PlumX Metrics
Embed PlumX Metrics

Tunable photoluminescence and room temperature ferromagnetism of InS:Dy,Tb nanoparticles

Physical Chemistry Chemical Physics, ISSN: 1463-9076, Vol: 19, Issue: 25, Page: 16758-16764
2017
  • 20
    Citations
  • 0
    Usage
  • 9
    Captures
  • 0
    Mentions
  • 0
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

  • Citations
    20
    • Citation Indexes
      20
  • Captures
    9

Article Description

Trivalent lanthanide-doped luminescent nanomaterials have unique spectral and magnetic properties, which have been extensively investigated due to their potential application prospects in a number of new technologies. The rare earth Dy and Tb ions co-doped β-InS dilute nanoparticles with different doping concentrations were successfully synthesized by a gas-liquid phase chemical deposition method. The band gap energy could be tuned by varying the doping concentration from 3.17 to 3.51 eV. The InS:Dy,Tb nanoparticles exhibited strong photoluminescence emission peaks and room temperature ferromagnetism. Under excitation at 352 nm, the intrinsic emission and transitions of D → F for Tb and F → H for Dy were observed. The saturation magnetizations presented an increasing trend and then decreased as the doping concentration increased. This can be ascribed to the fact that the enhanced antiferromagnetic interaction suppresses the ferromagnetic behavior after the doping concentration reaches a certain value. In addition, VASP first-principles calculations were used to further shed light on the magnetic origin and chemical bonding mechanism of the as-prepared samples. It was found that the magnetism could be attributed to In vacancies and the co-doped system is in favor of the formation of In vacancies. This study provides experimental and theoretical guidance for the design and synthesis of promising candidates for optical, magnetic, and spintronic applications.

Provide Feedback

Have ideas for a new metric? Would you like to see something else here?Let us know