Deep eutectic solvent as an effective tool for enhanced photocatalytic activity of Cu2S@MoS2 nano-assemblies: A green approach

Abstract

The scientific world has witnessed the emergence of plethora of green strategies to ameliorate the efficiency of nano-photocatalytic materials for waste water treatment applications. This work, for the first time, highlights the effect of ZnCl2 and urea-based DES on the morphology, electronic band structure and photocatalytic efficiency of Cu2S @MoS2 NPs compared to solvents like water, EDA and DETA. XRD and FT-IR analysis confirmed the formation of NPs and quite significant changes in the pattern of M-S bonds of Cu2S@MoS2 were observed upon variation of solvents. The FE-SEM analysis of NPs prepared in 1:1 composition of DES and water (Cu2S@MoS2 NPs - 1:1) showed entirely distinct nanoflower morphology compared to spherical arrangement shown by NPs prepared using other solvents. As a result, Cu2S@MoS2 NPs - 1:1 showed superior textural properties with a surface area of 89 m2/g in contrast to 7.4, 6.2 and 18 m2/g observed for NPs synthesized in water, EDA and DETA, respectively. Besides, wide band gap of 2.75 eV for Cu2S@MoS2 NPs - 1:1 induced favorable charge carrier recombination kinetics, which played an instrumental role in the degradation of tetracycline hydrochloride (TC) and rhodamine B (RB). Cu2S@MoS2 NPs - 1:1 showed best photocatalytic activity as 97% and 96% of TC and RB was removed after 90 min of visible light irradiation with no significant decline in removal efficiency till 5 cycles. Scavenger studies hinted towards the crucial role of h+ and ⋅ OH in degradation process and a mechanism was proposed accordingly. The superior photocatalytic activity of NPs prepared using DES compared to water and organic solvents showed that the inclusion of DES in synthesis schemes of NPs is an excellent strategy for improving their efficiency towards waste water treatment applications.