Abstract

Herein, the peculiarities of complex phosphate formation in self-fluxes of Cs-MII-Bi-P-O (MII = Ca, Sr, Ba and Pb) systems with Cs/P = 0.7-1.3 at fixed ratios of Bi/P = 0.2 and Bi/MII = 1.0 were studied and discussed. Three novel isostructural diphosphates with the general composition Cs3MIIBi(P2O7)2 (MII = Ca, Sr and Pb) and the original framework topology were synthesized and characterized via single-crystal and powder X-ray diffraction, SEM, DTA, and FTIR- and UV-VIS-spectroscopy. In addition, electronic structure (DFT) and Voronoi-Dirichlet polyhedra (VDP) characteristics calculations and crystallochemical analysis were performed. In the structure of the new compounds, the MIIO7 and BiO6 polyhedra are connected via common oxygen vertices forming infinite helical-like chains, which are linked by P2O7 groups into a 3D-framework with pentagonal tunnels, where the Cs+ cations are located. The structural peculiarities are discussed considering perspectives for the creation of new luminescent materials. The dielectric bandgaps, Eg, of the Cs3MIIBi(P2O7)2 crystals reveal an ∼0.2 eV low-energy shift in the Ca-Sr-Pb sequence of MII cations, which reveals the possibility to tune the optical absorbance spectra of the crystals via the synthesis of solid solutions with various contents of MII cations. The glass-ceramic synthetic approach is also proposed as a convenient method for the creation of new diphosphates, and the applicability of this method is verified for Cs3CaBi(P2O7)2.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.