标题:Selective determination of p-nitrophenol based on its unique voltammetric behavior on nanoporous gold
作者:Liu, Z.;Zhang, H.;Ma, H.;Hou, S.
作者机构:[Liu, Z] Key Laboratory for Colloid and Interface Chemistry of State Education Ministry, School of Chemistry and Chemical Engineering, Shandong Univer 更多
通讯作者:Ma, HY
通讯作者地址:[Ma, HY]Shandong Univ, Sch Chem & Chem Engn, Key Lab Colloid & Interface Chem, State Educ Minist, Jinan 250100, Peoples R China.
来源:Electroanalysis
出版年:2011
卷:23
期:12
页码:2851-2861
DOI:10.1002/elan.201100385
关键词:Cyclic voltammograms (CVs);Nanoporous gold (NPG);Nitrophenol (NP);Redox waves;Selectivity
摘要:In this paper, an unsupported nanoporous gold (us-NPG) was applied as a novel electrochemical sensor material for the selective detection of p-nitrophenol (p-NP) among its isomers in acid solution based on the distinct cyclic voltammetric behavior. To ascertain the ascription of each peak in cyclic voltammograms (CVs) of three nitrophenol isomers (NPs) on the us-NPG, contrast voltammetric studies of NPs were conducted at an ultrathin NPG film supported on glassy carbon substrate (NPG/GC) and a well-defined Au(111) electrode, respectively. Effects of potential scan rate and rotation speed of the electrode on the redox reaction of NPs were investigated to further confirm the reaction mechanisms. Interestingly, unlike those obtained on NPG/GC and Au(111) electrodes, the CVs of both o-nitrophenol (o-NP) and m-nitrophenol (m-NP) on us-NPG presented a new pair of redox waves separated very well from the redox waves of p-NP, indicating an obviously different mechanism involved in the redox process. Based on the voltammetric behavior, trace level determination of p-NP can be achieved on us-NPG electrode in the presence of o-NP and m-NP. Thus, the fast electron transfer, high selectivity and good sensitivity make us-NPG act as an ideal electrochemical sensor material in the selective determination of p-NP in aqueous solutions.
收录类别:SCOPUS;SCIE
WOS核心被引频次:17
Scopus被引频次:18
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-83355177604&doi=10.1002%2felan.201100385&partnerID=40&md5=680e13d0a9597199ee2d78b845d45b4f
TOP