TY - GEN A1 - Loebner, Sarah A1 - Jelken, Joachim A1 - Yadavalli, Nataraja Sekhar A1 - Sava, Elena A1 - Hurduc, Nicolae A1 - Santer, Svetlana T1 - Motion of adsorbed nano-particles on azobenzene containing polymer films N2 - We demonstrate in situ recorded motion of nano-objects adsorbed on a photosensitive polymer film. The motion is induced by a mass transport of the underlying photoresponsive polymer material occurring during irradiation with interference pattern. The polymer film contains azobenzene molecules that undergo reversible photoisomerization reaction from trans- to cis-conformation. Through a multi-scale chain of physico-chemical processes, this finally results in the macro-deformations of the film due to the changing elastic properties of polymer. The topographical deformation of the polymer surface is sensitive to a local distribution of the electrical field vector that allows for the generation of dynamic changes in the surface topography during irradiation with different light interference patterns. Polymer film deformation together with the motion of the adsorbed nano-particles are recorded using a homemade set-up combining an optical part for the generation of interference patterns and an atomic force microscope for acquiring the surface deformation. The particles undergo either translational or rotational motion. The direction of particle motion is towards the topography minima and opposite to the mass transport within the polymer film. The ability to relocate particles by photo-induced dynamic topography fluctuation offers a way for a non-contact simultaneous manipulation of a large number of adsorbed particles just in air at ambient conditions. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 352 KW - motion of adsorbed nano-particles KW - azobenzene containing polymer films KW - fluctuating surfaces Y1 - 2017 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-400423 ER - TY - JOUR A1 - Loebner, Sarah A1 - Jelken, Joachim A1 - Yadavalli, Nataraja Sekhar A1 - Sava, Elena A1 - Hurduc, Nicolae A1 - Santer, Svetlana T1 - Motion of Adsorbed Nano-Particles on Azobenzene Containing Polymer Films JF - Molecules N2 - We demonstrate in situ recorded motion of nano-objects adsorbed on a photosensitive polymer film. The motion is induced by a mass transport of the underlying photoresponsive polymer material occurring during irradiation with interference pattern. The polymer film contains azobenzene molecules that undergo reversible photoisomerization reaction from trans-to cis-conformation. Through a multi-scale chain of physico-chemical processes, this finally results in the macro-deformations of the film due to the changing elastic properties of polymer. The topographical deformation of the polymer surface is sensitive to a local distribution of the electrical field vector that allows for the generation of dynamic changes in the surface topography during irradiation with different light interference patterns. Polymer film deformation together with the motion of the adsorbed nano-particles are recorded using a homemade set-up combining an optical part for the generation of interference patterns and an atomic force microscope for acquiring the surface deformation. The particles undergo either translational or rotational motion. The direction of particle motion is towards the topography minima and opposite to the mass transport within the polymer film. The ability to relocate particles by photo-induced dynamic topography fluctuation offers a way for a non-contact simultaneous manipulation of a large number of adsorbed particles just in air at ambient conditions. KW - motion of adsorbed nano-particles KW - azobenzene containing polymer films KW - fluctuating surfaces Y1 - 2016 U6 - https://doi.org/10.3390/molecules21121663 SN - 1420-3049 VL - 21 SP - 397 EP - 411 PB - MDPI CY - Basel ER - TY - JOUR A1 - Jelken, Joachim A1 - Santer, Svetlana T1 - Light induced reversible structuring of photosensitive polymer films JF - RSC Advances N2 - In this paper we report on photoswitchable polymer surfaces with dynamically and reversibly fluctuating topographies. It is well known that when azobenzene containing polymer films are irradiated with optical interference patterns the film topography changes to form a surface relief grating. In the simplest case, the film shape mimics the intensity distribution and deforms into a wave like, sinusoidal manner with amplitude that may be as large as the film thickness. This