Single-crystalline PbTe film growth through reorientation

Jason Jung, Sander G. Schellingerhout, Orson A.H. Van Der Molen, Wouter H.J. Peeters, Marcel A. Verheijen, Erik P.A.M. Bakkers (Corresponding author)

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6 Citaten (Scopus)
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Samenvatting

Heteroepitaxy enables the engineering of novel properties, which do not exist in a single material. Two principal growth modes are identified for material combinations with a large lattice mismatch, Volmer-Weber, and Stranski-Krastanov. Both lead to the formation of three-dimensional islands, hampering the growth of flat defect-free thin films. This limits the number of viable material combinations. Here, we report a distinct growth mode found in molecular beam epitaxy of PbTe on InP initiated by pregrowth surface treatments. Early nucleation forms islands analogous to the Volmer-Weber growth mode, but film closure exhibits a flat surface with atomic terracing. Remarkably, despite multiple distinct crystal orientations found in the initial islands, the final film is single crystalline. This is possible due to a reorientation process occurring during island coalescence, facilitating high quality heteroepitaxy despite the large lattice mismatch, difference in crystal structures, and diverging thermal expansion coefficients of PbTe and InP. This growth mode offers a new strategy for the heteroepitaxy of dissimilar materials and expands the realm of possible material combinations.

Originele taal-2Engels
Artikelnummer023401
Aantal pagina's7
TijdschriftPhysical Review Materials
Volume7
Nummer van het tijdschrift2
DOI's
StatusGepubliceerd - feb. 2023

Bibliografische nota

Funding Information:
We thank NanoLab@TU/e for their help and support. This work has been supported by the European Research Council (TOCINA Grant No. 834290 and TOPSQUAD Grant No. 862046). We, furthermore, acknowledge Solliance, a solar energy R&D initiative of ECN, TNO, Holst, TU/e, IMEC and Forschungszentrum Jülich, and the Dutch Province of Noord-Brabant for funding the TEM facility.

Publisher Copyright:
© 2023 American Physical Society.

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