The influence of halides in polyoxotitanate cages; dipole moment, splitting and expansion of d-orbitals and electron-electron repulsion
Royal Society of Chemistry
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Hanf, S., Matthews, P. D., Li, N., Luo, H., & Wright, D. (2017). The influence of halides in polyoxotitanate cages; dipole moment, splitting and expansion of d-orbitals and electron-electron repulsion. Dalton Transactions, 46 (2), 578-585. https://doi.org/10.1039/C6DT04288K
Metal-doped polyoxotitanate (M-POT) cages have been shown to be efficient single-source precursors to metal-doped titania [TiO$_2$(M)] (state-of-the-art photocatalytic materials) as well as molecular models for the behaviour of dopant metal ions in bulk titania. Here we report the influence halide ions have on the optical and electronic properties of a series of halide-only, and cobalt halide-‘doped’ POT cages. In this combined experimental and computational study we show that halide ions can have several effects on the band gaps of halide-containing POT cages, influencing the dipole moment (hole–electron separation) and the structure of the valance band edge. Overall, the band gap behaviour stems from the effects of increasing orbital energy moving from F to I down Group 17, as well as crystal-field splitting of the d-orbitals, the potential effects of the Nephelauxetic influence of the halides and electron–electron repulsion.
We thank the EPSRC (Doctoral Prize for P. D. M.), A*STAR Singapore (Scholarship for N. L.), the Studienstiftung des deutschen Volkes, Fonds of the Chemical Industry (S. H.) for funding. The authors would like to acknowledge the use of the EPSRC UK National Service for Computational Chemistry Software (NSCCS) at Imperial College London and contributions from its staff in carrying out this work.
External DOI: https://doi.org/10.1039/C6DT04288K
This record's URL: https://www.repository.cam.ac.uk/handle/1810/270560
Attribution 4.0 International
Licence URL: http://creativecommons.org/licenses/by/4.0/
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