Synthesis and characterization of ZnO/SnO2 nanorods core–shell arrays for high performance gas sensors
In this work, three samples were synthesized; SnO 2 nanoparticles, ZnO nanorods and ZnO/SnO 2 core–shell nanorods. The preparation of the ZnO/SnO 2 composite included two steps, the first was to spin ZnO thin film as a seed layer. The second step is to grow ZnO/SnO 2 to produce core–shell nanorod de...
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Published in | Applied physics. A, Materials science & processing Vol. 127; no. 3 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.03.2021
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | In this work, three samples were synthesized; SnO
2
nanoparticles, ZnO nanorods and ZnO/SnO
2
core–shell nanorods. The preparation of the ZnO/SnO
2
composite included two steps, the first was to spin ZnO thin film as a seed layer. The second step is to grow ZnO/SnO
2
to produce core–shell nanorod devices. The structure and morphology of the prepared samples were characterized by X-ray diffraction (XRD) and field emission scanning electron microscopy (FE-SEM). Meanwhile, the optical properties were investigated by ultraviolet–visible (UV–Vis) and photoluminescence (PL) spectroscopy. The morphology of the prepared sample revealed that ZnO nanorods were capped by SnO
2
shell. The energy band gap of ZnO/SnO
2
is lower than that of both bare ZnO and SnO
2
. Evaluations to near-band (PL) emission of bare ZnO nanorod arrays were considerably reduced by capping with SnO
2
sell. The performance of the gas sensor was further examined on the basis of ZnO/SnO
2
. The response and sensitivity were measured to be 86.6 ( ± 0.5) at optimum operating temperature of 225 °C toward 100 ppm ethanol vapor, which is even higher than those of the bare ZnO nanorods. The local sites added by the SnO
2
shell layer could probably stop the excitons from becoming captured by intrinsic defects, leading to improved sensitivity of the gas sensor. |
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ISSN: | 0947-8396 1432-0630 |
DOI: | 10.1007/s00339-021-04357-4 |