process takes place in the glassy state without photo-induced softening. Here we report on an intriguing discovery regarding the formation of reliefs under special illumination conditions. We have developed a novel setup combining the optical part for creating interference patterns, an AFM for in situ acquisition of topography changes and diffraction efficiency signal measurements. In this way we demonstrate that these gratings can be “set in motion” like water waves or dunes in the desert. We achieve this by applying repetitive polarization changes to the incoming interference pattern. Such light responsive surfaces represent the prerequisite for providing practical applications ranging from conveyer or transport systems for adsorbed liquid objects and colloidal particles to generation of adaptive and dynamic optical devices. KW - surface-relief gratings KW - induced deformation KW - mass-transport KW - azobenzene elastomers KW - thin-films KW - birefringence KW - roughness KW - network KW - erasure Y1 - 2019 U6 - https://doi.org/10.1039/C9RA02571E SN - 2046-2069 VL - 9 IS - 35 SP - 20295 EP - 20305 PB - RSC Publishing CY - London ER - TY - GEN A1 - Jelken, Joachim A1 - Santer, Svetlana T1 - Light induced reversible structuring of photosensitive polymer films T2 - Postprints der Universität Potsdam Mathematisch-Naturwissenschaftliche Reihe N2 - In this paper we report on photoswitchable polymer surfaces with dynamically and reversibly fluctuating topographies. It is well known that when azobenzene containing polymer films are irradiated with optical interference patterns the film topography changes to form a surface relief grating. In the simplest case, the film shape mimics the intensity distribution and deforms into a wave like, sinusoidal manner with amplitude that may be as large as the film thickness. This process takes place in the glassy state without photo-induced softening. Here we report on an intriguing discovery regarding the formation of reliefs under special illumination conditions. We have developed a novel setup combining the optical part for creating interference patterns, an AFM for in situ acquisition of topography changes and diffraction efficiency signal measurements. In this way we demonstrate that these gratings can be “set in motion” like water waves or dunes in the desert. We achieve this by applying repetitive polarization changes to the incoming interference pattern. Such light responsive surfaces represent the prerequisite for providing practical applications ranging from conveyer or transport systems for adsorbed liquid objects and colloidal particles to generation of adaptive and dynamic optical devices. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 750 KW - surface-relief gratings KW - induced deformation KW - mass-transport KW - azobenzene elastomers KW - thin-films KW - birefringence KW - roughness KW - network KW - erasure Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-436432 SN - 1866-8372 IS - 750 SP - 20295 EP - 20305 ER - TY - JOUR A1 - Jelken, Joachim A1 - Pandiyarajan, Chinnayan Kannan A1 - Genzer, Jan A1 - Lomadze, Nino A1 - Santer, Svetlana T1 - Fabrication of flexible hydrogel sheets featuring periodically spaced circular holes with continuously adjustable size in realtime JF - ACS applied materials & interfaces N2 - We report on the formation of stimuli-responsive structured hydrogel thin films whose pattern geometry can be adjusted on demand and tuned reversibly by varying solvent quality or by changing temperature. The hydrogel films, similar to 100 nm in thickness, were prepared by depositing layers of random copolymers comprising N-isopropylacrylamide and ultraviolet (UV)-active methacryloyloxybenzophenone units onto solid substrates. A two-beam interference pattern technique was used to cross-link the selected areas of the film; any unreacted material was extracted using ethanol after UV light-assisted cross-linking. In this way, we produced nanoholes, perfectly ordered structures with a narrow size distribution, negligible tortuosity, adjustable periodicity, and a high density. The diameter of the circular holes ranged from a few micrometers down to several tens of nanometers; the hole periodicity could be adjusted readily by changing the optical period of the UV interference pattern. The holes were reversibly closed and opened by swelling/deswelling the polymer networks in the presence of ethanol and water, respectively, at various temperatures. The