Dr. M. Salado, Dr. R. Fernández de Luis, Dr. T. H. Smith, Dr. M. Hasanpoor, Prof. S. Lanceros-Mendez, Prof. M. Forsyth
{"title":"基于 MOFs 的锂金属电池准固转固电解质 (Q-SSE) 对锂传输的尺寸控制","authors":"Dr. M. Salado, Dr. R. Fernández de Luis, Dr. T. H. Smith, Dr. M. Hasanpoor, Prof. S. Lanceros-Mendez, Prof. M. Forsyth","doi":"10.1002/batt.202400134","DOIUrl":null,"url":null,"abstract":"<p>Nowadays, lithium-ion batteries (LIBs) are widely used in all walks of life and play a very important role. As complex systems composed of multiple materials with diverse chemical compositions, where different electrochemical reactions take place, battery interfaces are essential for determining the operation, performance, durability and safety of the battery. This work, set out to study the incorporation of lithium bis(fluorosulfonyl)amide (LiFSI) doped 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([EMIm][TFSI]) ionic liquid into an archetype Ti-based Metal Organic Framework (MOF) ((Ti) MIL125−NH<sub>2</sub>) to create a solid to quasi-solid (depending on the amount of IL in the system), and how it affects not only ionic transport but also the structural properties of the IL/MOF electrolyte. Remarkably high ionic conductivity values (2.13×10<sup>−3</sup> S ⋅ cm<sup>−1</sup> at room temperature) as well as a lithium transference number (t<sub>Li</sub>=0.58) were achieved, supported by pulsed field gradient (PFG) NMR experiments. Electrochemical characterization revealed reversible plating-stripping of lithium and lower overpotential after 750 h at 50 °C. Additionally, a proof-of-concept solid state battery was fabricated resulting in a discharge capacity of 160 mAh ⋅ g<sup>−1</sup> at 50 °C and 0.1 C rate after 50 cycles. This work presents a suitable strategy to dendrite suppression capability, allowing its implementation as interface modifiers in next-generation solid-state batteries.</p>","PeriodicalId":132,"journal":{"name":"Batteries & Supercaps","volume":"7 9","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2024-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/batt.202400134","citationCount":"0","resultStr":"{\"title\":\"Dimensionality Control of Li Transport by MOFs Based Quasi-Solid to Solid Electrolyte (Q-SSEs) for Li−Metal Batteries\",\"authors\":\"Dr. M. Salado, Dr. R. Fernández de Luis, Dr. T. H. Smith, Dr. M. Hasanpoor, Prof. S. Lanceros-Mendez, Prof. M. Forsyth\",\"doi\":\"10.1002/batt.202400134\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Nowadays, lithium-ion batteries (LIBs) are widely used in all walks of life and play a very important role. As complex systems composed of multiple materials with diverse chemical compositions, where different electrochemical reactions take place, battery interfaces are essential for determining the operation, performance, durability and safety of the battery. This work, set out to study the incorporation of lithium bis(fluorosulfonyl)amide (LiFSI) doped 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([EMIm][TFSI]) ionic liquid into an archetype Ti-based Metal Organic Framework (MOF) ((Ti) MIL125−NH<sub>2</sub>) to create a solid to quasi-solid (depending on the amount of IL in the system), and how it affects not only ionic transport but also the structural properties of the IL/MOF electrolyte. Remarkably high ionic conductivity values (2.13×10<sup>−3</sup> S ⋅ cm<sup>−1</sup> at room temperature) as well as a lithium transference number (t<sub>Li</sub>=0.58) were achieved, supported by pulsed field gradient (PFG) NMR experiments. Electrochemical characterization revealed reversible plating-stripping of lithium and lower overpotential after 750 h at 50 °C. Additionally, a proof-of-concept solid state battery was fabricated resulting in a discharge capacity of 160 mAh ⋅ g<sup>−1</sup> at 50 °C and 0.1 C rate after 50 cycles. 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Dimensionality Control of Li Transport by MOFs Based Quasi-Solid to Solid Electrolyte (Q-SSEs) for Li−Metal Batteries
Nowadays, lithium-ion batteries (LIBs) are widely used in all walks of life and play a very important role. As complex systems composed of multiple materials with diverse chemical compositions, where different electrochemical reactions take place, battery interfaces are essential for determining the operation, performance, durability and safety of the battery. This work, set out to study the incorporation of lithium bis(fluorosulfonyl)amide (LiFSI) doped 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([EMIm][TFSI]) ionic liquid into an archetype Ti-based Metal Organic Framework (MOF) ((Ti) MIL125−NH2) to create a solid to quasi-solid (depending on the amount of IL in the system), and how it affects not only ionic transport but also the structural properties of the IL/MOF electrolyte. Remarkably high ionic conductivity values (2.13×10−3 S ⋅ cm−1 at room temperature) as well as a lithium transference number (tLi=0.58) were achieved, supported by pulsed field gradient (PFG) NMR experiments. Electrochemical characterization revealed reversible plating-stripping of lithium and lower overpotential after 750 h at 50 °C. Additionally, a proof-of-concept solid state battery was fabricated resulting in a discharge capacity of 160 mAh ⋅ g−1 at 50 °C and 0.1 C rate after 50 cycles. This work presents a suitable strategy to dendrite suppression capability, allowing its implementation as interface modifiers in next-generation solid-state batteries.
期刊介绍:
Electrochemical energy storage devices play a transformative role in our societies. They have allowed the emergence of portable electronics devices, have triggered the resurgence of electric transportation and constitute key components in smart power grids. Batteries & Supercaps publishes international high-impact experimental and theoretical research on the fundamentals and applications of electrochemical energy storage. We support the scientific community to advance energy efficiency and sustainability.