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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

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