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Amperometric sensor for hydroxylamine based on hybrid nickel-cobalt hexacyanoferrate modified electrode
Shi, LH ; Wu, T ; He, P ; Li, D ; Sun, CY ; Li, JH
2010-05-06 ; 2010-05-06
关键词hybrid nickel-cobalt hexacyanoferrate amperometric sensor hydroxylamine modified electrode GLASSY-CARBON ELECTRODE PRUSSIAN BLUE ELECTROCHEMICAL PREPARATION ELECTROCATALYTIC ACTIVITY CERAMIC ELECTRODE HYDROGEN-PEROXIDE FILMS OXIDATION COPPER VOLTAMMETRY Chemistry, Analytical Electrochemistry
中文摘要Hybrid nickel-cobalt hexacyanoferrate (NiCoHCF) particles were immobilized onto a glassy carbon electrode by cyclic voltammetry. Characterization of these particles by Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction and electrochemistry revealed that NiCoHCF was a substitution-type hybrid hexacyanoferrate rather than a simple mixture system. As an important reducing agent, hydroxylamine could be electrocatalytically oxidized at the NiCoHCF modified electrode. The effects of the solution pH and the applied potential on the amperometric response of hydroxylamine were examined. Under optimum conditions, the catalytic peak current was proportional to the concentration of hydroxylamine in the range 2.0 x 10(-5)-1.0 x 10(-2) mol/L with a detection limit of 2.3 x 10(-7) mol/L. Furthermore, detection results obtained with this sensor showed high sensitivity fast response time, good stability and anti-interference ability.
语种英语 ; 英语
出版者WILEY-V C H VERLAG GMBH ; WEINHEIM ; PO BOX 10 11 61, D-69451 WEINHEIM, GERMANY
内容类型期刊论文
源URL[http://hdl.handle.net/123456789/13447]  
专题清华大学
推荐引用方式
GB/T 7714
Shi, LH,Wu, T,He, P,et al. Amperometric sensor for hydroxylamine based on hybrid nickel-cobalt hexacyanoferrate modified electrode[J],2010, 2010.
APA Shi, LH,Wu, T,He, P,Li, D,Sun, CY,&Li, JH.(2010).Amperometric sensor for hydroxylamine based on hybrid nickel-cobalt hexacyanoferrate modified electrode..
MLA Shi, LH,et al."Amperometric sensor for hydroxylamine based on hybrid nickel-cobalt hexacyanoferrate modified electrode".(2010).
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