dc.contributor.author | Bakken, Kristine | |
dc.contributor.author | Pedersen, Viviann Hole | |
dc.contributor.author | Blichfeld, Anders Bank | |
dc.contributor.author | Nylund, Inger-Emma | |
dc.contributor.author | Tominaka, Satoshi | |
dc.contributor.author | Ohara, Koji | |
dc.contributor.author | Grande, Tor | |
dc.contributor.author | Einarsrud, Mari-Ann | |
dc.date.accessioned | 2021-10-22T06:41:40Z | |
dc.date.available | 2021-10-22T06:41:40Z | |
dc.date.created | 2021-05-26T09:32:31Z | |
dc.date.issued | 2021 | |
dc.identifier.citation | ACS Omega. 2021, 6 9567-9576. | en_US |
dc.identifier.issn | 2470-1343 | |
dc.identifier.uri | https://hdl.handle.net/11250/2824851 | |
dc.description.abstract | Carbonate formation is a prevailing challenge in synthesis of BaTiO3, especially through wet chemical synthesis routes. In this work, we report the phase evolution during thermal annealing of an aqueous BaTiO3 precursor solution, with a particular focus on the structures and role of intermediate phases forming prior to BaTiO3 nucleation. In situ infrared spectroscopy, in situ X-ray total scattering, and transmission electron microscopy were used to reveal the decomposition, pyrolysis, and crystallization reactions occurring during thermal processing. Our results show that the intermediate phases consist of nanosized calcite-like BaCO3 and BaTi4O9 phases and that the intimate mixing of these along with their metastability ensures complete decomposition to form BaTiO3 above 600 °C. We demonstrate that the stability of the intermediate phases is dependent on the processing atmosphere, where especially enhanced CO2 levels is detrimental for the formation of phase pure BaTiO3. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | American Chemical Society | en_US |
dc.relation.uri | PMCID# PMC8047748 | |
dc.rights | Navngivelse 4.0 Internasjonal | * |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/deed.no | * |
dc.title | Structures and Role of the Intermediate Phases on the Crystallization of BaTiO3 from an Aqueous Synthesis Route | en_US |
dc.type | Peer reviewed | en_US |
dc.type | Journal article | en_US |
dc.description.version | publishedVersion | en_US |
dc.source.pagenumber | 9567-9576 | en_US |
dc.source.volume | 6 | en_US |
dc.source.journal | ACS Omega | en_US |
dc.identifier.doi | 10.1021/acsomega.1c00089 | |
dc.identifier.cristin | 1911854 | |
dc.relation.project | Norges forskningsråd: 250403 | en_US |
dc.relation.project | Norges forskningsråd: 245963/F50 | en_US |
dc.relation.project | Norges forskningsråd: 197405 | en_US |
cristin.ispublished | true | |
cristin.fulltext | original | |
cristin.qualitycode | 1 | |