The development of nanocomposites with tunable physicochemical properties is essential for tackling global challenges related to sustainable energy storage and environmental remediation. This study comprehensively investigated the impact of several solvents on the structural, textural, and electrical characteristics of MoS2/CdS nanocomposites (NCs), as well as their photocatalytic and electrochemical performance. The heterostructured MoS2/CdS NCs were synthesized via a one-pot solvothermal approach at 180 ℃ for 16 h using cadmium acetate dihydrate, sodium molybdate dihydrate, and thiourea as the precursors of Cd, Mo, and S, respectively. X-ray diffraction and N2 adsorption-desorption analyses confirmed the successful synthesis of the NCs and demonstrated that both crystallinity and BET surface area were strongly influenced by the solvent environment. The photocatalytic performance was evaluated by degrading methyl orange dye under solar irradiation, while electrochemical behavior was assessed for supercapacitor applications. Among the synthesized samples, the MoS2/CdS NC obtained using ethylene glycol solvent demonstrated superior photocatalytic efficiency, achieving approximately 99% degradation of methyl orange in just 15 minutes. This efficiency is attributed to its larger surface area and more effective separation of photogenerated charge carriers. Electrochemical measurements further revealed that this sample delivered an enhanced specific capacitance of 445 F/g, outperforming those synthesized with other solvents. This study demonstrates the critical importance of solvent selection in modulating the morphology, surface properties, and charge-transfer characteristics of CdS/MoS2 NCs. The findings demonstrate their strong potential as dual-function materials for high-efficiency pollutant degradation and advanced energy storage technologies.
Published in: 8th IEOM Bangladesh International Conference on Industrial Engineering and Operations Management, Dhaka, Bangladesh
Publisher: IEOM Society International
Date of Conference: December 20
-21
, 2025
ISBN: 979-8-3507-4441-5
ISSN/E-ISSN: 2169-8767