关键词: 多晶石墨烯/
拉伸/
断裂/
力学特性
English Abstract
Molecular dynamics study of the tensile mechanical properties of polycrystalline graphene
He Xin,Bai Qing-Shun,
Bai Jin-Xuan
1.School of Mechanical and Electrical Engineering, Harbin Institute of Technology, Harbin 150001, China
Fund Project:Project supported by the National Natural Science Foundation of China (Grant Nos. 51535003, 51575138).Received Date:19 January 2016
Accepted Date:13 March 2016
Published Online:05 June 2016
Abstract:Grain boundaries (GBs) are known to have an important influence on material properties, so understanding how GBs in graphene change its physical properties is important both scientifically and technologically. In this paper, we perform a series of molecular dynamics simulations to investigate the energies, mechanical properties and fracture process of 29 graphene GBs (symmetric and nonsymmetric) under tensile strains. With different arrangements of the pentagonal and heptagonal rings, the misorientation angle () ranges from 3.5 to 27.8. The GBs defects in graphene can produce a pre-strain that will lead to an increase of the energy of GBs. We study the atomic energy distribution around GBs and define a new parameter: single defect energy (Esingle) to calculate the average energy per GBs defect. It is found that Esingle shows a clear linear relation between and defect density (), because pre-strain filed can be cancelled out locally with the increase of defect density. And this pre-stain can reduce the strength of the C-C bond contained in GBs defects. Hence, with very few exceptions, mechanical failure always starts from the defective region. Furthermore, the energy of GBs can be used to reflect the strength of GBs indirectly. The simulated results show that the tensile strength of GBs is linearly related to the highest atomic energy (Emax), and it also depends on Esingle monotonically. Owing to the pre-strain, load distribution along GBs is uneven. Because some bonds are stretched while others are compressed, that is, the real number of bearing carbon bonds is less than the nominal number. Therefore, at the beginning of tension, the Young's modulus of polycrystalline graphene is significantly lower than that of the monocrystal one. But with the increase of strain, it becomes comparable to that of the monocrystal graphene at sufficiently large strain. The results of fracture process indicate that formation and propagation of crack are both dependent on strength GBs. For low GB strength, the fracture mechanism is transgranular fracture in the form of direct fracture of C-C bonds. When stress reaches a critical value, the weakest C-C bonds in GBs will breakdown and form a fracture site. Because of the uneven bearing condition, the C-C bonds in front of the crack possess considerable residual strength and could prevent crack from propagating. As a result, many other fracture sites in the GBs defect can be produced with the increase of strain, and finally, these sites emerge gradually along GBs and form a sawtooth crack. In contrast, the fracture process of high strength GBs is always accompanied with the variations of Stone-Wales (S-W) transformation and direct fracture of C-C bonds. Once the fracture site forms, the crack will propagate rapidly predominantly along armchair or zigzag direction and finally could cross GBs, this process can be called intergranular fracture. Our present work provides fundamental guidance for understanding how defects affect the mechanical behaviour, which is important for further research and application of graphene devices.
Keywords: polycrystalline graphene/
tensile/
fracture/
mechanical properties
