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	       <dc:title>The Enhanced Electrochemical Performance of Nanocrystalline Li[Li₀.₂₆Ni₀.₁₁Mn₀.₆₃]O₂ Synthesized by the Molten-Salt Method for Li-ion batteries</dc:title>
	       <dc:creator>ZhenYao, Wang; Biao, Li; Jin, Ma; DingGuo, Xia</dc:creator>
	       <dc:subject>37 INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; 77 NANOSCIENCE AND NANOTECHNOLOGY; CRYSTALS; DISTRIBUTION; ELECTRODES; EXTRACTION; LITHIUM; LITHIUM IONS; MOLTEN SALTS; NANOPARTICLES; NANOSTRUCTURES; OXIDES; PARTICLE SIZE; SYNTHESIS</dc:subject>
	       <dc:subjectRelated></dc:subjectRelated>
	       <dc:description>Nanocrystalline Li[Li₀.₂₆Ni₀.₁₁Mn₀.₆₃]O₂ were easily prepared by using Ni₀.₁₅Mn₀.₅(OH)₂ and Li₂CO₃ as precursors and KCl as melt-salt for the high capacity materials of Li-ion storage. The obtained nanoparticles showed same morphology of polygonal shape and the particle size distribution increased with increasing sinter temperature. The Li[Li₀.₂₆Ni₀.₁₁Mn₀.₆₃]O₂ electrode sintered at 800 °C for 12 h exhibits a reversible capacity of more than 300 mAh g⁻¹ at 0.1 C rate between 2 V and 4.8 V and the capacity retention remains 86% and 90% after 90 cycles at the rate of 0.5 C and 1 C, respectively. These superior electrochemical performances are discussed in detail and ascribed to the low dimension and well-crystallized particles. The low dimension provides a short diffusion path and fast transport channels for the lithium ion insertion/extraction reactions and the well-crystallized structure restrains the elimination of oxide ion vacancies and metal ions rearrangement during charge–discharge cycling.</dc:description>
	       <dcq:publisher></dcq:publisher>
	       <dcq:publisherResearch></dcq:publisherResearch>
	       <dcq:publisherAvailability>Available from http://dx.doi.org/10.1016/j.electacta.2013.11.124</dcq:publisherAvailability>
	       <dcq:publisherSponsor></dcq:publisherSponsor>
	       <dcq:publisherCountry>United Kingdom</dcq:publisherCountry>
		   <dc:contributingOrganizations></dc:contributingOrganizations>
	       <dc:date>2014-01-01</dc:date>
	       <dc:language>English</dc:language>
	       <dc:type>Journal Article</dc:type>
	       <dcq:typeQualifier></dcq:typeQualifier>
	       <dc:relation>Journal Name: Electrochimica Acta; Journal Volume: 117; Other Information: Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA)</dc:relation>
	       <dc:coverage></dc:coverage>
	       <dc:format>Medium: X; Size: page(s) 285-291</dc:format>
	       <dc:doi>https://doi.org/10.1016/J.ELECTACTA.2013.11.124</dc:doi>
	       <dc:identifier>PII: S0013-4686(13)02357-8</dc:identifier>
		   <dc:journalName>[]</dc:journalName>
		   <dc:journalIssue></dc:journalIssue>
		   <dc:journalVolume>117</dc:journalVolume>
	       <dc:identifierReport></dc:identifierReport>
	       <dcq:identifierDOEcontract></dcq:identifierDOEcontract>
	       <dc:identifierOther>Journal ID: ISSN 0013-4686; CODEN: ELCAAV; Other: PII: S0013-4686(13)02357-8; TRN: GB15R1009028068</dc:identifierOther>
	       <dc:source>INIS</dc:source>
	       <dc:rights></dc:rights>
	       <dc:dateEntry>2015-05-05</dc:dateEntry>
	       <dc:dateAdded></dc:dateAdded>
	       <dc:ostiId>22321859</dc:ostiId>
	       <dcq:identifier-purl></dcq:identifier-purl>
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