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Issue 39, 2017
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Room-temperature SO2 gas-sensing properties based on a metal-doped MoS2 nanoflower: an experimental and density functional theory investigation

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Abstract

This paper demonstrates a sulfur dioxide (SO2) gas sensor based on a transition-metal-doped molybdenum disulfide (MoS2) nanocomposite synthesized via a facile single-step hydrothermal route. The Ni-doped, Fe-doped, Co-doped, and pristine MoS2 film sensors were fabricated on a FR4 epoxy substrate with interdigital electrodes. The morphologies, microstructures, and compositions of as-prepared samples were fully examined using X-ray diffraction, energy dispersive spectroscopy, scanning electron microscopy, transmission electron microscope, and X-ray photoelectron spectroscopy. The gas-sensing properties of the four samples were systematically investigated at room temperature, and the Ni-doped MoS2 film sensor was screened out as the optimal SO2 sensor among the four sensors, exhibiting a relatively high response value, quick response/recovery time, and excellent stability toward SO2 gas. Furthermore, in order to explain the experimental results, we used Materials Studio software to construct molecular models of adsorption systems and calculate the geometry, energy, and charge parameters via density functional theory (DFT) based on first principles. The sensing mechanism is also discussed in depth. Through a comprehensive research approach of combining experimentation with DFT simulation, this work suggests that an Ni-doped MoS2 film sensor is able to detect SO2 gas at room temperature.

Graphical abstract: Room-temperature SO2 gas-sensing properties based on a metal-doped MoS2 nanoflower: an experimental and density functional theory investigation

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Article information


Submitted
08 Aug 2017
Accepted
06 Sep 2017
First published
06 Sep 2017

J. Mater. Chem. A, 2017,5, 20666-20677
Article type
Paper

Room-temperature SO2 gas-sensing properties based on a metal-doped MoS2 nanoflower: an experimental and density functional theory investigation

D. Zhang, J. Wu, P. Li and Y. Cao, J. Mater. Chem. A, 2017, 5, 20666
DOI: 10.1039/C7TA07001B

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