Repositório Institucional da Universidade de Aveiro > Departamento de Física > FIS - Artigos >
 Strain relaxation in GaN films as a function of growth direction and buffer layer measured by Raman spectroscopy
Please use this identifier to cite or link to this item http://hdl.handle.net/10773/6484

title: Strain relaxation in GaN films as a function of growth direction and buffer layer measured by Raman spectroscopy
authors: Seitz, R.
Monteiro, T.
Pereira, E.
Di Forte-Poisson, M.
keywords: Crystal orientation
Metallorganic chemical vapor deposition
Raman spectroscopy
issue date: 1999
publisher: Wiley-VCH Verlag Berlin GmbH
abstract: We studied the residual strain in hexagonal GaN epitaxial layers grown exactly or slightly off the (0001) direction on sapphire substrates with either GaN or AlN buffer layers (BLs). The residual strain was determined by Raman spectroscopy. The results were compared with photoluminescence (PL) measurements. We found that the samples with an AlN buffer layer show a residual compressive strain which depends on the misorientation between substrate and growth direction. The residual compressive strain decreases with increasing misorientation. A good correlation exists between Raman and PL measurements. Samples with GaN BL instead show a residual tensile strain which also depends slightly on the misorientation. The correlation between misorientation and residual strain can in this case only be established by Raman measurements.
URI: http://hdl.handle.net/10773/6484
ISSN: 0031-8965
publisher version/DOI: dx.doi.org/10.1002/(SICI)1521-396X(199911)
source: Physica Status Solidi (A) Applied Research
appears in collectionsFIS - Artigos

files in this item

file description sizeformat
PhysStat.pdfversão pdf do editor130.17 kBAdobe PDFview/open
Restrict Access. You can Request a copy!

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


Valid XHTML 1.0! RCAAP OpenAIRE DeGóis
ria-repositorio@ua.pt - Copyright ©   Universidade de Aveiro - RIA Statistics - Powered by MIT's DSpace software, Version 1.6.2