English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Perovskite-type oxynitrides  AB (O,N) 3  are potential candidates for photoelectrode materials in solar water splitting. A drawback of these materials is their low sintering tendency resulting in low electrical conductivities. Typically, they are prepared by ammonia treatment of insulating, wide band gap oxides. In this study, we propose an approach starting from small band gap oxides Eu 1− x  Ca  x  TiO 3−   δ   and then widen the band gaps in a controlled way by ammonolysis and partial Ca 2+  substitution. Both together induced a distortion of the octahedral network and dilution of the Eu4 f  and N2 p  levels in the valence band. The effect is the stronger the more Ca 2+  is present. Within the series of samples, Eu 0.4 Ca 0.6 Ti(O,N) 3  had the most suitable optical band gap ( E G   ≈ 2.2 eV) for water oxidation. However, its higher Eu content compared to Eu 0.1 Ca 0.9 Ti(O,N) 3  slowed down the charge carrier dynamics due to enhanced trapping and recombination as expressed by large accumulation ( τ  on ) and decay ( τ  off ) times of the photovoltage of up to 109 s and 486 s, respectively. In contrast, the highly Ca 2+ -substituted samples ( x  ≥ 0.7) were more prone to formation of TiN and oxygen vacancies also leading to Ti 3+  donor levels below the conduction band. Therefore, a precise control of the ammonolysis temperature is essential, since even small amounts of TiN can suppress the photovoltage generation by fast recombination processes. Water oxidation tests on Eu 0.4 Ca 0.6 Ti(O,N) 3  revealed a formation of 7.5 μmol O 2  from 50 mg powder together with significant photocorrosion of the bare material. Combining crystal structure, chemical composition, and optical and electronical band gap data, a first simplified model of the electronical band structure of Eu 1− x  Ca  x  Ti(O,N) 3  could be proposed.

Band Gap Adjustment in Perovskite-type Eu 1− x Ca x TiO 3 via Ammonolysis