In the present study, a green, scalable, and environmentally friendly approach was developed for the fabrication of Bi₂S₃-decorated CdS nanoparticles with an efficient hydrogen generation ability from the water. As a sulfur source, thiourea was used. The process was completed in two stages: mechanical activation and thermal annealing. The presence of spherical CdS nanoparticles and Bi₂S₃ nanorods in the CdS/Bi₂S₃ nanocomposite was confirmed and proved by XRD, Raman spectroscopy, SEM-EDS, and TEM. The synthesized CdS/Bi₂S₃ nanocomposites were evaluated for their photocatalytic hydrogen evolution capabilities. The CdS/Bi₂S₃ photocatalyst exhibited 25% higher photocatalytic activity compared to CdS, reaching a hydrogen evolution rate of 996.68 μmol h⁻¹g⁻¹ (AQE 0.87%) after 3.5 h under solar-light irradiation.

The efficient capture of carbon dioxide (CO₂) using polymer, supported ionic liquids (ILs) remains challenging due to limited understanding of atomic-scale interaction mechanisms. Here, a polystyrene (PS) oligomer supported by an amidinium chloride-based IL is proposed as a CO₂-absorbing material. Density functional theory (DFT) calculations were employed to investigate the structural, electronic, and intermolecular interaction energy characteristics of the PS oligomer, amidinium chloride ILs, CO₂, and their binary and ternary complexes. Molecular electrostatic potential maps (MEPs), reduced density gradient (RDG) plots with non-covalent interaction (NCI) snapshots, quantum theory of atoms in molecules critical point (CP) analysis, and electron localization function (ELF) analysis reveal pronounced hydrogen bonding and dispersion interactions between PS and IL that modulate the electronic environment of the IL anion, which is the primary CO₂ binding site. Interaction energy calculations show that the ternary PS–IL–CO₂ complex exhibits a significantly enhanced binding energy compared to the isolated IL–CO₂ complex, providing quantitative evidence for the cooperative role of the PS support. The results indicate enhanced CO₂ binding in the presence of PS supported by ILs, driven by cooperative electrostatic and dispersion interactions. These findings provide molecular-level insights into CO₂ capture mechanisms in polymer–IL hybrid systems.