reversible regulation of the hole diameter can be repeated many times within a few seconds. The hydrogel sheet with circular holes periodically arranged may also be transferred onto different substrates and be employed as tunable templates for the deposition of desired substances. KW - photosensitive polymers KW - PNIPAm KW - hydrogels KW - UV cross-linking KW - stimuli-responsive structured polymer films KW - azobenzene-containing molecules Y1 - 2018 U6 - https://doi.org/10.1021/acsami.8b09580 SN - 1944-8244 VL - 10 IS - 36 SP - 30844 EP - 30851 PB - American Chemical Society CY - Washington ER - TY - JOUR A1 - Jelken, Joachim A1 - Henkel, Carsten A1 - Santer, Svetlana T1 - Polarization controlled fine structure of diffraction spots from an optically induced grating JF - Applied physics letters N2 - We report on the remote control of the fine structure of a diffraction spot from optically induced dual gratings within a photosensitive polymer film. The material contains azobenzene in the polymer side chains and develops a surface relief under two-beam holographic irradiation. The diffraction of a polarized probe beam is sensitive to the orientation of the azobenzene groups forming a permanently stored birefringence grating within the film. We demonstrate that the fine structure of the probe diffraction spot switches from a Gaussian to a hollow or a hollow to a "Saturn"-like structure by a change in polarization. This makes it potentially useful in photonic devices because the beam shape can be easily inverted by an external stimulus. Y1 - 2020 U6 - https://doi.org/10.1063/1.5140067 SN - 0003-6951 SN - 1077-3118 VL - 116 IS - 5 PB - American Institute of Physics CY - Melville ER - TY - JOUR A1 - Jelken, Joachim A1 - Henkel, Carsten A1 - Santer, Svetlana T1 - Solving an old puzzle: fine structure of diffraction spots from an azo-polymer surface relief grating JF - Applied physics : B, Lasers and optics N2 - We report on the experimental and theoretical interpretation of the diffraction of a probe beam during inscription of a surface relief grating with an interference pattern into a photo-responsive polymer film. For this, we developed a set-up allowing for the simultaneous recording of the diffraction efficiency (DE), the fine structure of the diffraction spot and the topographical changes, in situ and in real time while the film is irradiated. The time dependence of the DE, as the surface relief deepens, follows a Bessel function exhibiting maxima and minima. The size of the probe beam relative to the inscribed grating (i.e., to the size of the writing beams) matters and has to be considered for the interpretation of the DE signal. It is also at the origin of a fine structure within the diffraction spot where ring-shaped features appear once an irradiation time corresponding to the first maximum of the DE has been exceeded. Y1 - 2019 U6 - https://doi.org/10.1007/s00340-019-7331-8 SN - 0946-2171 SN - 1432-0649 VL - 125 IS - 11 PB - Springer CY - Heidelberg ER - TY - JOUR A1 - Jelken, Joachim A1 - Henkel, Carsten A1 - Santer, Svetlana T1 - Formation of half-period surface relief gratings in azobenzene containing polymer films JF - Applied physics : B, Lasers and optics N2 - We study the peculiar response of photo-sensitive polymer films irradiated with a certain type of interference pattern where one interfering beam is S-polarized, while the second one is P-polarized. The polymer film, although in a glassy state, deforms following the local polarization distribution of the incident light, and a surface relief grating (SRG) appears whose period is half the optical one. All other types of interference patterns result in the matching of both periods. The topographical response is triggered by the alignment of photo-responsive azobenzene containing polymer side chains orthogonal to the local electrical field, resulting in a bulk birefringence grating (BBG). We investigate the process of dual grating formation (SRG and BBG) in a polymer film utilizing a dedicated set-up that combines probe beam diffraction and atomic force microscopy (AFM) measurements, and permits acquiring in situ and in real-time information about changes in local topography and birefringence. We find that the SRG maxima appear at the positions of linearly polarized light (tilted by 45 degrees relative to the grating vector), causing the formation of the half-period topography. This permits to inscribe symmetric and asymmetric topography gratings