Solid solutions between two isotypic host compounds: GdSr(2)AlO(5) and Sr(3)AlO(4)F; Gd(1-x)Sr(2+x)AlO(5-x)F(x):Ce(3+) (GSAF:Ce(3+)), have been prepared across the complete solid solution range x. Depending on x, the series display considerable optical tunability of emission wavelengths in the range 574 nm to 474 nm, which is attributed to the decreased crystal field splitting arising from increased host ionicity with fluorine addition. Applying the GSAF:Ce(3+) phosphors on InGaN LEDs (lambda (max) = 405 nm and 450 nm) permits white lighting sources to be prepared. The characteristics of these are reported.

International audienceAn approach is presented that enables the analysis and prediction of stacking sequences in intercalated lamellar vanadium phosphates. A comparison of previously reported vanadium phosphates reveals two modes of intercalation: (i) 3d transition metal ions intercalated between VOPO4 layers and (ii) alkali/alkaline earth metal ions between VOPO4·H2O layers. Both intercalations were investigated using DFT calculations in order to understand the relative shifts of the vanadium phosphate layers. These calculations in addition to an analysis of the stacking sequences in previously reported materials enable the prediction of the crystal structures of Mx(VOPO4)·yH2O (M = Cs+, Cd2+ and Sn2+). Experimental realization and structural determination of Cd(VOPO4)2·4H2O by single-crystal X-ray diffraction confirmed the predicted stacking sequences