scholarly journals Graphene-like Membranes: From Impermeable to Selective Sieves

2014 ◽  
Vol 1658 ◽  
Author(s):  
G. Brunetto ◽  
D. S. Galvao

ABSTRACTRecently, it was proposed that graphene membranes could act as impermeable atomic structures to standard gases. For some other applications, a higher level of porosity is needed, and the so-called Porous Graphene (PG) and Biphenylene Carbon (BPC) membranes are good candidates to effectively work as selective sieves. In this work we have used classical molecular dynamics simulations to study the dynamics of membrane permeation of He and Ar atoms and possible selectivity effects. For the graphene membranes we did not observe any leakage through the membrane and/or membrane/substrate interface until a critical pressure limit, then a sudden membrane detachment occurs. PG and BPC membranes are not impermeable as graphene ones, but there are significant energy barriers to diffusion depending on the atom type. Our results show that this kind of porous membranes can be effectively used as selective sieves for pure and mixtures of gases.

2015 ◽  
Vol 17 (36) ◽  
pp. 23619-23626 ◽  
Author(s):  
Boyao Wen ◽  
Chengzhen Sun ◽  
Bofeng Bai

The inhibition effect of a non-permeating component on gas permeability of nanoporous graphene membranes is identified using molecular dynamics simulations.


Nanoscale ◽  
2018 ◽  
Vol 10 (42) ◽  
pp. 19854-19862 ◽  
Author(s):  
Xiangjun Liu ◽  
Junfeng Gao ◽  
Gang Zhang ◽  
Yong-Wei Zhang

Using density functional theory calculations and molecular dynamics simulations, we systematically explore various possible atomic structures of phosphorene/graphene in-plane heterojunctions and their effects on interfacial thermal conductance (ITC).


2015 ◽  
Vol 17 (2) ◽  
pp. 1018-1024 ◽  
Author(s):  
Krzysztof Nieszporek ◽  
Mateusz Drach

The mechanism of alkane permeation across designed graphene nanopores has been studied using molecular dynamics simulations.


2013 ◽  
Vol 80 (4) ◽  
Author(s):  
Zhigong Song ◽  
Zhiping Xu ◽  
Xianliang Huang ◽  
Ji-Yeun Kim ◽  
Quanshui Zheng

We explore here the structural stability and fracture of supported graphene sheets under pressure loadings normal to the sheets by performing molecular dynamics simulations. The results show that, in absence of defects, supported graphene deforms into an inverse bubble shape and fracture is nucleated at the supported edges. The critical pressure decreases from ideal tensile strength of graphene in biaxial tension as the size of supporting pores increases. When nanoscale holes are created in the suspended region of graphene, the critical pressure is further lowered with the area of nanoholes, with additional dependence on their shapes. The results are explained by analyzing the deformed profile of graphene sheets under pressure and the stress state.


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