{"title":"Strain Coupled (110)-Oriented Lithium Anodes for High-Rate and High-Capacity Epitaxial Growth","authors":"Aoxuan Wang, Haoran Li, Zhibin Xu, Hao Chen, Xiaofan Lv, Yumeng Zhao, Dehua Xu, Zhenglin Hu, Qingtao Ma, Xingjiang Liu, Jiayan Luo","doi":"10.1021/acsnano.6c09189","DOIUrl":null,"url":null,"abstract":"<p>Lithium metal is considered as the ultimate anode for\r\nhigh-energy-density\r\nbatteries, yet its practical realization is thwarted by dendrite proliferation\r\nand chemomechanical interfacial instability. While epitaxial growth\r\non crystallographically textured substrates provides a template for\r\nordered deposition, sustaining this ordered growth under high capacities\r\nand current densities remains a formidable kinetic challenge. Herein,\r\nwe overcome this barrier by engineering an elastic (110)-oriented\r\nlithium anode (e-Li (110)) comprising a conductive polymer scaffold.\r\nThe e-Li (110) integrates preferred (110) crystallographic orientation\r\nwith a mechanically coupled strain corresponding to the optimized\r\n4% tensile-strain condition. Consequently, this strain-engineering\r\nstrategy enables a capacity of 30 mAh cm<sup>–2</sup> and current\r\ndensity of 25 mA cm<sup>–2</sup> before lithium epitaxial breakdown.\r\n5.9 Ah Li || LiNi<sub>0.8</sub>Co<sub>0.1</sub>Mn<sub>0.1</sub>O<sub>2</sub> (NCM811) pouch cells with a high energy density of 509.8\r\nWh kg<sup>–1</sup> show 90% capacity retention after 140 cycles.\r\nIn sulfide-based all-solid-state batteries (ASSBs), e-Li (110) anode\r\nenables stable cycling for over 1600 cycles at a rate of 5 C. By highlighting\r\nstrain as a critical parameter, our work provides a strategy for mechano-electrochemical\r\ncoupling in lithium metal anodes for high-rate, high-energy-density\r\nbatteries.</p>","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":"20 41","pages":"27762–27773"},"PeriodicalIF":17.3000,"publicationDate":"2026-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Nano","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsnano.6c09189","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/10/5 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Lithium metal is considered as the ultimate anode for
high-energy-density
batteries, yet its practical realization is thwarted by dendrite proliferation
and chemomechanical interfacial instability. While epitaxial growth
on crystallographically textured substrates provides a template for
ordered deposition, sustaining this ordered growth under high capacities
and current densities remains a formidable kinetic challenge. Herein,
we overcome this barrier by engineering an elastic (110)-oriented
lithium anode (e-Li (110)) comprising a conductive polymer scaffold.
The e-Li (110) integrates preferred (110) crystallographic orientation
with a mechanically coupled strain corresponding to the optimized
4% tensile-strain condition. Consequently, this strain-engineering
strategy enables a capacity of 30 mAh cm–2 and current
density of 25 mA cm–2 before lithium epitaxial breakdown.
5.9 Ah Li || LiNi0.8Co0.1Mn0.1O2 (NCM811) pouch cells with a high energy density of 509.8
Wh kg–1 show 90% capacity retention after 140 cycles.
In sulfide-based all-solid-state batteries (ASSBs), e-Li (110) anode
enables stable cycling for over 1600 cycles at a rate of 5 C. By highlighting
strain as a critical parameter, our work provides a strategy for mechano-electrochemical
coupling in lithium metal anodes for high-rate, high-energy-density
batteries.
金属锂被认为是高能量密度电池的终极阳极,但其实际实现受到枝晶增殖和化学力学界面不稳定性的阻碍。虽然晶体结构衬底上的外延生长为有序沉积提供了模板,但在高容量和高电流密度下维持这种有序生长仍然是一个巨大的动力学挑战。在这里,我们通过设计一个包含导电聚合物支架的弹性(110)取向锂阳极(e-Li(110))来克服这一障碍。e-Li(110)集成了优选(110)晶体取向和对应于优化的4%拉伸应变条件的机械耦合应变。因此,这种应变工程策略可以在锂外延击穿之前实现30 mAh cm-2的容量和25 mA cm-2的电流密度。LiNi0.8Co0.1Mn0.1O2 (NCM811)袋状电池具有509.8 Wh kg-1的高能量密度,经过140次循环后容量保持率达到90%。在硫化物基全固态电池(assb)中,e-Li(110)阳极能够以5℃的速率稳定循环超过1600次,通过强调应变作为关键参数,我们的工作为高速率,高能量密度电池的锂金属阳极的机械电化学耦合提供了一种策略。
期刊介绍:
ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.