微分脉冲伏安法
检出限
化学
电化学
催化作用
选择性
壳聚糖
石墨烯
共价键
基质(化学分析)
尿酸
酰胺
电化学气体传感器
循环伏安法
核化学
无机化学
电极
材料科学
纳米技术
色谱法
有机化学
物理化学
生物化学
作者
Halima Begum,Mohammad Shamsuddin Ahmed,S JEON
出处
期刊:ACS omega
[American Chemical Society]
日期:2017-06-29
卷期号:2 (6): 3043-3054
被引量:63
标识
DOI:10.1021/acsomega.7b00331
摘要
Amide-functionalized materials have emerged as promising nonprecious catalysts for electrochemical sensing and catalysis. The covalent immobilization of chitosan (CS) onto graphene sheet (GS) (denoted as CS-GS) has been done via higher degree of amidation reaction to develop an electrochemical sensing matrix for simultaneous determination of dopamine (DA) and uric acid (UA). The enhanced amidation between CS and GS has not been reported previously. However, electrochemical results have revealed that the CS-GS enhances the electrocatalytic performance in terms of the oxidation potential and peak current due to the higher degree of amide functionalization compared to that of CS/GS, which has a lower amidation. Differential pulse voltammetry-based studies have indicated that the CS-GS matrix works at a lower detection limit (0.14 and 0.17 μM) (S/N = 3) and over a longer linear range (1-700 and 1-800 μM), with a comparatively higher sensitivity (2.5 and 2.0 μA μM-1 cm-2), for DA and UA, respectively. In addition, the CS-GS matrix demonstrates good selectivity toward the detection of DA and UA in the presence of a 10-fold higher concentration of AA and glucose. The as-prepared three-dimensional porous CS-GS also endows selective determination toward DA and UA in various real samples.
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