Effect of Sb doping on structural and photoelectric properties of SnO2 thin films
Sb-doped SnO 2 (ATO) thin films were synthesized via the sol–gel dip-coating method on glass substrates. The XPS and XRD spectra showed that Sb atoms were successfully incorporated into the SnO 2 lattice and mostly existed in the form of Sb 5+ (~ 90%) in 1 at.% ATO thin films annealed in air and fur...
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Published in | Journal of materials science. Materials in electronics Vol. 31; no. 4; pp. 3289 - 3302 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.02.2020
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Sb-doped SnO
2
(ATO) thin films were synthesized via the sol–gel dip-coating method on glass substrates. The XPS and XRD spectra showed that Sb atoms were successfully incorporated into the SnO
2
lattice and mostly existed in the form of Sb
5+
(~ 90%) in 1 at.% ATO thin films annealed in air and further annealed in vacuum. The transmittance spectra revealed that the average transmittance was more than 75% at the wavelength range of 325–700 nm. The average sheet resistancewas 14.05 kΩ/□ in 1 at.% ATO thin films annealing in air and much less than undoped SnO
2
. The electric property was better when ATO thin films were further annealing vacuum compared to annealing in air. The average sheet resistance and resistivity of 1 at.% ATO thin films were 2.42 kΩ/□ and 0.035 Ω cm, respectively. The PL showed that electrons transition from a shallow level of
V
O
to the minimum level of conduction band (CBM) increased with increasing of Sb
3+
ions. The maximum level of valence band (VBM) and CBM level positions were mainly affected by Sb
3+
and Sb
5+
energy levels after air annealing, respectively. The behavior of surface carrier transport was investigated after further vacuum annealing. The CBM–VBM level position mainly was affected by
V
O
energy level after further vacuum annealing. It was further proved by the Hall carrier concentration and the electrochemical impedance spectroscopy (EIS). |
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ISSN: | 0957-4522 1573-482X |
DOI: | 10.1007/s10854-020-02877-y |