Advanced search
Start date
(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

The structure of graphene on graphene/C-60/Cu interfaces: a molecular dynamics study

Full text
Fonseca, Alexandre F. [1] ; Dantas, Socrates O. [1, 2] ; Galvao, Douglas S. [1, 3] ; Zhang, Difan [4, 5] ; Sinnott, Susan B. [5, 6]
Total Authors: 5
[1] Univ Estadual Campinas, Inst Phys Gleb Wataghin, Appl Phys Dept, BR-13083970 Campinas, SP - Brazil
[2] Univ Fed Juiz de Fora, Sci Inst, Phys Dept, BR-36036330 Juiz De Fora, MG - Brazil
[3] Univ Estadual Campinas, Ctr Comp Engn & Sci, BR-13083959 Campinas, SP - Brazil
[4] Univ Florida, Dept Mat Sci & Engn, Gainesville, FL 32611 - USA
[5] Penn State Univ, Dept Mat Sci & Engn, University Pk, PA 16801 - USA
[6] Penn State Univ, Dept Chem, University Pk, PA 16801 - USA
Total Affiliations: 6
Document type: Journal article
Source: Nanotechnology; v. 30, n. 50 DEC 13 2019.
Web of Science Citations: 0

Two experimental studies reported the spontaneous formation of amorphous and crystalline structures of C-60 molecules intercalated between graphene and a surface. The findings observed included interesting phenomena ranging from reaction between fullerene C(60)s ('C(60)s' stands for plural of C-60) under graphene to graphene sheets sagging between C(60)s and control of strain in these sheets. Motivated by this work, we performed fully atomistic reactive molecular dynamics simulations to investigate the formation and thermal stability of graphene sheet wrinkles as well as graphene attachment to and detachment from a surface when the sheet is laid over a previously distributed array of C-60 molecules on a copper surface at different temperatures. As graphene compresses the C(60)s against the surface, and graphene attachment to the surface in between C(60)s depends on the height of the wrinkles in the graphene sheet, configurations with both frozen and non-frozen fullerenes were investigated in the simulations in order to examine the experimental result of stable, sagged graphene sheets when the distance between C(60)s is about 4 nm and the height of the wrinkles in the sheet is about 0.8 nm. Below a distance of 4 nm between fullerenes, the graphene is predicted to become locally suspended and less strained. The simulations predict that this happens when the fullerenes can deform under the compressive action of the graphene sheet. If the fullerenes are kept frozen, spontaneous `blanketing' of graphene is predicted only when the distance between neighbouring C(60)s is equal to or great than about 7 nm. These predictions agree with a mechanical model relating the rigidity of a graphene sheet to the energy of graphene-surface adhesion. This work further reveals the structure of intercalated molecules and the role of stability and sheet wrinkling on the preferred configuration of graphene. This study thus might assist in the development of two-dimensional confined nanoreactors for chemical reactions. (AU)

FAPESP's process: 18/02992-4 - Carbon Nanostructures: Modeling and Simulations
Grantee:Alexandre Fontes da Fonseca
Support type: Regular Research Grants
FAPESP's process: 13/08293-7 - CCES - Center for Computational Engineering and Sciences
Grantee:Munir Salomao Skaf
Support type: Research Grants - Research, Innovation and Dissemination Centers - RIDC