Anti-poisoning electrode for real-time in-situ monitoring of hydrogen sulfide release

被引:18
|
作者
Jeromiyas, Nithiya [1 ]
Mani, Veerappan [1 ,2 ]
Chang, Pu-Chieh [1 ]
Huang, Chih-Hung [1 ]
Salama, Khaled Nabil [2 ]
Huang, Sheng-Tung [1 ]
机构
[1] Natl Taipei Univ Technol, Inst Biochem & Biomed Engn, Dept Chem Engn & Biotechnol, 1,Sect 3,Chung Hsiao East Rd, Taipei 106, Taiwan
[2] King Abdullah Univ Sci & Technol KAUST, Adv Membranes & Porous Mat Ctr AMPMC, Comp Elect Math Sci & Engn CEMSE Div, Sensors Lab, Thuwal 239556900, Saudi Arabia
来源
关键词
Nanocomposites; Real-time sensor; Gasotransmitters; Serum biomarker; Live cells; In-Situsensors; SCREEN-PRINTED ELECTRODE; ELECTROCHEMICAL OXIDATION; GRAPHENE; H2S; SENSOR; PERMSELECTIVITY; PROBES; GUIDE; FILMS;
D O I
10.1016/j.snb.2020.128844
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Electrode poisoning and interferences from complex biological environments are major challenges in the development of in-situ H2S sensors. To circumvent these issues, herein a robust electrode based on reduced graphene oxide-molybdenum disulfide nanohybrid (RGO-MoS2) and polymerized o-phenylenediamine (POPD) is developed. The POPD/RGO-MoS2-modified electrode catalyzed H2S oxidation at a minimized overpotential (+ 0.15 V vs. Ag/AgCl). A new strategy based on inherent material properties was implemented to alleviate the electrode-poisoning problem. The nano-tailored interface blocks 2.5-fold surplus levels of interferences because of its exclusive size-exclusion property and electrostatic interactions. Moreover, this method with a response time of fewer than 5s displayed a detection limit of 10 nM, which covers the endogenous H2S levels. Practicality tests in various biological media yielded valuable recoveries of 96.4-97.8%. The amounts of H2S released from the bacterial cells were quantified in real-time over a continuous time span of 5 h.
引用
收藏
页数:10
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