Details

Autor(en) / Beteiligte

• Kong, Wei
• Li, Huashan
• Qiao, Kuan
• Kim, Yunjo
• Lee, Kyusang
• Nie, Yifan
• Lee, Doyoon
• Osadchy, Tom
• Molnar, Richard J
• Gaskill, D. Kurt
• Myers-Ward, Rachael L.
• Daniels, Kevin M.
• Zhang, Yuewei
• Sundram, Suresh
• Yu, Yang
• Bae, Sang-hoon
• Rajan, Siddharth
• Shao-Horn, Yang
• Cho, Kyeongjae
• Ougazzaden, Abdallah
• Grossman, Jeffrey C.
• Kim, Jeehwan

Titel

Polarity governs atomic interaction through two-dimensional materials

Ist Teil von

• Nature materials, 2018-11, Vol.17 (11), p.999-1004

Ort / Verlag

London: Nature Publishing Group UK

Erscheinungsjahr

2018

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• The transparency of two-dimensional (2D) materials to intermolecular interactions of crystalline materials has been an unresolved topic. Here we report that remote atomic interaction through 2D materials is governed by the binding nature, that is, the polarity of atomic bonds, both in the underlying substrates and in 2D material interlayers. Although the potential field from covalent-bonded materials is screened by a monolayer of graphene, that from ionic-bonded materials is strong enough to penetrate through a few layers of graphene. Such field penetration is substantially attenuated by 2D hexagonal boron nitride, which itself has polarization in its atomic bonds. Based on the control of transparency, modulated by the nature of materials as well as interlayer thickness, various types of single-crystalline materials across the periodic table can be epitaxially grown on 2D material-coated substrates. The epitaxial films can subsequently be released as free-standing membranes, which provides unique opportunities for the heterointegration of arbitrary single-crystalline thin films in functional applications. Remote atomic interaction of crystalline materials through 2D materials is presented to depend on the polarity of both the 2D interlayers and underlying substrates, providing insights for the epitaxial growth of various materials on 2D crystals.