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- W2016297455 abstract "We present periodic DFT calculations to study the structure of the V2O5–TiO2 (anatase) catalyst. Linear and cyclic dimeric V2O5 species represent the active phase. The support TiO2 (anatase) is represented for the perfect (1 0 0) and (0 0 1) surfaces. The maximum interaction between the active phase and the support is favored, and low coverage is assumed. The most stable models allow the compensation of the surface dangling bonds, and can be understood as a continuation of the bulk anatase structure. The more suitable models for studying reactivity possess uncoordinated atoms available for reactivity, such as terminal oxygen atoms in V2O5. Relaxation plays an important role in the adsorption systems, and cannot be discarded when modeling the V2O5–anatase catalyst." @default.
- W2016297455 created "2016-06-24" @default.
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- W2016297455 date "2003-03-01" @default.
- W2016297455 modified "2023-10-18" @default.
- W2016297455 title "A periodic model for the V2O5–TiO2 (anatase) catalyst. Stability of dimeric species" @default.
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- W2016297455 doi "https://doi.org/10.1016/s0039-6028(02)02673-0" @default.
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