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	       <dc:title>Filming mechanism of lithium-carbon anodes in organic and inorganic electrolytes</dc:title>
	       <dc:creator>Besenhard, J O [Inst. fuer Chemische Technologie Anorganischer Stoffe, Technische Univ., Graz (Austria)]; Winter, M [Inst. fuer Chemische Technologie Anorganischer Stoffe, Technische Univ., Graz (Austria)]; Yang, J [Inst. fuer Chemische Technologie Anorganischer Stoffe, Technische Univ., Graz (Austria)]; Biberacher, W [Walther-Meissner-Inst. fuer Tieftemperaturforschung, Garching (Germany)]</dc:creator>
	       <dc:subject>25 ENERGY STORAGE; GRAPHITE; ANODES; CLATHRATES; LAYERS; ELECTRIC BATTERIES; LITHIUM; SULFUR DIOXIDE; THIONYL CHLORIDES; DME; CARBONIC ACID ESTERS; FILMS; LITHIUM PERCHLORATES; POLAROGRAPHY</dc:subject>
	       <dc:subjectRelated></dc:subjectRelated>
	       <dc:description>To study the filming mechanism of graphite-based LiC{sub n} electrodes, electrochemical reduction of graphite materials was carried out in 1 M LiClO{sub 4}/ethylene carbonate (EC)-1,2-dimethoxyethane (DME) (1:1 by volume). Due to film forming a peak at potentials around 0.8 V versus Li/Li{sup +} was observed during the first reduction. The reversibility of this peak was examined by cyclic voltammetry; in addition, the crystal expansion/contraction was checked by means of dilatometry. The results indicate that ternary solvated graphite-intercalation compounds (GICs) were formed at those potentials leading to drastic expansion of the graphite matrix (>150%). These Li(EC){sub y1}(DME){sub y2}C{sub n}-GICs decompose and build up a protective layer on the graphite that prevents further solvent co-intercalation. The beneficial effect of EC-containing electrolytes on the stability of lithium-carbon anodes seems to be related to inorganic films formed via secondary chemical decomposition of electrochemically formed EC-GICs. The key-role of inorganic films is also demonstrated by the fact that inorganic additives, such as carbon dioxide, suppress the formation of solvated GICs. Furthermore, it can be seen that lithium-carbon negatives can even be operated in inorganic electrolytes such as SO{sub 2} and SOCl{sub 2}. (orig.)</dc:description>
	       <dcq:publisher></dcq:publisher>
	       <dcq:publisherResearch></dcq:publisherResearch>
	       <dcq:publisherAvailability></dcq:publisherAvailability>
	       <dcq:publisherSponsor></dcq:publisherSponsor>
	       <dcq:publisherCountry>Switzerland</dcq:publisherCountry>
		   <dc:contributingOrganizations></dc:contributingOrganizations>
	       <dc:date>1995-04-01</dc:date>
	       <dc:language>English</dc:language>
	       <dc:type>Journal Article</dc:type>
	       <dcq:typeQualifier></dcq:typeQualifier>
	       <dc:relation>Journal Name: Journal of Power Sources; Journal Volume: 54; Journal Issue: 2; Conference: 7. international meeting on lithium batteries (IMLB-7), Cambridge, MA (United States), 15-20 May 1994; Other Information: PBD: Apr 1995</dc:relation>
	       <dc:coverage></dc:coverage>
	       <dc:format>Medium: X; Size: pp. 228-231</dc:format>
	       <dc:doi>https://doi.org/10.1016/0378-7753(94)02073-C</dc:doi>
	       <dc:identifier></dc:identifier>
		   <dc:journalName>[]</dc:journalName>
		   <dc:journalIssue>2</dc:journalIssue>
		   <dc:journalVolume>54</dc:journalVolume>
	       <dc:identifierReport>CONF-940568-</dc:identifierReport>
	       <dcq:identifierDOEcontract></dcq:identifierDOEcontract>
	       <dc:identifierOther>Journal ID: JPSODZ; ISSN 0378-7753; TRN: CH95GI367</dc:identifierOther>
	       <dc:source>CHF; SCA: 250903; PA: CHF-95:0GI367; EDB-95:147784; SN: 95001456422</dc:source>
	       <dc:rights></dc:rights>
	       <dc:dateEntry>2010-12-29</dc:dateEntry>
	       <dc:dateAdded></dc:dateAdded>
	       <dc:ostiId>123073</dc:ostiId>
	       <dcq:identifier-purl></dcq:identifier-purl>
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