Inorganic superionic conductor holds great promise for high-performance all-solid-state lithium batteries. However, the ionic conductivity of traditional inorganic solid electrolytes (ISEs) is always unsatisfactory owing to the grain boundary resistance and large thickness. Here, a 13 μm-thick laminar framework with ≈1.3 nm interlayer channels is fabricated by self-assembling rigid, hydrophilic vermiculite (Vr) nanosheets. Then, Li La TiO (LLTO) precursors are impregnated in interlayer channels and afterwards in situ sintered to large-size, oriented, and defect-free LLTO crystal. We demonstrate that the confinement effect permits ordered arrangement of LLTO crystal along the c-axis (the fastest Li transfer direction), permitting the resultant 15 μm-thick Vr-LLTO electrolyte an ionic conductivity of 8.22×10 S cm and conductance of 87.2 mS at 30 °C. These values are several times' higher than that of traditional LLTO-based electrolytes. Moreover, Vr-LLTO electrolyte has a compressive modulus of 1.24 GPa. Excellent cycling performance is demonstrated with all-solid-state Li/LiFePO battery.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/anie.202114220 | DOI Listing |
Int J Biol Macromol
January 2025
College of Materials Science and Engineering, Nanjing Tech University, Nanjing 211816, PR China. Electronic address:
The carboxymethyl chitosan (CMCS)-based porous beads are still criticized for their limited number of binding sites, which impairs their efficacy in removing aqueous pollutants. To overcome this challenge, this work introduces the production of covalently crosslinked CMCS-based beads containing SiO and poly(2-acrylamido-2-methylpropanesulfonic acid) (PAMPS). The porous composite beads not only possess remarkable stability under acidic conditions, but also have abundant active binding sites for adsorption.
View Article and Find Full Text PDFInorg Chem
January 2025
Departamento de Química Física and Instituto de Biocomputación y Física de Sistemas Complejos (BIFI), Universidad de Zaragoza, Zaragoza 50009, Spain.
The pentafluoroorthotellurate group (-OTeF, teflate) exhibits high electron-withdrawing properties. Indeed, it is often used as a bulky substitute for fluoride due to its high chemical stability and larger size, which reduces its tendency to act as a bridging ligand. These characteristics make it a valuable ligand in synthetic chemistry, facilitating the preparation of molecular structures analogous to polymeric fluoride-based compounds.
View Article and Find Full Text PDFNano Lett
January 2025
College of Materials Science and Engineering, Hunan Joint International Laboratory of Advanced Materials and Technology of Clean Energy, Hunan Province Key Laboratory for Advanced Carbon Materials and Applied Technology, Hunan University, Changsha 410082, China.
Solid-state metallic potassium batteries (SSMPBs) afresh have attracted incremental attention because of their potential to supplement solid-state metallic lithium batteries. However, SSMPBs suffer poor electrochemical performances due to the low ionic conductivity of solid electrolytes and huge electrode/electrolyte interfacial resistance. Herein, high-rate SSMPBs are achieved by in situ ring-opening polymerization of 1,3-dioxolane with succinonitrile as a plasticizer and Al(OTf) as the catalyst, where the succinonitrile enables short-chain polyether electrolytes.
View Article and Find Full Text PDFSci Adv
January 2025
Department of Mechanical Engineering, University of Delaware, Newark, DE 19716, USA.
Enhancing transport and chemomechanical properties in cathode composites is crucial for the performance of solid-state batteries. Our study introduces the filler-aligned structured thick (FAST) electrode, which notably improves mechanical strength and ionic/electronic conductivity in solid composite cathodes. The FAST electrode incorporates vertically aligned nanoconducting carbon nanotubes within an ion-conducting polymer electrolyte, creating a low-tortuosity electron/ion transport path while strengthening the electrode's structure.
View Article and Find Full Text PDFACS Nano
January 2025
Department of Chemistry, Pohang University of Science and Technology (POSTECH), Pohang 37673, Republic of Korea.
We present a strategy for enhancing Li conduction in block copolymer electrolytes by introducing trace amounts of Li salts into polystyrene--poly(ethylene oxide) (PS--PEO), wherein Li ions preferentially coordinate with the -OH end groups of the PEO chains, resulting in the formation of double primitive cubic (3̅) structures. Compared with TFSI anions in Li salts, smaller anions (PF and BF) could facilitate ion localization more effectively, expanding the salt concentration range for developing stable 3̅ structures. The 3̅ structures formed in PS--PEOs doped with LiBF at = 0.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!