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Synthesis of Monodisperse and Discrete Ultra-High Nickel LiNiCoMnO Octahedral Single Crystals via Single Crystal Intermediates for Li-Ion Batteries.

作者信息

Choi Seung Hyun, Hong Soon-Kie, Yun Byunghyun, Jung Junho, Baik Chanhyun, Kim Kanghyeon, Lee Kyu Tae

机构信息

School of Chemical and Biological Engineering, Institute of Chemical Processes, Institute of Engineering Research, Seoul National University, Seoul 08826, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2024 Nov 6;16(44):60298-60309. doi: 10.1021/acsami.4c13570. Epub 2024 Oct 28.

Abstract

Micrometer-sized single crystal cathodes have garnered significant interest as promising cathode materials for lithium-ion batteries due to their ability to reduce surface area exposure to electrolytes and suppress side reactions, thereby enhancing electrochemical performance. One of the challenging issues with single crystal cathode materials is synthesizing monodisperse and discrete single crystals rather than agglomerated quasi-single crystals. However, conventional solid-state synthesis of most single crystals results in severe agglomeration and cation mixing, as it requires high temperatures to promote particle growth to several micrometers. In this study, a novel morphology-conserving reaction strategy that employs octahedron single crystal intermediates is introduced to synthesize discrete, monodisperse LiNiCoMnO octahedron single crystals. This scalable and cost-effective approach involves using rock-salt NiCoMnO octahedrons as single crystal intermediates, which are transformed in unreactive unary lithium salt melts (LiCl and LiSO) from spherical NiCoMn(OH) obtained via coprecipitation. These intermediates are then subjected to a stoichiometric amount of Li precursor in a conventional solid-state synthesis to produce layered LiNiCoMnO. This process is a morphology-conserving lithiation reaction, leading to the formation of discrete and monodisperse LiNiCoMnO octahedron single crystals. The resultant LiNiCoMnO single crystals demonstrate superior electrochemical performance, including stable capacity retention over 150 cycles, which surpasses that of typical quasi-single crystals produced through conventional methods. This is attributed to negligible crack formation during cycling, in contrast to significant cracking observed in conventional quasi-single crystals. This implies that single-crystal forms are preferred over agglomerated quasi-single crystal forms for enhancing cycle performance. These findings provide valuable insights into the industrial synthesis of discrete and monodisperse ultrahigh-nickel oxide cathode materials.

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