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在α-丙氨酸功能化玻碳电极上电化学合成聚苯胺纳米网络及其在马心细胞色素c直接电化学中的应用。

Electrochemical synthesis of polyaniline nano-network on alpha-alanine functionalized glassy carbon electrode and its application for the direct electrochemistry of horse heart cytochrome c.

作者信息

Zhang Lei, Zhang Jing, Zhang Chunhua

机构信息

Department of Chemistry, College of Life and Environment Sciences, Shanghai Normal University, Guilin Road No. 100, Shanghai 200234, PR China.

出版信息

Biosens Bioelectron. 2009 Mar 15;24(7):2085-90. doi: 10.1016/j.bios.2008.10.025. Epub 2008 Nov 8.

DOI:10.1016/j.bios.2008.10.025
PMID:19084388
Abstract

Polyaniline (PAN) nano-particles, nano-fibrils, and nano-network have been synthesized via electrochemical polymerization of aniline using a three-step electrochemical deposition procedure on alpha-alanine (ALA)-monolayer functionalized glassy carbon electrode (GCE). The structure and properties of PAN nano-structures have been characterized using field emission scanning electron microscope (SEM), Fourier transform infrared spectra (FT-IR), and electrochemical techniques. The 3-dimensional (3D) PAN nano-network/ALA composite film coated GCE (PAN-ALA/GCE) leads to the direct electrochemistry of horse heart cytochrome c (Cyt c) immobilized on this electrode surface. The immobilized Cyt c maintains its activity, showing a surface-controlled electrode process with the electron transfer rate constant (k(s)) of 21.9s(-1) and the charge-transfer coefficient (alpha) of 0.37, and could be used for the electrocatalytic reduction of hydrogen peroxide (H(2)O(2)). The steady-state current response increases linearly with H(2)O(2) concentration from 2.5 x 10(-5) to 3.0 x 10(-4) moll(-1). The detection limit (3delta) is 8.2 x 10(-6) moll(-1).

摘要

通过三步电化学沉积法,在α-丙氨酸(ALA)单层功能化玻碳电极(GCE)上对苯胺进行电化学聚合,合成了聚苯胺(PAN)纳米颗粒、纳米纤维和纳米网络。利用场发射扫描电子显微镜(SEM)、傅里叶变换红外光谱(FT-IR)和电化学技术对PAN纳米结构的结构和性能进行了表征。三维(3D)PAN纳米网络/ALA复合膜包覆的GCE(PAN-ALA/GCE)实现了固定在该电极表面的马心细胞色素c(Cyt c)的直接电化学。固定化的Cyt c保持其活性,显示出表面控制的电极过程,电子转移速率常数(k(s))为21.9s(-1),电荷转移系数(α)为0.37,可用于过氧化氢(H(2)O(2))的电催化还原。稳态电流响应随H(2)O(2)浓度从2.5×10(-5)到3.0×10(-4) moll(-1)呈线性增加。检测限(3δ)为8.2×10(-6) moll(-1)。

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