with sub-wavelength period, while changing only slightly the polarization of one of the interfering beams. We demonstrate an easy generation of sawtooth profiles (blazed gratings) with adjustable shape. With these results, we have taken a significant step in understanding the photo-induced deformation of azo-polymer films. Y1 - 2020 U6 - https://doi.org/10.1007/s00340-020-07500-w SN - 0946-2171 SN - 1432-0649 VL - 126 IS - 9 PB - Springer CY - Heidelberg ER - TY - THES A1 - Jelken, Joachim T1 - Surface relief and bulk birefringence gratings in photo-sensitive polymer films T1 - Realzeit Observierung der Entstehung von Volumen- und Oberflächengittern in photosensitiven Polymerfilmen mittels der Rasterkraftmikroskopie und Messung der Beugungseffizienz BT - in-situ probing and manipulation in real time N2 - This thesis is focused on a better understanding of the formation mechanism of bulk birefringence gratings (BBG) and a surface relief gratings (SRG) in photo-sensitive polymer films. A new set-up is developed enabling the in situ investigation how the polymer film is being structured during irradiation with modulated light. The new aspect of the equipment is that it combines several techniques such as a diffraction efficiency (DE) set-up, an atomic force microscope (AFM) and an optical set-up for controlled illumination of the sample. This enables the simultaneous acquiring and differentiation of both gratings (BBG and SRG), while changing the irradiation conditions in desired way. The dissertation is based on five publications. The first publication (I) is focused on the description of the set-up and interpretation of the measured data. A fine structure within the 1st-order diffraction spot is observed, which is a result of the inhomogeneity of the inscribed gratings. In the second publication (II) the interplay of BBG and SRG in the DE is discussed. It has been found, that, dependent on the polarization of a weak probe beam, the diffraction components of the SRG and BBG either interfere constructively or destructively in the DE, altering the appearance of the intensity distribution within the diffracted spot. The third (III) and fourth (IV) publications describe the light-induced reconfiguration of surface structures. Special attention is payed to conditions influencing the erasure of topography and bulk gratings. This can be achieved via thermal treatment or illumination of the polymer film. Using the translation of the interference pattern (IP) in a controlled way, the optical erase speed is significantly increased. Additionally, a dynamic reconfigurable surface is generated, which could move surface attached objects by the continuous translation of the interference pattern during irradiation of the polymer films. The fifth publication (V) deals with the understanding of polymer deformation under irradiation with SP-IP, which is the only IP generating a half-period topography grating (compared to the period of the IP) on the photo-sensitive polymer film. This mechanism is used, e.g. to generate a SRG below the diffraction limit of light. It also represents an easy way of changing the period of the surface grating just by a small change in polarization angle of the interfering beams without adjusting the optical pass of the two beams. Additionally, complex surface gratings formed in mixed polarization- and intensity interference patterns are shown. I J. Jelken, C. Henkel and S. Santer, Applied Physics B, 125 (2019), 218 II J. Jelken, C. Henkel and S. Santer, Appl. Phys. Lett., 116 (2020), 051601 III J. Jelken and S. Santer, RSC Advances, 9 (2019), 20295 IV J. Jelken, M. Brinkjans, C. Henkel and S. Santer, SPIE Proceedings, 11367 (2020), 1136710 V J. Jelken, C. Henkel and S. Santer, Formation of Half-Period Surface Relief Gratings in Azobenzene Containing Polymer Films (submitted to Applied Physics B) N2 - In dieser kumulativen Dissertation, basierend auf fünf Publikationen, geht es darum ein Verständnis über die grundlegenden Mechanismen zu entwickeln, welche hinter der Entstehung von Oberflächen- und Volumengittern in amorphen photo-sensitiven Polymerfilmen stehen. Hierzu wurde ein neuer Versuchsaufbau entwickelt, welcher in situ (d.h. während der Belichtung mit einem Interferenzgitter) Messungen der zeitlichen Entwicklung (Entstehung oder Löschung) von Volumen- als auch Oberflächengittern unabhängig voneinander ermöglicht. Dies stellt einen erheblichen Vorteil gegenüber dem gängigen Verfahren der Beugungseffizienzmessung