Letter

Layer-by-layer assembly of two-dimensional materials into wafer-scale heterostructures

  • Nature volume 550, pages 229233 (12 October 2017)
  • doi:10.1038/nature23905
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Abstract

High-performance semiconductor films with vertical compositions that are designed to atomic-scale precision provide the foundation for modern integrated circuitry and novel materials discovery1,2,3. One approach to realizing such films is sequential layer-by-layer assembly, whereby atomically thin two-dimensional building blocks are vertically stacked, and held together by van der Waals interactions4,5,6. With this approach, graphene and transition-metal dichalcogenides—which represent one- and three-atom-thick two-dimensional building blocks, respectively—have been used to realize previously inaccessible heterostructures with interesting physical properties7,8,9,10,11. However, no large-scale assembly method exists at present that maintains the intrinsic properties of these two-dimensional building blocks while producing pristine interlayer interfaces12,13,14,15, thus limiting the layer-by-layer assembly method to small-scale proof-of-concept demonstrations. Here we report the generation of wafer-scale semiconductor films with a very high level of spatial uniformity and pristine interfaces. The vertical composition and properties of these films are designed at the atomic scale using layer-by-layer assembly of two-dimensional building blocks under vacuum. We fabricate several large-scale, high-quality heterostructure films and devices, including superlattice films with vertical compositions designed layer-by-layer, batch-fabricated tunnel device arrays with resistances that can be tuned over four orders of magnitude, band-engineered heterostructure tunnel diodes, and millimetre-scale ultrathin membranes and windows. The stacked films are detachable, suspendable and compatible with water or plastic surfaces, which will enable their integration with advanced optical and mechanical systems.

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Change history

  • Corrected online 21 November 2017

    In the HTML version of the Figure 2 legend, the AFM height image was corrected from '2 mm × 2 mm' to '2 μm × 2 μm'.

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Acknowledgements

We thank D. Talapin, P. L. McEuen and M. Guimaraes for discussions and for helping with preparing the manuscript. This work was mainly supported by the Air Force Office of Scientific Research (FA9550-16-1-0031, FA2386-13-1-4118) and the Nano Material Technology Development Program through the National Research Foundation of Korea funded by the Ministry of Science, ICT, and Future Planning (2012M3A7B4049887). Additional funding was provided by the National Science Foundation (NSF) through the Platform for the Accelerated Realization, Analysis, and Discovery of Interface Materials (PARADIM; DMR-1539918) and the Cornell Center for Materials Research (CCMR; NSF DMR-1120296). Material characterizations including electron microscopy were supported by the CCMR (NSF DMR-1120296) and the MRSEC Shared User Facilities at the University of Chicago (NSF DMR-1420709). Device fabrication and characterizations were performed at the Cornell Nanoscale Facility (Grant ECCS-1542081) and the Pritzker Nanofabrication Facility of the Institute for Molecular Engineering at the University of Chicago (NSF NNCI-1542205), both of which are members of the National Nanotechnology Coordinated Infrastructure supported by the National Science Foundation.

Author information

Author notes

    • Kibum Kang
    •  & Kan-Heng Lee

    These authors contributed equally to this work.

Affiliations

  1. Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, USA

    • Kibum Kang
    • , Hui Gao
    •  & Jiwoong Park
  2. Department of Chemistry, University of Chicago, Chicago, Illinois 60637, USA

    • Kibum Kang
    • , Hui Gao
    •  & Jiwoong Park
  3. James Franck Institute, University of Chicago, Chicago, Illinois 60637, USA

    • Kibum Kang
    •  & Jiwoong Park
  4. School of Applied and Engineering Physics, Cornell University, Ithaca, New York 14853, USA

    • Kan-Heng Lee
    • , Yimo Han
    • , Saien Xie
    •  & David A. Muller
  5. Institute for Molecular Engineering, University of Chicago, Chicago, Illinois 60637, USA

    • Kan-Heng Lee
    • , Saien Xie
    •  & Jiwoong Park
  6. Kavli Institute at Cornell for Nanoscale Science, Cornell University, Ithaca, New York 14853, USA

    • David A. Muller
    •  & Jiwoong Park

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Contributions

K.K. and K.-H.L. contributed equally to this work. K.K., K.-H.L. and J.P. conceived the experiments. K.K., H.G. and S.X. synthesized the monolayer TMD films. K.K., K.-H.L. and H.G. developed the PVS method. Y.H. and D.A.M. conducted the atomic-resolution STEM imaging and FIB milling. K.-H.L. fabricated and measured the tunnelling devices. K.K. and K.-H.L. performed the AFM, XRD and optical measurements. K.K., K.-H.L. and J.P. wrote the manuscript. All authors discussed the results and commented on the manuscript.

Competing interests

The authors declare no competing financial interests.

Corresponding author

Correspondence to Jiwoong Park.

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Supplementary information

PDF files

  1. 1.

    Supplementary Information

    This file contains Supplementary Methods, Supplementary Notes, Supplementary Table 1, Supplementary Tables 1-13 and Supplementary References. The Supplementary Methods contain a detailed description of preparation, characterization and applications of our samples, the Supplementary Notes contains additional characterization data supporting the large-scale uniformity, pristine interlayer interfaces and interlayer coupling of our stacked TMD films and additional description of our experimental observation, tunnel model and statistical method. Supplementary Table contains a list of combined characterizations and their length scales and the Supplementary Figures contains additional characterization data and schematics of our process.

Videos

  1. 1.

    Mechanical peeling of a 2-inch ML MoS2 film with TRT/PMMA from its growth substrate

    A video of mechanical peeling of a 2-inch ML MoS2 film with TRT/PMMA from its growth substrate (SiO2/Si in our experiment).

  2. 2.

    Delamination process of a ML MoS2 film from the substrate by dipping it into water with no polymer support or chemical treatment

    A video of delamination process of a ML MoS2 film from the substrate by dipping it into water with no polymer support or chemical treatment.

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