期刊
SENSORS AND ACTUATORS B-CHEMICAL
卷 326, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2020.128844
关键词
Nanocomposites; Real-time sensor; Gasotransmitters; Serum biomarker; Live cells; In-Situsensors
资金
- Ministry of Science and Technology (MOST) Taiwan (ROC) [107-2113-M-027-007, 108-2221-E-027-063]
- King Abdullah University of Science and Technology (KAUST), Saudi Arabia
A robust electrode based on RGO-MoS2 and POPD was developed to address electrode poisoning and interference challenges in H2S sensor development, enabling efficient detection of H2S and applications in various biological media. The method achieved a detection limit of 10 nM with a response time of less than 5 seconds, and practical tests showed valuable recoveries of 96.4-97.8% in different biological environments. Real-time quantification of H2S released from bacterial cells over a continuous 5-hour span was successfully demonstrated.
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.
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