Solution-processable Li10GeP2S12 solid electrolyte for a composite electrode in all-solid-state lithium batteries
文献信息
Genxi Yu, Yaping Wang, Kai Li, Daming Chen, Liguang Qin, Hui Xu, Jian Chen, Wei Zhang, Peigen Zhang, Zhengming Sun
Lithium-ion-conducting solid electrolytes (SEs) hold promise for enabling high-energy battery chemistries and circumventing safety issues of conventional lithium batteries. Among various solid electrolytes, the sulfide Li10GeP2S12 (LGPS) has received wide attention due to its high conductivity at room temperature. The performance of the battery using sulfide-based SEs is still challenged by the interfacial problems, such as large interfacial resistance originating from solid–solid contact, and contact failure within electrodes and/or between electrodes and SEs. In this work, LGPS–PVDF composite electrolytes were prepared by tape casting with thicknesses of ∼30 μm and showed an ionic conductivity of 2.64 × 10−4 S cm−1 at 50 °C and an electrochemical window of 5.0 V at room temperature. A solution-processable LGPS with a PVDF binder in N-methylpyrrolidone (NMP) was infiltrated into porous LiCoO2 (LCO) electrodes to form LGPS–PVDF and LCO composite (LGPS–PVDF@LCO) electrodes. The LGPS particle size is reduced by the NMP solvent treatment. The addition of PVDF into the LCO composite cathode benefits the formation of a dense structure which provides a continuous migration path for Li+ ions. The soft and elastic PVDF polymer can alleviate the large volume variation within the cathode or at the interface between the LCO cathode and LGPS electrolyte during cycling. Moreover, an interconnected 3D conductive network between the electrode materials and SEs has been developed in the composite electrodes, resulting in favorable conduction pathways for electrons and Li+ ions simultaneously. The LGPS–PVDF@LCO composite electrodes of solid-state lithium batteries show a reversible capacity of 120 mA h g−1 after 100 cycles at 0.1C and they maintain a discharge specific capacity of 76.3 mA h g−1 at 1.0C after 60 cycles, with a capacity retention of 71% at 50 °C. This composite electrode engineering strategy for all-solid-state batteries will not only provide a solution treatment method for LGPS, but will also provide a new insight into the ionic conduction between positive materials and solid electrolytes.
期刊推荐

