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Electrochemical delamination assisted transfer of molecular nanosheets

Abstract

Delamination and transfer of two-dimensional (2D) materials from their synthesis substrates onto target substrates is an important task for their implementation in both fundamental and applied research. To this end, the electrochemical delamination based transfer has been successfully applied for a variety of inorganic 2D materials grown on conducting substrates. However, this promising method has not yet been demonstrated for organic 2D materials, which recently gain a significant importance in the 2D materials family. Here, we present a transfer method of molecular nanosheets covalently bonded to the metal substrate based on the electrochemical delamination, which involves cleavage of Au-S bond and hydrogen evolution. We demonstrate a successful transfer of different types of carbon nanomembranes (CNMs) – about 1 nm thick molecular nanosheets – synthesized from aromatic thiol-based self-assembled monolayers on various polycrystalline gold substrates, onto new target substrates such as SiO2/Si wafers and transmission electron microscope grids. We analyze the subsequent nanofabrication steps, chemical and structural characteristics of the transferred supported and suspended CNMs by X-ray photoelectron spectroscopy (XPS), optical, atomic force (AFM) and scanning electron microscopy (SEM). The XPS analysis enables us to reveal the chemical mechanisms during the delamination process, whereas the complementary microscopy measurements confirm a high structural integrity of the transferred molecular nanosheets. We expect that the developed methodology can be applied for a broad variety of organic 2D materials synthetized on conducting substrates.

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Article information


Submitted
07 Feb 2020
Accepted
17 Mar 2020
First published
19 Mar 2020

Nanoscale, 2020, Accepted Manuscript
Article type
Communication

Electrochemical delamination assisted transfer of molecular nanosheets

Z. Tang, C. Neumann, A. Winter and A. Turchanin, Nanoscale, 2020, Accepted Manuscript , DOI: 10.1039/D0NR01084G

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