Metastable II–VI sulphides: Growth, characterization and stability

Among the II–VI compounds, many sulphides have the stable rocksalt structure, but can also be grown by MBE in the metastable zinc blende (ZB) form in epitaxial thin films, including MgS and MnS. By using a metal rich growth regime where sulphur is supplied from the evaporation of ZnS, we have shown...

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Veröffentlicht in:Journal of crystal growth 2011-05, Vol.323 (1), p.114-121
Hauptverfasser: Prior, K.A., Bradford, C., Davidson, I.A., Moug, R.T.
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creator Prior, K.A.
Bradford, C.
Davidson, I.A.
Moug, R.T.
description Among the II–VI compounds, many sulphides have the stable rocksalt structure, but can also be grown by MBE in the metastable zinc blende (ZB) form in epitaxial thin films, including MgS and MnS. By using a metal rich growth regime where sulphur is supplied from the evaporation of ZnS, we have shown that layers of both MgS and MnS up to 140nm thick can be grown in the ZB structure, allowing the production of different multilayer structures exploiting the properties of these novel semiconductors. This review concentrates on developments in MgS, which we have studied in greater detail than the other compounds and has proved a very versatile component of multilayer structures. These include the development of new metastable MgS-rich ZnMgSSe quaternary alloys, which we have been able to incorporate into structures with MgS and have used to develop a new lift off technology. Comparison of the growth of MgS, ZnMgS and ZnMgSSe has allowed us to determine the incorporation coefficients of Zn and Mg, which are approximately 0.03 and 0.4, respectively. The Zn flux appears to play a crucial role in the development of the film, by forming a ZnMgS surface layer, aiding transport of material across the surface and increasing the energy barrier to conversion to the stable rocksalt phase. TEM shows that occasionally both ZB and RS phases may be present simultaneously. The small RS inclusions seem to stabilise the ZB phase against relaxation and do not propagate through the crystal. Examination of the totally converted films suggests that they are composed of different rocksalt domains and may not have transformed via the mechanism which has been suggested as the lowest route for bulk MgS.
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Semiconducting II–VI materials</topic><topic>Condensed matter: structure, mechanical and thermal properties</topic><topic>Cross-disciplinary physics: materials science; rheology</topic><topic>Exact sciences and technology</topic><topic>Inclusions</topic><topic>Materials science</topic><topic>Methods of deposition of films and coatings; film growth and epitaxy</topic><topic>Molecular beam epitaxy</topic><topic>Molecular, atomic, ion, and chemical beam epitaxy</topic><topic>Multilayers</topic><topic>Other semiconductors</topic><topic>Physics</topic><topic>Quaternary alloys</topic><topic>Semiconductors</topic><topic>Specific materials</topic><topic>Structure and morphology; thickness</topic><topic>Sulfides</topic><topic>Sulfur</topic><topic>Surfaces and interfaces; thin films and whiskers (structure and nonelectronic properties)</topic><topic>Theory and models of film growth</topic><topic>Thin film structure and morphology</topic><topic>Zinc</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Prior, K.A.</creatorcontrib><creatorcontrib>Bradford, C.</creatorcontrib><creatorcontrib>Davidson, I.A.</creatorcontrib><creatorcontrib>Moug, R.T.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of crystal growth</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Prior, K.A.</au><au>Bradford, C.</au><au>Davidson, I.A.</au><au>Moug, R.T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metastable II–VI sulphides: Growth, characterization and stability</atitle><jtitle>Journal of crystal growth</jtitle><date>2011-05-15</date><risdate>2011</risdate><volume>323</volume><issue>1</issue><spage>114</spage><epage>121</epage><pages>114-121</pages><issn>0022-0248</issn><eissn>1873-5002</eissn><coden>JCRGAE</coden><abstract>Among the II–VI compounds, many sulphides have the stable rocksalt structure, but can also be grown by MBE in the metastable zinc blende (ZB) form in epitaxial thin films, including MgS and MnS. 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subjects A1. Morphological stability
A3. Molecular Beam Epitaxy
B1. Sulphides
B2. Semiconducting II–VI materials
Condensed matter: structure, mechanical and thermal properties
Cross-disciplinary physics: materials science
rheology
Exact sciences and technology
Inclusions
Materials science
Methods of deposition of films and coatings
film growth and epitaxy
Molecular beam epitaxy
Molecular, atomic, ion, and chemical beam epitaxy
Multilayers
Other semiconductors
Physics
Quaternary alloys
Semiconductors
Specific materials
Structure and morphology
thickness
Sulfides
Sulfur
Surfaces and interfaces
thin films and whiskers (structure and nonelectronic properties)
Theory and models of film growth
Thin film structure and morphology
Zinc
title Metastable II–VI sulphides: Growth, characterization and stability
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