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The adsorption of organic molecules
from solution onto a solid surface
has attracted tremendous attention
as it is fundamentally associated to
many phenomena of both industrial
and academic relevance. Governed
by an intricate balance between
adsorbate-substrate and adsorbate-
adsorbate interactions, spontaneous
self-organization of molecules at the
interface may lead to the formation of
delicate ultrathin fi lms with nanometer
scale ordered surface structures due
to the molecular-level packing in a
particular way. Various techniques
have been reported to investigate
those organic layers. For instance,
differential scanning calorimetry
(DSC) provides an effective means
to probe the surface phase behavior.
The structural information normal to
the interface, to some extent, can be
extracted from neutron refl ectivity
measurements. So far, the real time
3D structural characterization with
atomic or molecular scale details of
the assemblies especially the top
layer comes mainly from scanning
probe microscopy techniques.
In this application brief, the capability
of atomic force microscopy (AFM) to
directly visualize soft thin fi lm materials
with true molecular resolution is
demonstrated using self-assembly of
n-C36H74 molecules on graphite as an
example. All the data displayed here
are acquired from an Agilent 5600LS
system with a 90 µm large scanner.
A typical AFM topographic image of
n-C36H74 upon adsorption on HOPG
is shown in Figure 1, from which
rich information about this sample is
revealed. First, molecules are aligned
on the substrate with long-range
order and exhibit a striped morphology.
Second, existence of local defect areas
is captured. As can be seen, the whole
image is divided into four segments
by two long and one short domain
boundaries and a protrusion island is
observed near the bottom location.
Those surface features correspond to
adsorbed molecules in an amorphous
state. Third, two different orientations
of the molecular packing are identifi ed.
The stripes in the left-upper corner
are exactly 60° rotated with respect to
those in the remaining three domains,
refl ecting the impact of underneath
substrate (i.e., the 6-fold symmetry
graphite) on n-C36H74 alignment on the
surface. Figure 2 is another n-C36H74 /
graphite topography image with a larger
magnifi cation to deliver important
information at single molecular level.
It shows that the stripe width is about
4.5 nm, which is matching well with the
molecular length of n-C36H74 with a fully
extended confi guration. Furthermore,
the linear backbones (i.e., hydrocarbon
chains with an all-tans confi guration)
of individual n-C36H74 molecules are
resolved at lower part of the image.
These results unambiguously illustrate
that n-C36H74 molecules are lying
down and orderly aligned on graphite
to form a lamellar packing structure.
from solution onto a solid surface
has attracted tremendous attention
as it is fundamentally associated to
many phenomena of both industrial
and academic relevance. Governed
by an intricate balance between
adsorbate-substrate and adsorbate-
adsorbate interactions, spontaneous
self-organization of molecules at the
interface may lead to the formation of
delicate ultrathin fi lms with nanometer
scale ordered surface structures due
to the molecular-level packing in a
particular way. Various techniques
have been reported to investigate
those organic layers. For instance,
differential scanning calorimetry
(DSC) provides an effective means
to probe the surface phase behavior.
The structural information normal to
the interface, to some extent, can be
extracted from neutron refl ectivity
measurements. So far, the real time
3D structural characterization with
atomic or molecular scale details of
the assemblies especially the top
layer comes mainly from scanning
probe microscopy techniques.
In this application brief, the capability
of atomic force microscopy (AFM) to
directly visualize soft thin fi lm materials
with true molecular resolution is
demonstrated using self-assembly of
n-C36H74 molecules on graphite as an
example. All the data displayed here
are acquired from an Agilent 5600LS
system with a 90 µm large scanner.
A typical AFM topographic image of
n-C36H74 upon adsorption on HOPG
is shown in Figure 1, from which
rich information about this sample is
revealed. First, molecules are aligned
on the substrate with long-range
order and exhibit a striped morphology.
Second, existence of local defect areas
is captured. As can be seen, the whole
image is divided into four segments
by two long and one short domain
boundaries and a protrusion island is
observed near the bottom location.
Those surface features correspond to
adsorbed molecules in an amorphous
state. Third, two different orientations
of the molecular packing are identifi ed.
The stripes in the left-upper corner
are exactly 60° rotated with respect to
those in the remaining three domains,
refl ecting the impact of underneath
substrate (i.e., the 6-fold symmetry
graphite) on n-C36H74 alignment on the
surface. Figure 2 is another n-C36H74 /
graphite topography image with a larger
magnifi cation to deliver important
information at single molecular level.
It shows that the stripe width is about
4.5 nm, which is matching well with the
molecular length of n-C36H74 with a fully
extended confi guration. Furthermore,
the linear backbones (i.e., hydrocarbon
chains with an all-tans confi guration)
of individual n-C36H74 molecules are
resolved at lower part of the image.
These results unambiguously illustrate
that n-C36H74 molecules are lying
down and orderly aligned on graphite
to form a lamellar packing structure.
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- 图片：AS5600L_IM000268_1-00.PNG
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- 框图：AS5600L_BD000385_1-00.jpg
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