The advancement of multidrug-resistant bacterial strains and their adverse effects is one of the most significant global health issues. The perovskite nanomaterial with combined antioxidant and antibacterial activities in one molecule has the potential for improved therapeutic solutions. In this work, Yttrium-doped Lanthanum Titanate (LaTi_1 −xY_xO₃, where x = 0, 0.05, and 0.1) was synthesized using auto combustion technique. Excellent crystalline structure with a tetragonal system is revealed by X-ray diffraction analysis (XRD). UV–Visible diffuse reflectance spectroscopy (UV–Vis DRS), Fourier transform infrared (FTIR), and photoluminescence (PL) were used to study its optical characteristics. The field emission scanning electron microscope (FE-SEM) shows rod-like pellet-shaped Yttrium-doped nanostructures, and the elements present were confirmed with the Energy Dispersive X-Ray Analysis (EDAX). Various concentrations of the synthesized materials were tested for antibacterial activity against Gram-positive (Staphylococcus aureus 902) and Gram-negative (E. coli 443) strains using the agar-well diffusion method with gentamicin antibiotic as a positive control. High antibacterial activity of 87.1% and 83.3% was shown by 10% Yttrium-doped LaTiO₃ (LY(0.1)TO) at 500 mg/mL against both positive and negative stains, respectively. Moreover, the antioxidant properties of synthesized materials were assessed with IC50 values of 352.33 µg/mL, 458.055 µg/mL, and 440.163 µg/mL for samples LaTi_1 − xY_xO₃, where x = 0, 0.05, and 0.1 respectively. The antibacterial and antioxidant capabilities of the proposed samples illustrate their applicability in various biomedical applications.

A high perovskite activity is sought for use in magnetic applications. In this paper, we present the simple synthesis of (2.5% and 5%) Tellurium-impregnated-LaCoO₃ (Te-LCO), Te and LaCoO₃ (LCO) by using a ball mill, chemical reduction, and hydrothermal synthesis, respectively. We also explored the structure stability along with the magnetic properties of Te-LCO. Te has a rhombohedral crystal structure, whereas Te-LCO has a hexagonal crystal system. The reconstructed Te was imbued with LCO that was produced by hydrothermal synthesis; as the concentration of the imbuing agent grew, the material became magnetically preferred. According to the X-ray photoelectron spectra, the oxidation state of the cobaltite is one that is magnetically advantageous. As a result of the fact that the creation of oxygen-deficient perovskites has been shown to influence the mixed (Te^4+/2−) valence state of the incorporated samples, it is abundantly obvious that this process is of utmost significance. The TEM image confirms the inclusion of Te in LCO. The samples start out in a paramagnetic state (LCO), but when Te is added to the mixture, the magnetic state shifts to a weak ferromagnetic one. It is at this point that hysteresis occurs due to the presence of Te. Despite being doped with Mn in our prior study, rhombohedral LCO retains its paramagnetic characteristic at room temperature (RT). As a result, the purpose of this study was to determine the impacts of RT field dependency of magnetization (M-H) for Te-impregnated LCO in order to improve the magnetic properties of RT because it is a low-cost material for advanced multi-functional and energy applications.

Enhanced photo-induced electron utilization leads to efficient photocatalytic hydrogen production. The inefficient separation of photo-induced electron–hole pairs has hindered this process. This study introduces a synergistic approach using defect-rich SnS₂ and Ti₃C₂ MXene as cocatalysts in a two-step hydrothermal process to address this challenge. By integrating these materials with TiO₂ nanosheets, we create a novel composite, SnS₂/Ti₃C₂/TiO₂ (STT), that significantly boosts photocatalytic hydrogen evolution. The defect-rich SnS₂ provides abundant active sites for hydrogen generation, while Ti₃C₂ MXene facilitates photo-induced charge separation. The synergistic combination of charge carrier diffusion enhances chromophore absorption, thereby increasing the overall photocatalytic hydrogen-production rate, achieving several grams of hydrogen per hour per gram of double cocatalysts with molybdenum vacancies. Characterization techniques confirm the phase composition of the composite (STT). Compared to pristine TiO₂ and other composites, the STT composite, optimized with a 150 °C hydrothermal treatment, shows a photocatalytic H₂-production rate nearly 192 times higher than that of pure TiO₂ and 6 times higher than that of other composites. The presence of molybdenum vacancies in SnS₂ further enhances its specific activity for hydrogen evolution by suppressing carrier recombination and providing additional active sites. Moreover, Ti₃C₂ MXene and SnS₂ act as dual cocatalysts, improving electronic conductivity and electron-transfer efficiency. Our findings demonstrate the potential of combining defect-rich SnS₂ and Ti₃C₂ MXene to develop highly efficient and sustainable photocatalysts for hydrogen production. TiO₂ has been in situ grown on highly conductive Ti₃C₂ MXene, and SnS₂, rich in molybdenum vacancies, is uniformly distributed on the TiO₂/Ti₃C₂ composite through the two-step hydrothermal method. The presence of molybdenum vacancies in SnS₂ further enhances its specific activity for hydrogen evolution by suppressing carrier recombination and providing additional active sites. Moreover, Ti₃C₂ MXene and SnS₂ act as dual cocatalysts, improving electronic conductivity and electron-transfer efficiency. Our findings demonstrate the potential of combining defect-rich SnS₂ and Ti₃C₂ MXene to develop highly efficient and sustainable photocatalysts for hydrogen production.

This review reveals the parameters of next-generation fuel cells for portable applications such as cellular phones, laptops, automobiles, etc. Disputes over issues such as design, fluid dynamics, channel dimensions, thermal management, and water management must be overcome for practical applications. We examine techniques such as microfabrication, material selection for membranes and electrodes, and integration challenges in small-scale devices, in addition to issues like methanol crossover, low efficiency at high methanol concentrations, thermal management, and the cost of materials. The advancements in micro-DMFC stacks and prototype developments are presented, and the challenges relating to micro-DMFCs are also identified and reviewed in detail. The challenges in the development of micro-DMFC applications are also presented, including the need for a better understanding of the anode and cathode catalyst structure and for high catalyst loadings in oxidation-and-reduction reactions. Also, a comprehensive and highly valuable database for advancing innovations and enhancing the understanding of micro-DMFCs for potential applications is provided.