TY - JOUR
T1 - Directed self-assembled crystalline oligomer domains on graphene and graphite
T2 - Paper
AU - Balzer, Frank
AU - Henrichsen, Henrik Hartmann
AU - Klarskov, Mikkel Buster
AU - Booth, Tim
AU - Sun, Rong
AU - Parisi, Jürgen
AU - Schiek, Manuela
AU - Bøggild, Peter
PY - 2014
Y1 - 2014
N2 - We observe the formation of thin films of fibre-like aggregates from the prototypical organic semiconductor molecule para-hexaphenylene (p-6P) on graphite thin flakes and on monolayer graphene. Using atomic force microscopy, scanning electron microscopy, x-ray diffraction, polarized fluorescence microscopy, and bireflectance microscopy, the molecular orientations on the surface are deduced and correlated to both the morphology as well as to the high-symmetry directions of the graphitic surface: the molecules align with their long axis at ±11° with respect to a high-symmetry direction. The results show that the graphene surface can be used as a growth substrate to direct the self-assembly of organic molecular thin films and nanofibres, both with and without lithographical processing.
AB - We observe the formation of thin films of fibre-like aggregates from the prototypical organic semiconductor molecule para-hexaphenylene (p-6P) on graphite thin flakes and on monolayer graphene. Using atomic force microscopy, scanning electron microscopy, x-ray diffraction, polarized fluorescence microscopy, and bireflectance microscopy, the molecular orientations on the surface are deduced and correlated to both the morphology as well as to the high-symmetry directions of the graphitic surface: the molecules align with their long axis at ±11° with respect to a high-symmetry direction. The results show that the graphene surface can be used as a growth substrate to direct the self-assembly of organic molecular thin films and nanofibres, both with and without lithographical processing.
U2 - 10.1088/0957-4484/25/3/035602
DO - 10.1088/0957-4484/25/3/035602
M3 - Journal article
C2 - 24356510
SN - 0957-4484
VL - 25
SP - 035602
JO - Nanotechnology
JF - Nanotechnology
IS - 3
ER -