Effects of electrostatic interactions on Kapitza resistance in hexagonal boron nitride-water interfaces

Abstract

Electrostatic interactions in nanoscale systems can influence the heat transfer mechanism and interfacial properties. This study uses molecular dynamics simulations to investigate the impact of various electrostatic interactions on the Kapitza resistance ($R_k$) on a hexagonal boron nitride-water system. The Kapitza resistance at hexagonal boron nitride nanotube (hBNNT)-water interface reduces with an increase in diameter of the nanotube due to more aggregation of water molecules per unit surface area. An increase in the partial charges on boron and nitride caused the reduction in $R_k$. With the increase in partial charge, a better hydrogen bonding between hBNNT and water was observed, whereas the structure and order of the water molecules remain the same. Nevertheless, the addition of NaCl salt into water does not have any influence on interfacial thermal transport. $R_k$ remains unchanged with electrolyte concentration since the cumulative Coulombic interaction between the ions, and the hBNNT is significantly less when compared with water molecules. Furthermore, the effect of electric field strength on interfacial heat transfer is also investigated by providing uniform positive and negative surface charges on the outermost hBN layers. $R_k$ is nearly independent of the practical range of applied electric fields and decreases with an increasing electric field for extreme field strengths until the electro-freezing phenomenon occurs. The ordering of water molecules towards the charged surface leads to an increase in the layering effect, causing the reduction in $R_k$ in the presence of an electric field.

arXiv comment35 pages, 9 figures

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• Nanofluidics, from bulk to interfaces
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• Energy Dissipation and Transport in Nanoscale Devices
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Cited by in corpus (2)

• Interfacial Thermal Transport and Electrical Performance of Supercapacitors with Graphene/Carbon Nanotube Composite Electrodes
• A review of heat transport in solvated gold nanoparticles: Molecular dynamics modeling and experimental perspectives