Control of Anion Ordering in Perovskite Oxyhydrides by High-Pressure and High-Temperature Treatment
Crystallographic order-disorder transitions are of fundamental interest due to the intimate relationship between structure and properties, while controlling anion ordering in oxide-based compounds has been less achieved. Here, we report anion-order-disorder structural control in primitive perovskite oxyhydrides. Anion-disordered vanadium perovskite oxyhydride with cubic symmetry was obtained by quenching the sample from 1000 °C to room temperature within five minutes under high pressure, while anion-ordered ones with tetragonal symmetry emerge through slow cooling from 1000 °C over 10 hours. In addition, the sign of the order-disorder structural change was also found in chromium perovskite oxyhydride. This study presents a novel synthetic route to anion-ordered oxyhydrides, enabling the future achievement of desirable properties.
Authors
- Takafumi Yamamoto (ORCID: https://orcid.org/0000-0002-7960-1014)
- Teppei Nagase (ORCID: https://orcid.org/0000-0001-5974-5208)
- Hiroki Sahara
- Hiroyuki Saitoh (ORCID: https://orcid.org/0000-0002-2146-5152)
- Masaki Azuma (ORCID: https://orcid.org/0000-0002-8378-321X)
- Haruki Tochizawa
- Yuki Sakai
- Takumi Nishikubo
- Takashi Honda
Institutions
- High Energy Accelerator Research Organization (JP)
- Kyoto University (JP)
- Shanghai Institute for Science of Science (CN)
- National Institutes for Quantum Science and Technology (JP)
- Institute of Science Tokyo (JP)
Publication Details
- Journal
- Inorganic Chemistry
- Published
- 2026-02-13
- DOI
- https://doi.org/10.1021/acs.inorgchem.5c04760
- Primary Topic
- Thermal Expansion and Ionic Conductivity
- Type
- article
- Field-Weighted Citation Impact
- 0.00