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Fabrication of a p-type Cu2O thin-film via UV-irradiation of a patternable molecular-precursor film containing Cu(II) complexes
•Cu2O crystal formation by UV-irradiation onto the molecular precursor film involving Cu(II) complexes at room temperature.•Novel patterning method utilizing water as the remover of the selective portion UV-shielded by a Na-free glass plate.•Fabrication of patterned thin film consisting of p-type Cu...
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Published in: | Journal of crystal growth 2019-03, Vol.509, p.112-117 |
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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: | •Cu2O crystal formation by UV-irradiation onto the molecular precursor film involving Cu(II) complexes at room temperature.•Novel patterning method utilizing water as the remover of the selective portion UV-shielded by a Na-free glass plate.•Fabrication of patterned thin film consisting of p-type Cu2O crystals, with high mobility of positive charge.
A patterned p-type Cu2O thin-film was fabricated using 4-mW cm−2 ultraviolet (UV) irradiation onto a preheated precursor-film formed on a Na-free glass by spin-coating a solution containing Cu(II) complexes of propylamine and ethylenediamine, and post-annealing. After a small Na-free glass plate was placed on the spin-coated and preheated precursor-film to provide a UV-shielded area, the film was UV-irradiated for 6 h at room temperature. X-ray diffraction measurement indicated that the UV-irradiation converted the Cu(II) complexes to crystallized Cu2O. The patterned film obtained by removal of the UV-shielded portion with immersion into water was then post-annealed at 400 °C for 3 min in an Ar-gas flow. The Hall effect measurement of the resultant film of a 90 nm thickness showed that the electrical resistivity, carrier concentration, and hole mobility were 1.4(2) × 102 Ω cm, 8(3) × 1016 cm−3, and 0.9(3) cm2 V−1 s−1, respectively. |
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ISSN: | 0022-0248 1873-5002 |
DOI: | 10.1016/j.jcrysgro.2018.12.036 |