book of abstracts - IM2NP
book of abstracts - IM2NP
book of abstracts - IM2NP
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Z[nm]<br />
A B S T R A C T S WEDNESDAY, JUNE 30 N A N O S E A 2 0 1 0<br />
sulfonato groups (SO3-) point towards the electrophilic surface. The three<br />
oxygen atoms interact with three adjacent Si adatoms thanks to an attractive<br />
electrostatic force. However, molecules are stabilized at an equilibrium distance<br />
above the surface due to the repulsive interaction between (SO3-) and the<br />
negatively charged rest-atom.<br />
Fig.1 STM image <strong>of</strong> MSP on Si(111)-7x7surface (I=0.013 nA, V=1.7 v)<br />
3 – Conclusion:<br />
A large molecular organic paving has been achieved at room temperature by two dimensional template<br />
effects <strong>of</strong> the highly reactive Si(111)-7×7. We have demonstrated that the MSP molecules are adsorbed onto<br />
the surface by electrostatic interactions between the local charges <strong>of</strong> the Si atoms and the negative sulfonato<br />
groups.<br />
12H00-12H20<br />
Block Copolymer Self-Assembly on Nanostructured Surfaces.<br />
DIRANI Ali, DIKA Ihab, SOPPERA Olivier (Institut de Sciences des Matériaux de Mulhouse<br />
(IS2M –CNRS LRC7228) 15, rue Jean Starcky, BP 2488, 68057 MULHOUSE Cedex, France)<br />
olivier.soppera@uha.fr, ali.dirani@uha.fr<br />
Block copolymer lithography harnesses the power <strong>of</strong> chemistry to reduce feature size even further,<br />
potentially smaller than 10 nm. Block copolymers have been proposed for many applications based<br />
Image 500 nm x 500 nm<br />
Topography<br />
2<br />
1.5<br />
1<br />
0.5<br />
0<br />
0<br />
20<br />
40<br />
35 nm<br />
60<br />
80<br />
X[nm]<br />
100<br />
120<br />
Block copo<br />
PS-PMMA<br />
140<br />
160<br />
Au<br />
180<br />
300 nm<br />
principally on their ability to form regular nanometer-scale<br />
patterns. These self-assembled patterns have been considered<br />
as nanolithographic masks as well as templates for the further<br />
synthesis <strong>of</strong> inorganic or organic structures. So far, the main<br />
limitation for practical applications has been due to the lack <strong>of</strong><br />
order at long distance and much work has been done to control<br />
the self-assembly and orientation <strong>of</strong> block copolymers.<br />
Patterned substrates with length scales comparable to the<br />
natural periodicity <strong>of</strong> the block copolymer were used to<br />
control the orientation <strong>of</strong> the nanodomains <strong>of</strong> the block<br />
copolymer.<br />
Au patterns with trenches ranging from 100 to 1000 nm were<br />
prepared by DUV lithography, Au deposition and lift-<strong>of</strong>f.<br />
Block copolymer thin films were deposited on these<br />
nanopatterned substrates and annealed. They consisted in P(Sb-MMA)<br />
block copolymers with various molecular weights.<br />
The typical lateral size <strong>of</strong> the blocks was 35 nm.<br />
Image 500 nm x 500 nm<br />
Phase<br />
Image 2µm x 10 µm<br />
Phase<br />
69