Abstract

Undoped and Fe3+ doped Li2Ba3(P2O7)2 pyrophosphate nanopowders were produced by a solid-state reaction process. The prepared samples underwent characterizations using XRD, SEM with EDS, HR-TEM with SAED, FTIR, Raman, UV-Vis, EPR and PL techniques. The XRD analysis confirms the orthorhombic crystal structure of the prepared samples and unit cell parameters were evaluated. The samples exhibited stone-like structures with low aggregation based on the micrographs obtained from SEM and HR-TEM images. Additionally, the grain and particle sizes of the powder samples were evaluated. The elements Li, O, P, Ba and Fe were confirmed to be present in the produced samples by EDS spectra. FT-IR and Raman spectral investigation revealed the fundamental vibrational and bending modes of various phosphate groups. The energy bands, identified as characteristic bands of Fe3+ ions, were produced in the UV–visible region of the optical absorption spectrum for the doped sample. The crystal field and inter-electronic parameters (Dq = 915, B = 700 and C = 2715 cm−1) were also evaluated. Furthermore, the refractive index and metallization criteria properties were calculated using energy bandgap values of 4.46 and 4.38 eV of the produced samples. The doping of Fe3+ ions led to a reduction in the bandgap energy, resulting in a red-shift. A resonance signal was observed in the EPR spectrum at g = 2.05, which can be ascribed to iron ions entering the host lattice at a distorted octahedral symmetry sites and this was also supported by optical absorption studies. The produced sample showed emission peaks at 354, 440 and 530 nm in the ultraviolet, blue and green regions of its photoluminescence spectrum. Photometric parameters, such as CCT, CRI and CIE chromatic coordinates, reveal that the prepared samples could bee used in LEDs applications. This work offers novel visions into diphosphate compounds doped with transition metal ions.

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