Issue 46, 2018

Phase transformation in two-dimensional covalent organic frameworks under compressive loading

Abstract

As a new class of two-dimensional (2D) materials, 2D covalent organic frameworks (COFs) are proven to possess remarkable electronic and magnetic properties. However, their mechanical behaviours remain almost unexplored. In this work, taking the recently synthesised dimethylmethylene-bridged triphenylamine (DTPA) sheet as an example, we investigate the mechanical behaviours of 2D COFs based on molecular dynamics simulations together with density functional theory calculations. A novel phase transformation is observed in DTPA sheets when a relatively large in-plane compressive strain is applied to them. Specifically, the crystal structures of the transformed phases are topographically different when the compressive loading is applied in different directions. The compression-induced phase transformation in DTPA sheets is attributed to the buckling of their kagome lattice structures and is found to have significant impacts on their material properties. After the phase transformation, Young's modulus, band gap and thermal conductivity of DTPA sheets are greatly reduced and become strongly anisotropic. Moreover, a large in-plane negative Poisson's ratio is found in the transformed phases of DTPA sheets. It is expected that the results of the compression-induced phase transformation and its influence on the material properties observed in the present DTPA sheets can be further extended to other 2D COFs, since most 2D COFs are found to possess a similar kagome lattice structure.

Graphical abstract: Phase transformation in two-dimensional covalent organic frameworks under compressive loading

Supplementary files

Article information

Article type
Paper
Submitted
25 Aug 2018
Accepted
01 Nov 2018
First published
02 Nov 2018

Phys. Chem. Chem. Phys., 2018,20, 29462-29471

Phase transformation in two-dimensional covalent organic frameworks under compressive loading

J. Zhang, Phys. Chem. Chem. Phys., 2018, 20, 29462 DOI: 10.1039/C8CP05410J

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