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Temperature Dependent Raman Spectroscopy and Sensing Behavior of Few Layer SnSe 2 Nanosheets
Author(s) -
Pawbake Amit S.,
Date Abhijit,
Jadkar Sandesh R.,
Late Dattatray J.
Publication year - 2016
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201601347
Subject(s) - raman spectroscopy , materials science , relative humidity , softening , humidity , atmospheric temperature range , active layer , analytical chemistry (journal) , layer (electronics) , spectroscopy , tin , optoelectronics , nanotechnology , optics , composite material , chemistry , chromatography , quantum mechanics , meteorology , metallurgy , thermodynamics , thin film transistor , physics
Two‐ dimensional (2D) tin diselenide (SnSe 2 ) nanosheets were synthesized using solvothermal route in one step and perform its humidity sensing, photo sensing and temperature dependant Raman spectroscopy studies. The sensor devices based on few layer SnSe 2 nanosheets were prepared and which shows fast response as well as recovery time along with good long‐term stability and high sensitivity. The photo sensing behavior shows the typical response time and recovery time to be ∼ 310 ms and ∼ 340 ms respectively for visible light illumination. The room temperature humidity sensing behaviors were studied in the range of 11–97 % relative humidity (RH). The observed sensitivity of ∼ 81 % with response time of ∼ 74 sec and recovery time of ∼ 30 sec were calculated for the few layer SnSe 2 nanosheets based humidity sensor. The humidity sensing results confirms the high stability of the device even after six months of time. The temperature dependent Raman spectroscopy investigation in the range of 80 K to 593 K were carried out which shows the negative temperature coefficient and softening of Raman modes as we increases the temperature. The softening modes of SnSe 2 nanosheets due to temperature were explained on the basis of a double resonance process which is more active in an atomically thin sample.