A direct and selective electrochemical hydrogen sulfide sensor

被引:64
|
作者
Brown, Micah D. [1 ]
Hall, Jackson R. [1 ]
Schoenfisch, Mark H. [1 ]
机构
[1] Univ N Carolina, Dept Chem, CB 3290, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
Hydrogen sulfide; Sulfur poisoning; Surface conditioning; Electropolymerized film; Phenylenediamine; Anti-biofouling; NITRIC-OXIDE; ELECTROPOLYMERIZED FILMS; VERTEBRATE BLOOD; SULFUR-COMPOUNDS; GOLD ELECTRODES; CARBON-MONOXIDE; H2S; GASOTRANSMITTER; SYSTEM; PERMSELECTIVITY;
D O I
10.1016/j.aca.2018.08.054
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Continuous, in situ detection of hydrogen sulfide (H2S) in biological milieu is made possible with electrochemical methods, but direct amperometry is constrained by the generation of elemental sulfur as an oxidative byproduct. Deposition of a sulfur layer passivates the working electrode, reducing sensitivity and causing performance variability. Herein, we report on the use of a surface preconditioning procedure to deposit elemental sulfur on a glassy carbon electrode prior to measurement and evaluate performance with common analytical metrics. The lack of traditional anti-poisoning techniques (e.g. redox mediators, cleaning pulses) also allowed for facile surface modification with electropolymerized films. For the first time, a series of electropolymerized films were characterized for their H2S permselective behavior against common biological interferents. Highly selective, film-modified electrodes were then evaluated for their anti-biofouling ability in simulated wound fluid. The final optimized electrode was capable of measuring H2S with a low detection limit (i.e., <100 nM) and similar to 80% of its initial sensitivity in proteinaceous media. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:67 / 76
页数:10
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