The carbon chain growth during the onset of CVD graphene formation on γ-Al 2 O 3 is promoted by unsaturated CH 2 ends.

Chemical vapor deposition of methane onto a template of alumina (Al 2 O 3 ) nanoparticles is a prominent synthetic strategy of graphene meso-sponge, a new class of nano porous carbon materials consisting of single-layer graphene walls. However, the elementary steps controlling the early stages of graphene growth on Al 2 O 3 surfaces are still not well understood. In this study, density functional theory calculations provide insights into the initial stages of graphene growth. We have modelled the mechanism of CH 4 dissociation on the (111), (110), (100), and (001) γ-Al 2 O 3 surfaces. Subsequently, we have considered the reaction pathway leading to the formation of a C6 ring. The γ-Al 2 O 3 (110) and γ-Al 2 O 3 (100) are both active for CH 4 dissociation, but the (100) surface has higher catalytic activity towards the carbon growth reaction. The overall mechanism involves the formation of the reactive intermediate CH 2 * that then can couple to form C n H 2 n * ( n = 2-6) intermediates with unsaturated CH 2 ends. The formation of these species, which are not bound to the surface-active sites, promotes the sustained carbon growth in a nearly barrierless process. Also, the short distance between terminal carbon atoms leads to strong interactions, which might lead to the high activity between unsaturated CH 2 * of the hydrocarbon chain. Analysis of the electron localization and geometries of the carbon chains reveals the formation of C-Al-σ bonds with the chain growing towards the vacuum rather than C-Al-π bonds covering the γ-Al 2 O 3 (100) surface. This growth behaviour prevents catalyst poisoning during the initial stage of graphene nucleation.