Bi26Mo10O69–based solid solution with nonmetal dopants: Synthesis and properties
A series of S- and P- doped Bi26Mo10O69 was synthesized by conventional solid state method and studied. Chemical analysis detected closeness of experimental and theoretical ratios of bismuth, molybdenum and dopant for P-doped samples and 50% deficiency of sulfur for S-doped samples. The solid soluti...
Saved in:
| Published in: | Solid state ionics Vol. 331; pp. 30 - 36 |
|---|---|
| Main Authors: | , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
Amsterdam
Elsevier B.V
01.03.2019
Elsevier BV |
| Subjects: | |
| ISSN: | 0167-2738, 1872-7689 |
| Online Access: | Get full text |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Summary: | A series of S- and P- doped Bi26Mo10O69 was synthesized by conventional solid state method and studied. Chemical analysis detected closeness of experimental and theoretical ratios of bismuth, molybdenum and dopant for P-doped samples and 50% deficiency of sulfur for S-doped samples. The solid solutions ranges were determined to be x = 0–0.7 for Bi26Mo10−2xP2xO69−d and x = 0–0.6 for Bi26Mo10−2xSxO69−d. Stabilization of the monoclinic form is observed when x > 0.1 for P and x > 0.4 for S doping. The IR FT spectroscopy and Rietveld whole profile structure refinement at X-Ray diffraction data showed substitution of Mo by S and P forming SO4 and PO4 groups. The geometrical sizes of particles were determined to be in the range of 1–20 μm. Materials under study are characterized with total ionic conductivity of the 1 × 10−4 − 9 × 10−3 S cm−1 at 273–1073 K.
•S and doped Bi26Mo10O69−d solid solutions were synthesized by solid sate method.•Chemical analysis gave Bi26Mo10−2xP2xO69−d and Bi26Mo10−2xSxO69−d formulae.•Infrared spectroscopy detected SO4 and PO4 groups.•Impedance spectroscopy showed a modest increase in conductivity. |
|---|---|
| Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
| ISSN: | 0167-2738 1872-7689 |
| DOI: | 10.1016/j.ssi.2018.12.014 |