Issue 28, 2019

Disparate strain response of the thermal transport properties of bilayer penta-graphene as compared to that of monolayer penta-graphene

Abstract

In this study, strain modulation of the lattice thermal conductivity of monolayer and bilayer penta-graphene (PG) at room temperature was investigated using first-principles calculations combined with the phonon Boltzmann transport equation. The thermal conductivities of both the monolayer and the bilayer PG exhibit a robust nonmonotonic up-and-down behavior under strain despite the effect of van der Waals (vdW) interactions, and the thermal conductivities of bilayer PG under strain are significantly reduced by up to 87%. Using phonon-level systematic analysis, the variation of thermal conductivity with the increasing strain was determined by increasing the phonon lifetime in specific phonon modes, and that with the reduction of strain was determined by the decrease of both phonon group velocity and phonon lifetime. Moreover, bilayer PG shows an unexpectedly different response to strain when compared with monolayer PG, and a significantly larger reduction (>60%) in the thermal conductivity of bilayer PG is achieved when the strain reaches 10% because the interlayer interactions enhance the phonon anharmonicity of the phonon modes of ultra-low frequency. Our study shows that bilayer PG will have tremendous opportunities for application in thermal management and two-dimensional nanoscale electronic devices owing to its largely tunable thermal conductivity.

Graphical abstract: Disparate strain response of the thermal transport properties of bilayer penta-graphene as compared to that of monolayer penta-graphene

Supplementary files

Article information

Article type
Paper
Submitted
07 May 2019
Accepted
18 Jun 2019
First published
21 Jun 2019

Phys. Chem. Chem. Phys., 2019,21, 15647-15655

Disparate strain response of the thermal transport properties of bilayer penta-graphene as compared to that of monolayer penta-graphene

Z. Sun, K. Yuan, X. Zhang, G. Qin, X. Gong and D. Tang, Phys. Chem. Chem. Phys., 2019, 21, 15647 DOI: 10.1039/C9CP02574J

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