Chapter 3. Microscopic mechanisms at the origin of the photo-induced deformation inazobenzene-containing thin <strong>films</strong> 92experiments with different assisting beam intensities. In order to vary the polarizationmodulation from zero we consider the case of p-assisted s-polarized interference for whichthere is no modulation of the polarization when the assisting beam is off (see 3.4.1).In Figure 3.27 we show the deformation kinetics obtained on a sol-gel sample 19 (quantitativedata are reported in Table 3.3) for different power densities of the p-polarizedassisting beam, while the s-polarized interfering beams have always the same powerdensity of 1 mW/mm 2 per beam. In this experiment, the interfering and the assistingbeams are switched on simultaneously at t = 0, in order to measure the full evolution ofthe assisted photoinduced deformation. The growth rate is the slope of the deformationkinetics: for the matrix photoexpansion mechanism it is measured at t = 0, while forthe mass migration mechanism it is measured over the first 100 s of irradiation, duringwhich the deformation amplitude is quasi-linear.pastel-00527388, version 1 - 19 Oct 2010With no assisting beam (Figure 3.27(a)), the photoinduced deformation is only dueto photoexpansion, which is characterized by a high rate and a low efficiency with a maximumdeformation of ≃ 7 nm. Using 0.4 mW p-polarized assisting beam (Figure 3.27(b))is sufficient to activate the matter migration with a low SRG growth rate of 0.04 nm/s.In this case, as the light intensity contrast 20 is ≃ 90%, we measure a smaller deformationdue to the photoexpansion (≃ 4 nm). When increasing the intensity of the assistingbeam (hence reducing the contrast), the photoexpansion contribution to the deformationvanishes (it almost disappears in (d) where the optical contrast is ≃ 78%), while mattermigration is more and more efficient (d-f). At the maximum power density availablefor the assisting beam, 2.1 mW/mm 2 , where the ratio between the assisting and theincident beams power densities is ≃ 1, we obtain a higher SRG growth rate of 2.1 nm/s.Let us define the spatial modulation of the polarization as E pol = min{E‖ 0 , E0 ⊥ } (byanalogy with section 3.3.2). The parallel component is provided only by the assistingbeam 21 (E‖0 = √ I assist ) while the perpendicular component is given by the interferingbeams (E⊥ 0 = √ I interf ). For assisting beam intensities smaller than the intensity interferencepattern amplitude, we have: E pol = E‖ 0 = √ I assist . So, we expect that the efficiencyof the SRG formation increases as √ I assist .In Figure 3.28 we compare the SRG growth rate experimentally observed (□) andthe corresponding values of √ I assist .The close correlation between the experimental19 In this experiment we used a 450 nm thick sol-gel sample, as we wanted to better discriminatebetween the photoexpansion and the matter migration mechanisms. As shown in [9], the photoexpansionmechanism is dependent on the thickness, while [15] matter migration efficiency doesn’t significantlychange using a 200 nm or a 450 nm thick sample.20 Defined asImax − IminI max, where I max and I min are the maximum and the minimum intensity valuesof the total light field.21 We recall that the p-polarized assisting beam is in normal incidence on the sample.
Chapter 3. Microscopic mechanisms at the origin of the photo-induced deformation inazobenzene-containing thin <strong>films</strong> 93pastel-00527388, version 1 - 19 Oct 2010a)b)c)d)e)f)deformation amplitude (nm)A (nm)deformation amplitude (nm)A (nm)deformation amplitude (nm)A (nm)deformation amplitude (nm)A (nm)deformation amplitude (nm)A (nm)deformation amplitude (nm)A (nm)4030201004030201004030201004030201004030201004030201000 100 200time (s)20081205_130 100 200time (s)20081205_150 100 200time (s)20081205_70 100 200time (s)20081205_80 100 200time (s)20081205_90 100 200time (s)time (s))#*"20081205_1100000deformation growth rate speed (nm/s) (nm/s) deformation growth rate speed (nm/s) (nm/s) deformation growth rate speed (nm/s) (nm/s) deformation growth rate speed (nm/s) (nm/s) deformation growth rate speed (nm/s) (nm/s) deformation growth rate speed (nm/s) (nm/s)0,60,40,20-1 0 1 2 3single = P photoexp.beam power (mW/mm 2 )0,60,40,20-1 0 1 2 3single = P mass beam power migr. (mW/mm 2 )0,60,40,20-1 0 1 2 3single P beam power (mW/mm 2 )0,60,40,20-1 0 1 2 30,60,40,2!"#$%## &"0.4 mW%## &0.7 mW%## &1.1 mW%## &single P beam power (mW/mm 2 )0-1 0 1 2 30,60,40,21.7 mW%## &single P beam power (mW/mm 2 )&'("#$%## & "0-1 0 1 2 3single P beam power (mW/mmassisting beam2 )(mW/mm 2 )DEFORMATION AMPLITUDE OPTICS TOPOGRAPHY GROWTH RATEFigure 3.27: p-assisted s-polarized interfering beams: dependence of the photodeformationmechanisms on the assisting beam power density. Interfering beams’ powerdensity: 1 mW/mm 2 per beam (λ = 473 nm; assisting beam (λ = 532 nm): (a) 0,(b) 0.4, (c) 0.7, (d) 1.1, (e) 1.7, (f) 2.1 mW/mm 2 . From the top to the bottom: thephotoinduced deformation corresponding to various p-polarized beam power densities(mW/mm 2 ). From left to right : the kynetics of the grating formation, the optical nearfieldimage and the corresponding shear-force topography image (x-range = 5 µm). TheSRG growth rate is reported in the last column on the right: squares indicate the SRGgrowth rate due to photoexpansion, while circ<strong>les</strong> indicate the SRG growth rate due tomatter migration (in each plot are reported in grey the values of the previous cases, forcomparison).
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Thèse de doctorat de l’Ecole Pol
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AcknowledgementsAt the beginning it
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vpastel-00527388, version 1 - 19 Oc
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ContentsAbstractiAcknowledgementsii
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List of Figures1.1 The trans/cis ph
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List of Figuresxiipastel-00527388,
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Introduction 2In this work, we stud
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Bibliography[1] A. Natansohn, P. Ro
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Introduction 6azobenzene-containing
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"##$%&'()')*#'+(%,-.(/#'011'2'"(%)(
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Chapter 1. The azobenzene molecules
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Chapter 1. The azobenzene molecules
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Chapter 1. The azobenzene molecules
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Chapter 1. The azobenzene molecules
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Chapter 1. The azobenzene molecules
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Chapter 1. The azobenzene molecules
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Chapter 1. The azobenzene molecules
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Chapter 2. Experimental setup and s
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Chapter 5. Nanostructured hybrid sy
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Chapter 5. Nanostructured hybrid sy
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Bibliography[1] A. Natansohn, P. Ro
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Conclusionspastel-00527388, version
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Bibliography[1] Chi-Ming Che et Al.
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Appendix A 156⎛ ⎞ ⎛n g sinθ
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Appendix A 158hence for each compon
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Appendix BPhotoisomerization dynami
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Appendix B 162( 1Since λ 2 = −(
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Appendix C 164L = 5000 nmu = 1 nmL!
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Appendix D 166n. light power densit
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Bibliography 170azobenzene-containi
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Bibliography 172as estimated from a
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Bibliography 174[53] C. Barrett, A.