An effective metal-organic framework-based electrochemical non-enzymatic glucose sensor

被引:39
作者
Daud, A. D. [1 ]
Lim, H. N. [1 ,2 ]
Ibrahim, I. [1 ]
Endot, N. A. [2 ]
Gowthaman, N. S. K. [1 ]
Jiang, Z. T. [3 ]
Cordova, Kyle E. [1 ,2 ,4 ]
机构
[1] Univ Putra Malaysia, Inst Nanosci & Nanotechnol ION2, Foundry Reticular Mat Sustainabil Forms Lab, Upm Serdang 43400, Selangor, Malaysia
[2] Univ Putra Malaysia, Fac Sci, Dept Chem, Upm Serdang 43400, Selangor, Malaysia
[3] Murdoch Univ, Surface Anal & Mat Engn Res Grp, Coll Sci Hlth Engn & Educ, Murdoch, WA 6150, Australia
[4] Royal Sci Soc, Mat Discovery Res Unit, Adv Res Ctr, Amman 11941, Jordan
关键词
Metal-organic frameworks; Chemosensor; Glucose; Electrochemical activity; Non-enzymatic sensing; Reticular chemistry; MOF NANOSHEET ARRAY; NI; CARBON; ZIF-67; CU;
D O I
10.1016/j.jelechem.2022.116676
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Herein, we report a non-enzymatic glucose sensor based on a metal-organic framework (MOF) as alternative approach for long-term glucose monitoring. Specifically, nickel-based MOFs were solvothermally synthesized using either 2-amino-1,4-benzenedicarboxylic acid (BDC-NH2) or 2-hydroxy-1,4-benzenedicarboxylic acid (H2BDC-OH), both of which were characterized by different physicochemical techniques. The electrochemical performance of both electrodes towards glucose sensing was investigated and Ni-BDC-NH2 exhibited a significantly better electrocatalytic behaviour towards oxidation of glucose than bare Ni-BDC or Ni-BDC-OH in an alkaline media. This was attributed to a favourable multi-layered sheet-like structure that allowed diffusion for entrapment of glucose and the incorporation of -NH2 functional groups attached to the BDC linker which, were responsible for electrochemical adsorption of glucose molecules. Ni-BDC-NH2 displayed a lower detection limit (3.82 mu M), higher stability (> 180 days), and remarkable sensitivity (308 mu A mM(-1) cm(-2)). Additionally, a molecular sieve effect for Ni-BDC-NH2 led to a noteworthy anti-interference ability and the sensor displays a fast response time of 5.4 s towards glucose detection. These results indicate that the as-synthesized non-enzymatic glucose sensor operates with a longer lifetime and is viable for use as an intensive monitoring system.
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页数:9
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