4.7 Article

Hierarchical MnS@MoS2 architectures on tea bag filter paper for flexible, sensitive, and selective non-enzymatic hydrogen peroxide sensors

Journal

JOURNAL OF ALLOYS AND COMPOUNDS
Volume 855, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2020.157103

Keywords

Analyte utilization rate; Core@shell architecture; Flexibility; Micro cubes; Nanosheets

Funding

  1. Department of Science and Technology, New Delhi [DST/TMD/HFC/2K18/52(C)]
  2. Deanship of Scientific Research at King Khalid University [R.G.P.1/177/41]

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In this study, MnO2 nanorods coated tea bag filter paper were developed as a self-standing, bendable, and disposable electrochemical probe for sensitive and selective H2O2 detection. By addressing challenges in H2O2 sensing and utilizing core@shell architecture with MoS2, the MnS@MoS2/TBFP probe showed low detection limit, excellent sensitivity, and wide linear range for H2O2 detection. The non-enzymatic H2O2 detection performances of MnS/MoS2/TBFP were found to be selective, decisive, repeatable, and stable, making them promising for practical applications.
We report here the rational development of MnO2 nanorods coated tea bag filter paper (TBFP) as a self-standing, bendable, and disposable electrochemical probe for the sensitive and selective H2O2 detection and addresses their challenges in H2O2 sensing via the replacement of 'O' with 'S' in the form of MnS microcubes and its core@shell architecture with MoS2. The as-configured MnS@MoS2/TBFP overwhelms the constrains of conventional electrochemical probes including time and cost consumed electrode surface renewability and catalyst loading progression, and the practice of an insulating binder. The hierarchical open porous architectures of MoS2-shell favour the diffusion of H2O2 into the core-MnS microcubes, facilitating an analyte utilization efficacy at both the core and shell architectures. The impacts of core@shell morphological features, replacement of 'O' with 'S', surface defects, and lattice distribution of MnS@MoS2 toward non-enzymatic H2O2 sensing performances are elucidated using variant electrochemical techniques. With the synergism of uniformly implanted and exposed metallic active sites, efficient electron transfer rate, and high analyte utilization efficiency, MnS@MoS2/TBFP exposes the low detection limit (120 nM), excellent sensitivity (650 mu A mM(-1) cm(-2)), and wide linear range (500 nM-5 mM) on H2O2 detection. Furthermore, the scrutinized non-enzymatic H2O2 detection concerts of MnS/MoS2/TBFP are selective, decisive, repeatable, and stable, constructing the excellent recovery rates in human urine sample analyses. Thus, the collective benefits of free-standing, flexible, binder-less, refunctional, and cost-efficient MnS@MoS2/TBFP probe actualize the evolution of affordable and high performance H2O2 sensors. (C) 2020 Elsevier B.V. All rights reserved.

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