5d-level energies of Ce and the crystalline environment. II. Chloride, bromide, and iodide compounds

نویسنده

  • P. Dorenbos
چکیده

Information on the energy of 5d levels of Ce in chloride, bromide, and iodide compounds has been collected. From this, values for the centroid shift and the crystal field splitting of the 5d configuration are obtained. The centroid shift will be related to the polarizability of the anions and further analyzed by means of the ligand polarization model. The crystal field splitting is to a large extent determined by the shape and size of the anion polyhedron coordinating Ce. It will be analyzed in terms of the crystal field Bq k parameters. By combining centroid shift and crystal field splitting, the spectroscopic redshift of the first electric dipole-allowed f d transition in Ce-doped halide compounds will be interpreted. The observed trends provide insights into the relationship between the spectroscopic properties of Ce 5d levels and the crystalline environment.

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تاریخ انتشار 2000