A base-stable metal-organic framework for sensitive and non-enzymatic electrochemical detection of hydrogen peroxide

被引:92
|
作者
Lopa, Nasrin Siraj [1 ]
Rahman, Md. Mahbubur [2 ]
Ahmed, Faiz [1 ]
Sutradhar, Sabuj Chandra [1 ]
Ryu, Taewook [1 ]
Kim, Whangi [1 ]
机构
[1] Konkuk Univ, Dept Appl Chem, Chungju 380701, South Korea
[2] Konkuk Univ, Dept Appl Life Sci, Coll Biomed & Hlth Sci, Chungju 380701, South Korea
基金
新加坡国家研究基金会;
关键词
MIL-53-Cr; Chemical and electrochemical stability; Glassy carbon electrode; Non-enzymatic detection; H2O2; IMPRINTED POLYMER NANOPARTICLES; REDUCED GRAPHENE OXIDE; ULTRA-TRACE; GLUCOSE DETECTION; CARBON ELECTRODE; SENSOR; PERFORMANCE; OXIDATION; REDUCTION; IONS;
D O I
10.1016/j.electacta.2018.03.148
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Stability of metal-organic frameworks (MOFs) in aqueous medium and extreme solution conditions (acidic or basic) are important for the development of stable, reproducible, and sensitive electrochemical biosensors. Herein, a base-stable chromium(III) dicarboxylate MOF was synthesized by microwave assisted solvothermal method for non-enzymatic detection of hydrogen peroxide (H2O2). The as-synthesized MOF exhibited excellent base stability without any obvious changes in crystallinity, morphology, and spectroscopic behaviors after base treatment. This MOF-modified glassy carbon electrode showed negligible change in charge transfer resistance at the electrode vertical bar electrolyte interface after redox cycling and good catalytic activity for the reduction of H2O2 in 0.1M NaOH(aq.). The enhanced catalytic activity of H2O2 reduction is enabled by the redox process of Cr-III/II in the chromium (III) dicarboxylate. The sensor showed the sensitivity of ca. 11.9 mu A mM(-1), wide linear range from 25 to 500 mu M, and a method detection limit of ca. 3.52 mu M. The validation of this sensing platform was evaluated by standard addition method. Thus, the present biosensor could be used for the point of care detection of H2O2. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:49 / 56
页数:8
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