IMN

Biblio. IMN

Référence en vue solo

Almoussawi, B., Sen, S., Saitzek, S., Roussel, P. & Kabbour, H. (2023) Designing Visible-Light Photoactive Thioapatites Using Thiovanadate Groups: The Ba5(VO4-alphaSalpha)3X (X = F, Cl, I) Phases. Inorg. Chem. 62 18970–18981. 
Added by: Richard Baschera (2023-12-15 08:44:17)   Last edited by: Richard Baschera (2024-01-24 09:28:08)
Type de référence: Article
DOI: 10.1021/acs.inorgchem.3c02592
Numéro d'identification (ISBN etc.): 0020-1669
Clé BibTeX: Almoussawi2023
Voir tous les détails bibliographiques
Catégories: MIOPS
Créateurs: Almoussawi, Kabbour, Roussel, Saitzek, Sen
Collection: Inorg. Chem.
Consultations : 1/114
Indice de consultation : 17%
Indice de popularité : 4.25%
Liens URLs     https://doi.org/10 ... .inorgchem.3c02592
Résumé     
The new thioapatite Ba5(VO4−αSα)3X (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−αSα, 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 Pb5(VO4)3I, 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.
  
Notes     
Publisher: American Chemical Society
  
wikindx 4.2.2 ©2014 | Références totales : 2859 | Requêtes métadonnées : 48 | Exécution de script : 0.13015 secs | Style : Harvard | Bibliographie : Bibliographie WIKINDX globale