The NO2 response in the range of 200 ppb to 1 ppm of a chemoresistive WS2-decorated rGO sensor has been investigated at operating temperatures of 25 °C and 50 °C in dry and humid air (40% RH) under dark and Purple Blue (PB) light conditions (λ = 430 nm). Few-layers WS2, exfoliated by ball milling and sonication technique, with average dimensions of 200 nm, have been mixed with rGO flakes (average dimension 700 nm) to yield WS2-decorated rGO, deposited on Si3N4 substrates, provided with platinum (30 μm gap distance) finger-type electrodes. TEM analysis showed the formation of homogeneous and well-dispersed WS2 flakes distributed over a thin, continuous and uniform underlying layer of interconnected rGO flakes. XPS and STEM revealed a partial oxidation of WS2 flakes leading to the formation of 18% amorphous WO3 over the WS2 flakes. PB-light irradiation and mild heating of the sensor at 50 °C substantially enhanced the baseline recovery yielding improved adsorption/desorption rates, with detection limit of 400 ppb NO2 and reproducible gas responses. Cross sensitivity tests with humid air interfering vapor highlighted a negligible influence of water vapor on the NO2 response. A charge carrier mechanism between WS2 and rGO is proposed and discussed to explain the overall NO2 and H2O response of the WS2-rGO hybrids.

Near room temperature light-activated ws2-decorated rgo as no2 gas sensor

Paolucci V.
Methodology
;
Emamjomeh S. M.
Methodology
;
Ottaviano L.
Supervision
;
Cantalini C.
Supervision
2019-01-01

Abstract

The NO2 response in the range of 200 ppb to 1 ppm of a chemoresistive WS2-decorated rGO sensor has been investigated at operating temperatures of 25 °C and 50 °C in dry and humid air (40% RH) under dark and Purple Blue (PB) light conditions (λ = 430 nm). Few-layers WS2, exfoliated by ball milling and sonication technique, with average dimensions of 200 nm, have been mixed with rGO flakes (average dimension 700 nm) to yield WS2-decorated rGO, deposited on Si3N4 substrates, provided with platinum (30 μm gap distance) finger-type electrodes. TEM analysis showed the formation of homogeneous and well-dispersed WS2 flakes distributed over a thin, continuous and uniform underlying layer of interconnected rGO flakes. XPS and STEM revealed a partial oxidation of WS2 flakes leading to the formation of 18% amorphous WO3 over the WS2 flakes. PB-light irradiation and mild heating of the sensor at 50 °C substantially enhanced the baseline recovery yielding improved adsorption/desorption rates, with detection limit of 400 ppb NO2 and reproducible gas responses. Cross sensitivity tests with humid air interfering vapor highlighted a negligible influence of water vapor on the NO2 response. A charge carrier mechanism between WS2 and rGO is proposed and discussed to explain the overall NO2 and H2O response of the WS2-rGO hybrids.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11697/139659
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