Solid oxide fuel cells (SOFC) are promising, environmentally friendly energy sources. Many works are devoted to the study of materials, individual aspects of SOFC operation, and the development of devices based on them. However, there is no work covering the entire spectrum of SOFC concepts and designs. In the present review, an attempt is made to collect and structure all types of SOFC that exist today. Structural features of each type of SOFC have been described, and their advantages and disadvantages have been identified. A comparison of the designs showed that among the well-studied dual-chamber SOFC with oxygen-ion conducting electrolyte, the anode-supported design is the most suitable for operation at temperatures below 800 °C. Other SOFC types that are promising for low-temperature operation are SOFC with proton-conducting electrolyte and electrolyte-free fuel cells. However, these recently developed technologies are still far from commercialization and require further research and development.

The design of metal-supported solid oxide fuel cells (MS-SOFCs) has again aroused interest in recent years due to their low cost of materials, strength, and resistance to thermal cycling, as well as the advantages of manufacturability. MS-SOFCs are promising electrochemical devices for hydrogen energy. Compared to SOFCs, where ceramic electrodes or electrolytes are used as a carrier base, they are of great interest due to their fast start-up capability, greater reliability, mechanical stability, and resistance to the thermal cycle. MS-SOFCs have many advantages over conventional ceramic-based SOFCs, with the selection of metal-based electrode materials (anode, cathode) and their degradation processes being some of the biggest challenges facing researchers. Therefore, this review reports on the state of the latest research on MS-SOFCs with various structures, discusses the corresponding electrode materials and their existing problems, and puts forward topical issues that need to be addressed in MS-SOFCs.

This review presents thermoelectric phenomena in copper chalcogenides substituted with sodium and lithium alkali metals. The results for other modern thermoelectric materials are presented for comparison. The results of the study of the crystal structure and phase transitions in the ternary systems Na-Cu-S and Li-Cu-S are presented. The main synthesis methods of nanocrystalline copper chalcogenides and its alloys are presented, as well as electrical, thermodynamic, thermal, and thermoelectric properties and practical application. The features of mixed electron–ionic conductors are discussed. In particular, in semiconductor superionic copper chalcogenides, the presence of a “liquid-like phase” inside a “solid” lattice interferes with the normal propagation of phonons; therefore, superionic copper chalcogenides have low lattice thermal conductivity, and this is a favorable factor for the formation of high thermoelectric efficiency in them.

In this study, α-cellulose was extracted from lignocellulosic simpor leaf residue as a sustainable alternative to conventional cellulose sources. The extraction process involved the removal of hemicellulose, lignin, and other phytocompounds using alkali (NaOH) treatment and bleaching with hydrogen peroxide (H₂O₂). The nanocrystalline cellulose (NCC) was isolated from α-cellulose using sulfuric acid hydrolysis treatment followed by ultrasonication. The extracted α-cellulose and isolated NCC were characterized using Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and dynamic light scattering (DLS). The obtained results confirmed that the extracted NCC exhibited characteristic cellulose functional groups and a crystallinity index of 64.7%, indicating the effective removal of amorphous regions through sulfuric acid hydrolysis. The thermal stability of the extracted cellulose increased to 332 °C due to the elimination of extractives. DLS analysis showed that the extracted NCC exhibited high colloidal stability in polar solvents, characterized by a zeta potential of −70.8 mV and an average particle size of 251.7 nm. This study highlights an environmentally friendly approach for converting low-value biomass waste into high-value cellulose materials with potential applications in sustainable packaging, biomedical applications and composite reinforcement.

Conventional solvents remain the most used media for lignocellulosic biomass valorization. However, these solvents exhibit many limitations and have a negative environmental impact. In the last decade, Deep Eutectic Solvents (DESs) have emerged as a multifaceted tool in biomass valorization, with a promising perspective in the application of lignocellulosic biomass valorization. DESs have gained attention in the last decade as an alternative solvent in biomass valorization and biorefinery processes due to their high efficiency; eco-friendliness; low cost; and numerous other advantages, such as recyclability, non-volatility, and stability. This paper discusses the latest research on the potential applications of DESs in the valorization of secondary lignocellulosic biomass.

Kazakhstan possesses significant natural resources, including coal, oil, natural gas, and uranium, and also has substantial potential for utilizing renewable energy sources such as wind, solar, hydropower, and biomass. However, the country currently relies heavily on fossil fuels for electricity...