Decomposition of LiGdF4 scheelite at high pressures
The high-pressure behaviour of LiGdF4 scheelite (I41/a, Z = 4) was studied by measuring its angle-dispersive x-ray powder diffraction patterns as a function of pressure and temperature in a diamond anvil cell and a large-volume Paris–Edinburgh cell using a synchrotron radiation source. Upon compress...
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Veröffentlicht in: | Journal of physics. Condensed matter 2004-11, Vol.16 (43), p.7779-7786 |
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creator | Grzechnik, Andrzej Crichton, Wilson A Bouvier, Pierre Dmitriev, Vladimir Weber, Hans-Peter Gesland, Jean-Yves |
description | The high-pressure behaviour of LiGdF4 scheelite (I41/a, Z = 4) was studied by measuring its angle-dispersive x-ray powder diffraction patterns as a function of pressure and temperature in a diamond anvil cell and a large-volume Paris–Edinburgh cell using a synchrotron radiation source. Upon compression to about 11 GPa at room temperature, the stable structure is of the scheelite type. At higher pressures and T = 298 K, new reflections occur that cannot be explained with the fergusonite structural model previously observed for LiY F4. Associated with this is the growth of an amorphous component. All the transformations are largely irreversible upon decompression. Annealing of the sample at 13.1 GPa led to a nucleation of a solid solution series LiyGd1−yF3−2y (P63/mmc, Z = 2) and traces of LiF. The new material LiyGd1−yF3−2y (P63/mmc, Z = 2) was recovered to ambient conditions but back-transformed to a Y F3-type phase (Pnma, Z = 4) after regrinding at room temperature for several hours. These observations are discussed in relation to the high-pressure high-temperature systematics of the AMX4-type compounds. |
doi_str_mv | 10.1088/0953-8984/16/43/017 |
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Upon compression to about 11 GPa at room temperature, the stable structure is of the scheelite type. At higher pressures and T = 298 K, new reflections occur that cannot be explained with the fergusonite structural model previously observed for LiY F4. Associated with this is the growth of an amorphous component. All the transformations are largely irreversible upon decompression. Annealing of the sample at 13.1 GPa led to a nucleation of a solid solution series LiyGd1−yF3−2y (P63/mmc, Z = 2) and traces of LiF. The new material LiyGd1−yF3−2y (P63/mmc, Z = 2) was recovered to ambient conditions but back-transformed to a Y F3-type phase (Pnma, Z = 4) after regrinding at room temperature for several hours. These observations are discussed in relation to the high-pressure high-temperature systematics of the AMX4-type compounds.</description><identifier>ISSN: 0953-8984</identifier><identifier>EISSN: 1361-648X</identifier><identifier>DOI: 10.1088/0953-8984/16/43/017</identifier><identifier>CODEN: JCOMEL</identifier><language>eng</language><publisher>Bristol: IOP Publishing</publisher><subject>Chemical Sciences ; Condensed matter: structure, mechanical and thermal properties ; Crystalline state (including molecular motions in solids) ; Crystallographic aspects of phase transformations; pressure effects ; Exact sciences and technology ; Material chemistry ; Physics ; Structure of solids and liquids; crystallography</subject><ispartof>Journal of physics. Condensed matter, 2004-11, Vol.16 (43), p.7779-7786</ispartof><rights>2004 INIST-CNRS</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0003-1882-6786</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://iopscience.iop.org/article/10.1088/0953-8984/16/43/017/pdf$$EPDF$$P50$$Giop$$H</linktopdf><link.rule.ids>230,314,780,784,885,27915,27916,53821,53901</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16211240$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00417895$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Grzechnik, Andrzej</creatorcontrib><creatorcontrib>Crichton, Wilson A</creatorcontrib><creatorcontrib>Bouvier, Pierre</creatorcontrib><creatorcontrib>Dmitriev, Vladimir</creatorcontrib><creatorcontrib>Weber, Hans-Peter</creatorcontrib><creatorcontrib>Gesland, Jean-Yves</creatorcontrib><title>Decomposition of LiGdF4 scheelite at high pressures</title><title>Journal of physics. Condensed matter</title><description>The high-pressure behaviour of LiGdF4 scheelite (I41/a, Z = 4) was studied by measuring its angle-dispersive x-ray powder diffraction patterns as a function of pressure and temperature in a diamond anvil cell and a large-volume Paris–Edinburgh cell using a synchrotron radiation source. Upon compression to about 11 GPa at room temperature, the stable structure is of the scheelite type. At higher pressures and T = 298 K, new reflections occur that cannot be explained with the fergusonite structural model previously observed for LiY F4. Associated with this is the growth of an amorphous component. All the transformations are largely irreversible upon decompression. Annealing of the sample at 13.1 GPa led to a nucleation of a solid solution series LiyGd1−yF3−2y (P63/mmc, Z = 2) and traces of LiF. The new material LiyGd1−yF3−2y (P63/mmc, Z = 2) was recovered to ambient conditions but back-transformed to a Y F3-type phase (Pnma, Z = 4) after regrinding at room temperature for several hours. These observations are discussed in relation to the high-pressure high-temperature systematics of the AMX4-type compounds.</description><subject>Chemical Sciences</subject><subject>Condensed matter: structure, mechanical and thermal properties</subject><subject>Crystalline state (including molecular motions in solids)</subject><subject>Crystallographic aspects of phase transformations; pressure effects</subject><subject>Exact sciences and technology</subject><subject>Material chemistry</subject><subject>Physics</subject><subject>Structure of solids and liquids; crystallography</subject><issn>0953-8984</issn><issn>1361-648X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNptkEFLw0AQhRdRsFZ_gZdcPCik2dndZDfHUm0VAl4UvC3TZGJW0iZko-C_d0OlF73MwMz3hjePsWvgC-DGJDxPZWxyoxLIEiUTDvqEzUBmEGfKvJ2y2ZE4Zxfef3DOlZFqxuQ9ld2u77wbXbePujoq3KZaq8iXDVHrRopwjBr33kT9QN5_hnLJzmpsPV399jl7XT-8rB7j4nnztFoWcSOEHGOtZUoVoJI6GNmm9eSnCn54zinFbEtAVW0wx0pLRCTgILTAVEhOWyI5Z7eHuw22th_cDodv26Gzj8vCTrPwBGiTp18Q2JsD26Mvsa0H3JfOH1WQCQCheODuDpzr-uN2CsdO4QTOKmlDfLav6gAv_sLA7ZT5fyL5A1mAcAs</recordid><startdate>20041103</startdate><enddate>20041103</enddate><creator>Grzechnik, Andrzej</creator><creator>Crichton, Wilson A</creator><creator>Bouvier, Pierre</creator><creator>Dmitriev, Vladimir</creator><creator>Weber, Hans-Peter</creator><creator>Gesland, Jean-Yves</creator><general>IOP Publishing</general><general>Institute of Physics</general><general>IOP Publishing [1989-....]</general><scope>IQODW</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-1882-6786</orcidid></search><sort><creationdate>20041103</creationdate><title>Decomposition of LiGdF4 scheelite at high pressures</title><author>Grzechnik, Andrzej ; Crichton, Wilson A ; Bouvier, Pierre ; Dmitriev, Vladimir ; Weber, Hans-Peter ; Gesland, Jean-Yves</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h223t-7735ed1a437361b5f1361d648090e5a6be1edf8a9ad73aaae101272a5230ebee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Chemical Sciences</topic><topic>Condensed matter: structure, mechanical and thermal properties</topic><topic>Crystalline state (including molecular motions in solids)</topic><topic>Crystallographic aspects of phase transformations; pressure effects</topic><topic>Exact sciences and technology</topic><topic>Material chemistry</topic><topic>Physics</topic><topic>Structure of solids and liquids; crystallography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grzechnik, Andrzej</creatorcontrib><creatorcontrib>Crichton, Wilson A</creatorcontrib><creatorcontrib>Bouvier, Pierre</creatorcontrib><creatorcontrib>Dmitriev, Vladimir</creatorcontrib><creatorcontrib>Weber, Hans-Peter</creatorcontrib><creatorcontrib>Gesland, Jean-Yves</creatorcontrib><collection>Pascal-Francis</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of physics. Condensed matter</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grzechnik, Andrzej</au><au>Crichton, Wilson A</au><au>Bouvier, Pierre</au><au>Dmitriev, Vladimir</au><au>Weber, Hans-Peter</au><au>Gesland, Jean-Yves</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decomposition of LiGdF4 scheelite at high pressures</atitle><jtitle>Journal of physics. Condensed matter</jtitle><date>2004-11-03</date><risdate>2004</risdate><volume>16</volume><issue>43</issue><spage>7779</spage><epage>7786</epage><pages>7779-7786</pages><issn>0953-8984</issn><eissn>1361-648X</eissn><coden>JCOMEL</coden><abstract>The high-pressure behaviour of LiGdF4 scheelite (I41/a, Z = 4) was studied by measuring its angle-dispersive x-ray powder diffraction patterns as a function of pressure and temperature in a diamond anvil cell and a large-volume Paris–Edinburgh cell using a synchrotron radiation source. Upon compression to about 11 GPa at room temperature, the stable structure is of the scheelite type. At higher pressures and T = 298 K, new reflections occur that cannot be explained with the fergusonite structural model previously observed for LiY F4. Associated with this is the growth of an amorphous component. All the transformations are largely irreversible upon decompression. Annealing of the sample at 13.1 GPa led to a nucleation of a solid solution series LiyGd1−yF3−2y (P63/mmc, Z = 2) and traces of LiF. The new material LiyGd1−yF3−2y (P63/mmc, Z = 2) was recovered to ambient conditions but back-transformed to a Y F3-type phase (Pnma, Z = 4) after regrinding at room temperature for several hours. These observations are discussed in relation to the high-pressure high-temperature systematics of the AMX4-type compounds.</abstract><cop>Bristol</cop><pub>IOP Publishing</pub><doi>10.1088/0953-8984/16/43/017</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-1882-6786</orcidid></addata></record> |
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subjects | Chemical Sciences Condensed matter: structure, mechanical and thermal properties Crystalline state (including molecular motions in solids) Crystallographic aspects of phase transformations pressure effects Exact sciences and technology Material chemistry Physics Structure of solids and liquids crystallography |
title | Decomposition of LiGdF4 scheelite at high pressures |
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