Design of High-Voltage Stable Hybrid Electrolyte with an Ultrahigh Li Transference Number
Source abstract
Abstract
Considering the high energy consumption during processing, and the low compliance and adhesion of ceramic electrolytes, the integration of polymer into ceramic electrolytes provides a way to mitigate the interfacial issues. However, the severe ion concentration gradient, low ionic conductivity, and instability toward Li metal and high-voltage cathodes become the major concerns in applying hybrid electrolytes. In this work, we report a single-ion-conducting hybrid electrolyte (SIE-LLZO) with 64 wt % Li7La3Zr2O12(LLZO) particles embedded in a fluoroboron-centered Li-conductive polymer framework (LiBFSIE). The SIE-LLZO electrolyte exhibited a high Li transference number of 0.94 and electrochemical stability up to 5.6 V vs Li/Li+. Promising averaged Coulombic efficiencies of 99.97% and 99.91% were achieved in cells with LiNi0.8Co0.15Al0.05O2 and LiNi0.6Mn0.2Co0.2O2 cathodes for 400 and 200 cycles, respectively. The Li-conducting pathway in the hybrid electrolyte was further investigated by a 6Li-to-7Li isotope replacement method, indicating that Li transport mainly relies on the LLZO and interface between LiBFSIE and LLZO.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced Battery Technologies Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Chemical Sciences and Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue, Lemont, Illinois 60439, United States
Department of Mechanical Engineering, University of Arkansas, Fayetteville, Arkansas 72701, United States
Applied Materials Division, Argonne National Laboratory, 9700 S. Cass Ave., Lemont, Illinois 60564, United States
Joint Center for Energy Storage Research, Lemont, Illinois 60439, United States
Funding
Argonne National Laboratory
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