Ionic liquids (ILs) have emerged as active pharmaceutical ingredients because of their excellent antibacterial and biological activities. Herein, we used the green-chemistry-synthesis procedure, also known as the metathesis method, to develop three series of ionic liquids using 1-methyl-3-butyl imidazolium, butyl pyridinium, and diethyldibutylammonium as cations, and bromide (Br⁻), methanesulfonate (CH₃SO₃⁻), bis(trifluoromethanesulfonyl)imide (NTf₂⁻), dichloroacetate (CHCl₂CO₂⁻), tetrafluoroborate (BF₄⁻), and hydrogen sulfate (HSO₄⁻) as anions. Spectroscopic methods were used to validate the structures of the lab-synthesized ILs. We performed an agar well diffusion assay by using pathogenic bacteria that cause various infections (Escherichia coli; Enterobacter aerogenes; Klebsiella pneumoniae; Proteus vulgaris; Pseudomonas aeruginosa; Streptococcus pneumoniae; Streptococcus pyogenes) to scrutinize the in vitro antibacterial activity of the ILs. It was established that the nature and unique combination of the cations and anions were responsible for the antibacterial activity of the ILs. Among the tested ionic liquids, the imidazolium cation and NTf₂⁻ and HSO₄⁻ anions exhibited the highest antibacterial activity. The antibacterial potential was further investigated by in silico studies, and it was observed that bis(trifluoromethanesulfonyl)imide (NTf₂⁻) containing imidazolium and pyridinium ionic liquids showed the maximum inhibition against the targeted bacterial strains and could be utilized in antibiotics. These antibacterial activities float the ILs as a promising alternative to the existing antibiotics and antiseptics.

The ongoing challenge of water pollution necessitates innovative approaches to remove organic contaminants from wastewater. In this work, new two-dimensional S-scheme heterojunction photocatalysts Bi₂O₃/CdS and MoS₂/Bi₂O₃/CdS that are intended for the effective photocatalytic destruction of 4-nitrophenol, a dangerous organic pollutant, are synthesized and characterized. Utilizing a solvothermal method, successfully generated these ternary nanocomposites, which were characterized through various techniques including X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), high resolution transmission electronmicroscopy (HRTEM), Brunauer-Emmett-Telle (BET) and diffuse reflectance spectroscopy (DRS). Our results demonstrated that the Bi₂O₃/CdS heterojunction achieved an 86% degradation rate of 4-nitrophenol, while the MoS₂/Bi₂O₃/CdS composite exhibited exceptional photocatalytic performance, achieving nearly complete degradation (99%) within 120 min under visible light irradiation. Most importantly the improved photocatalytic activity of MoS₂/Bi₂O₃/CdS heterojunction originated from the release of internal electric field in S-scheme heterojunction. This enhanced activity is attributable to the synergistic effects of the heterojunctions that facilitate more effective charge separation and generation with more OP and RP confirmed the composite synthesis using S-scheme. The S-scheme is further confirmed by XPS, DRS, XPS-VB and photocurrent response. These findings highlight the promising application of these advanced photocatalysts in real-world wastewater treatment processes, offering a sustainable solution to combat water pollution.