Self-organized twist-heterostructures via aligned van der Waals epitaxy and solid-state transformations
Abstract
Abstract Vertical van der Waals (vdW) heterostructures of 2D crystals with defined interlayer twist are of interest for band-structure engineering via twist moiré superlattice potentials. To date, twist-heterostructures have been realized by micromechanical stacking. Direct synthesis is hindered by the tendency toward equilibrium stacking without interlayer twist. Here, we demonstrate that growing a 2D crystal with fixed azimuthal alignment to the substrate followed by transformation of this intermediate enables a potentially scalable synthesis of twisted heterostructures. Microscopy during growth of ultrathin orthorhombic SnS on trigonal SnS 2 shows that vdW epitaxy yields azimuthal order even for non-isotypic 2D crystals. Excess sulfur drives a spontaneous transformation of the few-layer SnS to SnS 2 , whose orientation – rotated 30° against the underlying SnS 2 crystal – is defined by the SnS intermediate rather than the substrate. Preferential nucleation of additional SnS on such twisted domains repeats the process, promising the realization of complex twisted stacks by bottom-up synthesis.
- Authors:
- Publication Date:
- Research Org.:
- Univ. of Nebraska, Lincoln, NE (United States)
- Sponsoring Org.:
- USDOE; USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22). Materials Sciences & Engineering Division
- OSTI Identifier:
- 1619600
- Alternate Identifier(s):
- OSTI ID: 1579958
- Grant/Contract Number:
- SC0016343
- Resource Type:
- Published Article
- Journal Name:
- Nature Communications
- Additional Journal Information:
- Journal Name: Nature Communications Journal Volume: 10 Journal Issue: 1; Journal ID: ISSN 2041-1723
- Publisher:
- Nature Publishing Group
- Country of Publication:
- United Kingdom
- Language:
- English
- Subject:
- 36 MATERIALS SCIENCE
Citation Formats
Sutter, Peter, Ibragimova, Rina, Komsa, Hannu-Pekka, Parkinson, Bruce A., and Sutter, Eli. Self-organized twist-heterostructures via aligned van der Waals epitaxy and solid-state transformations. United Kingdom: N. p., 2019.
Web. doi:10.1038/s41467-019-13488-5.
Sutter, Peter, Ibragimova, Rina, Komsa, Hannu-Pekka, Parkinson, Bruce A., & Sutter, Eli. Self-organized twist-heterostructures via aligned van der Waals epitaxy and solid-state transformations. United Kingdom. https://doi.org/10.1038/s41467-019-13488-5
Sutter, Peter, Ibragimova, Rina, Komsa, Hannu-Pekka, Parkinson, Bruce A., and Sutter, Eli. Wed .
"Self-organized twist-heterostructures via aligned van der Waals epitaxy and solid-state transformations". United Kingdom. https://doi.org/10.1038/s41467-019-13488-5.
@article{osti_1619600,
title = {Self-organized twist-heterostructures via aligned van der Waals epitaxy and solid-state transformations},
author = {Sutter, Peter and Ibragimova, Rina and Komsa, Hannu-Pekka and Parkinson, Bruce A. and Sutter, Eli},
abstractNote = {Abstract Vertical van der Waals (vdW) heterostructures of 2D crystals with defined interlayer twist are of interest for band-structure engineering via twist moiré superlattice potentials. To date, twist-heterostructures have been realized by micromechanical stacking. Direct synthesis is hindered by the tendency toward equilibrium stacking without interlayer twist. Here, we demonstrate that growing a 2D crystal with fixed azimuthal alignment to the substrate followed by transformation of this intermediate enables a potentially scalable synthesis of twisted heterostructures. Microscopy during growth of ultrathin orthorhombic SnS on trigonal SnS 2 shows that vdW epitaxy yields azimuthal order even for non-isotypic 2D crystals. Excess sulfur drives a spontaneous transformation of the few-layer SnS to SnS 2 , whose orientation – rotated 30° against the underlying SnS 2 crystal – is defined by the SnS intermediate rather than the substrate. Preferential nucleation of additional SnS on such twisted domains repeats the process, promising the realization of complex twisted stacks by bottom-up synthesis.},
doi = {10.1038/s41467-019-13488-5},
journal = {Nature Communications},
number = 1,
volume = 10,
place = {United Kingdom},
year = {Wed Dec 04 00:00:00 EST 2019},
month = {Wed Dec 04 00:00:00 EST 2019}
}
https://doi.org/10.1038/s41467-019-13488-5
Web of Science
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