Ti3C2-MXene/NiO Nanocomposites-Decorated CsPbI3 Perovskite Active Materials under UV-Light Irradiation for the Enhancement of Crystal-Violet Dye Photodegradation.

Ti3C2-MXene material, known for its strong electronic conductivity and optical properties, has emerged as a promising alternative to noble metals as a cocatalyst for the development of efficient photocatalysts used in environmental cleanup. In this study, we investigated the photodegradation of crystal-violet (CV) dye when exposed to UV light using a newly developed photocatalyst known as Ti3C2-MXene/NiO nanocomposite-decorated CsPbI3 perovskite, which was synthesized through a hydrothermal method. Our research investigation into the structural, morphological, and optical characteristics of the Ti3C2-MXene/NiO/CsPbI3 composite using techniques such as FTIR, XRD, TEM, SEM-EDS mapping, XPS, UV-Vis, and PL spectroscopy. The photocatalytic efficacy of the Ti3C2-MXene/NiO/CsPbI3 composite was assessed by evaluating its ability to degrade CV dye in an aqueous solution under UV-light irradiation. Remarkably, the Ti3C2-MXene/NiO/CsPbI3 composite displayed a significant improvement in both the degradation rate and stability of CV dye when compared to the Ti3C2-MXene/NiO nanocomposite and CsPbI3 perovskite materials. Furthermore, the UV-visible absorption spectrum of the Ti3C2-MXene/NiO/CsPbI3 composite demonstrated a reduced band gap of 2.41 eV, which is lower than that of Ti3C2-MXene/NiO (3.10 eV) and Ti3C2-MXene (1.60 eV). In practical terms, the Ti3C2-MXene/NiO/CsPbI3 composite achieved an impressive 92.8% degradation of CV dye within 90 min of UV light exposure. We also confirmed the significant role of photogenerated holes and radicals in the CV dye removal process through radical scavenger trapping experiments. Based on our findings, we proposed a plausible photocatalytic mechanism for the Ti3C2-MXene/NiO/CsPbI3 composite. This research may open up new avenues for the development of cost-effective and high-performance MXene-based perovskite photocatalysts, utilizing abundant and sustainable materials for environmental remediation.

Synthesis of nickel-doped ceria nanospheres for in situ profiling of Warfarin sodium in biological media.

Venous thromboembolism is one of the major disorders, which is significantly increased the mortality and morbidity rate. Warfarin sodium (WFS) is the most extensively prescribed drug for the prevention of thromboembolic diseases however, it has a narrow therapeutic index. Recently, many methods for detecting and monitoring the level of WFS have been proposed. However, the electrochemical method has gained more interest than the other traditional method due to its ease of operation. This article describes the hydrothermal synthesis of nickel-doped cerium oxide (CeO2@Ni) nanospheres for the selective electrochemical determination of WFS. Various spectroscopic techniques have been used to analyze the chemical composition, and surface morphology of CeO2@Ni nanospheres. Further, the prepared CeO2@Ni nanospheres modified electrode demonstrated excellent electrocatalytic behavior for WFS detection, with an ultralow detection limit of 6.3 × 10-9 M, a linear range of 1.0 × 10-8 M to 1.51 × 10-4 M and 1.51 × 10-4 M to 9.51 × 10-4 M, and a higher sensitivity of 2.9986 µA µM-1 cm2. Therefore, we believe that the CeO2@Ni nanosphere electrocatalyst can serve as a potential electrode catalyst for the sensing of WFS in real-time applications.

Multi-biological combined system: A mechanistic approach for removal of multiple heavy metals.

In this work, interactions of diverse fungal species by the manipulation of cell concentrations has been utilized as the driving feature for the removal of hazardous multi-metals from the aqueous solutions. This study is focused on the exploitation of internal structures of microbes as a repository of lead (Pb(II)) and nickel (Ni(II)). For the concerned purpose 24 heavy metal resistant fungi are isolated from different industrial waste sites to form different microbial combinations as a single unit 'consortia' for achieving highest possible removal rates. Polymerase chain reaction and DNA sequencing are involved for the biochemical characterization and phylogenetic analysis of the screened isolates. The identification and screening studies reveal isolated strains as two Pb resistant fungi viz. K1SF-Pb15 (Aspergillus terreus) and SEF-Pb (Talaromyces islandicus) which have shown metal removal up to 93% and two Ni(II) tolerant fungal isolates namely, MEF-Ni-11 (Neurospora crassa) and Ni-1 (Aspergillus flavus) with removal efficiency of more than 91%. Relationship has been validated between the biosorption capacity and efficiency of the novel consortium under the influence of variable pH, time duration, initial concentration of Pb(II) and Ni(II), and inoculum size which has led to the foundation of effective and economical parameters for its exploitation in practical fields. The fungal consortia when applied on various industrial effluents has exhibited more than 95% of removal for both Pb(II) and Ni(II) simultaneously. The detailed mechanistic insight has shown the involvement of physical, chemical and ionic forces for the removal of heavy metals. So the designed novel multi-biological combined system acted as a repository for Pb(II) and Ni(II) ions with a greater potential which can be guided by the mechanistic methodology for the retrieval and remediation of multiple heavy metals from the real waste water samples.