Zesen Gao, Shijie Yang, Yan Yang, Futing Sun, Tianshuo Zhang, Yunluo Wang, Tianrui Zhou, Lang Tao, Hucheng Song, Haijie Chen
{"title":"A three-in-one strategy enables improved kinetics in an LLZTO solid electrolyte for Li-CO2 batteries with high energy efficiency","authors":"Zesen Gao, Shijie Yang, Yan Yang, Futing Sun, Tianshuo Zhang, Yunluo Wang, Tianrui Zhou, Lang Tao, Hucheng Song, Haijie Chen","doi":"10.1039/d5qi00659g","DOIUrl":null,"url":null,"abstract":"Solid-state Li-CO<small><sub>2</sub></small> batteries possess unique merits, including high environmental friendliness, extremely high energy density, and wide operational temperature range. In this work, we used the garnet-type Li<small><sub>6.4</sub></small>La<small><sub>3</sub></small>Zr<small><sub>1.4</sub></small>Ta<small><sub>0.6</sub></small>O<small><sub>12</sub></small> (LLZTO) as the solid electrolyte for Li-CO<small><sub>2</sub></small> batteries. By a simple solid-state reaction under vacuum, LLZTO was tightly composited with organic materials. Detailed analysis confirms that a three-in-one effect was achieved, resulting in additional Li<small><sup>+</sup></small> migration pathways, improved mechanical properties of the electrolyte, and more active sites for Li<small><sub>2</sub></small>CO<small><sub>3</sub></small> decomposition. This contributes to accelerated Li<small><sup>+</sup></small> transport and fast CO<small><sub>2</sub></small> reaction kinetics. A solid-state Li-CO<small><sub>2</sub></small> cell was assembled using a Ru@C cathode and an integrated layer of LLZTO@PVDF interfaced with an artificial molten salt. An exceptionally low charging overpotential (below 3.0 V) was achieved, maintaining a charge potential retention rate of over 99%. This work introduces LLZTO as a promising electrolyte for solid-state Li-CO<small><sub>2</sub></small> batteries, shedding light on the advancement of next-generation Li-CO<small><sub>2</sub></small> battery technologies.","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":"11 1","pages":""},"PeriodicalIF":6.1000,"publicationDate":"2025-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5qi00659g","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
Solid-state Li-CO2 batteries possess unique merits, including high environmental friendliness, extremely high energy density, and wide operational temperature range. In this work, we used the garnet-type Li6.4La3Zr1.4Ta0.6O12 (LLZTO) as the solid electrolyte for Li-CO2 batteries. By a simple solid-state reaction under vacuum, LLZTO was tightly composited with organic materials. Detailed analysis confirms that a three-in-one effect was achieved, resulting in additional Li+ migration pathways, improved mechanical properties of the electrolyte, and more active sites for Li2CO3 decomposition. This contributes to accelerated Li+ transport and fast CO2 reaction kinetics. A solid-state Li-CO2 cell was assembled using a Ru@C cathode and an integrated layer of LLZTO@PVDF interfaced with an artificial molten salt. An exceptionally low charging overpotential (below 3.0 V) was achieved, maintaining a charge potential retention rate of over 99%. This work introduces LLZTO as a promising electrolyte for solid-state Li-CO2 batteries, shedding light on the advancement of next-generation Li-CO2 battery technologies.