Charge-transfer transition in Au-induced quantum wires on Si(553)

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OriginalspracheEnglisch
Aufsatznummer045419
FachzeitschriftPhysical Review B
Jahrgang100
Ausgabenummer4
PublikationsstatusVeröffentlicht - 24 Juli 2019

Abstract

The Si(553)-Au system resembles a heteroatomic chain ensemble with a delicate spin-charge interplay. The ordering of the ×3 reconstruction vanishes via a phase transition taking place at Tc=100 K. Our directional-dependent surface transport measurements showed that this order-disorder phase transition is not driven by the formation of a charge-density wave, as previously suggested. Instead, at 65 K there is a pronounced increase of the surface-state conductivity along the wires. We attribute this to activated charge transfer between the localized Si dangling bond states and the proximate Au bands revealing a ×2 periodicity. Apparently, a quasiorthogonality between the wave functions of the two proximal reconstructions is also responsible for a missing ×6 periodicity along the wires. The electronic charge transfer is in agreement with recent band-structure calculations.

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Charge-transfer transition in Au-induced quantum wires on Si(553). / Edler, Frederik; Miccoli, Ilio; Pfnür, Herbert et al.
in: Physical Review B, Jahrgang 100, Nr. 4, 045419, 24.07.2019.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Edler F, Miccoli I, Pfnür H, Tegenkamp C. Charge-transfer transition in Au-induced quantum wires on Si(553). Physical Review B. 2019 Jul 24;100(4):045419. doi: 10.1103/physrevb.100.045419
Edler, Frederik ; Miccoli, Ilio ; Pfnür, Herbert et al. / Charge-transfer transition in Au-induced quantum wires on Si(553). in: Physical Review B. 2019 ; Jahrgang 100, Nr. 4.
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AU - Miccoli, Ilio

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AU - Tegenkamp, Christoph

N1 - Funding information: We gratefully acknowledge the fruitful discussions with B. Hafke and M. Horn-von Hoegen (University of Duisburg–Essen, Germany), C. Braun and W. Gero Schmidt (University of Paderborn, Germany), S. Sanna (University of Gießen, Germany), as well as the financial support by the Deutsche Forschungsgemeinschaft through our Research Unit FOR1700 (Project Te/386 10-2).

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