Loading…
Interfacial Phase Stability in TiV Multilaminate Thin Films
The influence of the interfacial energy on the material phase stability is investigated for a series of TiV multilaminate thin films. Experiments reveal that at a higher layer thickness, the α (hcp) phase is the most stable. As the layer thickness is reduced, a transformation from the α (hcp) phase...
Saved in:
Published in: | Journal of physical chemistry. C 2009-12, Vol.113 (51), p.21383-21388 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-a259t-380f71254368d17ad8f3393fa8fec5855457cd1bfb15b2c69db9e31a041f06ca3 |
---|---|
cites | cdi_FETCH-LOGICAL-a259t-380f71254368d17ad8f3393fa8fec5855457cd1bfb15b2c69db9e31a041f06ca3 |
container_end_page | 21388 |
container_issue | 51 |
container_start_page | 21383 |
container_title | Journal of physical chemistry. C |
container_volume | 113 |
creator | Stott, Amanda C Abel, Phillip B Bozzolo, Guillermo H Dixon, David A |
description | The influence of the interfacial energy on the material phase stability is investigated for a series of TiV multilaminate thin films. Experiments reveal that at a higher layer thickness, the α (hcp) phase is the most stable. As the layer thickness is reduced, a transformation from the α (hcp) phase to the β (bcc) phase occurs. Atomic-scale characterization of the transformed specimen by atom probe tomography reveals V interfacial diffusion between the layers. Equivalent crystal theory based calculations confirm the V interfacial diffusion mechanism. The predicted segregation profiles match those obtained experimentally. |
doi_str_mv | 10.1021/jp907807k |
format | article |
fullrecord | <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_jp907807k</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c486333613</sourcerecordid><originalsourceid>FETCH-LOGICAL-a259t-380f71254368d17ad8f3393fa8fec5855457cd1bfb15b2c69db9e31a041f06ca3</originalsourceid><addsrcrecordid>eNptj8FLwzAYxYMoOKcH_4NcPHio5muaJsWTDKeDiYLVa_maJiw160aSHfbfW5ns5Ok9Hj8e7xFyDewOWA73_bZiUjH5fUImUPE8k4UQp0dfyHNyEWPPmOAM-IQ8LIZkgkXt0NP3FUZDPxK2zru0p26gtfuirzufnMe1GzAZWq_GeO78Ol6SM4s-mqs_nZLP-VM9e8mWb8-L2eMyw1xUKeOKWQm5KHipOpDYKct5xS0qa7RQQhRC6g5a24Joc11WXVsZDsgKsKzUyKfk9tCrwybGYGyzDW6NYd8Aa35fN8fXI3tzYFHHpt_swjAu-4f7ARS3VZA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Interfacial Phase Stability in TiV Multilaminate Thin Films</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)</source><creator>Stott, Amanda C ; Abel, Phillip B ; Bozzolo, Guillermo H ; Dixon, David A</creator><creatorcontrib>Stott, Amanda C ; Abel, Phillip B ; Bozzolo, Guillermo H ; Dixon, David A</creatorcontrib><description>The influence of the interfacial energy on the material phase stability is investigated for a series of TiV multilaminate thin films. Experiments reveal that at a higher layer thickness, the α (hcp) phase is the most stable. As the layer thickness is reduced, a transformation from the α (hcp) phase to the β (bcc) phase occurs. Atomic-scale characterization of the transformed specimen by atom probe tomography reveals V interfacial diffusion between the layers. Equivalent crystal theory based calculations confirm the V interfacial diffusion mechanism. The predicted segregation profiles match those obtained experimentally.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/jp907807k</identifier><language>eng</language><publisher>American Chemical Society</publisher><subject>C: Surfaces, Interfaces, Catalysis</subject><ispartof>Journal of physical chemistry. C, 2009-12, Vol.113 (51), p.21383-21388</ispartof><rights>Copyright © 2009 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a259t-380f71254368d17ad8f3393fa8fec5855457cd1bfb15b2c69db9e31a041f06ca3</citedby><cites>FETCH-LOGICAL-a259t-380f71254368d17ad8f3393fa8fec5855457cd1bfb15b2c69db9e31a041f06ca3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Stott, Amanda C</creatorcontrib><creatorcontrib>Abel, Phillip B</creatorcontrib><creatorcontrib>Bozzolo, Guillermo H</creatorcontrib><creatorcontrib>Dixon, David A</creatorcontrib><title>Interfacial Phase Stability in TiV Multilaminate Thin Films</title><title>Journal of physical chemistry. C</title><addtitle>J. Phys. Chem. C</addtitle><description>The influence of the interfacial energy on the material phase stability is investigated for a series of TiV multilaminate thin films. Experiments reveal that at a higher layer thickness, the α (hcp) phase is the most stable. As the layer thickness is reduced, a transformation from the α (hcp) phase to the β (bcc) phase occurs. Atomic-scale characterization of the transformed specimen by atom probe tomography reveals V interfacial diffusion between the layers. Equivalent crystal theory based calculations confirm the V interfacial diffusion mechanism. The predicted segregation profiles match those obtained experimentally.