In this work, sustainable Li‐based battery separators are prepared starting from a waste material from the glass industry, viz . polyvinyl butyral (PVB) widely used as a sacrificial interlayer in high impact‐resistant windows. First, polymeric membranes are prepared via the phase‐inversion method using commercial PVB as the backbone and 4,4′‐methylenebis(cyclohexylisocyanate) as a crosslinking agent. They are characterized from a physicochemical viewpoint by thermomechanical analysis, infrared spectroscopy, and scanning electron microscopy, and are successfully tested as separators in Li‐metal cells with LP30 electrolyte. Electrical and electrochemical properties are evaluated by impedance spectroscopy and galvanostatic cycling, providing comparable results with commercial Celgard 25 µm monolayer microporous polypropylene separator. As a proof‐of‐concept, for the first time, recycled PVB‐based polymer membranes from wasted car glasses are prepared, adjusting the synthesis protocol to account for the presence of plasticizers and contaminants. They show a dense elastomeric appearance and proved to be compatible with Li metal and stable upon 600 h of Li plating/stripping. The electrochemical window is compatible with the LiFePO ₄ cathode, as demonstrated by prolonged galvanostatic cycling (250 cycles) in laboratory‐scale cells. Preliminary results are highly encouraging and pave the way to developing novel separators for safe, low‐cost, and sustainable energy storage devices.

Configurational entropy stabilizes P2-type Na _x MO ₂ layered cathodes by suppressing TM migration and P2–O2 gliding. High-entropy compositions distribute redox activity, improving structural reversibility and cycling stability in Na-ion batteries.

Nowadays, face masks play an essential role in limiting coronavirus diffusion. However, their disposable nature represents a relevant environmental issue. In this work, we propose the utilization of two types of disposed (waste) face masks to prepare hard carbons (biochar) by pyrolytic conversion in mild conditions. Moreover, we evaluated the application of the produced hard carbons as anode materials in Na-ion batteries. Pristine face masks were firstly analyzed through infrared spectroscopy and thermogravimetric analysis. The pyrolysis of both mask types resulted in highly disordered carbons, as revealed by field-emission scanning electron microscopy and Raman spectroscopy, with a very low specific surface area. Anodes prepared with these carbons were tested in laboratory-scale Na-metal cells through electrochemical impedance spectroscopy, cyclic voltammetry and galvanostatic cycling, displaying an acceptable specific capacity along a wide range of current regimes, with a good coulombic efficiency (>98% over at least 750 cycles). As a proof of concept, the anodes were also used to assemble a Na-ion cell in combination with a Na₃V₂(PO₄)₂F₃ (NVPF) cathode and tested towards galvanostatic cycling, with an initial capacity of almost 120 mAhg⁻¹ (decreasing at about 47 mAhg⁻¹ after 50 cycles). Even though further optimization is required for a real application, the achieved electrochemical performances represent a preliminary confirmation of the possibility of repurposing disposable face masks into higher-value materials for Na-ion batteries.

The urgent demand for sustainable energy solutions in the face of climate change and resource depletion has catalyzed a global shift toward cleaner energy production and more efficient storage technologies. Lithium-ion batteries (LIBs), as the cornerstone of modern portable electronics, electric vehicles, and grid-scale storage systems, are continually evolving to meet the growing performance requirements. In this dynamic context, two-dimensional (2D) materials have emerged as highly promising candidates for use in electrodes due to their layered structure, tunable electronic properties, and high theoretical capacity. Among 2D materials, molybdenum disulfide (MoS₂) has gained increasing attention as a promising low-dimensional candidate for LIB anode applications. This review provides a comprehensive yet concise overview of recent advances in the application of MoS₂ in LIB electrodes, with particular attention to its unique electrochemical behavior at the nanoscale. We critically examine the interplay between structural features, charge-storage mechanisms, and performance metrics—chiefly the specific capacity, rate capability, and cycling stability. Furthermore, we discuss current challenges, primarily poor intrinsic conductivity and volume fluctuations, and highlight innovative strategies aimed at overcoming these limitations, such as through nanostructuring, composite formation, and surface engineering. By shedding light on the opportunities and hurdles in this rapidly progressing field, this work offers a forward-looking perspective on the role of MoS₂ in the next generation of high-performance LIBs.

Asymmetric thioether-TFSI Li salts plasticize PEO SPEs, suppress crystallinity, and retain conductivity, Li ⁺ transference, and stability. They also passivate Al, improving Li-metal compatibility and enabling stable Li∥LiFePO ₄ cycling.