Structure and optical properties of Er3+ doped ZnSe nanoparticles.

ZnSe: x %Er3+ (0 ≤ x ≤ 1.8) thin films were deposited on the glass substrates using a photo-assisted chemical bath deposition method. The X-ray diffraction investigation revealed that the samples exhibited a hexagonal crystalline structure. The undoped ZnSe had a crystallite size of 21 nm, which decreased to 4 nm as the concentration of Er3+ increased. The Scanning electron microscopy images showed that the shape of the particles changed from nanoflakes to glass-like particles after the introduction of Er3+. The expected elemental composition was determined using energy-dispersive spectroscopy. The ultraviolet–visible spectroscopy analysis revealed that increasing the concentration of Er3+ modified the band gap energy within the range of 2.75–4.09 eV. The photoluminescence investigation revealed two distinguishable emission peaks at the energy of 1.79 and 2.34 eV when stimulated with an energy of 5.68 eV. These emission peaks were attributed to the presence of impurities in the host material. The Commission Internationale de l'Eclairage revealed that increasing Er3+ concentration shift the yellow emission from the host towards the light blue region. Incorporating Er³⁺ dopant into the ZnSe lattice significantly alters the structure and optical properties. [Display omitted] • Limited studies have explored the effect of Er3+ ions doped ZnSe on structural and optical properties. • A photo-assisted chemical bath deposition method prepared ZnSe: x %Er3+ (0 ≤ x ≤ 1.8) thin films. • The UV–vis results showed an energy band gap (E g) modification from 2.75 to 4.18 eV by varying Er3+ concentration. • The results revealed exponential luminescence intensity enhancement with increasing Er3+ concentration. • The CIE coordinates show ZnSe: x %Er3+ (0 ≤ x ≤ 1.8) thin films are tunable from yellow to light blue region. [ABSTRACT FROM AUTHOR]