Designing Visible-Light Photoactive Thioapatites Using Thiovanadate Groups: The Ba5(VO4-αSα)3X (X = F, Cl, I) Phases

The new thioapatite Ba-5(VO4-alpha S alpha)(3)X (X = F, Cl, I) series of compounds was prepared and characterized. Compared to known apatite phases built from unconnected vanadate VO4 groups separated by Ba2+ cations delimiting halide-filled channels, their crystal structure is built from mixed anion thiovanadate VO4-alpha S alpha, where V5+ is surrounded by both O and S, therefore exhibiting a triple anion lattice. Here, the strategy consisting in incorporating a chalcogenide anion aims at raising the valence band to bring the band gap to the visible range in order to reach photoactive materials under visible light. Both the halide anion nature and the S/O ratio impact the materials' photoconductivity. While the photocurrent response is comparable to that found in the recently investigated apatite phase Pb-5(VO4)(3)I, a short carrier lifetime is detected as well as a shift of the activity toward the visible light. This apatite series combining thiovanadate and halide-filled channels opens new perspectives in the extended field of apatites and their applications.

Automated summary

The new series of thioapatite compounds Ba-5(VO4-alpha S alpha)(3)X (X = F, Cl, I) were prepared and characterized. The crystal structure of these compounds is built from mixed anion thiovanadate VO4-alpha S alpha, showing a triple anion lattice. The incorporation of a chalcogenide anion aims at raising the valence band to bring the band gap to the visible range for photoactive materials.