Abstract
Herein, we report Dy3+-activated ZrO2 phosphors synthesized via the sol-gel technique. The structural, morphological, and optical properties of the synthesized powder samples annealed at 900 °C were investigated. The monoclinic phase of the synthesized phosphor was confirmed by recording the X-ray powder diffraction (XRPD) pattern. Ultraviolet–visible analysis was performed for the reflectance and bandgap measurements of the phosphors. Field emission scanning electron microscope and X-ray energy dispersive spectroscopy analyses were used to study the morphology and elemental composition of the phosphors, respectively. The distribution of ions in the undoped and Dy3+-doped samples was confirmed using time-of-flight secondary ion mass spectroscopy. The photoluminescence (PL) behavior of the synthesized phosphors was investigated by recording the excitation and emission spectra. When the synthesized phosphors were exposed to UV light at 353 nm, we observed characteristic blue and yellow Dy3+ PL emissions, corresponding to the transition 4F9/2 → 6H15/2 and 4F9/2 → 6H13/2, respectively. Additionally, we observed low-intensity red and brown-red emission peaks corresponding to 4F9/2 → 6H11/2 and 4F9/2 → 6H9/2. These observations indicate that the non-aqueous sol-gel route, coupled with the suitable post-synthesis heat treatment, resulted in the development of a monophase (monoclinic) zirconia. This makes it a strong candidate for phosphor applications due to its high room temperature stability and efficient characteristic features of the monoclinic phase. These findings strongly suggest that Dy3+-doped ZrO2 can serve as a superior phosphor material for white light-emitting diode applications.
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