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Synthesis and Crystal Structure of δ-TaON, a Metastable Polymorph of Tantalum Oxide Nitride

Tobias LüdtkeInstitut für Chemie, TU Berlin, Straße des 17. Juni 135, D-10623 Berlin, GermanyAlexander SchmidtInstitut für Chemie, TU Berlin, Straße des 17. Juni 135, D-10623 Berlin, GermanyCaren GöbelInstitut für Chemie, TU Berlin, Straße des 17. Juni 135, D-10623 Berlin, GermanyAnna FischerInstitut für Chemie, TU Berlin, Straße des 17. Juni 135, D-10623 Berlin, GermanyNils B. BeckerInstitut für Anorganische Chemie, RWTH Aachen University, Landoltweg 1, D-52056 Aachen, GermanyChristoph ReimannInstitut für Physikalische und Theoretische Chemie, Universität Bonn, Wegelerstraße 12, D-53115 Bonn, GermanyThomas BredowInstitut für Physikalische und Theoretische Chemie, Universität Bonn, Wegelerstraße 12, D-53115 Bonn, GermanyRichard DronskowskiInstitut für Anorganische Chemie, RWTH Aachen University, Landoltweg 1, D-52056 Aachen, GermanyMartin LerchInstitut für Chemie, TU Berlin, Straße des 17. Juni 135, D-10623 Berlin, Germany
2014en
ABI

Аннотация

δ-TaON was prepared by reaction of gaseous ammonia with an amorphous tantalum oxide precursor. As a representative of the anatase structure (aristotype) it crystallizes in the tetragonal crystal system with lattice parameters a = 391.954(16) pm and c = 1011.32(5) pm. At temperatures between 800 and 850 °C an irreversible phase transformation to baddeleyite-type β-TaON is observed. While quantum-chemical calculations confirm the metastable character of δ-TaON, its transformation to β-TaON is kinetically controlled. The anion distribution of the anatase-type phase was studied theoretically. In agreement with previous studies, it was found that a configuration with maximal N-N distances is most stable. The calculated band edge energies indicate that δ-TaON is a promising photocatalytic material for redox reactions, e.g., water splitting.

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