Comparative analysis of oxide phase formation and its effects on electrical properties of SiO2/InSb metal-oxide-semiconductor structures
- Authors
- Lee, Jaeyel; Park, Sehun; Kim, Jungsub; Yang, Changjae; Kim, Sujin; Seok, Chulkyun; Park, Jinsub; Yoon, Euijoon
- Issue Date
- Jun-2012
- Publisher
- Elsevier Sequoia
- Keywords
- InSb; SiO2; PECVD; Interface; XPS
- Citation
- Thin Solid Films, v.520, no.16, pp 5382 - 5385
- Pages
- 4
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- Thin Solid Films
- Volume
- 520
- Number
- 16
- Start Page
- 5382
- End Page
- 5385
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/165396
- DOI
- 10.1016/j.tsf.2012.04.007
- ISSN
- 0040-6090
- Abstract
- We report on the changes in the interfacial phases between SiO2 and InSb caused by various deposition temperatures and heat treatments. X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy were used to evaluate the relative amount of each phase present at the interface. The effect of interfacial phases on the electrical properties of SiO2/InSb metal-oxide-semiconductor (MOS) structures was investigated by capacitance-voltage (C-V) measurements. The amount of both In and Sb oxides increased with the deposition temperature. The amount of interfacial In oxide was larger for all samples, regardless of the deposition and annealing temperatures and times. In particular, the annealed samples contained less than half the amount of Sb oxide compared with the as-deposited samples, indicating a strong interfacial reaction between Sb oxide and the InSb substrate during annealing. The interface trap density sharply increased for deposition temperatures above 240 degrees C. The C-V measurements and Raman spectroscopy indicated that elemental Sb accumulation due to the interfacial reaction of Sb oxide with InSb substrate was responsible for the increased interfacial trap densities in these SiO2/InSb MOS structures.
- Files in This Item
-
Go to Link
- Appears in
Collections - 서울 공과대학 > 서울 융합전자공학부 > 1. Journal Articles

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.