Related Experiment Video
Updated: May 16, 2025

A Technical Guide for Performing Spectroscopic Measurements on Metal-Organic Frameworks
Published on: April 28, 2023
Elucidation of the Ta(O,N)6 Octahedral Arrangement in Flux-Grown BaTaO2N Photocatalysts by Experimental and
Tetsuya Yamada1,2, Hiroh Miyagawa1, Tomohito Sudare1
1Research Initiative for Supra-Materials, Shinshu University, 4-17-1 Wakasato, Nagano 380-8553, Japan.
Abstract:
BaTaO2N (BTON) is a visible-light-responsive photocatalyst used for water splitting. The flux method, which involves the use of a molten salt, is an effective synthetic strategy for achieving a high photocatalytic activity. Fluxes with alkali metal cations strongly affect the photocatalytic activity of the BTON crystals. In particular, RbCl flux-grown BTON exhibits hydrogen evolution activity over several times higher than that grown in other chloride fluxes, such as NaCl, under visible-light irradiation. One factor of this difference is presumably owing to the change in the Ta(O,N)6 octahedral arrangement in the BTON triggered by the doping of alkali metal ions into the crystal lattice. However, the precise Ta(O,N)6 octahedral arrangement remains unclear. Herein, X-ray absorption spectroscopy, structural analysis by neutron diffraction, and computational structural modeling based on comprehensive structural energy predictions were performed for two types of BTONs. The results suggested that the configuration manners of Ta(O,N)6 octahedral units strongly depend on the flux composition. Specifically, in NaCl-flux-grown BTON crystals, the number of N20 cis planes parallel to the (100), (010), and (001) crystal planes in a TaO4N2 unit is anisotropic, resulting in differences in their electron-hole conduction characteristics. The findings indicate that in addition to lattice defects, the interconnections of mixed-anion units such as Ta(O,N)6 should be taken into account to improve the photocatalytic activity of BTONs and develop other mixed-anion compounds.
Related Concept Videos
Keto–Enol Tautomerism: Mechanism
SN1 Reaction: Mechanism
Firstly, the haloalkane ionizes to generate a carbocation intermediate and a halide ion. This heterolytic cleavage is highly endothermic with large activation energy. The ionization of the substrate, facilitated by a...
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
Acid-Catalyzed α-Halogenation of Aldehydes and Ketones
In the first step of the mechanism, the acid protonates the carbonyl oxygen resulting in a resonance-stabilized cation, which subsequently loses an α-hydrogen to form an enol tautomer. The C=C bond in an enol is highly nucleophilic because of the electron-donating nature of the –OH group. Consequently, the double bond attacks an electrophilic...
Enolate Mechanism Conventions
Nucleophilic Aromatic Substitution: Elimination–Addition

