Abstract

Core–shell based nanostructures are attractive candidates for photocatalysis owing to their tunable physicochemical properties, their interfacial contact effects, and their efficacy in charge-carrier separation. This study reports, for the first time, on the synthesis of mesoporous silica@nickel phyllosilicate/titania (mSiO2@NiPS/TiO2) core–shell nanostructures. The TEM results showed that the mSiO2@NiPS composite has a core–shell nanostructure with a unique flake-like shell morphology. XPS analysis revealed the successful formation of 1:1 nickel phyllosilicate on the SiO2 surface. The addition of TiO2 to the mSiO2@NiPS yielded the mSiO2@NiPS/TiO2 composite. The bandgap energy of mSiO2@NiPS and of mSiO2@NiPS/TiO2 were estimated to be 2.05 and 2.68 eV, respectively, indicating the role of titania in tuning the optoelectronic properties of the SiO2@nickel phyllosilicate. As a proof of concept, the core–shell nanostructures were used as photocatalysts for the degradation of methyl violet dye and the degradation efficiencies were found to be 72% and 99% for the mSiO2@NiPS and the mSiO2@NiPS/TiO2 nanostructures, respectively. Furthermore, a recyclability test revealed good stability and recyclability of the mSiO2@NiPS/TiO2 photocatalyst with a degradation efficacy of 93% after three cycles. The porous flake-like morphology of the nickel phyllosilicate acted as a suitable support for the TiO2 nanoparticles. Further, a coating of TiO2 on the mSiO2@NiPS surface greatly affected the surface features and optoelectronic properties of the core–shell nanostructure and yielded superior photocatalytic properties.

Highlights

  • Textile dyes and organic compounds are major water pollutants, which create an environmental hazard to aquatic systems and humanity

  • SEM images show the spherical morphology of the mSiO2 and mSiO2@NiPS nanostructures (Supporting Information File 1, Figure S1a,b)

  • Ni3Si2O5(OH)4 corresponding to 1:1 nickel phyllosilicate comprises a brucitic sheet of Ni(II) cations that are octahedrally coordinated and connected to an interlinked SiO4 tetrahedra layer

Read more

Summary

Introduction

Textile dyes and organic compounds are major water pollutants, which create an environmental hazard to aquatic systems and humanity. The addition of TiO2 (51 m2/g) as expected, led to a lower surface area of the mSiO2@NiPS/TiO2 composite (103 m2/g) compared to the mSiO2@NiPS core–shell nanostructures. The presence of TiO2 on the shell of the mSiO2@NiPS surface played a role in increasing the bandgap energy of the core–shell nanostructure.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call