Geometry, electronic structure, morphology, and photoluminescence emissions of BaW1-xMoxO4 (x = 0, 0.25, 0.50, 0.75, and 1) solid solutions: Theory and experiment in concert

• Published in: Applied surface science 2019-01, Vol.463, p.907-917
• Main Authors: Oliveira, Marisa Carvalho, Andrés, Juan, Gracia, Lourdes, de Oliveira, Michelle Suzane M.P., Mercury, Jose Manuel R., Longo, Elson, Nogueira, Içamira Costa
• Format: Article
• Language: English
• Subjects: BaW1-xMoxO4 solid solutions; Co-precipitation; DFT; Morphology; Photoluminescence
• ISSN: 0169-4332; 1873-5584
• DOI: 10.1016/j.apsusc.2018.08.146

[Display omitted] •Theoretical characterization (DFT) of the structural bulk and surfaces of BaW1-xMoxO4 solid solutions.•Rationalizing of the crystal morphologies from FE-SEM images by means of Wulff construction.•Enhancement of the electron-transfer process by the substitution of W6+ by Mo6+.•Simple co-precipitation method was reported for the first time in the formation of solid solutions. The design of a solid solution with tunable electro-optical properties and multifunctionality is a promising strategy for developing novel materials. In this work, BaW1-xMoxO4 (x = 0, 0.25, 0.5, 0.75, and 1) solid solutions have been successfully prepared for the first time by a co-precipitation method. Their crystal structure and phase composition were determined by X-ray diffraction and Rietveld refinements. Fourier transform infrared and micro Raman spectroscopy in combination with field-emission scanning electron microscopy (FE-SEM) were used to describe the microstructures and chemical compositions of the synthesized materials. The influence of chemical composition on morphology and photoluminescence (PL) emission has been analyzed. The geometry, electronic structures, and morphologies of BaW1-xMoxO4 (x = 0, 0.25, 0.5, 0.75, and 1) solid solutions were investigated by first-principles quantum-mechanical calculations based on the density functional theory. By using Wulff construction and the values of the surface energies for the (1 1 2), (0 0 1), (1 1 0), (1 0 1), (1 0 0), and (1 1 1) crystal faces, a complete map of the available morphologies for the BaW1-xMoxO4 solid solutions was obtained. These results show a qualitative agreement between the experimental morphologies obtained using the FE-SEM images and the computational models. The substitution of W6+ by Mo6+ enhances the electron-transfer process due to a stronger Mo(4d)-O(2p) hybridization compared to W(5d)-O(2p) for the W/Mo-O superficial bonds, and is responsible for the change in morphology from BaWO4 to BaMoO4. Such a fundamental study, which combines multiple experimental methods and first-principles calculations, has provided valuable insight into obtaining a basic understanding of the local structures, bonding, morphologies, band gaps, and electronic and optical properties of the BaW1-xMoxO4 (x = 0, 0.25, 0.5, 0.75, and 1) solid solutions.