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contributor authorQian
contributor authorGuannan;Zan
contributor authorGuibin;Li
contributor authorJizhou;Zhang
contributor authorJin;Pianetta
contributor authorPiero;Liu
contributor authorYijin
date accessioned2022-08-18T12:52:18Z
date available2022-08-18T12:52:18Z
date copyright6/6/2022 12:00:00 AM
date issued2022
identifier issn2381-6872
identifier otherjeecs_19_4_041002.pdf
identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4287007
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.
publisherThe American Society of Mechanical Engineers (ASME)
titleIn-Situ Visualization of the Transition Metal Dissolution in Layered Cathodes
typeJournal Paper
journal volume19
journal issue4
journal titleJournal of Electrochemical Energy Conversion and Storage
identifier doi10.1115/1.4054584
journal fristpage41002-1
journal lastpage41002-6
page6
treeJournal of Electrochemical Energy Conversion and Storage:;2022:;volume( 019 ):;issue: 004
contenttypeFulltext


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