Development of deep red-emitting CaBiVO5:Pr3+ phosphor for multifunctional optoelectronic applications

Orthorhombic Pr3+-doped calcium bismuth vanadate (CBV: Pr3+) phosphors have been synthesized successfully via a citrate-gel method. The single-phase formation of CBV: Pr3+ phosphor has been endorsed by X-ray diffraction (XRD) analysis. The scanning electron microscopy (SEM) image reveals dense-particle packaging with the quasi-spherical shape for the prepared CBV: Pr3+ phosphors. Under blue light excitation, CBV: Pr3+ phosphors exhibit intense red emission bands located at 608 and 656 nm wavelengths, overlapping with the absorption spectrum of P-R phytochrome, which is present in plants. To achieve the maximum red intensity, the Pr3+ ion concentration is optimized to be 1.25 mol% in the CBV host, after which the emission intensity ceases due to concentration quenching. Dexter's theory disclosed the possibility of d-d multipolar interaction among Pr3+ ions at higher concentrations of Pr3+ ions in the CBV host. The CIE coordinates are found to be positioned in the pure red region for CBV: Pr3+ phosphor and in the proximity of red-emitting commercial phosphor. The temperature-dependent spectral studies manifest substantial thermal stability of the as-synthesized phosphor. All the studies mentioned above specify the tremendous potentiality of thermally stable CBV: Pr3+ phosphor in agricultural lighting and w-LED applications.

Automated summary

Pr3+-doped calcium bismuth vanadate phosphors were successfully synthesized using a citrate-gel method, showing intense red emission bands and concentration quenching at higher Pr3+ ion concentrations. The phosphors exhibited CIE coordinates in the red region and demonstrated significant thermal stability in temperature-dependent spectral studies.