</description><subject>C: Surfaces, Interfaces, Catalysis</subject><issn>1932-7447</issn><issn>1932-7455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNptj8FLwzAYxYMoOKcH_4NcPHio5muaJsWTDKeDiYLVa_maJiw160aSHfbfW5ns5Ok9Hj8e7xFyDewOWA73_bZiUjH5fUImUPE8k4UQp0dfyHNyEWPPmOAM-IQ8LIZkgkXt0NP3FUZDPxK2zru0p26gtfuirzufnMe1GzAZWq_GeO78Ol6SM4s-mqs_nZLP-VM9e8mWb8-L2eMyw1xUKeOKWQm5KHipOpDYKct5xS0qa7RQQhRC6g5a24Joc11WXVsZDsgKsKzUyKfk9tCrwybGYGyzDW6NYd8Aa35fN8fXI3tzYFHHpt_swjAu-4f7ARS3VZA</recordid><startdate>20091224</startdate><enddate>20091224</enddate><creator>Stott, Amanda C</creator><creator>Abel, Phillip B</creator><creator>Bozzolo, Guillermo H</creator><creator>Dixon, David A</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20091224</creationdate><title>Interfacial Phase Stability in TiV Multilaminate Thin Films</title><author>Stott, Amanda C ; Abel, Phillip B ; Bozzolo, Guillermo H ; Dixon, David A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a259t-380f71254368d17ad8f3393fa8fec5855457cd1bfb15b2c69db9e31a041f06ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>C: Surfaces, Interfaces, Catalysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stott, Amanda C</creatorcontrib><creatorcontrib>Abel, Phillip B</creatorcontrib><creatorcontrib>Bozzolo, Guillermo H</creatorcontrib><creatorcontrib>Dixon, David A</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of physical chemistry. C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stott, Amanda C</au><au>Abel, Phillip B</au><au>Bozzolo, Guillermo H</au><au>Dixon, David A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interfacial Phase Stability in TiV Multilaminate Thin Films</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2009-12-24</date><risdate>2009</risdate><volume>113</volume><issue>51</issue><spage>21383</spage><epage>21388</epage><pages>21383-21388</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>The influence of the interfacial energy on the material phase stability is investigated for a series of TiV multilaminate thin films. Experiments reveal that at a higher layer thickness, the α (hcp) phase is the most stable. As the layer thickness is reduced, a transformation from the α (hcp) phase to the β (bcc) phase occurs. Atomic-scale characterization of the transformed specimen by atom probe tomography reveals V interfacial diffusion between the layers. Equivalent crystal theory based calculations confirm the V interfacial diffusion mechanism. The predicted segregation profiles match those obtained experimentally.</abstract><pub>American Chemical Society</pub><doi>10.1021/jp907807k</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-7447 |
ispartof | Journal of physical chemistry. C, 2009-12, Vol.113 (51), p.21383-21388 |
issn | 1932-7447 1932-7455 |
language | eng |
recordid | cdi_crossref_primary_10_1021_jp907807k |
source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | C: Surfaces, Interfaces, Catalysis |
title | Interfacial Phase Stability in TiV Multilaminate Thin Films |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T12%3A48%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Interfacial%20Phase%20Stability%20in%20TiV%20Multilaminate%20Thin%20Films&rft.jtitle=Journal%20of%20physical%20chemistry.%20C&rft.au=Stott,%20Amanda%20C&rft.date=2009-12-24&rft.volume=113&rft.issue=51&rft.spage=21383&rft.epage=21388&rft.pages=21383-21388&rft.issn=1932-7447&rft.eissn=1932-7455&rft_id=info:doi/10.1021/jp907807k&rft_dat=%3Cacs_cross%3Ec486333613%3C/acs_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a259t-380f71254368d17ad8f3393fa8fec5855457cd1bfb15b2c69db9e31a041f06ca3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |