Defect and Surface Area Control in Hydrothermally Synthesized LiMn0.8Fe0.2PO4 Using a Phosphate Based Structure Directing Agent
As confirmed by ion coupled plasma-optical emission spectroscopy and powder X-ray diffraction, stoichiometrically pure samples of olivine type LiFe0.2Mn0.8PO4 in the presence of a phosphoric acid ester based structure directing agent have been prepared. A Rietveld analysis of X-ray and n0 diffractio...
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Veröffentlicht in: | Crystal growth & design 2015-09, Vol.15 (9), p.4213-4218 |
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creator | Schoiber, Jürgen Tippelt, Gerold Redhammer, Günther J Yada, Chihiro Dolotko, Oleksandr Berger, Raphael J. F Hüsing, Nicola |
description | As confirmed by ion coupled plasma-optical emission spectroscopy and powder X-ray diffraction, stoichiometrically pure samples of olivine type LiFe0.2Mn0.8PO4 in the presence of a phosphoric acid ester based structure directing agent have been prepared. A Rietveld analysis of X-ray and n0 diffraction data suggests that the solids are largely free of defect occupation of Fe at the lithium sites. This is confirmed by 57Fe-Mößbauer spectroscopic investigations. The use of the structure directing surfactant results in significantly higher specific surface areas (SSA) and smaller particle sizes as compared to samples prepared without using a surfactant. |
doi_str_mv | 10.1021/acs.cgd.5b00324 |
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The use of the structure directing surfactant results in significantly higher specific surface areas (SSA) and smaller particle sizes as compared to samples prepared without using a surfactant.</description><identifier>ISSN: 1528-7483</identifier><identifier>EISSN: 1528-7505</identifier><identifier>DOI: 10.1021/acs.cgd.5b00324</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Crystal growth & design, 2015-09, Vol.15 (9), p.4213-4218</ispartof><rights>Copyright © 2015 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.cgd.5b00324$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.cgd.5b00324$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,27076,27924,27925,56738,56788</link.rule.ids></links><search><creatorcontrib>Schoiber, Jürgen</creatorcontrib><creatorcontrib>Tippelt, Gerold</creatorcontrib><creatorcontrib>Redhammer, Günther J</creatorcontrib><creatorcontrib>Yada, Chihiro</creatorcontrib><creatorcontrib>Dolotko, Oleksandr</creatorcontrib><creatorcontrib>Berger, Raphael J. 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Growth Des</addtitle><date>2015-09-02</date><risdate>2015</risdate><volume>15</volume><issue>9</issue><spage>4213</spage><epage>4218</epage><pages>4213-4218</pages><issn>1528-7483</issn><eissn>1528-7505</eissn><abstract>As confirmed by ion coupled plasma-optical emission spectroscopy and powder X-ray diffraction, stoichiometrically pure samples of olivine type LiFe0.2Mn0.8PO4 in the presence of a phosphoric acid ester based structure directing agent have been prepared. A Rietveld analysis of X-ray and n0 diffraction data suggests that the solids are largely free of defect occupation of Fe at the lithium sites. This is confirmed by 57Fe-Mößbauer spectroscopic investigations. The use of the structure directing surfactant results in significantly higher specific surface areas (SSA) and smaller particle sizes as compared to samples prepared without using a surfactant.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.cgd.5b00324</doi><tpages>6</tpages></addata></record> |
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title | Defect and Surface Area Control in Hydrothermally Synthesized LiMn0.8Fe0.2PO4 Using a Phosphate Based Structure Directing Agent |
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