{"publication_status":"published","author":[{"full_name":"Li, Chunmei","last_name":"Li","first_name":"Chunmei"},{"full_name":"Fontaine, Olivier","last_name":"Fontaine","first_name":"Olivier"},{"first_name":"Stefan Alexander","last_name":"Freunberger","full_name":"Freunberger, Stefan Alexander","orcid":"0000-0003-2902-5319","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425"},{"full_name":"Johnson, Lee","last_name":"Johnson","first_name":"Lee"},{"full_name":"Grugeon, Sylvie","last_name":"Grugeon","first_name":"Sylvie"},{"last_name":"Laruelle","first_name":"Stéphane","full_name":"Laruelle, Stéphane"},{"full_name":"Bruce, Peter G.","last_name":"Bruce","first_name":"Peter G."},{"full_name":"Armand, Michel","last_name":"Armand","first_name":"Michel"}],"publication":"The Journal of Physical Chemistry C","publication_identifier":{"issn":["1932-7447","1932-7455"]},"month":"01","doi":"10.1021/jp4093805","date_published":"2014-01-29T00:00:00Z","quality_controlled":"1","issue":"7","language":[{"iso":"eng"}],"date_created":"2020-01-15T12:17:28Z","article_processing_charge":"No","_id":"7301","date_updated":"2021-01-12T08:12:53Z","extern":"1","intvolume":"       118","citation":{"mla":"Li, Chunmei, et al. “Aprotic Li–O2 Battery: Influence of Complexing Agents on Oxygen Reduction in an Aprotic Solvent.” <i>The Journal of Physical Chemistry C</i>, vol. 118, no. 7, ACS, 2014, pp. 3393–401, doi:<a href=\"https://doi.org/10.1021/jp4093805\">10.1021/jp4093805</a>.","ista":"Li C, Fontaine O, Freunberger SA, Johnson L, Grugeon S, Laruelle S, Bruce PG, Armand M. 2014. Aprotic Li–O2 battery: Influence of complexing agents on oxygen reduction in an aprotic solvent. The Journal of Physical Chemistry C. 118(7), 3393–3401.","chicago":"Li, Chunmei, Olivier Fontaine, Stefan Alexander Freunberger, Lee Johnson, Sylvie Grugeon, Stéphane Laruelle, Peter G. Bruce, and Michel Armand. “Aprotic Li–O2 Battery: Influence of Complexing Agents on Oxygen Reduction in an Aprotic Solvent.” <i>The Journal of Physical Chemistry C</i>. ACS, 2014. <a href=\"https://doi.org/10.1021/jp4093805\">https://doi.org/10.1021/jp4093805</a>.","apa":"Li, C., Fontaine, O., Freunberger, S. A., Johnson, L., Grugeon, S., Laruelle, S., … Armand, M. (2014). Aprotic Li–O2 battery: Influence of complexing agents on oxygen reduction in an aprotic solvent. <i>The Journal of Physical Chemistry C</i>. ACS. <a href=\"https://doi.org/10.1021/jp4093805\">https://doi.org/10.1021/jp4093805</a>","ama":"Li C, Fontaine O, Freunberger SA, et al. Aprotic Li–O2 battery: Influence of complexing agents on oxygen reduction in an aprotic solvent. <i>The Journal of Physical Chemistry C</i>. 2014;118(7):3393-3401. doi:<a href=\"https://doi.org/10.1021/jp4093805\">10.1021/jp4093805</a>","short":"C. Li, O. Fontaine, S.A. Freunberger, L. Johnson, S. Grugeon, S. Laruelle, P.G. Bruce, M. Armand, The Journal of Physical Chemistry C 118 (2014) 3393–3401.","ieee":"C. Li <i>et al.</i>, “Aprotic Li–O2 battery: Influence of complexing agents on oxygen reduction in an aprotic solvent,” <i>The Journal of Physical Chemistry C</i>, vol. 118, no. 7. ACS, pp. 3393–3401, 2014."},"day":"29","volume":118,"status":"public","year":"2014","type":"journal_article","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","article_type":"original","page":"3393-3401","title":"Aprotic Li–O2 battery: Influence of complexing agents on oxygen reduction in an aprotic solvent","publisher":"ACS","abstract":[{"lang":"eng","text":"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."}],"oa_version":"None"}