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A comparative study on gas-sensing behavior of reduced graphene oxide (rGO) synthesized by chemical and environment-friendly green method
This paper presents a comparative study on gas-sensing behavior of reduced graphene oxide (rGO) synthesized by chemical and green synthesis route. GO is synthesized by Hummers method and then reduced employing two reducing agents hydrazine hydrate [represented by (rGO) 1 ] and l -citrulline [represe...
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Published in: | Applied nanoscience 2020-02, Vol.10 (2), p.517-528 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | This paper presents a comparative study on gas-sensing behavior of reduced graphene oxide (rGO) synthesized by chemical and green synthesis route. GO is synthesized by Hummers method and then reduced employing two reducing agents hydrazine hydrate [represented by (rGO)
1
] and
l
-citrulline [represented by (rGO)
2
]. Synthesized products were then obtained in the form of thin films, and tested for 10 ppm NO
2
and CO at operating temperatures of 50, 100, and 150 °C. The green-synthesized reduced graphene oxide (rGO)
2
exhibits higher relative response of 254.7% as compared to conventionally synthesized (rGO)
1
(93.9%) and GO (22.7%) for 10 ppm NO
2
at operating temperature of 150 °C. Furthermore, a switching of conductivity from usual p-type behavior to n-type on exposure of NO
2
is observed at all operating temperatures (50, 100, and 150 °C) for GO, (rGO)
1
, and (rGO)
2
. The XRD, FTIR, and Raman confirm the oxidation and reduction process. (rGO)
2
shows high thermal stability as observed through TGA. FESEM and TEM images show wrinkled sheet structure for GO as well (rGO)
1
and (rGO)
2
. The data observed from the characterization of resultant products have made it possible to explain better reduction of GO through green-reducing agent and enhanced gas-sensing performance of green-synthesized reduced graphene oxide. |
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ISSN: | 2190-5509 2190-5517 |
DOI: | 10.1007/s13204-019-01138-7 |