Origin of surface and subband states at the InAs(111)A surface

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The atomic structure of surfaces and interfaces plays a vital role in the electronic quality and properties of quantum devices. The interplay between the surface and confined bulk subband states in terms of their susceptibility has been investigated in relation to crystal defects on an InAs(111)A-(2×2) reconstructed surface, using low-temperature scanning tunneling microscopy and spectroscopy. We measure the two-dimensional quantized subband states arising from the confined potential imposed by downward bending of the conduction band edge. Furthermore, we show evidence of the existence of surface Bloch states within the confined bulk band gap projected on the surface spectrum which have originated from the surface reconstruction. As expected, larger confined bulk band gaps at the surface and conduction band offset are measured to be 0.58 and 0.31 eV, respectively. We further show the scattering of these quantum states at different surface defects and demonstrate that surface states are more susceptible to the defect potential when compared with the corresponding subband states. This apparent contrast follows from the length scale at which these defect potentials actively interact on or near the surface. Our observed experimental results are supported by empirical tight-binding simulations for the subband states and first-principles density functional theory simulations for the surface states present on the surface.

OriginalsprogEngelsk
Artikelnummer066201
TidsskriftPhysical Review Materials
Vol/bind7
Udgave nummer6
Antal sider10
ISSN2475-9953
DOI
StatusUdgivet - 20 jun. 2023

Bibliografisk note

Funding Information:
We gratefully acknowledge discussions with Kasper Grove-Rasmussen, Jan Gukelberger, and Sergej Schuwalow and support from Microsoft Quantum. Work at CMU was funded by the National Science Foundation (NSF) through Grant No. OISE-1743717. This research used resources of the National Energy Research Scientific Computing Center (NERSC), a DOE Office of Science User Facility supported by the Office of Science of the U.S. Department of Energy under Contract No. DE-AC02-05CH11231.

Publisher Copyright:
© 2023 American Physical Society.

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