TY - JOUR

T1 - Nanomechanical mapping of graphene layers and interfaces in suspended graphene nanostructures grown via carbon diffusion

AU - Robinson, Benjamin

AU - Rabot, Caroline

AU - Mazzocco, Riccardo

AU - Delamoreanu, A

AU - Zenasni, Aziz

AU - Kolosov, Oleg

PY - 2014/1/1

Y1 - 2014/1/1

N2 - Graphene’s remarkable mechanical, electronic and thermal properties are strongly determined by both the mechanism of its growth and its interaction with the underlying substrate. Evidently, in order to explore the fundamentals of these mechanisms, efficient nanoscale methods are needed that enable observation of features hidden underneath the immediate surface. In this paper we use nanomechanical mapping via ultrasonic force microscopy that employs MHz frequency range ultrasonic vibrations and allows the observation of surface composition and subsurface interfaces with nanoscale resolution, to elucidate the morphology of few layer graphene (FLG) films produced via a recently reported method of carbon diffusion growth (CDG) on platinum-metal based substrate. CDG is known to result in FLG suspended over large areas, which could be of high importance for graphene transfer and applications where a standalone graphene film is required. This study directly reveals the detailed mechanism of CDG three-dimensional growth and FLG film detachment, directly linking the level of graphene decoupling with variations of the substrate temperature during the annealing phase of growth. We also show that graphene initially preferentially decouples at the substrate grain boundaries, likely due to its negative expansion coefficient at cooling, forming characteristic “nano-domes” at the intersections of the grain boundaries. Furthermore, quantitative nanomechanical mapping of flexural stiffness of suspended FLG “nano-domes” using kHz frequency range force modulation microscopy, uncovers the progression of “nano-domes” stiffness from single to bi-modal distribution as CDG growth progresses, suggesting growth instability at advanced CDG stages.

AB - Graphene’s remarkable mechanical, electronic and thermal properties are strongly determined by both the mechanism of its growth and its interaction with the underlying substrate. Evidently, in order to explore the fundamentals of these mechanisms, efficient nanoscale methods are needed that enable observation of features hidden underneath the immediate surface. In this paper we use nanomechanical mapping via ultrasonic force microscopy that employs MHz frequency range ultrasonic vibrations and allows the observation of surface composition and subsurface interfaces with nanoscale resolution, to elucidate the morphology of few layer graphene (FLG) films produced via a recently reported method of carbon diffusion growth (CDG) on platinum-metal based substrate. CDG is known to result in FLG suspended over large areas, which could be of high importance for graphene transfer and applications where a standalone graphene film is required. This study directly reveals the detailed mechanism of CDG three-dimensional growth and FLG film detachment, directly linking the level of graphene decoupling with variations of the substrate temperature during the annealing phase of growth. We also show that graphene initially preferentially decouples at the substrate grain boundaries, likely due to its negative expansion coefficient at cooling, forming characteristic “nano-domes” at the intersections of the grain boundaries. Furthermore, quantitative nanomechanical mapping of flexural stiffness of suspended FLG “nano-domes” using kHz frequency range force modulation microscopy, uncovers the progression of “nano-domes” stiffness from single to bi-modal distribution as CDG growth progresses, suggesting growth instability at advanced CDG stages.

KW - Graphene

KW - Carbon diffusion growth

KW - Ultrasonic Force Microscopy

KW - Graphene Nano-domes

KW - Nanomechanics

U2 - 10.1016/j.tsf.2013.10.093

DO - 10.1016/j.tsf.2013.10.093

M3 - Journal article

VL - 550

SP - 472

EP - 479

JO - Thin Solid Films

JF - Thin Solid Films

SN - 0040-6090

ER -