dar, weil dort die Anteile der beiden Gitter durch aufwendige mathematische Behandlung voneinander getrennt werden müssen. Hierzu wurde ein Rasterkraftmikroskop (AFM, atomic force microscope) in einen optischen Aufbau zur Erzeugung eines Interferenzgitters, welches zur Belichtung des Polymerfilms benutzt wird, integriert. Zusätzlich wurde außerdem die Beugung eines Sondenstrahls an den entstehenden Gittern detektiert. Die erste Publikation (I) beschäftigt sich mit der grundsätzlichen Interpretation der mit diesem neuen Messaufbau erzielten Ergebnisse. Es wurde eine Feinstruktur in dem räumlichen Profil der ersten Beugungsordnung gemessen, deren Ursprung aus der Inhomogenität der erzeugten Gitter herrührt. In der zweiten Publikation (II) wird die Kopplung von Oberflächen- und Volumengitter in der aufgezeichneten Beugungseffizienz untersucht. Es wird gezeigt, dass, abhängig von der Polarisation des Sondierungsstrahls, diese Kopplung sowohl konstruktiv als auch destruktiv sein kann, was auch die in der ersten Publikation beschriebene Feinstruktur beeinflusst. Die dritte (III) und vierte (IV) Publikation beschäftigen sich mit dem dynamischen Umbau von Oberflächenstrukturen. Hierzu muss das erzeugte Oberflächengitter möglichst schnell wieder gelöscht werden können. Dies kann sowohl thermisch, als auch optisch erfolgen. Durch eine definierte Translation des Interferenzgitters konnte hier die optische Löschgeschwindigkeit signifikant gesteigert werden. Zum anderen wird auch die Möglichkeit des Transports oberflächenadsorbierter Objekte durch die Erzeugung einer dynamisch modulierten Oberfläche (mittels einer kontinuierlichen Translation des Interferenz- und dadurch des Oberflächengitters) aufgezeigt. Die Hypothese des Massentransports wird hierbei kritisch untersucht. Die fünften Publikation (V) widmet sich dem SP-Interferenzgitter, welches als einziges Gitter eine Periode der Oberflächenstruktur ausbildet, die der Hälfte der Periode des optischen Interferenzgitters entspricht. Diese Eigenschaft kann zum einen für die Erzeugung von Oberflächengittern unterhalb der optischen Auflösungsgrenze benutzt werden, zum anderen erlaubt sie die Periode der Oberflächenstruktur einfach zu ändern, indem die Beleuchtung zu einem anderen Interferenzgitter geschaltet wird. Zusätzlich wird auch die Erzeugung von komplexen Oberflächengittern durch Misch-Interferenzgitter (Mischung aus Polarisations- und Intensitäts-Interferenzgitter) diskutiert. I J. Jelken, C. Henkel and S. Santer, Applied Physics B, 125 (2019), 218 II J. Jelken, C. Henkel and S. Santer, Appl. Phys. Lett., 116 (2020), 051601 III J. Jelken and S. Santer, RSC Advances, 9 (2019), 20295 IV J. Jelken, M. Brinkjans, C. Henkel and S. Santer, SPIE Proceedings, 11367 (2020), 1136710 V J. Jelken, C. Henkel and S. Santer, Formation of Half-Period Surface Relief Gratings in Azobenzene Containing Polymer Films (eingereicht bei Applied Physics B) KW - photosensitive Polymer KW - Surface Relief Grating (SRG) KW - sub-diffraction gratings KW - azobenzene containing molecules KW - Atomic Force Microscope KW - diffraction efficiency KW - photo-structuring of polymer films KW - Rasterkraftmikroskopie KW - Beugungseffizienz KW - Oberflächengitter KW - Azobenzol enthaltende Moleküle KW - Photostrukturierung von Polymerfilmen KW - Photopolymer Y1 - 2020 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-483988 ER - TY - JOUR A1 - Bekir, Marek A1 - Jelken, Joachim A1 - Jung, Se-Hyeong A1 - Pich, Andrij A1 - Pacholski, Claudia A1 - Kopyshev, Alexey A1 - Santer, Svetlana T1 - Dual responsiveness of microgels induced by single light stimulus JF - Applied physics letters N2 - We report on the multiple response of microgels triggered by a single optical stimulus. Under irradiation, the volume of the microgels is reversibly switched by more than 20 times. The irradiation initiates two different processes: photo-isomerization of the photo-sensitive surfactant, which forms a complex with the anionic microgel, rendering it photo-responsive; and local heating due to a thermo-plasmonic effect within the structured gold layer on which the microgel is deposited. The photo-responsivity is related to the reversible accommodation/release of the photo-sensitive surfactant depending on its photo-isomerization state, while the thermo-sensitivity is intrinsically built in. We show that under exposure to green light, the thermo-plasmonic effect generates a local hot spot in the gold layer, resulting