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Open AccessArticle

Impact of Oxalate Ligand in Co-Precipitation Route on Morphological Properties and Phase Constitution of Undoped and Rh-Doped BaTiO3 Nanoparticles

1
Department of High-Temperature and Functional Coatings, Institute of Materials Research, German Aerospace Center, 51147 Cologne, Germany
2
Division of Materials Science, Department of Engineering Sciences and Mathematics, Luleå University of technology, 97187 Luleå, Sweden
3
Department of Molecular Sciences and Nanosystems, Ca’ Foscari University of Venice, Via Torino 155, 30172 Venezia Mestre, Italy
*
Authors to whom correspondence should be addressed.
Nanomaterials 2019, 9(12), 1697; https://doi.org/10.3390/nano9121697
Received: 11 October 2019 / Revised: 21 November 2019 / Accepted: 22 November 2019 / Published: 28 November 2019
(This article belongs to the Special Issue Titanate Nanostructures)
In order to design and tailor materials for a specific application like gas sensors, the synthesis route is of great importance. Undoped and rhodium-doped barium titanate powders were successfully synthesized by two routes; oxalate route and classic route (a modified conventional route where solid-state reactions and thermal evaporation induced precipitation takes place). Both powders were calcined at different temperatures. X-ray diffraction (XRD), Raman spectroscopy, scanning electron microscopy (SEM), energy-dispersive x-ray spectroscopy (EDX) and Brunauer-Emmet-Teller (BET) analyses are employed to identify the phases and polymorphs, to determine the morphology, the chemical composition and the specific surface area of the synthesized materials, respectively. The so-called oxalate route yields pure BaTiO3 phase for undoped samples at 700 °C and 900 °C (containing both cubic and tetragonal structures), while the classic route-synthesized powder contains additional phases such as BaCO3, TiO2 and BaTi2O5. Samples of both synthesis routes prepared by the addition of Rh contain no metallic or oxide phase of rhodium. Instead, it was observed that Ti was substituted by Rh at temperatures 700 °C and 900 °C and there was some change in the composition of BaTiO3 polymorph (increase of tetragonal structure). Heat-treatments above these temperatures show that rhodium saturates out of the perovskite lattice at 1000 °C, yielding other secondary phases such as Ba3RhTi2O9 behind. Well-defined and less agglomerated spherical nanoparticles are obtained by the oxalic route, while the classic route yields particles with an undefined morphology forming very large block-like agglomerates. The surface area of the synthesized materials is higher with the oxalate route than with the classic route (4 times at 900 °C). The presence of the oxalate ligand with its steric hindrance that promotes the uniform distribution and the homogeneity of reactants could be responsible for the great difference observed between the powders prepared by two preparation routes. View Full-Text
Keywords: Rh-doped BaTiO3; nanoparticles; synthesis route; co-precipitation; perovskite Rh-doped BaTiO3; nanoparticles; synthesis route; co-precipitation; perovskite
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MDPI and ACS Style

Lontio Fomekong, R.; You, S.; Enrichi, F.; Vomiero, A.; Saruhan, B. Impact of Oxalate Ligand in Co-Precipitation Route on Morphological Properties and Phase Constitution of Undoped and Rh-Doped BaTiO3 Nanoparticles. Nanomaterials 2019, 9, 1697.

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