Effects of lithium perchlorate on the electrochemical performance of PVDF-HFP/CA composite-based solid-state electrolytes

Composite-based polymer electrolytes have attracted considerable attention due to their high ionic conductivity and excellent electrochemical performance in energy storage applications. This study explores the influence of Lithium Perchlorate (LiClO 4 ) loading on the electrochemical performance of composite-based solid-state electrolytes (SSEs) based on a composite of poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and 20% cellulose acetate (CA), referred to as PVDF-HFP/20%CA. Utilizing a solution casting method, four SSE samples were fabricated: a control (0% LiClO 4 ) and three samples with varying LiClO 4 concentrations (5%, 10%, and 15%). Comprehensive characterizations, including scanning electron microscopy (SEM), Fourier-transform infrared (FTIR), physical characterization, and electrochemical impedance spectroscopy (EIS) were conducted to assess the impact of LiClO 4 on the composites. The Nyquist plot and DC ionic conductivity analysis further validate the superior performance of PH20CA-15Li (PVDF-HFP/20% cellulose acetate with 15% LiClO 4 ), with ionic conductivity increasing from 1.15 × 10 −6 S cm −1 for the control sample to 3.7 × 10 −6 S cm −1 . Loss Tangent and Cyclic Voltammetry analyses underscore the dynamic electrochemical behavior and stability of PH20CA-15Li, with the voltage window expanding from 0.996 V in the control sample to 1.398 V, highlighting its enhanced dielectric properties and energy storage capabilities. Electrolyte uptake and porosity analyses reveal a decrease in both parameters with increased LiClO 4 content, suggesting a trade-off between electrochemical performance and physical properties. SEM and FTIR analyses show structural and chemical changes, confirming the interaction between LiClO 4 and the composite matrix. The study concludes that 15% LiClO 4 loading optimally balances conductivity with physical properties, making it a promising candidate for advanced solid-state electrolyte applications.

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Journal
Energy & Environment
Published
2025-06-16
DOI
https://doi.org/10.1177/0958305x251349483
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
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article

Effects of lithium perchlorate on the electrochemical performance of PVDF-HFP/CA composite-based solid-state electrolytes

Sairul Izwan Safie, Muhammad Remanul Islam, Sam Toan, Maryam Firouzi et al.
Energy & Environment
Advanced Battery Materials and Technologies
article

Effects of lithium perchlorate on the electrochemical performance of PVDF-HFP/CA composite-based solid-state electrolytes

Sairul Izwan Safie, Muhammad Remanul Islam, Sam Toan, Maryam Firouzi, Ahmad Naim Ahmad Yahaya, Izuan Nasib
article en

Abstract

Composite-based polymer electrolytes have attracted considerable attention due to their high ionic conductivity and excellent electrochemical performance in energy storage applications. This study explores the influence of Lithium Perchlorate (LiClO 4 ) loading on the electrochemical performance of composite-based solid-state electrolytes (SSEs) based on a composite of poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and 20% cellulose acetate (CA), referred to as PVDF-HFP/20%CA. Utilizing a solution casting method, four SSE samples were fabricated: a control (0% LiClO 4 ) and three samples with varying LiClO 4 concentrations (5%, 10%, and 15%). Comprehensive characterizations, including scanning electron microscopy (SEM), Fourier-transform infrared (FTIR), physical characterization, and electrochemical impedance spectroscopy (EIS) were conducted to assess the impact of LiClO 4 on the composites. The Nyquist plot and DC ionic conductivity analysis further validate the superior performance of PH20CA-15Li (PVDF-HFP/20% cellulose acetate with 15% LiClO 4 ), with ionic conductivity increasing from 1.15 × 10 −6 S cm −1 for the control sample to 3.7 × 10 −6 S cm −1 . Loss Tangent and Cyclic Voltammetry analyses underscore the dynamic electrochemical behavior and stability of PH20CA-15Li, with the voltage window expanding from 0.996 V in the control sample to 1.398 V, highlighting its enhanced dielectric properties and energy storage capabilities. Electrolyte uptake and porosity analyses reveal a decrease in both parameters with increased LiClO 4 content, suggesting a trade-off between electrochemical performance and physical properties. SEM and FTIR analyses show structural and chemical changes, confirming the interaction between LiClO 4 and the composite matrix. The study concludes that 15% LiClO 4 loading optimally balances conductivity with physical properties, making it a promising candidate for advanced solid-state electrolyte applications.

Energy & Environment
University of British Columbia (CA), University of Minnesota, Duluth (US), University of Kuala Lumpur (MY), Okanagan University College (CA)
Openalex Percentile: Top 87%
Advanced Battery Materials and Technologies
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