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| Main Authors: | , , , , , , , , , , |
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| Format: | Preprint |
| Published: |
2025
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| Subjects: | |
| Online Access: | https://arxiv.org/abs/2507.18985 |
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| _version_ | 1866913959681982464 |
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| author | Jung, Ju-Hyun Zhao, Chao Yang, Seong-Jun Park, Jun-Ho Lee, Woo-Ju Song, Su-Beom Kim, Jonghwan Hwang, Chan-Cuk Baek, Seung-Hwa Ding, Feng Kim, Cheol-Joo |
| author_facet | Jung, Ju-Hyun Zhao, Chao Yang, Seong-Jun Park, Jun-Ho Lee, Woo-Ju Song, Su-Beom Kim, Jonghwan Hwang, Chan-Cuk Baek, Seung-Hwa Ding, Feng Kim, Cheol-Joo |
| contents | Insulating hexagonal boron nitride (hBN) films with precisely controlled thickness are ideal dielectric components to modulate various interfaces in electronic devices. To achieve this, high-quality hBN with controlled atomic configurations must be able to form pristine interfaces with various materials in devices. However, previously reported large-scale hBN films with uniform thickness either are polycrystalline or are not suitable for atomically clean assembly via mechanical exfoliation, limiting their applications in device technology. Here, we report the large-scale growth of monolayer single crystalline hBN films on Ge(110) substrates by using chemical vapor deposition (CVD). Vicinal Ge(110) substrates are used for the step-directed epitaxial growth of hBN, where Ge atomic steps act as the hBN nucleation sites, guiding the uni-directional alignments of multiple hBN domains. Density functional theory (DFT) calculations reveal that the optimum hydrogen passivations on both hBN edges and Ge surfaces enable the epitaxial coupling between hBN and the Ge step edges and the single crystallinity of the final hBN films. Using epitaxially grown monolayer hBN films, we fabricate a few hBN films with controlled stacking orders and pristine interfaces through a layer-by-layer assembly process. These films function as high-quality dielectrics to enhance carrier transport in graphene and MoS<sub>2</sub> channels. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2507_18985 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | Step-directed Epitaxy of Uni-directional Hexagonal Boron Nitride on Vicinal Ge(110) Jung, Ju-Hyun Zhao, Chao Yang, Seong-Jun Park, Jun-Ho Lee, Woo-Ju Song, Su-Beom Kim, Jonghwan Hwang, Chan-Cuk Baek, Seung-Hwa Ding, Feng Kim, Cheol-Joo Materials Science Insulating hexagonal boron nitride (hBN) films with precisely controlled thickness are ideal dielectric components to modulate various interfaces in electronic devices. To achieve this, high-quality hBN with controlled atomic configurations must be able to form pristine interfaces with various materials in devices. However, previously reported large-scale hBN films with uniform thickness either are polycrystalline or are not suitable for atomically clean assembly via mechanical exfoliation, limiting their applications in device technology. Here, we report the large-scale growth of monolayer single crystalline hBN films on Ge(110) substrates by using chemical vapor deposition (CVD). Vicinal Ge(110) substrates are used for the step-directed epitaxial growth of hBN, where Ge atomic steps act as the hBN nucleation sites, guiding the uni-directional alignments of multiple hBN domains. Density functional theory (DFT) calculations reveal that the optimum hydrogen passivations on both hBN edges and Ge surfaces enable the epitaxial coupling between hBN and the Ge step edges and the single crystallinity of the final hBN films. Using epitaxially grown monolayer hBN films, we fabricate a few hBN films with controlled stacking orders and pristine interfaces through a layer-by-layer assembly process. These films function as high-quality dielectrics to enhance carrier transport in graphene and MoS<sub>2</sub> channels. |
| title | Step-directed Epitaxy of Uni-directional Hexagonal Boron Nitride on Vicinal Ge(110) |
| topic | Materials Science |
| url | https://arxiv.org/abs/2507.18985 |