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dc.contributor.authorWu, Junru
dc.contributor.authorWang, Xianshu
dc.contributor.authorLiu, Qi
dc.contributor.authorWang, Shuwei
dc.contributor.authorZhou, Dong
dc.contributor.authorKang, Feiyu
dc.contributor.authorShanmukaraj, Devaraj
dc.contributor.authorArmand, Michel
dc.contributor.authorRojo Aparicio, Teófilo ORCID
dc.contributor.authorLi, Baohua
dc.contributor.authorWang, Guoxiu
dc.date.accessioned2021-11-18T08:38:54Z
dc.date.available2021-11-18T08:38:54Z
dc.date.issued2021-09-30
dc.identifier.citationNature Communications 12(1) : (2021) // Article ID 5746es_ES
dc.identifier.issn2041-1723
dc.identifier.urihttp://hdl.handle.net/10810/53802
dc.description.abstract[EN]The energy content increase is of paramount importance for the development of future Li-based batteries. Here, the authors propose a gel polymer electrolyte in combination with a positive electrode comprising of a Li-rich oxide active material and graphite to produce a high-energy Li metal cell. The current Li-based battery technology is limited in terms of energy contents. Therefore, several approaches are considered to improve the energy density of these energy storage devices. Here, we report the combination of a heteroatom-based gel polymer electrolyte with a hybrid cathode comprising of a Li-rich oxide active material and graphite conductive agent to produce a high-energy "shuttle-relay" Li metal battery, where additional capacity is generated from the electrolyte's anion shuttling at high voltages. The gel polymer electrolyte, prepared via in situ polymerization in an all-fluorinated electrolyte, shows adequate ionic conductivity (around 2 mS cm(-1) at 25 degrees C), oxidation stability (up to 5.5 V vs Li/Li+), compatibility with Li metal and safety aspects (i.e., non-flammability). The polymeric electrolyte allows for a reversible insertion of hexafluorophosphate anions into the conductive graphite (i.e., dual-ion mechanism) after the removal of Li ions from Li-rich oxide (i.e., rocking-chair mechanism).es_ES
dc.description.sponsorshipProf. B. Li would like to acknowledge the support funded by the National Nature Science Foundation of China (No. 51872157), Shenzhen Key Laboratory (ZDSYS201707271615073), and Guangdong Technical Plan Project (No. 2017B090907005). Prof. G. Wang would like to acknowledge the support from Australian Research Council (ARC) Discovery Projects (DP200101249 and DP210101389) and the ARC Research Hub for Integrated Energy Storage Solutions (IH180100020). We would like to thank Prof. Atsuo Yamada from The University of Tokyo for giving valuable advice on this work.es_ES
dc.language.isoenges_ES
dc.publisherNature Researches_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectgraphite/electrolyte interfacees_ES
dc.subjectsolvation sheathes_ES
dc.subjectelectrolyteses_ES
dc.subjectperformancees_ES
dc.subjectstoragees_ES
dc.subjectcostes_ES
dc.subjectli+es_ES
dc.titleA synergistic exploitation to produce high-voltage quasi-solid-state lithium metal batterieses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://www.nature.com/articles/s41467-021-26073-6es_ES
dc.identifier.doi10.1038/s41467-021-26073-6
dc.departamentoesQuímica Orgánica e Inorgánicaes_ES
dc.departamentoeuKimika Organikoa eta Ez-Organikoaes_ES


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This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Except where otherwise noted, this item's license is described as This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.