Published June 2021 | Version v1
Journal article

Effect of co-doped (Ni2+:Co2+) in CdS nanoparticles. Investigation on structural and magnetic properties

  • 1. Department of Physics, Meenakshi College of Engineering, West K. K. Nagar, 60007, Chennai, Tamil Nadu (India)
  • 2. Department of Physics, Thanthai Hans Roever College, 621220, Perambalur (India)
  • 3. Centre for Nanoscience and Nanotechnology, Sathyabama Institute of Science and Technology, 600119, Chennai, Tamil Nadu (India)

Description

Facile chemical precipitation method was used to synthesize Ni (4%) doped and Co (4%): Ni (4%) co-doped CdS nanoparticles. Polyvinylpyrrolidone (PVP) was used as a surfactant to control the particles size and growth rate. The synthesized co-doped sample showed mixed structures of cubic and hexagonal which was confirmed by X-ray diffraction (XRD) study. Average crystallite size is to be 4.2 nm and 3.3 nm for Ni doped and Co:Ni co-doped CdS nanoparticles, respectively. Transmission electron microscopy (TEM) results showed spherical shape with homogeneous particle size distribution of the samples. Due to reduction the particle size, the absorption peak of co-doped CdS shows a significant blue shifting compared to the single metal ion doped CdS nanoparticles. Electron paramagnetic resonance (EPR) spectroscopy was used to study the magnetic g-factor, covalency parameter and magnetic properties of the samples. Anti-ferromagnetic magnetic signal was observed for doped and co-doped samples using Vibrating Sample Magnetometer (VSM) at room temperature. Thermal stability and lattice deformation of the samples were studied using Thermo Gravimetric-Differential Thermal Analysis (TG-DTA). The obtained room temperature based magnetic properties of CdS:Co:Ni nanoparticles demonstrate it could be suitable for spintronic and optoelectronic applications.

Additional details

Identifiers

Publishing Information

Journal Title
Applied Physics. A, Materials Science and Processing (Print)
Journal Volume
127
Journal Issue
6
Journal Page Range
vp.
ISSN
0947-8396
CODEN
APAMFC

Optional Information

Notes
AID: 400