Natália Magalhães

This study explores the preparation of lithium iron phosphate (LFP) electrodes for lithium-ion batteries (LIBs), focusing on electrode loadings, dispersion techniques, and drying methods. Using a three-roll mill for LFP slurry dispersion, good electrochemical properties were achieved with loadings of 5–8 mg·cm⁻² (0.8–1.2 mAh·cm⁻² areal capacity). Adding polyvinylidene fluoride (PVDF) during the final milling stage reduced performance due to premature solidification in-between rolls. Vacuum-free drying improved ionic conductivity, stability against lithium metal, and discharge capacity, whereas vacuum-dried samples exhibited higher initial resistance and lower capacity retention. These findings highlight critical parameters for enhancing LFP electrode performance, paving the way for high-performance, and sustainable energy-storage solutions.

To effectively use (Li) lithium metal anodes, it is becoming increasingly necessary to create membranes with high lithium conductivity, electrochemical and thermal stabilities, as well as adequate mechanical properties. Composite gel polymer electrolytes (CGPE) have emerged as a promising strategy, offering improved ionic conductivity and structural performance compared to polymer electrolytes. In this study, a simple and scalable approach was developed to fabricate a crosslinked polyethylene oxide (PEO)-based membrane, comprising two different glass fiber reinforcements, in terms of morphology and thickness. The incorporation of a solvated ionic liquid into the developed membrane enhances the ionic conductivity and reduces flammability in the resulting CGPE. Galvanostatic cycling experiments demonstrate favorable performance of the composite membrane in symmetric Li cells. Furthermore, the CGPE demonstrated electrochemical stability, enabling the cell to cycle continuously for more than 700 h at a temperature of 40 °C without short circuits. When applied in a half-cell configuration with lithium iron phosphate (LFP) cathodes, the composite membrane enabled cycling at different current densities, achieving a discharge capacity of 144 mAh·g⁻¹. Overall, the findings obtained in this work highlight the potential of crosslinked PEO-based composite membranes for high-performance Li metal anodes, with enhanced near room temperature conductivity, electrochemical stability, and cycling capability.

Solid-state electrolytes are a promising family of materials for the next generation of high-energy rechargeable lithium batteries. Polymer electrolytes (PEs) have been widely investigated due to their main advantages, which include easy processability, high safety, good mechanical flexibility, and low weight. This review presents recent scientific advances in the design of versatile polymer-based electrolytes and composite electrolytes, underlining the current limitations and remaining challenges while highlighting their technical accomplishments. The recent advances in PEs as a promising application in structural batteries are also emphasized.