Publications by authors named "Katsunori Kodato"

Orthorhombic Mo-V oxide is one of the most active solid-state catalysts for selective oxidation of alkane, and revealing its detailed structure is important for understanding reaction mechanisms and for the design of better catalysts. We report the single-crystal X-ray structure analysis of orthorhombic Mo-V oxide heated under a N flow; V is present in 6-membered rings with partial occupancy, similar to the structure reported by Trunschke's group for orthorhombic Mo-V oxide heated under an Ar flow (Trunschke, ACS Catal.2017, 7, 3061).

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We demonstrated that the sorption behavior of orthorhombic Mo-V oxide (Mo(29)V(11)O(112-x)) is continually and reversibly tunable by redox treatment.

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In this work, we structurally characterize defects, grain boundaries, and intergrowth phases observed in various Mo-V-O materials using aberration-corrected high-angle annular dark-field (HAADF) imaging within a scanning transmission electron microscope (STEM). Atomic-level imaging of these preparations clearly shows domains of the orthorhombic M1-type phase intergrown with the trigonal phase. Idealized models based on HAADF imaging indicate that atomic-scale registry at the domain boundaries can be seamless with several possible trigonal and M1-type unit cell orientation relationships.

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Mix and match: The pentagonal [Mo(6)O(21)](n-) polyoxomolybdate building block assembles with other sources of Mo, V, and Sb ions to form an orthorhombic Mo-V-Sb oxide. The first single-crystal X-ray analysis of an orthorhombic Mo-V-based oxide, a promising catalyst for light alkane selective oxidation known as the "M1 phase", revealed the structure of the compound.

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