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240716s2024 xx |||||o 00| ||eng c |
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|a 10.1002/adma.202404983
|2 doi
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|a pubmed24n1538.xml
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|a (NLM)39011787
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|a DE-627
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|e rakwb
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|a eng
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|a Hao, Zhimin
|e verfasserin
|4 aut
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|a Unveiling the In Situ Evolution of Li2O-Rich Solid Electrolyte Interface on CoOx Embedded Carbon Fibers as Li Anode Host
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|c 2024
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|a Text
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|a ƒaComputermedien
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|2 rdamedia
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|a ƒa Online-Ressource
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|a Date Revised 18.09.2024
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|a published: Print-Electronic
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|a ErratumIn: Adv Mater. 2024 Sep 18:e2411621. doi: 10.1002/adma.202411621. - PMID 39291886
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|a Citation Status PubMed-not-MEDLINE
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|a © 2024 Wiley‐VCH GmbH.
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|a Modification of three-dimensional (3D) carbon hosts with metal oxides has been considered as advantageous for the formation of Li2O-rich solid electrolyte interface (SEI), which can show fast Li+ diffusion, and meanwhile alleviate dendrite problems caused by fragility and nonuniformity of native SEIs. However, the lack of convincing experimental evidence has made it difficult to unveil the true origin of oxygen in Li2O-rich SEIs until now. Herein, CoOx embedded carbon nanofibers (CNF-CoOx) are successfully prepared as high-performance Li anode hosts. By employing 18O isotope labeling, the role of CoOx during SEI evolution is elucidated, revealing that CoOx contributes significantly to Li2O formation by delivering oxygen. Benefiting from the rich Li2O content, the as-formed SEIs greatly improve the Li+ migration kinetics, and therefore, the CNF-CoOxLi anode can exhibit excellent cycling stability in half, symmetrical, and full cells
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|a Journal Article
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|a CoOx
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|a Li anode host
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|a carbon nanofibers
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|a isotope labeling
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|a solid electrolyte interface
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|a Liu, Dapeng
|e verfasserin
|4 aut
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|a Zuo, Xintao
|e verfasserin
|4 aut
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|a Yu, Haohan
|e verfasserin
|4 aut
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|a Zhang, Yu
|e verfasserin
|4 aut
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|i Enthalten in
|t Advanced materials (Deerfield Beach, Fla.)
|d 1998
|g 36(2024), 36 vom: 16. Sept., Seite e2404983
|w (DE-627)NLM098206397
|x 1521-4095
|7 nnns
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|g volume:36
|g year:2024
|g number:36
|g day:16
|g month:09
|g pages:e2404983
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|u http://dx.doi.org/10.1002/adma.202404983
|3 Volltext
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