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弹性晶格助力高容量氧化锰阴极中可逆四面体锂存储位点的形成

Elastic Lattice Enabling Reversible Tetrahedral Li Storage Sites in a High-Capacity Manganese Oxide Cathode.

作者信息

Huang Weiyuan, Yang Luyi, Chen Zhefeng, Liu Tongchao, Ren Guoxi, Shan Peizhao, Zhang Bin-Wei, Chen Shiming, Li Shunning, Li Jianyuan, Lin Cong, Zhao Wenguang, Qiu Jimin, Fang Jianjun, Zhang Mingjian, Dong Cheng, Li Fan, Yang Yong, Sun Cheng-Jun, Ren Yang, Huang Qingzhen, Hou Guangjin, Dou Shi-Xue, Lu Jun, Amine Khalil, Pan Feng

机构信息

School of Advanced Materials, Peking University Shenzhen Graduate School, Shenzhen, 518055, P. R. China.

Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, IL, 60439, USA.

出版信息

Adv Mater. 2022 Jul;34(30):e2202745. doi: 10.1002/adma.202202745. Epub 2022 Jun 23.

Abstract

The key to breaking through the capacity limitation imposed by intercalation chemistry lies in the ability to harness more active sites that can reversibly accommodate more ions (e.g., Li ) and electrons within a finite space. However, excessive Li-ion insertion into the Li layer of layered cathodes results in fast performance decay due to the huge lattice change and irreversible phase transformation. In this study, an ultrahigh reversible capacity is demonstrated by a layered oxide cathode purely based on manganese. Through a wealth of characterizations, it is clarified that the presence of low-content Li MnO domains not only reduces the amount of irreversible O loss; but also regulates Mn migration in LiMnO domains, enabling elastic lattice with high reversibility for tetrahedral sites Li-ion storage in Li layers. This work utilizes bulk cation disorder to create stable Li-ion-storage tetrahedral sites and an elastic lattice for layered materials, with a reversible capacity of 600 mA h g , demonstrated in th range 0.6-4.9 V versus Li/Li at 10 mA g . Admittedly, discharging to 0.6 V might be too low for practical use, but this exploration is still of great importance as it conceptually demonstrates the limit of Li-ions insertion into layered oxide materials.

摘要

突破嵌入化学所带来的容量限制的关键在于能够利用更多的活性位点,这些活性位点能够在有限的空间内可逆地容纳更多的离子(例如锂离子)和电子。然而,过量的锂离子插入层状阴极的锂层会由于巨大的晶格变化和不可逆的相变而导致快速的性能衰减。在本研究中,一种纯锰层状氧化物阴极展现出了超高的可逆容量。通过大量的表征,明确了低含量的LiMnO域的存在不仅减少了不可逆的氧损失量;而且还调节了LiMnO域中的锰迁移,使得晶格具有弹性,能够在锂层中为四面体位置的锂离子存储提供高可逆性。这项工作利用体阳离子无序为层状材料创造了稳定的锂离子存储四面体位置和弹性晶格,在10 mA g的电流密度下,相对于Li/Li在0.6 - 4.9 V的电压范围内,展现出了600 mA h g的可逆容量。诚然,放电至0.6 V对于实际应用来说可能过低,但这种探索仍然非常重要,因为它从概念上证明了锂离子插入层状氧化物材料的极限。

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