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High-performance free-standing hybrid solid electrolyte membrane combined with Li6.28Al0.24La3Zr2O12 and hexagonal-BN for all-solid-state lithium-based batteries

Authors
Kim, Ji-HwanPark, Deok-HyeJang, Jae-SungShin, Jae-HoonKim, Min-CheolKim, Sung-BeomMoon, Sang-HyunLee, Seong-NamPark, Kyung-Won
Issue Date
Oct-2022
Publisher
ELSEVIER SCIENCE SA
Keywords
Al doping; hexafluoropropylene); h-BN; Hybrid solid electrolyte membrane; Hybrid solid electrolyte membrane All-solid-state lithium based batteries
Citation
CHEMICAL ENGINEERING JOURNAL, v.446
Journal Title
CHEMICAL ENGINEERING JOURNAL
Volume
446
URI
http://scholarworks.bwise.kr/ssu/handle/2018.sw.ssu/42402
DOI
10.1016/j.cej.2022.137035
ISSN
1385-8947
Abstract
Hybrid solid electrolytes (HSEs) have received intensive attentions for all-solid-state lithium-based batteries (ASSBs) because of their high ionic conductivity, high mechanical strength, improved electrochemical stability, and effective lithium dendrite suppression capability. In this study, free-standing HSE membranes were fabricated using a poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) matrix and Li6.28Al0.24La3Zr2O12 (LALZO)/hexagonal-BN (h-BN) composite ceramic fillers with different amounts of h-BN. The optimal proportion of h-BN (10 wt%) in the HSE membrane reduces the crystallinity of PVDF-HFP matrix, increases the proportion of the electroactive beta phase, and enhances the mechanical strength of the HSE membrane. Furthermore, the PVDFHFP/LALZO/h-BN 10% HSE membrane exhibited improved electrochemical properties, for example, a lithium ion transference number of 0.63 at 55 C, ionic conductivity of 1.1 x 10(-4) S cm(-1) at 25 C, electrochemical stability window of-5.0 V vs. Li/Li+, and effective lithium dendrite suppression capability. The ASSB consisting of a LiFePO4 cathode, PVDF-HFP/LALZO/h-BN 10% HSE, and Li metal anode delivered improved battery performance with an average capacity of 131 mAh g(-1) at 0.2C, > 99% coulombic efficiency, and a capacity retention of 92% after 100 cycles.
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PARK, KYUNG WON
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