The deposition mechanisms of smooth laminar (SL) and rough laminar (RL) pyr
ocarbons from propane are found to be very different, as evidenced by (i) g
as phase analysis, (ii) nucleation experiments and (iii) analysis of the de
posit composition and nanostructure. SL pyrocarbon results mainly from alip
hatic species; its nucleation needs surface reactive sites where chemisorpt
ion and hydrogen abstraction occur; its growth leads to extended but highly
distorted graphene layers which can enclose internal nanoporosity. RL pyro
carbon results mainly from polycyclic aromatic hydrocarbons (PAH); its nucl
eation, which does not depend on the substrate, occurs widely by physisorpt
ion of PAH; the corresponding graphene layers are not very extended but par
allel to each other and parallel to the anisotropy plane.