Perovskites-Based Nanomaterials for Chemical Sensors

The perovskite structure is adopted by many compounds in solid-state chemistry. The sensitivity, selectivity, and stability of many perovskite nanomaterials have been devoted the most attention for chemical sensors. They are capable to sense the level of small molecules such as O2, NO, and CO. This chapter provides a comprehensive overview of perovskite nanoscale materials that concentrate on chemical sensors. The perovskite structure, with two differently sized cations, is amenable to a variety of dopant additions. This flexibility allows for the control of transport and catalytic properties, which are important for improving sensor performance. We devote the most attention on the synthesis, structural information, and sensing mechanism. We will later elaborate on the development mechanism of chemical sensors based on perovskite nanomaterials. We conclude this chapter with the personal perspectives on the directions toward future works on a novelty of nanostructured chemical sensors

Enhanced hydrogen storage performance of zinc and magnesium cobaltite nanocomposites

Renewable and sustainable energies are vital for the near future. Hydrogen, as a clean energy carrier, is a potential candidate for supplying energy in the foreseeable future. Nowadays, hydrogen storage technology has become a significant issue in the energy sector. In this study, ZnCo2O4/ZnO and MgCo2O4/MgO nanocomposites have been synthesized using the sol-gel method with stearic acid as a complexing agent. Different analyses were studied to examine the crystal structure, morphology, and physical properties of the as-prepared samples, including X-ray diffraction (XRD), Fourier transforms infrared (FT-IR), field emission scanning electron microscopy (FESEM), diffuse reflectance spectroscopy (DRS), and vibrating sample magnetometer (VSM). Various methods have been utilized for hydrogen storage technology. In a pioneering approach, the electrochemical hydrogen storage of samples was compared by the chronopotentiometry technique in KOH (4 M) electrolyte solution. The results reveal that ZnCo2O4/ZnO and MgCo2O4/MgO nanocomposites exhibit excellent discharge capacities of 4240 and 3529 mAh/g, respectively, after 11 cycles

Multi-wall carbon Nanotube surface-based functional nanoparticles for stimuli-responsive dual pharmaceutical compound delivery

Carbon nanotubes (CNTs) have the potential to serve as delivery systems for medicinal substances and gene treatments, particularly in cancer treatment. Co-delivery of curcumin (CUR) and Methotrexate (MTX) has shown promise in cancer treatment, as it uses fewer drugs and has fewer side effects. This study used MTX-conjugated albumin (BSA)-based nanoparticles (BSA-MTX) to enhance and assess the efficiency of CUR. In-vitro cytotoxicity tests, DLS, TEM, FTIR, UV/Vis, SEM, and DSC studies assessed the formulations' physical and chemical properties. The Proteinase K enzyme was used to severe amidic linkages between MTX and BSA. The findings demonstrated the efficacy of using ƒ-MWCNT-CUR-BSA-MTX as a vehicle for efficient co-delivery of CUR and MTX in cancer treatment. The MTT colorimetric method was used to evaluate the effect of chemical and medicinal compounds. Cell division was studied using the MTT method to investigate the effect of pure MWCNT, pure CUR, MTX-BSA, and ƒ-MWCNT-CUR-MTX-BSA. Studies on cell lines have shown that the combination of curcumin and MTX with CNT can increase and improve the effectiveness of both drugs against cancer. A combination of drugs curcumin and methotrexate simultaneously had a synergistic effect on MCF-7 cells, which indicated that these drugs could potentially be used as a strategy for both prevention and treatment of breast cancer. Also, ƒ-MWCNT-CUR-MTX-BSA was found to have a significant effect on cancer treatment with minimal toxicity compared to pure curcumin, pure MTX-BSA, MTX, and ƒ-MWCNT alone. Unique properties such as a high ratio of specific surface area to volume, high chemical stability, chemical adsorption ability, high capacity of drug and biomolecules of carbon nanotubes, as well as multiple drug loading at the same time The combination of ƒ-MWCNT-CUR-BSA MTX significantly impacts cancer therapy), are desirable as an alternative option for targeted drug delivery and high therapeutic efficiency

Sol-gel synthesis, characterization, and electrochemical evaluation of magnesium aluminate spinel nanoparticles for high-capacity hydrogen storage

In this research, we successfully synthesized magnesium aluminate (MgAl2O4) spinel nanoparticles using a sol-gel process, with stearic acid serving as a capping agent. The synthesis process involved calcination at 900 °C for 4 h, resulting in the formation of nanoparticles with an average crystallite size of approximately 12 nm, as determined through Debye–Scherrer analysis and X-ray diffraction (XRD) data. The optical band gap was measured as 2.84 eV using Diffuse Reflectance Spectroscopy (DRS) analysis. Additionally, we found the mean pore size of the nanoparticles to be 20.2 nm through Brunauer–Emmett–Teller (BET) analysis. We characterized the resulting powders using various techniques, including Fourier Transform Infrared (FTIR) spectroscopy, Field Emission Scanning Electron Microscopy (FESEM), Energy-Dispersive X-ray Spectroscopy (EDS), and Vibrating Sample Magnetometry (VSM). We conducted electrochemical investigations utilizing the Chronopotentiometry (CP) technique. The electrochemical analysis demonstrated that MgAl2O4 spinel nanoparticles exhibit a noteworthy hydrogen storage capacity of 4000 mAh/g, highlighting their potential as promising candidates for hydrogen storage applications. This comprehensive study underscores the successful synthesis, thorough characterization, and exceptional electrochemical performance of MgAl2O4 spinel nanoparticles, firmly positioning them as valuable materials for advancing hydrogen storage technologies

FeAl2O4 Nanopowders; Structural Analysis and Band Gap Energy

AbstractNanoscale FeAl2O4 was successfully synthesized via sol–gel method. The sol constituents containing iron and aluminum cations were formed homogenously in stearic acid gel (formation of organic precursor). The pure structural analysis and the size of the spinels were confirmed by X-ray diffraction (XRD). It was observed that the size of the nanoscale materials obtained at around 30–40nm. The micrographs of FeAl2O4 evidenced the homogenous and nanosize formation of spinel. The semiconducting behavior of this mixed metal oxide was observed at 3.14eV based on the band gap energy (Eg). The final nanoscale materials exhibited a superparamagnetic behavior with a saturation magnetization of 9.8 emu/g at applied field of 10 kOe.</jats:p