Cross-Linked Polyamide-Integrated Argyrodite Li6PS5Cl for All-Solid-State Lithium Metal Batterie

IF 13 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Small Pub Date : 2024-11-22 DOI:10.1002/smll.202408824
Yang Xu, Zhiqiang Fang, Junyi Yue, Limin Wang, Zaifa Wang, Simeng Zhang, Mengzhu Liu, Zimujun Ye, Ran Liu, Xiaolong Yan, Xu Han, Yueyue Wang, Changtai Zhao, Biwei Xiao, Xianbao Wang, Wei Xiao, Xiaona Li, Tao Mei, Jianwen Liang
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Abstract

Lithium dendrite growth has become a significant barrier to realizing high-performance all-solid-state lithium metal batteries. Herein, an effective approach is presented to address this challenge through interphase engineering by using a cross-linked polyamide (negative electrostatic potential) that is chemically anchored to the surface of Li6PS5Cl (positive electrostatic potential). This method improves contact between electrolyte particles and strategically modifies the local electronic structure at the grain boundary. This innovation effectively suppresses lithium dendrite formation and enhances the overall interface stability. As a result, the critical current density of the Li6PS5Cl sulfide electrolyte is dramatically boosted from 0.4 to 1.6 mA cm−2, representing a remarkable fourfold improvement. Moreover, Li–Li symmetric batteries demonstrate exceptional stability, enduring over 10,000 h of consistent Li+ deposition/stripping at a high areal capacity of 3 mAh cm−2. Impressively Li–LiNi0.89Mn0.055Co0.055O2 full cells exhibited outstanding cycle stability and rate performance, maintaining over 80% capacity retention after 750 cycles at a demanding 1C rate. Pouch cells produced using dry-process electrodes demonstrate strong potential for commercialization. The interphase engineering strategy offers a promising solution to the persistent challenge of dendrite growth, enabling the full realization of sulfide electrolytes' capabilities in next-generation battery technologies.

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用于全固态金属锂电池的交联聚酰胺集成阿基洛代石 Li6PS5Cl
锂枝晶的生长已成为实现高性能全固态锂金属电池的一大障碍。本文提出了一种有效的方法,通过使用交联聚酰胺(负静电位)化学锚定到 Li6PS5Cl(正静电位)表面,进行相间工程来应对这一挑战。这种方法改善了电解质颗粒之间的接触,并战略性地改变了晶界的局部电子结构。这一创新有效地抑制了锂枝晶的形成,并增强了界面的整体稳定性。因此,硫化锂-6PS5Cl 电解质的临界电流密度从 0.4 mA cm-2 大幅提高到 1.6 mA cm-2,显著提高了四倍。此外,锂-锂对称电池还表现出了卓越的稳定性,在 3 mAh cm-2 的高电容条件下,锂+沉积/剥离持续时间超过 10,000 小时。令人印象深刻的是,锂-镍0.89Mn0.055Co0.055O2全电池表现出卓越的循环稳定性和速率性能,在苛刻的 1C 速率下循环 750 次后,容量保持率仍超过 80%。使用干法电极生产的袋装电池具有很强的商业化潜力。相间工程策略为解决枝晶生长这一长期难题提供了可行的解决方案,使硫化物电解质在下一代电池技术中的能力得以充分发挥。
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来源期刊
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
期刊介绍: Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments. With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology. Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.
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