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dc.contributor.authorQian
dc.contributor.authorGuannan;Zan
dc.contributor.authorGuibin;Li
dc.contributor.authorJizhou;Zhang
dc.contributor.authorJin;Pianetta
dc.contributor.authorPiero;Liu
dc.contributor.authorYijin
dc.date.accessioned2022-08-18T12:52:18Z
dc.date.available2022-08-18T12:52:18Z
dc.date.copyright6/6/2022 12:00:00 AM
dc.date.issued2022
dc.identifier.issn2381-6872
dc.identifier.otherjeecs_19_4_041002.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4287007
dc.description.abstractTransition metal dissolution in layered cathodes is one of the most intractable issues that deteriorate the battery performance and lifetime. It not only aggravates the structure degradation in cathode but also damages the solid electrolyte interphase in anode and even induces the formation of lithium dendrites. In this work, we investigate the dissolution behaviors of polycrystalline and single-crystalline layered cathode via operando X-ray imaging techniques. The cathode particle morphology appears to have a significant impact on the evolution of the dissolution dynamics. As a mitigation strategy, we reveal that doping with a trace amount of Zr in the layered cathode could improve its robustness against the transition metal dissolution. Our finding provides valuable insights for designing the next-generation highly stable layered battery cathodes.
dc.publisherThe American Society of Mechanical Engineers (ASME)
dc.titleIn-Situ Visualization of the Transition Metal Dissolution in Layered Cathodes
dc.typeJournal Paper
dc.journal.volume19
dc.journal.issue4
dc.journal.titleJournal of Electrochemical Energy Conversion and Storage
dc.identifier.doi10.1115/1.4054584
dc.journal.fristpage41002-1
dc.journal.lastpage41002-6
dc.page6
dc.treeJournal of Electrochemical Energy Conversion and Storage:;2022:;volume( 019 ):;issue: 004
dc.contenttypeFulltext


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