{"title":"Achieving 766.5 Wh kg–1 Electrode-Level Energy Density via Solid-State Cathode Integrating Ultrahigh Nickel Oxide and Lithium Iron Chloride","authors":"Zi-Wei Wang, Shun Xiang, Jin-Da Luo, Zhangqin Shi, Ye-Chao Wu, Hao-Yuan Tan, Xiaobin Cheng, Mei-Yu Zhou, Xu-Dong Hao, Chen-Peng Luo, Chuan Wan, Min Ge, Linjun Wang, Limin Sun, Zheng Liang*, Yi-Chen Yin* and Hong-Bin Yao*, ","doi":"10.1021/acs.nanolett.5c03012","DOIUrl":null,"url":null,"abstract":"<p >Coupling chloride solid electrolytes (SEs) with ultrahigh-nickel oxide cathodes (LiNi<sub><i>x</i></sub>Co<sub><i>y</i></sub>Mn<sub>1-x-y</sub>O<sub>2</sub>, <i>x</i> > 0.9) exhibits higher interfacial stability and better safety than traditional sulfide SE-based cathodes. However, the inevitable ∼30 wt% addition of inactive chloride SEs for sufficient Li<sup>+</sup> percolation sacrifices the electrode-level energy density. Herein, using ion-conductive and electrochemically active Li<sub>2</sub>FeCl<sub>4</sub> (LFC) to pair ultrahigh-nickel cathode LiNi<sub>0.92</sub>Co<sub>0.05</sub>Mn<sub>0.03</sub>O<sub>2</sub> (Ni92), we fabricate an all-active-cathode Ni92@LFC which unlocks an extra 22% capacity in comparison to Ni92@Li<sub>3</sub>InCl<sub>6</sub>, thus realizing a remarkable electrode energy density of 766.5 Wh kg<sup>–1</sup>. We demonstrate that the lithium-deficient LFC exhibits sufficient ionic conductivity to achieve a higher capacity of Ni92@LFC than Ni92@Li<sub>3</sub>InCl<sub>6</sub> cathode at 3 C (114 mAh g<sup>–1</sup> vs 86 mAh g<sup>–1</sup>). More attractively, we observe an <i>in-situ</i> formed Li<sub><i>x</i></sub>FeOCl interphase with rapid dynamics and high stability, facilitating durable cycling with 83.4% capacity retention after 1000 cycles. Our all-active-cathode design paves the way to higher-energy-density all-solid-state cathodes.</p>","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"25 34","pages":"12930–12937"},"PeriodicalIF":9.1000,"publicationDate":"2025-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nano Letters","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.nanolett.5c03012","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Coupling chloride solid electrolytes (SEs) with ultrahigh-nickel oxide cathodes (LiNixCoyMn1-x-yO2, x > 0.9) exhibits higher interfacial stability and better safety than traditional sulfide SE-based cathodes. However, the inevitable ∼30 wt% addition of inactive chloride SEs for sufficient Li+ percolation sacrifices the electrode-level energy density. Herein, using ion-conductive and electrochemically active Li2FeCl4 (LFC) to pair ultrahigh-nickel cathode LiNi0.92Co0.05Mn0.03O2 (Ni92), we fabricate an all-active-cathode Ni92@LFC which unlocks an extra 22% capacity in comparison to Ni92@Li3InCl6, thus realizing a remarkable electrode energy density of 766.5 Wh kg–1. We demonstrate that the lithium-deficient LFC exhibits sufficient ionic conductivity to achieve a higher capacity of Ni92@LFC than Ni92@Li3InCl6 cathode at 3 C (114 mAh g–1 vs 86 mAh g–1). More attractively, we observe an in-situ formed LixFeOCl interphase with rapid dynamics and high stability, facilitating durable cycling with 83.4% capacity retention after 1000 cycles. Our all-active-cathode design paves the way to higher-energy-density all-solid-state cathodes.
氯化物固体电解质(SEs)与超高镍氧化物阴极(LiNixCoyMn1-x-yO2, x > 0.9)耦合,比传统的硫化物se基阴极具有更高的界面稳定性和更好的安全性。然而,为了充分的Li+渗透,不可避免地要加入~ 30 wt%的非活性氯se,牺牲了电极级的能量密度。本研究利用离子导电性和电化学活性的Li2FeCl4 (LFC)与超高镍阴极lini0.92 co0.05 mn0.030 o2 (Ni92)偶联,制备了一种全活性阴极Ni92@LFC,其容量比Ni92@Li3InCl6多解锁22%,从而实现了766.5 Wh kg-1的显著电极能量密度。我们证明,在3c下,缺乏锂的LFC具有足够的离子电导率,比Ni92@Li3InCl6阴极具有更高的Ni92@LFC容量(114 mAh g-1 vs 86 mAh g-1)。更吸引人的是,我们观察到原位形成的LixFeOCl界面具有快速动态和高稳定性,促进持久循环,1000次循环后容量保留率为83.4%。我们的全有源阴极设计为更高能量密度的全固态阴极铺平了道路。
期刊介绍:
Nano Letters serves as a dynamic platform for promptly disseminating original results in fundamental, applied, and emerging research across all facets of nanoscience and nanotechnology. A pivotal criterion for inclusion within Nano Letters is the convergence of at least two different areas or disciplines, ensuring a rich interdisciplinary scope. The journal is dedicated to fostering exploration in diverse areas, including:
- Experimental and theoretical findings on physical, chemical, and biological phenomena at the nanoscale
- Synthesis, characterization, and processing of organic, inorganic, polymer, and hybrid nanomaterials through physical, chemical, and biological methodologies
- Modeling and simulation of synthetic, assembly, and interaction processes
- Realization of integrated nanostructures and nano-engineered devices exhibiting advanced performance
- Applications of nanoscale materials in living and environmental systems
Nano Letters is committed to advancing and showcasing groundbreaking research that intersects various domains, fostering innovation and collaboration in the ever-evolving field of nanoscience and nanotechnology.