DC Field | Value | Language |
---|---|---|
dc.contributor.author | Cha, Jong-Ho | ko |
dc.contributor.author | Shin, Kyuchul | ko |
dc.contributor.author | Choi, Sukjeong | ko |
dc.contributor.author | Lee, Sangyong | ko |
dc.contributor.author | Lee, Huen | ko |
dc.date.accessioned | 2009-05-07T02:15:53Z | - |
dc.date.available | 2009-05-07T02:15:53Z | - |
dc.date.created | 2012-02-06 | - |
dc.date.created | 2012-02-06 | - |
dc.date.issued | 2008-09 | - |
dc.identifier.citation | JOURNAL OF PHYSICAL CHEMISTRY C, v.112, no.35, pp.13332 - 13335 | - |
dc.identifier.issn | 1932-7447 | - |
dc.identifier.uri | http://hdl.handle.net/10203/8885 | - |
dc.description.abstract | The unique and specific interaction of ionic guests with the surrounding cage framework might play a key role in promoting the electrochemical properties of ionic clathrate hydrates. In this work we focus on addressing (1) structural transformation simply due to an increase of water content, (2) structure-dependent ionic conductivity, (3) the existence of maximum ionic conductivity at a specific hydration number, and (4) proton migration through channels in the crystalline hydrate matrix. The melting temperature and ionic conductivity of hexafluorophosphoric acid hexahydrate (HPF6-6.0H(2)O) are found to be approximately 29.5 degrees C and 10(-1) S.cm(-1). respectively, showing that HPF6 center dot 6.0H(2)O possesses desirable features as a solid proton conductor. | - |
dc.description.sponsorship | This work was supported by the Korea Science and Engineering Foundation (KOSEF) through the National Research Laboratory Program funded by the Ministry of Education, Science and Technology (R0A-2005-000-10074-0(2008)) and partially supported by the Brain Korea 21 Project. | en |
dc.language | English | - |
dc.language.iso | en_US | en |
dc.publisher | AMER CHEMICAL SOC | - |
dc.subject | STRUCTURE TRANSITION | - |
dc.subject | PATTERN | - |
dc.subject | ACID | - |
dc.title | Maximized proton conductivity of the HPF6 clathrate hydrate by structural transformation | - |
dc.type | Article | - |
dc.identifier.wosid | 000258800700006 | - |
dc.identifier.scopusid | 2-s2.0-52649127341 | - |
dc.type.rims | ART | - |
dc.citation.volume | 112 | - |
dc.citation.issue | 35 | - |
dc.citation.beginningpage | 13332 | - |
dc.citation.endingpage | 13335 | - |
dc.citation.publicationname | JOURNAL OF PHYSICAL CHEMISTRY C | - |
dc.identifier.doi | 10.1021/jp805510g | - |
dc.embargo.liftdate | 9999-12-31 | - |
dc.embargo.terms | 9999-12-31 | - |
dc.contributor.localauthor | Lee, Huen | - |
dc.contributor.nonIdAuthor | Lee, Sangyong | - |
dc.type.journalArticle | Letter | - |
dc.subject.keywordPlus | STRUCTURE TRANSITION | - |
dc.subject.keywordPlus | PATTERN | - |
dc.subject.keywordPlus | ACID | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.