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Restraining lithium dendrite formation in all-solid-state Li-metal batteries via the surface modification of the ceramic filler
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- Title
- Restraining lithium dendrite formation in all-solid-state Li-metal batteries via the surface modification of the ceramic filler
- Issued Date
- 2023-04
- Citation
- Jamal, Hasan. (2023-04). Restraining lithium dendrite formation in all-solid-state Li-metal batteries via the surface modification of the ceramic filler. Sustainable Materials and Technologies, 35, e00548. doi: 10.1016/j.susmat.2022.e00548
- Type
- Article
- Author Keywords
- Filled polymers ; Fillers ; Hydrophobicity ; Interface states ; Lithium-ion batteries ; Polyelectrolytes ; Scanning electron microscopy ; Silicones ; Solid electrolytes ; Surface chemistry ; X ray photoelectron spectroscopy ; Zeolites
- Keywords
- COMPOSITE POLYMER ELECTROLYTES ; IONIC-CONDUCTIVITY ; ELECTROCHEMICAL PERFORMANCE ; ENHANCEMENT ; INTERFACE ; MEMBRANES ; SIO2 ; PEO
- ISSN
- 2214-9937
- Abstract
-
Polymer-based all-solid-state Li-metal batteries (ASSLMBs) have acquired considerable attention owing to their applicability to various systems and their enhanced safety characteristics. Hence, ASSLMBs can potentially replace flammable organic-liquid-electrolyte-based Li-ion batteries. However, owing to the interfacial instability and Li dendrite formation, ASSLMBs exhibit low capacity deprivation. To overcome this limitation, in this study, the hydrophilic nature of SSZ-13 zeolite was altered to hydrophobic using OH-functional silicone-modified polyacrylate (BYK-SILCLEAN 3700). A hydrophobic surface-modified zeolite filler (SSZ-13, MZLT) was incorporated into a polyethylene oxide (PEO) matrix, which permitted considerable Li salt adsorption and ensured the uniform distribution of MZLT in the PEO matrix. This resulted in a substantially improved ionic conductivity (σ) of the electrolyte, thereby enhancing the performance and durability of ASSLMBs. Furthermore, excellent σ (3.46 × 10−2 S cm−1 at 60 °C) was achieved through the surface modification of the filler, resulting in a Li transference number of 0.83. The Li plating–stripping results (for 1800 h of cycling at a discharge current of 100 μA cm−2) suggested satisfactory compatibility of the electrolyte with the Li metal. Scanning electron microscopy and X-ray photoelectron spectroscopy results confirmed that the growth of Li dendrites was significantly suppressed, leading to a retention rate of 98.5% after 200 cycles. Additionally, the fire retardancy was considerably improved. The findings of this study highlight the potential of composite-electrolyte-based ASSLMBs as candidates for energy storage devices. © 2022 Elsevier B.V.
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- Publisher
- Elsevier BV
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