Three-dimensional graphene-like carbon frameworks as a new electrode material for electrochemical determination of small biomolecules

被引:46
|
作者
Deng, Wenfang [1 ]
Yuan, Xiaoyan [1 ]
Tan, Yueming [1 ]
Ma, Ming [1 ]
Xie, Qingji [1 ]
机构
[1] Hunan Normal Univ, Coll Chem & Chem Engn, Minist Educ China, Key Lab Chem Biol & Tradit Chinese Med Res, Changsha 410081, Hunan, Peoples R China
来源
BIOSENSORS & BIOELECTRONICS | 2016年 / 85卷
基金
中国国家自然科学基金;
关键词
Three-dimensional graphene-like carbon frameworks; Ascorbic acid; Dopamine; Uric acid; ASCORBIC-ACID; URIC-ACID; FUNCTIONALIZED GRAPHENE; SENSITIVE DETERMINATION; PARKINSONS-DISEASE; DOPAMINE; OXIDE; SUPERCAPACITORS; NETWORKS; NANOTUBES;
D O I
10.1016/j.bios.2016.05.065
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Three-dimensional (3D) graphene-like carbon frameworks (3DGLCFs) were facilely prepared via copyrolysis of polyaniline and nickel nitrate powder, followed by acid etching. The as-prepared 3DGLCFs possess graphene-like network structure, high specific surface area, and high content nitrogen dopant. Because these features enable large electrochemically active surface area, rapid electron transfer, and fast transport of analytes to electrode surface, the 3DGLCFs modified glassy carbon electrode (GCE) shows current response much higher than commercial graphene (CG) modified GCE towards the oxidation of ascorbic acid (AA), dopamine (DA) and uric acid (UA). The anodic peak separations at 3DGLCFs/GCE are 0.23 V between AA and DA, 0.13 V between DA and UA, and 036 V between AA and UA. For the simultaneous electrochemical determination of AA, DA and UA using differential pulse voltammetry, the 3DGLCFs/GCE shows linear response ranges of 1.25 x 10(-5)-4 x 10(-4) M for AA, 5 x 10(-8)-1.0 x 10(-5) M for DA, and 5 x 10(-8)-1.5 x 10(-5) M for UA, with low detection limits of 2 x 10(-6) M for AA, 1 x 10(-8) M for DA, and 1 x 10(-8) M for UA. The 3DGLCFs/GCE was also applied for the measurement of human serum, exhibiting satisfactory recoveries. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:618 / 624
页数:7
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