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γ-GeSe: A New Hexagonal Polymorph from Group IV-VI Monochalcogenides

  • Sol Lee
  • , Joong Eon Jung
  • , Han Gyu Kim
  • , Yangjin Lee
  • , Je Myoung Park
  • , Jeongsu Jang
  • , Sangho Yoon
  • , Arnab Ghosh
  • , Minseol Kim
  • , Joonho Kim
  • , Woongki Na
  • , Jonghwan Kim
  • , Hyoung Joon Choi
  • , Hyeonsik Cheong
  • , Kwanpyo Kim
  • Yonsei University
  • Korea Basic Science Institute
  • Sogang University
  • Pohang University of Science and Technology
  • Institute for Basic Science

Research output: Contribution to journalArticlepeer-review

96 Scopus citations

Abstract

The family of group IV-VI monochalcogenides has an atomically puckered layered structure, and their atomic bond configuration suggests the possibility for the realization of various polymorphs. Here, we report the synthesis of the first hexagonal polymorph from the family of group IV-VI monochalcogenides, which is conventionally orthorhombic. Recently predicted four-atomic-thick hexagonal GeSe, so-called γ-GeSe, is synthesized and clearly identified by complementary structural characterizations, including elemental analysis, electron diffraction, high-resolution transmission electron microscopy imaging, and polarized Raman spectroscopy. The electrical and optical measurements indicate that synthesized γ-GeSe exhibits high electrical conductivity of 3 × 105 S/m, which is comparable to those of other two-dimensional layered semimetallic crystals. Moreover, γ-GeSe can be directly grown on h-BN substrates, demonstrating a bottom-up approach for constructing vertical van der Waals heterostructures incorporating γ-GeSe. The newly identified crystal symmetry of γ-GeSe warrants further studies on various physical properties of γ-GeSe.

Original languageEnglish
Pages (from-to)4305-4313
Number of pages9
JournalNano Letters
Volume21
Issue number10
DOIs
StatePublished - 26 May 2021
Externally publishedYes

Bibliographical note

Publisher Copyright:
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Funding

This work was mainly supported by the Basic Science Research Program of the National Research Foundation of Korea (NRF-2017R1A5A1014862, NRF-2017R1C1B2012729, NRF-2019R1C1C1003643, 2020R1A2C3013673, and 2019R1A2C3006189) and by the Institute for Basic Science (IBS-R026-D1). Y.L. received support from the Basic Science Research Program at the National Research Foundation of Korea, which was funded by the Ministry of Education (NRF-2020R1A6A3A13060549), and Ministry of Science and ICT (NRF-2021R1C1C2006785). A.G. acknowledges the support from the Yonsei University Research Fund (Post-Doctoral Researcher Supporting Program) of 2019 (2019-12-0033). Computational resources were provided by the KISTI Supercomputing Center (Project No. KSC-2019-CRE-0195). Experiments at PLS-II were supported in part by MSIT and POSTECH.

FundersFunder number
Yonsei University Research Fund2019-12-0033
Pohang University of Science and Technology
Ministry of EducationNRF-2020R1A6A3A13060549
Ministry of Science, ICT and Future PlanningNRF-2021R1C1C2006785
National Research Foundation of Korea2019R1A2C3006189, 2020R1A2C3013673, NRF-2019R1C1C1003643, NRF-2017R1C1B2012729, NRF-2017R1A5A1014862
Institute for Basic ScienceIBS-R026-D1
National Supercomputing Center, Korea Institute of Science and Technology InformationKSC-2019-CRE-0195

    Keywords

    • Hexagonal GeSe
    • group IV-VI monochalcogenides
    • new polymorph
    • polarized Raman spectroscopy
    • transmission electron microscopy

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