Effects of the Post-Annealing Treatment on the Properties of Ga-Doped SnOx Thin Films

We investigated the effects of the post-annealing treatment (PAT) on the properties of Ga-doped tin-oxide (Ga-SnO x ) thin films grown at room temperature by using a radio-frequency magnetron sputtering technique. On the basis of X-ray photoelectron spectroscopy (XPS), dynamic secondaryion mass spec...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of the Korean Physical Society 2019, 75(8), , pp.561-568
Hauptverfasser: Bang, Hyo In, Yun, Eui-Jung, Bae, Byung Seong
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:We investigated the effects of the post-annealing treatment (PAT) on the properties of Ga-doped tin-oxide (Ga-SnO x ) thin films grown at room temperature by using a radio-frequency magnetron sputtering technique. On the basis of X-ray photoelectron spectroscopy (XPS), dynamic secondaryion mass spectrometry, X-ray diffraction (XRD), and Hall Effect measurements, we conclude that n -type SnO 2 is the dominant phase in all samples regardless of PAT at low temperatures (25–200 °C). The Sn 2+ area decreased to 32.5% with increasing temperature up to 150 °C, with a simultaneous increase in the Sn 4+ area to 59%. This was attributed to a decrease and an increase in the Ga and the oxygen contents in the samples, respectively, which also caused a decrease in the number of oxygen vacancies in the samples treated at higher temperatures. In contrast, XPS on the samples post-annealed at temperatures higher than 150 °C showed results opposite to those of the samples treated at temperatures lower than 150 °C. This indicates that the Ga ions in Ga-doped SnO x films act as hole acceptors and that heat treatment is useful for controlling the number of oxygen vacancies, Sn 2+ ions, and Sn 4+ ions in Ga-doped SnO x films. In addition, XRD showed that post-annealing did not affect the amorphous phase in the samples.
ISSN:0374-4884
1976-8524
DOI:10.3938/jkps.75.561