Abstract

Relative energies of 4f n electronic states and crystal band states are important for a fundamental understanding of rare-earth-doped optical materials and a practical understanding of each material's potential performance in specific applications. With this motivation, the 4f n ground state binding energies of rare earth ions have been studied in the gallium garnets using resonant photoemission spectroscopy and compared with the aluminum and iron garnets. The 4d–4f photoemission resonance was used to separate and identify the 4f n and valence band components of the spectra, and theoretical 4f photoemission spectra were fit to experimental results to accurately determine electron binding energies. A two-parameter empirical model was used to successfully describe the relative energies of the 4f n ground states in these materials. The success of this empirical model indicates that measurements on as few as two different rare earth ions in a host are sufficient to predict the energies of all rare earth ions in that host. This analysis shows that systematic shifts in the relative energies of 4f n states and crystal band states between different garnets arise entirely from shifts of the band states, while each rare earth ion maintains the same absolute binding energy for all garnets studied. These results suggest that further studies of additional host compounds using both photoemission and optical spectroscopy will rapidly lead to a broader picture of the host crystal's effect on 4f electron binding energies.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.