2016
DOI: 10.1007/s11664-016-4816-7
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Fabrication and Characterization of p-Type SnO Thin Film with High c-Axis Preferred Orientation

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Cited by 16 publications
(11 citation statements)
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“…To avoid confusion from the contamination and possible oxidation of the film surface during the air exposure before the XPS analysis, the thin surface layer (2–3 nm) was in situ etched using an accelerated (1 kV) Ar + ion before the spectrum acquisition. The Sn 3d peaks could be deconvoluted to two components with binding energies of 484.7 eV (Sn 0 ) and 486.2 eV (Sn 2+ ), without involving the peak at 486.9 eV, which corresponds to Sn 4+ even in the case of zero Sn dc power. The binding energy was calibrated with the C 1s peak position (284.6 eV). Therefore, it can be understood that the possible formation of SnO 2 was well-suppressed under the entire process conditions.…”
Section: Resultsmentioning
confidence: 99%
“…To avoid confusion from the contamination and possible oxidation of the film surface during the air exposure before the XPS analysis, the thin surface layer (2–3 nm) was in situ etched using an accelerated (1 kV) Ar + ion before the spectrum acquisition. The Sn 3d peaks could be deconvoluted to two components with binding energies of 484.7 eV (Sn 0 ) and 486.2 eV (Sn 2+ ), without involving the peak at 486.9 eV, which corresponds to Sn 4+ even in the case of zero Sn dc power. The binding energy was calibrated with the C 1s peak position (284.6 eV). Therefore, it can be understood that the possible formation of SnO 2 was well-suppressed under the entire process conditions.…”
Section: Resultsmentioning
confidence: 99%
“…76 On the other hand, Pei et al reported highly stable SnO layers reaching their highest crystalline quality during RTA (with unspecified annealing time) at 700 • C in nitrogen. 16 Interestingly, Yabuta et al demonstrated that a SiO x capping layer preseves the SnO layer by preventing oxygen exchange with the environment using annealing experiments in nitrogen, oxygen and air at 400 • C. 77 We note, however, that a capping layer cannot prevent disproportionation of the film at temperatures above ≈ 400 • C (cf. Fig1).…”
Section: Stability Of the Sno Phase After Growthmentioning
confidence: 86%
“…10 The observed p-type conductivity of unintentionally doped (UID) SnO has been correlated by first-principle calculations with Sn vacancies 14 or their complexes with hydrogen 15 acting as shallow acceptors, whereas oxygen interstitials were predicted to be electrically inactive. 14,15 SnO thin films have been grown by various methods, such as electron-beam evaporation 16 or reactive DC magnetron sputtering, 13 both followed by thermal annealing, reactive ion beam sputter deposition, 9 pulsed laser deposition (PLD) from an oxide target 10,12,17 or a metallic Sn target 18 , and molecular beam epitaxy (MBE). 8,19,20 The largest challenge for the growth of phase pure SnO is its metastability with respect to its stable relatives Sn and SnO 2 .…”
Section: Introductionmentioning
confidence: 99%
“…19,20 High-quality few-layer SnO has been successfully obtained experimentally via conventional thin-film fabrication methods such as atomic layer deposition 13 and electron beam evaporation. 21 In a study by Saji et al, the growth of SnO has also been reportedly achieved with single-layer precision on sapphire and SiO 2 substrates using pulsed laser deposition. 22 Tin (II) oxide has been widely explored as a p-type channel layer for high-performance TFTs, with field effect mobilities of as high as 1.9 cm 2 V −1 s −1 .…”
Section: Introductionmentioning
confidence: 99%