A polymer/ionic liquid thermoplastic solid electrolyte based on poly(ethylene oxide) (PEO), modified sepiolite (TPGS-S), lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), and 1-Butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide (PYR₁₄TFSI) ionic liquid is prepared using solvent free extrusion method. Its physical-chemical, electrical, and electrochemical properties are comprehensively studied. The investigated solid electrolyte demonstrates high ionic conductivity together with excellent compatibility with lithium metal electrode. Finally, truly Li-LiFePO₄ solid state coin cell with the developed thermoplastic solid electrolyte demonstrates promising electrochemical performance during cycling under 0.2 C/0.5 C protocol at 60 °C.

The development of novel solid electrolytes, which can be processed using solvent-free methods, is one of the keys for successful industrialization of solid state batteries and their further implementation in electrical vehicles. Here, we study thermoplastic solid state electrolytes based on polyethylene oxide (PEO), 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide (PYR₁₄TFSI), lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) and two inorganic fillers with different morphology and nature (modified sepiolite (TPGS-S) and garnet-type Li₇La₃Zr_1.75Nb_0.25O₁₂ (LLZNO) prepared by solvent free extrusion method. Several thermoplastic polymer electrolytes (TPEs) are prepared and comprehensively studied. Composite thermoplastic electrolyte TPE-S10G10 containing 10 wt% of TPGS-S and 10 wt% of LLZNO fillers shows the best electrochemical performance in Li-LiFePO₄ solid state batteries operating under 0.2C/0.5D cycling conditions at 60 °C. Solid state cell with TPE-S10G10 electrolyte retains 80% of initial discharge capacity after 540 cycles. Thus, a synergetic effect of using two different fillers, which can be exploited during the development of TPEs, is clearly demonstrated.

A series of thermoplastic polymer electrolytes have been prepared employing poly(ethylene oxide) (PEO) as a polymer matrix, bis(trifluoromethane sulfonimide) (LiTFSI), and different room-temperature ionic liquids (RTIL) with bis(fluorosulfonyl)imide (FSI) or TFSI anions. This formulation makes them safe and non-flammable. The electrolytes have been processed in the absence of solvents by melt compounding at 120 °C, using sepiolite modified with d-α-tocoferol-polyethyleneglycol 1000 succinate (TPGS-S) as a physical cross-linker of PEO. Several concentrations of RTILs, lithium salt, and TPGS-S have been tested in order to obtain the highest ionic conductivity (σ) without losing electrolytes’ mechanical stability. The materials’ rheology and ionic conductivity have been extensively characterized. The excellent crosslinking ability of TPGS-S makes the electrolytes behave as thermoplastic materials, even those with the highest liquid concentration. The electrolytes with the highest concentrations of FSI anion present a σ over 10⁻³ S·cm⁻¹ at 25 °C and close to 10⁻² S·cm⁻¹ at 70 °C, and notably behave as solids at temperatures up to 90 °C despite over 65 wt % of their formulation being liquid. The electrolytes thus obtained are safe solid thermoplastics prepared by industrially scalable procedures and are suitable for energy storage devices, proving the adequacy of polymer-based materials as solid electrolytes for batteries or supercapacitors.

Nanomaterials are attractive materials for researchers because they have essential characteristics in terms of their properties. Carbon has an ample range of crystalline allotropes. Some, such as graphite and diamond, have been known since ancient times, while new forms of carbon with potential for various applications have been discovered in recent decades. Since the discovery of graphene 20 years ago, research has increased on composite materials that take advantage of carbon structures for their electrical, thermal, and mechanical properties and their ability to be synthesized at the nanometer scale. Graphene has stood out above other nanomaterials due to its surprising properties and high impact on technological research, so its uses have diversified in different areas of science such as medicine, electronics, engineering, etc. This work aims to show some new and innovative applications of graphene, on which we can see its versatility as engineering material. It also seeks to show its potential in research and development processes for its use. These are key components of advanced graphene-based materials systems under active development, with an eye on the future of advanced materials science and technology.

Proper and innovative waste management methods still pose a major concern in our present world. Continuous accumulation of biowaste from bio-processing industries, household, organic residues and so on makes the environment polluted and endangers the health of man and other animals. The common waste management methods which include direct dumping into water bodies, open-air combustion, and as land fillers are obsolete and are the major causes of environmental pollution. Conversion of biowastes into valuable materials aids proper waste management, and helps to attain a cleaner environment, in addition to the fact that wastes are turned into wealth. Biowastes are rich in carbon and can serve as excellent precursors for the synthesis of important carbon materials such as activated carbon, graphene, carbon nanotubes etc. Three important methods of converting biowastes into carbon materials are discussed in this review. The electrochemical, adsorption, and electrocatalytic properties of the materials and the applications in electrochemical energy storage devices are also discussed in brief. This review focuses on the synthesis of carbon materials from biowaste residues and their use in developing electrode materials for batteries and supercapacitors. Future perspectives on the need to exploit greener technology for the conversion of biowastes into important carbon materials should be considered.

Composite materials of conjugated polymers/cellulose were fabricated by incorporating different polythiophene-derivative polymers: Poly(3,4-ethylenedioxythiophene) (PEDOT) and an alkylated derivative of poly(3,4-propylenedioxythiophene) (PProDOT). These conjugated polythiophenes were deposited by casting or spray coating methodologies onto three different cellulose substrates: Conventional filters papers as cellulose acetate, cellulose grade 40 Whatman^® and cellulose membranes prepared from cellulose microfibers. The preparation of composite materials was carried out by two methodologies: (i) by employing in-situ polymerization of 3,4-ethylenedioxithiophene (EDOT) or (ii) by depositing solutions of poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) or lab-synthetized PProDOT. Composite materials were studied in terms of electrical conductivity and surface morphology assessed by impedance spectroscopy, surface conductivity, SEM, and 3D optical profilometry. In-situ composite materials prepared by spray coating using iron trifluoromethane sulfonate as oxidizing agent can be handled and folded as the original cellulose membranes displaying a surface conductivity around 1 S∙cm⁻¹. This versatile procedure to prepare conductive composite materials has the potential to be implemented in flexible electrodes for energy storage applications.