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Graphyne–graphene (nitride) heterostructure as nanocapacitor
[Display omitted] •Binding energy of heterostructures indicates the exothermic nature.•Increasing electric field enhances charge and energy stored in the system.•The external electric fields amplify the charge transfer between two flakes.•The capacitance value gets saturated above a certain electric...
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Published in: | Chemical physics 2016-10, Vol.478, p.73-80 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Binding energy of heterostructures indicates the exothermic nature.•Increasing electric field enhances charge and energy stored in the system.•The external electric fields amplify the charge transfer between two flakes.•The capacitance value gets saturated above a certain electric field.
A nanoscale capacitor composed of heterostructure derived from finite size graphyne flake and graphene (nitride) flake has been proposed and investigated using density functional theory (DFT). The exothermic nature of formation process of these heterostructures implies their stability. Significant charge transfer between two flakes generates permanent dipole in this heterostructures. The amount of charge transfer is tunable under the application of external electric field which enhances their applicability in electronics. We have specifically focused on the capacitive properties of different heterostructure composed of graphyne flake and graphene (nitride) flake, i.e., graphyne/graphene, graphyne/h-BN, graphyne/AlN, graphyne/GaN. The charge stored by each flake, energy storage, and capacitance are switchable under external electric field. Thus, our modeled heterostructures are a good candidate as nanoscale capacitor and can be used in nanocircuit. We found that the charge stored by each flake, energy storage, and capacitance value are highest for graphyne/GaN heterostructures. |
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ISSN: | 0301-0104 |
DOI: | 10.1016/j.chemphys.2016.05.004 |