Direct electron transfer of hemoglobin in a CdS nanorods and Nafion composite film on carbon ionic liquid electrode

被引:71
|
作者
Sun, Wei [1 ]
Wang, Dandan [1 ]
Li, Guicun [2 ]
Zhai, Ziqin [1 ]
Zhao, Ruijun [1 ]
Jiao, Kui [1 ]
机构
[1] Qingdao Univ Sci & Technol, Key Lab Ecochem Engn, Minist Educ, Coll Chem & Mol Engn, Qingdao 266042, Peoples R China
[2] Qingdao Univ Sci & Technol, Key Lab Nanostruct Mat, Qingdao 266042, Peoples R China
基金
中国国家自然科学基金;
关键词
1-butyl-3-methylimidazolium; hexafluorophosphate; hemoglobin; direct electrochemistry; carbon paste electrode; ionic liquid;
D O I
10.1016/j.electacta.2008.06.021
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this paper the direct electron transfer of hemoglobin (Hb) was carefully investigated by using a room temperature ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate(BMIMPF6) modified carbon paste electrode (CILE) as the basal working electrode. Hb was immobilized on the surface of CILE with the nanocomposite film composed of Nafion and CdS nanorods by a step-by-step method. UV-vis and Fr-IR spectra showed that Hb in the composite film remained its native structure. The direct electrochemical behaviors of Hb in the composite film were further studied in a pH 7.0 phosphate buffer solution (PBS). A pair of well-defined and quasi-reversible cyclic voltammetric peaks of Hb was obtained with the formal potential (E-0') at -0.295 V (vs. SCE), which was the characteristic of heme Fe(III)/Fe(II) redox couples. The direct electrochemistry of Hb was achieved on the modified electrode and the apparent heterogeneous electron transfer rate constant (k(s)) was calculated to be 0.291 s(-1). The formal potentials of Hb Fe(III)/Fe(II) couple shifted negatively with the increase of buffer pH and a slope value of -45.1 mV/pH was got, which indicated that one electron transfer accompanied with one proton transportation. The fabricated Hb sensor showed good electrocatalytic manner to the reduction of trichloroacetic acid (TCA). (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:8217 / 8221
页数:5
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