ABSTRACT
Our study specifically explores the biosynthesis of copper-silver bimetallic nanoparticles (Cu-Ag BMNPs) using Argyreia nervosa (AN) plant leaf green extract as a versatile agent for capping, reducing, and stabilizing. This biosynthesis method is characterized by its simplicity and cost-effectiveness, utilizing silver nitrate (AgNO3) and cupric oxide (CuO) as precursor materials. Our comprehensive characterization of the Cu-Ag BMNPs, employing techniques such as X-ray diffraction (XRD), UV-Vis spectrometry, scanning electron microscopy (SEM), Zetasizer, and Fourier transformed infrared spectrometry (FTIR). FTIR analysis reveals biofunctional groups and chemical bands, while SEM and XRD analyses provide morphological and structural details. To evaluate the antimicrobial properties of the Cu-Ag BMNPs, we conducted disc diffusion and minimum inhibitory concentration (MIC) assays against Escherichia coli (E. coli), with results compared to the standard gentamicin antibiotic. It is observed that the 2% and 5% CuO concentrations of AN Cu-Ag BMNPs exhibit substantial antibacterial activity in comparison to AN extract when tested on EPEC. Among these, the Cu-Ag BMNPs at a 2% concentration demonstrate higher antibacterial activity, potentially attributed to the enhanced dispersion of BMNPs facilitated by the lower CuO doping concentration. These two assays showcased the improved antimicrobial activity of Cu-Ag BMNPs, highlighting their synergistic effect, characterized by high MIC values and a broad zone of inhibition in the disc diffusion tests against E. coli. These results emphasize the significant antibacterial potential of the synthesized BMNPs, with a medicinal plant AN leaf extract playing a pivotal role in enhancing antibacterial activity.
ABSTRACT
Perovskites have achieved immense progression in optoelectronic device applications owing to their fascinating intrinsic properties. However, the integration of perovskites in lighting applications has been retarded due to the challenges involved in achieving their deep blue light-emitting diodes (LEDs). Unlike other color counterparts, obtaining a stable, defect-tolerant, and high-band gap perovskite material for deep blue emission is an arduous task. Moreover, the ambient stability and efficient charge injection in the device are bottlenecks for the established perovskite emissive materials. Among all the dimensional perovskite counterparts, quasi-two-dimensional perovskites (Q2DPes) with hydrophobic ligands can exhibit better stability, and also, facile tunability of the properties can overcome the associated challenges. In this paper, for the first time, we demonstrate Ruddlesden-Popper-based Q2DPes that are pure deep blue emissive in the 450 nm region, stable, and can facilitate decent charge injection in LEDs. We have also demonstrated systematic modulations in the properties of the material, concerning the organic cation concentration.
