Variation of the charge dynamics in bandwidth- and filling-controlled metal-insulator transitions of pyrochlore-type molybdates

  • The systematics of the bandwidth- and filling-controlled metal-insulator transitions (MITs) have been investigated for R2Mo2O7 family (R=Nd, Sm, Eu, Gd, Dy, and Ho) by infrared spectroscopy. The substantial role of electron correlation in driving the MIT is verified. With changing the R ionic radius (r) or equivalently the one-electron bandwidth (W), the MIT occurs in a continuous manner at rc≈r(R=Gd). The T=0K gap continuously vanishes as Δ∝(rc−r), while at the metallic side the linear decrease of Drude weight is followed toward rc. In the metallic compounds, some of the infrared-active phonon modes show remarkably large Fano asymmetry correlating with the Drude weight. These Mo-O-Mo bending modes strongly couple to the conduction electrons via effective modulation of the bandwidth. Even for r≲rc a minimal level of hole doping closes the correlation gap, for example, the barely insulating Gd2Mo2O7 is turned to an incoherent metal by 5% partial substitution of Gd3+ with Ca2+. However,The systematics of the bandwidth- and filling-controlled metal-insulator transitions (MITs) have been investigated for R2Mo2O7 family (R=Nd, Sm, Eu, Gd, Dy, and Ho) by infrared spectroscopy. The substantial role of electron correlation in driving the MIT is verified. With changing the R ionic radius (r) or equivalently the one-electron bandwidth (W), the MIT occurs in a continuous manner at rc≈r(R=Gd). The T=0K gap continuously vanishes as Δ∝(rc−r), while at the metallic side the linear decrease of Drude weight is followed toward rc. In the metallic compounds, some of the infrared-active phonon modes show remarkably large Fano asymmetry correlating with the Drude weight. These Mo-O-Mo bending modes strongly couple to the conduction electrons via effective modulation of the bandwidth. Even for r≲rc a minimal level of hole doping closes the correlation gap, for example, the barely insulating Gd2Mo2O7 is turned to an incoherent metal by 5% partial substitution of Gd3+ with Ca2+. However, even on further doping no coherent electronic states are formed, indicating the role of the disorder-induced localization effect besides the dominant correlation effects.show moreshow less

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Metadaten
Author:István KézsmárkiORCiDGND, N. Hanasaki, K. Watanabe, S. Iguchi, Y. Taguchi, S. Miyasaka, Y. Tokura
URN:urn:nbn:de:bvb:384-opus4-442101
Frontdoor URLhttps://opus.bibliothek.uni-augsburg.de/opus4/44210
ISSN:1098-0121OPAC
ISSN:1550-235XOPAC
Parent Title (English):Physical Review B
Publisher:American Physical Society (APS)
Type:Article
Language:English
Year of first Publication:2006
Publishing Institution:Universität Augsburg
Release Date:2018/11/29
Volume:73
Issue:12
First Page:125122
DOI:https://doi.org/10.1103/physrevb.73.125122
Institutes:Mathematisch-Naturwissenschaftlich-Technische Fakultät
Mathematisch-Naturwissenschaftlich-Technische Fakultät / Institut für Physik
Mathematisch-Naturwissenschaftlich-Technische Fakultät / Institut für Physik / Lehrstuhl für Experimentalphysik V
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 53 Physik / 530 Physik
Licence (German):Deutsches Urheberrecht