.1016/J.ELECTACTA.2007.03.065
[2]   CAUSE OF RESIDUAL CAPACITY IN NICKEL OXYHYDROXIDE ELECTRODES [J].
BARNARD, R ;
CRICKMORE, GT ;
LEE, JA ;
TYE, FL .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1980, 10 (01) :61-70
[3]   Nickel hydroxide as an active material for the positive electrode in rechargeable alkaline batteries [J].
Chen, J ;
Bradhurst, DH ;
Dou, SX ;
Liu, HK .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1999, 146 (10) :3606-3612
[4]   A facile and novel synthetic route to Ni(OH)2 nanoflowers [J].
Cheng, Zhipeng ;
Xu, Jiming ;
Zhong, Hui ;
Li, Dong ;
Zhu, Pengcheng ;
Yang, Yi .
SUPERLATTICES AND MICROSTRUCTURES, 2010, 48 (02) :154-161
[5]   Synthesis hexagonal -Ni(OH)2 nanosheets for use in electrochemistry sensors [J].
Fang, Bin ;
Gu, Aixia ;
Wang, Guangfeng ;
Li, Bo ;
Zhang, Cuihong ;
Fang, Yongyi ;
Zhang, Xiaojun .
MICROCHIMICA ACTA, 2009, 167 (1-2) :47-52
[6]   Synthetically Directed Self-Assembly and Enhanced Surface-Enhanced Raman Scattering Property of Twinned Crystalline Ag/Ag Homojunction Nanoparticles [J].
Feng, Xiumei ;
Ruan, Fangxiong ;
Hong, Ruijin ;
Ye, Jianshan ;
Hu, Jianqiang ;
Hu, Guanqi ;
Yang, Zhilin .
LANGMUIR, 2011, 27 (06) :2204-2210
[7]   AMPEROMETRIC DETERMINATION OF DOPAMINE ON AN ENZYMATICALLY MODIFIED CARBON-PASTE ELECTRODE [J].
FORZANI, ES ;
RIVAS, GA ;
SOLIS, VM .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1995, 382 (1-2) :33-40
[8]   An unusual H2O2 electrochemical sensor based on Ni(OH)2 nanoplates grown on Cu substrate [J].
Gu, Aixia ;
Wang, Guangfeng ;
Gu, Jing ;
Zhang, Xiaojun ;
Fang, Bin .
ELECTROCHIMICA ACTA, 2010, 55 (24) :7182-7187
[9]   Synthesis of α-Cobalt Hydroxides with Different Intercalated Anions and Effects of Intercalated Anions on Their Morphology, Basal Plane Spacing, and Capacitive Property [J].
Hu, Zhong-Ai ;
Xie, Yu-Long ;
Wang, Yao-Xian ;
Xie, Li-Jing ;
Fu, Guo-Rui ;
Jin, Xiao-Qing ;
Zhang, Zi-Yu ;
Yang, Yu-Ying ;
Wu, Hong-Ying .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (28) :12502-12508
[10]   A novel hydrogen peroxide biosensor based on the immobilization of horseradish peroxidase onto Au-modified titanium dioxide nanotube arrays [J].
Kafi, A. K. M. ;
Wu, Guosheng ;
Chen, Aicheng .
BIOSENSORS & BIOELECTRONICS, 2008, 24 (04) :566-571