Abstract

Ba2Zn2La4(1−x)O10:4xSm3+ (0.5–6 mol%) nanophosphor series synthesized successfully via solution combustion approach were crystallized into tetragonal lattice (I4/mcm (140) space group symmetry). The qualitative and quantitative phase information was obtained by performing Rietveld refinement technique. Morphological studies were carried out via scanning and transmission electron microscopy (SEM & TEM) observations. The energy-gap values for Ba2Zn2La4O10(5.58 eV) and Ba2Zn2La3.88Sm0.12O10(5.42 eV) powder samples were determined from diffuse reflectance (DR) studies. The near ultra-violet (NUV) excitation (λex = 410 nm) of Sm3+-doped nanophosphors revealed strong reddish-orange (603 nm) emission accredited to 4G5/2→6H7/2 (most prominent) transition. The Blasse’s relation provided critical distance (16.39 A) for energy transfer process amid adjacent activator centres and shortlisted the actual interaction type (dipole–quadrupole) behind concentration quenching behaviour. Non-radiative relaxation rate (78.7701 s− 1), radiative lifetime (1.61 ms) and quantum efficiency (89%) of 4G5/2 emitting state were obtained by detailed analysis of fluorescence decay curves of Ba2Zn2La4(1−x)O10:4xSm3+ series. Furthermore, the CIE chromaticity diagram provides strong reddish-orange luminescence in visible region, which displays the auspicious applications of Ba2Zn2La4O10:Sm3+ nanophosphor in NUV-based white LEDs.

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