<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Zhao, Yan</dc:creator>
  <dc:creator>Zhou, Tianhong</dc:creator>
  <dc:creator>Baster, Dominika</dc:creator>
  <dc:creator>El Kazzi, Mario</dc:creator>
  <dc:creator>Choi, Jang Wook</dc:creator>
  <dc:creator>Coskun, Ali</dc:creator>
  <dc:date>2023-06-27</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Understanding the degradation pathways and reactivity of electrolytes is the key to address the shortcomings of conventional electrolytes and to develop new electrolytes for high-voltage lithium metal batteries (LMBs). Accordingly, while 1,3-dioxolane (DOL) exhibits desired features such as good compatibility with Li metal, low viscosity, and high ionic conductivity, it suffers from poor oxidation stability, mainly from its ring-opening polymerization. In an effort to control the reactivity of DOL by tuning its electronic properties, we introduced methyl and trifluoromethyl groups to the ethyl moiety of DOL and developed 4-methyl-1,3-dioxolane (MDOL) and 4-(trifluoromethyl)-1,3-dioxolane (TFDOL) as solvents, respectively. Whereas the MDOL-based electrolyte exhibited serious side reactions toward metallic Li, the TFDOL-based electrolyte showed oxidation stability up to 5.0 V. Moreover, the inorganic-rich solid electrolyte interphase induced by the weak solvation power of TFDOL along with high oxidation stability enabled a robust cycling stability in a Li|NCM811 full cell (20 μm Li foil, N/P ratio of 2.5).</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/325452</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/325452/files/acsenergylett.3c01004.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1021/acsenergylett.3c01004</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/issn/2380-8195</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>Rights reserved</dc:rights>
  <dc:source>ACS Energy Letters. - American Chemical Society (ACS). - 2023, vol. 8, no. 30, p. 3180-3187</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Materials Chemistry</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Energy Engineering and Power Technology</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Fuel Technology</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Renewable Energy</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Sustainability and the Environment</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Chemistry (miscellaneous)</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns7="xml" ns7:lang="en">Targeted Functionalization of Cyclic Ether Solvents for Controlled Reactivity in High-Voltage Lithium Metal Batteries</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
