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   	<dc:title>Aprotic Li–O2 battery: Influence of complexing agents on oxygen reduction in an aprotic solvent</dc:title>
   	<dc:creator>Li, Chunmei</dc:creator>
   	<dc:creator>Fontaine, Olivier</dc:creator>
   	<dc:creator>Freunberger, Stefan Alexander ; https://orcid.org/0000-0003-2902-5319</dc:creator>
   	<dc:creator>Johnson, Lee</dc:creator>
   	<dc:creator>Grugeon, Sylvie</dc:creator>
   	<dc:creator>Laruelle, Stéphane</dc:creator>
   	<dc:creator>Bruce, Peter G.</dc:creator>
   	<dc:creator>Armand, Michel</dc:creator>
   	<dc:description>Several problems arise at the O2 (positive) electrode in the Li-air battery, including solvent/electrode decomposition and electrode passivation by insulating Li2O2. Progress partially depends on exploring the basic electrochemistry of O2 reduction. Here we describe the effect of complexing-cations on the electrochemical reduction of O2 in DMSO in the presence and absence of a Li salt. The solubility of alkaline peroxides in DMSO is enhanced by the complexing-cations, consistent with their strong interaction with reduced O2. The complexing-cations also increase the rate of the 1-electron O2 reduction to O2•– by up to six-fold (k° = 2.4 ×10–3 to 1.5 × 10–2 cm s–1) whether or not Li+ ions are present. In the absence of Li+, the complexing-cations also promote the reduction of O2•– to O22–. In the presence of Li+ and complexing-cations, and despite the interaction of the reduced O2 with the latter, SERS confirms that the product is still Li2O2.</dc:description>
   	<dc:publisher>ACS</dc:publisher>
   	<dc:date>2014</dc:date>
   	<dc:type>info:eu-repo/semantics/article</dc:type>
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   	<dc:type>text</dc:type>
   	<dc:type>http://purl.org/coar/resource_type/c_2df8fbb1</dc:type>
   	<dc:identifier>https://research-explorer.ista.ac.at/record/7301</dc:identifier>
   	<dc:source>Li C, Fontaine O, Freunberger SA, et al. Aprotic Li–O2 battery: Influence of complexing agents on oxygen reduction in an aprotic solvent. &lt;i&gt;The Journal of Physical Chemistry C&lt;/i&gt;. 2014;118(7):3393-3401. doi:&lt;a href=&quot;https://doi.org/10.1021/jp4093805&quot;&gt;10.1021/jp4093805&lt;/a&gt;</dc:source>
   	<dc:language>eng</dc:language>
   	<dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1021/jp4093805</dc:relation>
   	<dc:relation>info:eu-repo/semantics/altIdentifier/issn/1932-7447</dc:relation>
   	<dc:relation>info:eu-repo/semantics/altIdentifier/issn/1932-7455</dc:relation>
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