Nanocomposite of polymerized ionic liquid and graphene used as modifier for direct electrochemistry of cytochrome c and nitric oxide biosensing

被引:25
作者
Chen, Huamao [1 ]
Zhao, Guangchao [1 ]
机构
[1] Anhui Normal Univ, Sch Chem & Mat Sci, Anhui Key Lab Chem Biosensing, Wuhu 241000, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Graphene; Polymerized ionic liquid; Nitric oxide; Cytochrome c; Biosensor; GLASSY-CARBON ELECTRODE; GOLD NANOPARTICLES; CHITOSAN; ELECTROCATALYSIS; HEMOGLOBIN; BEHAVIOR; SHEETS; ALCOHOL; HYBRID;
D O I
10.1007/s10008-012-1769-5
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In the present work, nanocomposite of polymerized ionic liquid (PIL), poly (1-vinyl-3-ethyl imidazolium) bromide, modified graphene nanosheet (PIL-Gr) was prepared. The PIL-Gr nanosheet composite was evaluated using scanning electron microscopy, transmission electron microscopy, and Fourier transform infrared spectroscopy. Then, a robust and effective sensing strategy based on the nanocomposite for cytochrome c (Cyt c) immobilization on basal plane graphite (BPG) electrode surface was proposed. Direct electrochemistry and electrocatalysis of immobilized Cyt c were investigated in detail. The cyclic voltammogram results indicated that the PIL-Gr nanocomposite film showed an obvious promotion for the direct electron transfer between Cyt c and the underlying electrode. The immobilized Cyt c exhibited an excellent electrocatalytic activity towards the reduction of nitric oxide (NO). The fabricated biosensor exhibited a fast response and a good electrochemical activity for NO with comparable liner range and low detection limit. The low apparent Michaelis-Menten constant indicated the affinity of PIL-Gr and Cyt c. Moreover, the modified electrode displayed a rapid response to NO and possessed good stability and reproducibility. Based on the nanocomposite, a third-generation reagentless biosensor could be constructed for the determination of NO. The present work broadens the applications of graphene and ionic liquid in biosensor field.
引用
收藏
页码:3289 / 3297
页数:9
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