ABSTRACT
In this work, heterostructures of coupled TiO2@MoS2with different phases of MoS2were synthesized via hydrothermal technique. The prepared materials were thoroughly characterized using various techniques, including XRD, SEM, transmission electron microscopy, Brunauer-Emmet-Teller, XPS, Zeta potential and UV-vis spectroscopy. The optimized nanocomposites were tested for the photocatalytic degradation of methyl Orange (MO) under visible light as well as the adsorption of Rhodamine b (RhB) and methelene blue (MB) dyes. The TiO2@1T/2H-MoS2heterostructures exhibited a narrow bandgap compared to the other studied nanomaterials. A remarkable photodegradation efficiency of TiO2@1T/2H-MoS2was observed, which completely degraded 20 ppm of MO after 60 min with high stability over four successive cycles. This can be assigned to the formation of unique heterostructures with aligned energy bands between MoS2nanosheets and TiO2nanobelts. The formation of these novel interfaces promoted the electron transfer and increased the separation efficiency of carriers, resulting in high photocatalytic degradation. Furthermore, the adsorption efficiency of TiO2@1T/2H-MoS2was unique, 20 ppm solutions of RhB and MB were removed after 1 and 2 min, respectively. The superior adsorption performance of the TiO2@1T/2H-MoS2can be attributed to its high surface area (279.9 m2g-1) and the rich concentration of active sites. The kinetics and the isothermal analysis revealed that the TiO2@1T/2H MoS2heterstructures have maximum adsorption capacity of 1200 and 970 mg g-1for RhB and MB, respectively. This study provides a powerful way for designing an effective photocatalyst and adsorbent TiO2-based nanocomposites for water remediation.
ABSTRACT
Herein, different phases of MoS2 nanosheets were synthesized, characterized and tested for dye removal from water. The influence of the MoS2 phases as well as the 1T concentration on the adsorption performance of organic dyes MO, RhB and MB was deeply investigated. The results revealed that the 1T-rich MoS2 nanosheets have superior adsorption performance compared to other 2H and 3R phases. The kinetic results of the adsorption process demonstrate that the experimental data followed the pseudo-second order equation. Meanwhile, the adsorption of dyes over the obtained materials was fitted with several isotherm models. The Langmuir model gives the best fitting to the experimental data with maximum a adsorption capacity of 787 mg g-1. The obtained capacity is significantly higher than that of all previous reports for similar MoS2 materials. Computational studies of the 2H and 1T/2H-MoS2 phases showed that the structural defects present at the 1T/2H grain boundaries enhance the binding of hydroxide and carboxyl groups to the MoS2 surface which in turn increase the adsorption properties of the 1T/2H-MoS2 phase.
ABSTRACT
MoS2 is a 2D material that has been widely used in supercapacitor applications because of its layered structure that provides a large surface area and allows for high electric double-layer charge storage. To enhance the cycling stability and capacitance of MoS2, it is usually mixed with carbon materials. However, the dependence of the charge storage mechanism on the structure of the carbon material is still unclear in literature. Herein, the effect of the structure of the carbon material on the charge storage mechanism in 2H flower-shaped MoS2 is investigated in detail. Specifically, 2H MoS2 was mixed with either 8 nm-diameter carbon nanotubes (CNTs) or graphene nanoflakes (GNFs) in different weight ratios. Also, a composite of MoS2, CNTs, and GNFs (1:1:1) was also studied. The charge storage mechanism was found to depend on the structure and content of the carbon material. Insights into the possible storage mechanism(s) were discussed. The MoS2/CNT/GNF composite showed a predominant pseudocapacitive charge storage mechanism where the diffusion current was â¼89%, with 88.31% of the resulted capacitance being due to faradic processes.
