Remediation of phenanthrene by highly efficient CdS-SnS photocatalyst and its cytotoxic assessments.

Cadmium sulfide-tin sulfide (CdS-SnS) nanoparticles are a novel kind of photocatalyst. These CdS-SnS nanoparticles are synthesized and characterized using UV-Vis, FT-IR, XRD, SEM-EDX, and DLS techniques, to understand their size distribution, crystalline nature, morphology, shape, optical properties, and elemental composition. This research offers insight into the efficient photocatalytic degradation of Phenanthrene (PHE) using CdS-SnS. The CdS-SnS NPs as photocatalyst can effectively photodegrade the polycyclic aromatic hydrocarbons (PAH) such as phenanthrene under simulated solar and UV light. UV-vis spectra of these nanoparticles exhibit peaks at 365 and 546 cm respectively, the mean size of the CdS-SnS NPs in DLS is determined to be 78 nm. The CdS-SnS stretching frequency was observed at wave numbers below 700 cm, the absorption peak at 1123 cm indicates the presence of C-N stretch or CS bond of thiourea, while the peak at 1350.38 cm corresponds to the tris-amine C-N stretch in FT-IR. Additionally, the peaks observed at 2026  indicate the presence of isothiocyanate (NCS). 1456.23 cm represents the asymmetric scissor deformation vibration. EDAX revealed the presence of elemental Cd and Sn oxides. The antimicrobial studies showed that the CdS-SnS NPs at the concentration of 150 μg/mL, exhibit maximum inhibition (15 ± 1.25 mm) against the strains Proteus mirabilis followed by Staphylococcus epidermidis and Clostridium spp. Among fungal strains Colletotrichum spp. exhibits the maximum zone of inhibition (9 ± 0.25). This research also observed the cytotoxic effects of CdS-SnS NPs on HepG2 and ZF4 cells. HepG2 cells exhibited 50% inhibition at 50 μg/mL and 70% inhibition at 100 μg/mL concentrations, while ZF4 cells exhibited 50% inhibition at 50 μg/mL and 78% inhibition at 100 μg/mL concentrations, respectively. The parameters like concentration of PHE, concentration of CdS-SnS NPs, pH, and sources of irradiation on batch adsorption were examined to maximize the efficiency of the photodegradation process.