| Literature DB >> 27877521 |
Takayoshi Yokoya1, Rikiya Yoshida2, Yuki Utsumi3, Koji Tsubota2, Hiroyuki Okazaki4, Takanori Wakita1, Yoshikazu Mizuguchi5, Yoshihiko Takano5, Takayuki Muro6, Yukako Kato6, Hiroshi Kumigashira7, Masaharu Oshima7, Hisatomo Harima8, Yoshihiro Aiura9, Hitoshi Sato10, Akihiro Ino11, Hirofumi Namatame12, Masaki Taniguchi13, Masaaki Hirai1, Yuji Muraoka1.
Abstract
We have characterized the electronic structure of FeSe1-x Te x for various x 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 x. HRPES exhibits systematic x dependence of the structure near the Fermi level (EF): its splitting near EF and filling of the pseudogap in FeSe. IPES shows two features, near EF and approximately 6 eV above EF; 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 EF 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.Entities:
Keywords: FeSe(1−x)Tex; electronic structure; high-resolution photoemission spectroscopy; inverse photoemission spectroscopy; soft x-ray photoemission spectroscopy
Year: 2012 PMID: 27877521 PMCID: PMC5099622 DOI: 10.1088/1468-6996/13/5/054403
Source DB: PubMed Journal: Sci Technol Adv Mater ISSN: 1468-6996 Impact factor: 8.090