Revealing the role of the 1T phase on the adsorption of organic dyes on MoS nanosheets

Herein, different phases of MoS 2 nanosheets were synthesized, characterized and tested for dye removal from water. The influence of the MoS 2 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...

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Veröffentlicht in:RSC advances 2019-09, Vol.9 (49), p.28345-28356
Hauptverfasser: Omar, Asmaa M, Metwalli, Ossama I, Saber, Mohamed R, Khabiri, Gomaa, Ali, Mohamed E. M, Hassen, Arafa, Khalil, Mostafa M. H, Maarouf, Ahmed A, Khalil, Ahmed S. G
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Zusammenfassung:Herein, different phases of MoS 2 nanosheets were synthesized, characterized and tested for dye removal from water. The influence of the MoS 2 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 MoS 2 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 MoS 2 materials. Computational studies of the 2H and 1T/2H-MoS 2 phases showed that the structural defects present at the 1T/2H grain boundaries enhance the binding of hydroxide and carboxyl groups to the MoS 2 surface which in turn increase the adsorption properties of the 1T/2H-MoS 2 phase. The high adsorption capacity of dyes onto the 1T-rich MoS 2 samples is due to the strong binding between the hydroxide/carboxyl groups and the 1T active sites. The capacity can be tuned by controlling the ratio between 1T and 2H phases of MoS 2 nanosheets.
ISSN:2046-2069
DOI:10.1039/c9ra05427h