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Photoluminescent enhancement by the incorporation of Bi3+ in Ba2CaWO6: Eu3+ phosphors

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Abstract

A series of Bi3+-doped Ba2CaWO6: Eu3+ phosphors were prepared by the conventional high-temperature solid-state reaction method. The structure, composition and morphology of the prepared phosphor samples were analysed through XRD, XPS, EDS, FTIR, SEM and TEM analysis. Using the recorded photoluminescence excitation and emission profiles, the luminescence properties of Ba2CaWO6: Eu3+, Bi3+ phosphors were investigated thoroughly. Judd–Ofelt intensity parameters were also estimated from the emission spectra. An enhancement in emission intensity peaks was observed in the luminescence spectra of Ba2CaWO6: Eu3+ phosphors due to the incorporation of Bi3+ ions and the intense emission peak at 595 nm owes to the 5D0 → 7F1 magnetic dipole transition, thus confirming the occupancy of Eu3+ ion in the centrosymmetric site of Ba2CaWO6 matrix. Energy transfer from Bi3+ to Eu3+ ions occurred through the dipole–dipole interaction. The optimum doping concentration of Bi3+ is found to be 0.008 wt%. The co-doping of Bi3+ into Ba2CaWO6: Eu3+ matrix introduces a wide absorption band centred at 330 nm and a red shift from 314 to 330 nm. The decay profiles are well fitted with bi-exponential function. The efficient energy transfer from Bi3+ to Eu3+ ions within the Ba2CaWO6 matrix results in a strong reddish-orange emission from the prepared set of samples.

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Acknowledgements

The authors are thankful to UGC (Govt. of India) for financial assistance through SAP-DRS [No.F.530/12/DRS/2009 (SAP-1)] and DST-PURSE [SR/S9/Z-23/2010/22(C, G)] programmes. The authors gratefully acknowledge MoU-DAE-BRNS Project (No. 2009/34/36/BRNS/3174), Department of Physics, S.V. University, Tirupati, India for providing their instrumentation facilities for characterization.

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Sreeja, E., Gopi, S., Krishnapriya, T. et al. Photoluminescent enhancement by the incorporation of Bi3+ in Ba2CaWO6: Eu3+ phosphors. J Mater Sci: Mater Electron 33, 1851–1863 (2022). https://doi.org/10.1007/s10854-021-07384-2

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