Te concentration dependent photoemission and inverse-photoemission study of FeSeTe.

Sci Technol Adv Mater

The Graduate School of Natural Science and Technology, Okayama University, 3-1-1 Tsushima-naka, Okayama 700-8530, Japan; Japan Science and Technology Agency-Transformative Research Project on Iron Pnictides (JST-TRIP), Tsukuba, Ibaraki 305-0047, Japan; Core Research for Evolutional Science and Technology (CREST) Japan Science and Technology Agency, Okayama 700-8530, Japan; Research Laboratory for Surface Science, Okayama University, 3-1-1 Tsushima-naka, Okayama 700-8530, Japan.

Published: October 2012

We have characterized the electronic structure of FeSe Te for various values using soft x-ray photoemission spectroscopy (SXPES), high-resolution photoemission spectroscopy (HRPES) and inverse photoemission spectroscopy (IPES). The SXPES valence band spectral shape shows that the 2 eV feature in FeSe, which was ascribed to the lower Hubbard band in previous theoretical studies, becomes less prominent with increasing . HRPES exhibits systematic dependence of the structure near the Fermi level (): its splitting near and filling of the pseudogap in FeSe. IPES shows two features, near and approximately 6 eV above ; the former may be related to the Fe 3d states hybridized with chalcogenide p states, while the latter may consist of plane-wave-like and Se d components. In the incident electron energy dependence of IPES, the density of states near for FeSe and FeTe has the Fano lineshape characteristic of resonant behavior. These compounds exhibit different resonance profiles, which may reflect the differences in their electronic structures. By combining the PES and IPES data the on-site Coulomb energy was estimated at 3.5 eV for FeSe.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5099622PMC
http://dx.doi.org/10.1088/1468-6996/13/5/054403DOI Listing

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