A nonlinear optical phosphate Ba5P6O20 was rationally developed by a tailored synthetic approach based on the use of flexible [P3O10](5-) units. The phosphate exhibits a very short absorption edge of λ=167 nm, which is among the shortest known in phase-matchable phosphates. First-principles electronic structure analysis elucidated the origin of the changes in the optical properties, and specifically in the absorption edge, of the material. Such a tailored synthetic approach provides a new opportunity to design nonlinear optical materials with short absorption edges.
Tuning CO 2 hydrogenation selectivity to obtain targeted value-added chemicals and fuels has attracted increasing attention. However,af undamental understanding of the way to control the selectivity is still lacking, posing achallenge in catalyst design and development. Herein, we report our new discovery in ambient pressure CO 2 hydrogenation reaction where selectivity can be completely reversed by simply changing the crystal phases of TiO 2 support (anatase-or rutile-TiO 2) or changing metal loadings on anatase-TiO 2 .O perando spectroscopyand NAP-XPS studies reveal that the determining factor is adifferent electron transfer from metal to the support, most probably as ar esult of the different extents of hydrogen spillover,w hichc hanges the adsorption and activation of the intermediate of CO.Based on this new finding,wecan not only regulate CO 2 hydrogenation selectivity but also tune catalytic performance in other important reactions,t hus opening up ad oor for efficient catalyst development by rational design.
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