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Polymer Congress 2018

Polymer Sciences

ISSN: 2471-9935

Page 26

June 04-05, 2018

London, UK

4

th

Edition of International Conference on

Polymer Science and

Technology

M

any organic and hybrid thin film electronic devices (e.g.

solar cells, light emitting diodes and sensors) contain a

layer of a functional or responsive material based on a blend

of polymeric or small-molecular components. Depending on

the desired functionality, phase separation between the blend

components during solution processing is desired or not.

Predictive models that establish a link between processing

dynamics and device performance have been highly desired

to avoid trial-and-error experimentation. We study solution-

stage spinodal decomposition of such blends under

evaporative conditions using a combination of experimental

and theoretical approaches. We provide an explanation for

the decrease in the early stage spinodal wavelength under

steady solvent evaporation. Scaling relations are derived

that express the dependence of the emerging structure size

and demixing time scale on evaporation rate. Besides giving

experimental examples and summarizing our linearized theory,

this contribution provides discussion on the experimental

validation of the latter and in what way the dynamics change

if instead of only one, two blend components are non-mass

conserved. This scenario arises when water vapor condenses

as a non-solvent into an evaporating polymer solution, e.g.

during processing of thin-film memory elements based on

multifluorinated polyhydrocarbons.

Recent Publications

1. Kouijzer S et al. (2013) Predicting morphologies of

solution processed polymer: fullerene blends. J. Am.

Chem. Soc. 135(32):12057-12067.

2. Van Breemen A et al. (2015) Surface directed phase

separation of semiconductor ferroelectric polymer

blends and their use in non-volatile memories. Adv.

Func. Mater. 25(2):278-286.

3. Schaefer C, van der Schoot P and Michels J J (2015)

Structuring of polymer solutions upon solvent

evaporation. Phys. Rev. E 91(2):022602.

4. Schaefer C, Michels J J and van der Schoot P (2016)

Structuring of thin-film polymer mixtures upon solvent

evaporation. Macromolecules. 49(18):6858-6870.

5. Sharifi Dehsari H, Michels J J and Asadi K

(2017) Processing of ferroelectric polymers for

microelectronics: from morphological analysis to

functional devices. J. Mater. Chem. C. 5(40):10490-

10497.

Biography

Jasper Michels completed his PhD at the University of Twente (The Neth-

erlands) in at the Supramolecular Chemistry and Technology group of Pro-

fessor D N Reinhoudt, where he received his PhD Degree in 2001. After his

graduation he held a Postdoctoral Research position for two years in the

group of Professsor H L Anderson at Oxford University, UK. In 2003 he start-

ed working at TNO Science and Industry in Eindhoven, to join Holst Centre

in 2006 as a Senior Scientist. In the period 2006-2016 he has been mem-

ber and vice-chairman of the advisory board for IOP Self-Healing Materials

program in The Netherlands. In September 2014 he joined the Department

of Molecular Electronics at the Max Planck Institute for Polymer Research

as a Group Leader. His research activities include modeling and simulation

of phase transitions in semiconducting thin films that find applications in

organic and hybrid electronics.

michels@mpip-mainz.mpg.de

Evaporative structuring of solutions of active blends for

molecular electronics applications

Jasper Michels

Max Planck Institute for Polymer Research, Germany

Jasper Michels, Polym Sci 2018, Volume 4

DOI: 10.4172/2471-9935-C2-011

Figure 1:

Left: calculated Phase diagramof a polymer/water/solvent blendwith com-

position trajectories followed during solvent evaporation; Right: numerical simulation of

spinodal decomposition of a polymer solution under conditions of simultaneous solvent

evaporation andwater condensation.