in the shrinkage of the microgel. This process competes with the simultaneous photo-induced swelling. Depending on the position of the laser spot, the spatiotemporal control of reversible particle shrinking/swelling with a predefined extent on a per-second base can be implemented. Y1 - 2021 U6 - https://doi.org/10.1063/5.0036376 SN - 0003-6951 SN - 1077-3118 VL - 118 IS - 9 PB - American Institute of Physics CY - Melville ER - TY - JOUR A1 - Arya, Pooja A1 - Jelken, Joachim A1 - Lomadze, Nino A1 - Santer, Svetlana A1 - Bekir, Marek T1 - Kinetics of photo-isomerization of azobenzene containing surfactants JF - The journal of chemical physics : bridges a gap between journals of physics and journals of chemistry N2 - We report on photoisomerization kinetics of azobenzene containing surfactants in aqueous solution. The surfactant molecule consists of a positively charged trimethylammonium bromide head group, a hydrophobic spacer connecting via 6 to 10 CH2 groups to the azobenzene unit, and the hydrophobic tail of 1 and 3CH(2) groups. Under exposure to light, the azobenzene photoisomerizes from more stable trans- to metastable cis-state, which can be switched back either thermally in dark or by illumination with light of a longer wavelength. The surfactant isomerization is described by a kinetic model of a pseudo first order reaction approaching equilibrium, where the intensity controls the rate of isomerization until the equilibrated state. The rate constants of the trans-cis and cis-trans photoisomerization are calculated as a function of several parameters such as wavelength and intensity of light, the surfactant concentration, and the length of the hydrophobic tail. The thermal relaxation rate from cis- to trans-state is studied as well. The surfactant isomerization shows a different kinetic below and above the critical micellar concentration of the trans isomer due to steric hindrance within the densely packed micelle but does not depend on the spacer length. KW - genomic DNA conformation KW - water-interface KW - light photocontrol KW - driven KW - manipulation KW - photoisomerization KW - molecules Y1 - 2020 U6 - https://doi.org/10.1063/1.5135913 SN - 0021-9606 SN - 1089-7690 VL - 152 IS - 2 PB - American Institute of Physics CY - Melville ER - TY - JOUR A1 - Arya, Pooja A1 - Jelken, Joachim A1 - Feldmann, David A1 - Lomadze, Nino A1 - Santer, Svetlana T1 - Light driven diffusioosmotic repulsion and attraction of colloidal particles JF - The journal of chemical physics : bridges a gap between journals of physics and journals of chemistr N2 - In this paper, we introduce the phenomenon of light driven diffusioosmotic long-range attraction and repulsion of porous particles under irradiation with UV light. The change in the inter-particle interaction potential is governed by flow patterns generated around single colloids and results in reversible aggregation or separation of the mesoporous silica particles that are trapped at a solid surface. The range of the interaction potential extends to several times the diameter of the particle and can be adjusted by varying the light intensity. The "fuel" of the process is a photosensitive surfactant undergoing photo-isomerization from a more hydrophobic trans-state to a rather hydrophilic cis-state. The surfactant has different adsorption affinities to the particles depending on the isomerization state. The trans-isomer, for example, tends to accumulate in the negatively charged pores of the particles, while the cis-isomer prefers to remain in the solution. This implies that when under UV irradiation cis-isomers are being formed within the pores, they tend to diffuse out readily and generate an excess concentration near the colloid's outer surface, ultimately resulting in the initiation of diffusioosmotic flow. The direction of the flow depends strongly on the dynamic redistribution of the fraction of trans- and cis-isomers near the colloids due to different kinetics of photo-isomerization within the pores as compared to the bulk. The unique feature of the mechanism discussed in the paper is that the long-range mutual repulsion but also the attraction can be tuned by convenient external optical stimuli such as intensity so that a broad variety of experimental situations for manipulation of a particle ensemble can be realized. Y1 - 2020 U6 - https://doi.org/10.1063/5.0007556 SN - 0021-9606 SN - 1089-7690 VL - 152 IS - 19 PB - American Institute of Physics CY - Melville, NY ER -