Russian Journal of Coordination Chemistry

Russian Journal of Applied Chemistry

Russian Journal of General Chemistry

Russian Journal of Organic Chemistry

Acta Materialia

Organic Process Research & Development

Chemical Communications

Chemistry Education Research and Practice

Drug Discovery Today

Current Opinion in Colloid & Interface Science
相关文献
Construction of di-scFv through a trivalent alkyne–azide 1,3-dipolar cycloaddition
Arutselvan Natarajan, Wenjun Du, Cheng-Yi Xiong, Gerald L. DeNardo, Sally J. DeNardo, Jacquelyn Gervay-Hague
DOI: 10.1039/B611636A
Non-covalent interactions of a drug molecule encapsulated in a hybrid silica gel
Geo Paul, Stefan Steuernagel, Hubert Koller
DOI: 10.1039/B711105C
Rapid intramolecular heterolytic dihydrogen activation by a four-membered heterocyclic phosphane–borane adduct
Patrick Spies, Gerhard Erker, Gerald Kehr, Klaus Bergander, Roland Fröhlich, Stefan Grimme, Douglas W. Stephan
DOI: 10.1039/B710475H
From inconsistent results to high speed hydrosilylation
Virginie Comte, Cédric Balan, Pierre Le Gendre, Claude Moïse
DOI: 10.1039/B617413B
New insights into the enantioselectivity in the hydrogenation of prochiral ketones
Samuel A. French, Devis Di Tommaso, Antonio Zanotti-Gerosa, Fred Hancock
DOI: 10.1039/B616210J
High-connectivity networks: characterization of the first uninodal 9-connected net and two topologically novel 7-connected nets
J. Jacob Morris, Bruce C. Noll, Kenneth W. Henderson
DOI: 10.1039/B711668C
Efficient proton conduction in dry nanofilms of amorphous aluminosilicate
Yoshitaka Aoki, Emi Muto, Shinya Onoue, Toyoki Kunitake
DOI: 10.1039/B618920B
An unprecedented (6,8)-connected self-penetrating network based on two distinct zinc clusters
Ya-Qian Lan, Xin-Long Wang, Shun-Li Li, Zhong-Min Su, Kui-Zhan Shao, En-Bo Wang
DOI: 10.1039/B709835A
您可能还喜欢
奥美沙坦酯杂质4(CAS号:95579-71-8)的主要用途是什么?
奥美沙坦酯杂质4在药物工业中并无特定用途,主要作为生产和质量控制中的监控指标,以确保产品质量和符合相关规范。它具有一定的化学活性,因此在生产过程中需要严格控制其...
如何储存C3bot (154-182)(CAS号:1246280-79-4)?
C3bot (154-182)应储存在干燥、阴凉、通风良好的环境中,避免阳光直射。具体储存条件需要参考其相关安全数据表(SDS)中的储存信息。建议使用密闭容器存...
在合成中是否有4-吡唑甲酸乙酯(CAS号:37622-90-5)的替代品?
在合成过程中,可以考虑使用类似结构的化合物作为替代品,例如4-吡唑甲酸甲酯或其他吡唑类化合物。这些替代品在性质上相似,可以用于相似的合成反应中,但需根据具体应用...
(2-溴乙基)三甲基硅烷(CAS号:18156-67-7)的主要用途是什么?
(2-溴乙基)三甲基硅烷主要用作有机合成中的溴代试剂,特别是在硅化学领域中,用于制备硅烷衍生物和硅基功能材料。它也用于表面改性、催化剂合成、医药中间体合成以及分...
如何处理含有2-(4-broMophenyl)-1,1,1-trifluoropropan-2-ol(CAS号:122243-28-1)的废料?
含该化合物的废料需按照危险废物管理规定进行分类和处理。首先,应尽量减少废料的产生,通过改进生产工艺实现废物最小化。对于不可避免的废料,建议采用安全的收集方法,避...
什么是1,1,1-三氟-6-苯基-5-(e)-己烯-2,4-二酮(CAS号:18931-64-1)?
1,1,1-三氟-6-苯基-5-(e)-己烯-2,4-二酮是一种有机化合物,化学式为C14H8F3O2。它是一种具有特定立体结构的芳香族化合物,属于酮类。
2-(2-甲基哌啶-1-基)-2-氧代-乙酸(CAS号:77654-61-6)的主要用途是什么?
2-(2-甲基哌啶-1-基)-2-氧代-乙酸主要用于药物合成、有机合成及作为化学试剂。它在医药领域有一定的应用,可用于合成某些药物中间体。此外,它还用于实验室研...
如何储存(R)-1-(3-Chlorophenyl)-2,2,2-trifluoroethanamine(CAS号:1213627-66-7)?
应将(R)-1-(3-氯苯基)-2,2,2-三氟乙胺储存在阴凉、干燥、通风良好的地方,远离火源和热源。应使用密封的容器储存,并避免光照。储存温度应控制在室温范围...
N-亚硝基-N,N-二壬基胺(CAS号:84424-96-4)的市场或研究趋势如何?
N-亚硝基-N,N-二壬基胺目前主要应用于有机合成和药物化学领域。市场趋势显示,随着有机合成技术的进步,该化合物在新药研发中的应用将更加广泛。新兴研究领域包括其...
5-Chloro-2-methoxy-3-(2,2,2-trifluoroethoxy)pyridine(CAS号:1280786-68-6)的市场或研究趋势如何?
该化合物在医药、农药等领域有潜在应用价值,但市场需求较小。目前研究趋势主要集中在探索其在特定领域的应用潜力,如作为药物合成中的中间体。随着研究的深入,预计未来市...


![(2S)-2-({N-[(2S)-2-Ammonio-4-methylpentanoyl]glycyl}amino)-3-phenylpropanoate structure (2S)-2-({N-[(2S)-2-Ammonio-4-methylpentanoyl]glycyl}amino)-3-phenylpropanoate structure](https://cnstatic.chemtradehub.com/structs/429/4294-25-1-0842.webp)
![Ethyl 5-[({[(2-methyl-2-propanyl)oxy]carbonyl}amino)methyl]-1,2-oxazole-3-carboxylate structure Ethyl 5-[({[(2-methyl-2-propanyl)oxy]carbonyl}amino)methyl]-1,2-oxazole-3-carboxylate structure](https://cnstatic.chemtradehub.com/structs/253/253196-37-1-8450.webp)
![2-Methyl-2-propanyl 4-[3-(aminomethyl)phenyl]-1-piperazinecarboxylate structure 2-Methyl-2-propanyl 4-[3-(aminomethyl)phenyl]-1-piperazinecarboxylate structure](https://cnstatic.chemtradehub.com/structs/889/889948-55-4-5c12.webp)
![4-[(2-Fluoro-4-methylphenyl)amino]-6-[4-(2-hydroxyethyl)-1-piperazinyl]-7-methoxy-3-cinnolinecarboxamide structure 4-[(2-Fluoro-4-methylphenyl)amino]-6-[4-(2-hydroxyethyl)-1-piperazinyl]-7-methoxy-3-cinnolinecarboxamide structure](https://cnstatic.chemtradehub.com/structs/104/1041852-85-0-fb1c.webp)