Studies show that dynamical properties of ultra-thin polymer films deviate from those of bulk materials. Despite some controversial issues, there is growing evidence indicating that the interfacial properties play a key role for observed dynamical anomalies. However, how and how much the interfacial properties affect the average dynamics of the nanometer scale systems are still elusive. In this work, we developed several novel techniques to investigate near-free-surface dynamics of thin polymer films. We studied surface dynamics of glassy i-PMMA films using a nano surface hole relaxation technique: a strong substrate property dependence and an unexpected molecular weight dependence were observed; we found that a local Tg of ~40K below bulk Tg could be assigned to the surface region. We used nano gold particle embedding to study PS surface dynamics: enhanced surface dynamics and weak temperature dependence were observed for the surface region; a depth profile with the nm resolution was observed; viscous liquid-like and soft solid-like properties were observed in the first 5.5nm and next 3.3 nm regions in PS films; no molecualr weight dependence was found in glassy PS films. We built a low level noise measurement system to study the thermal polarization noise in PVAc films: cooperative rearranging dynamics were evidenced; the noise power spectral density (PSD) is found to fluctuate around a certain average level without discernable peak shift; we observed some relatively big jumps or fluctuations in successive integrated PSD’s, which indicate some energy exchange between different microscopic domains in glassy polymer systems. We developed a novel nano rheology AFM technique to study the near-free-surface dynamics of thin polymer films: enhanced near-free-surface dynamics with weak temperature dependence are observed for PVAc films, which is similar with the PS case.

Studies show that dynamical properties of ultra-thin polymer films deviate from those of bulk materials. Despite some controversial issues, there is growing evidence indicating that the interfacial properties play a key role for observed dynamical anomalies. However, how and how much the interfacial properties affect the average dynamics of the nanometer scale systems are still elusive. In this work, we developed several novel techniques to investigate near-free-surface dynamics of thin polymer films. We studied surface dynamics of glassy i-PMMA films using a nano surface hole relaxation technique: a strong substrate property dependence and an unexpected molecular weight dependence were observed; we found that a local Tg of ~40K below bulk Tg could be assigned to the surface region. We used nano gold particle embedding to study PS surface dynamics: enhanced surface dynamics and weak temperature dependence were observed for the surface region; a depth profile with the nm resolution was observed; viscous liquid-like and soft solid-like properties were observed in the first 5.5nm and next 3.3 nm regions in PS films; no molecualr weight dependence was found in glassy PS films. We built a low level noise measurement system to study the thermal polarization noise in PVAc films: cooperative rearranging dynamics were evidenced; the noise power spectral density (PSD) is found to fluctuate around a certain average level without discernable peak shift; we observed some relatively big jumps or fluctuations in successive integrated PSD’s, which indicate some energy exchange between different microscopic domains in glassy polymer systems. We developed a novel nano rheology AFM technique to study the near-free-surface dynamics of thin polymer films: enhanced near-free-surface dynamics with weak temperature dependence are observed for PVAc films, which is similar with the PS case.

Les liquides confinés présentent beaucoup de comportements fascinants, très différents de ceux qui sont observés dans leur volume. Le confinement peut induire un déplacement de l'équilibre des phases (par exemple de la transition liquide-vapeur, aussi appelé condensation capillaire), il peut modifier la température de transition vitreuses des polymères, ou bien imposer un ordre dans l'arrangement moléculaire du fluide. Les modifications des propriétés mécaniques des liquides aux interfaces sont particulièrement importantes au niveau des applications. Cependant au niveau de la compréhension, le simple cas des liquides newtoniens est toujours sujet à controverse, avec d'une part des simulations numériques montrant que la viscosité ne devrait pas être modifiée pour des confinements supérieurs à quelques tailles moléculaires, et d'autre part des expériences non unanimes, montrant parfois des modifications qualitatives des propriétés rhéologiques sous confinement. Récemment nous avons montré que les méthodes d'impédance hydrodynamique en géométrie sphère-plan constituent une méthode privilégiée, non-intrusive et non-ambigüe, pour aborder la nano-mécanique des liquides aux interfaces (1,2). S'agissant d'interphases, cad de couches fluides dont les propriétés sont modifiées par la proximité d'un solide, il est possible d'accéder à leur module sans contact, donc sans la perturbation apportée par une seconde surface. S'agissant de l'effet du confinement sur la rhéologie, nous avons montré que la déformation élastique à l'échelle du pico-mètre des surfaces confinantes, donne une forte modification de la rhéologie apparente du fluide, même en l'absence de tout effet intrinsèque. Le sujet de thèse vise à mettre en oeuvre les méthodes d'impédance hydrodynamique pour étudier la rhéologie de solutions de polymères confinés. On étudiera plus précisément deux systèmes modèles d'importance fondamentale aussi bien que pratique : les brosses de polymères greffés, dont les propriétés mécaniques sont un enjeu dans les applications de lubrification aussi bien que pour les écoulements biologiques, et les solutions de polymères hydro-solubles d'intérêt pour la récupération assistée du pétrole, en vue de comprendre les effets de fluidification sous confinement et de faire la part entre modification de la viscosité et couche de déplétion induite par l'écoulement. Au niveau instrumental, un des enjeux de la thèse sera de mettre en oeuvre les mesures d'impédance hydrodynamique sur deux types d'instruments complémentaires au niveau de l'échelle de la sonde: l'appareil de mesure de forces dynamique (SFA) du Liphy, et l'AFM à détection interférométrique développé à l'Institut Néel. Ces différentes échelles d'investigation devront permettre de préciser les propriétés moyennes mécaniques moyennes des liquides confinés et leurs gradients au voisinage de la paroi. Une perspective du travail sera de mettre en regard les propriétés mécaniques et rhéologiques intrinsèques des brosses polymères déterminées directement sur SFA ou AFM, avec leur propriétés fonctionnelles: propriétés de lubrification des contacts frottants, ou de modification des écoulements des dans micro-canaux. Ceci sera poursuivi sur la plateforme expérimentale mise en place par Lionel Bureau au Liphy : SFA de friction, systèmes micro-fluidiques à visée biomimétique (parois fonctionnalisées par des brosses polymères). L'enjeu sera alors de comprendre comment les propriétés mécaniques et rhéologiques des brosses déterminent celles des systèmes dans lesquels elles interviennent. / Liquids confined present many fascinating behaviors very different from those observed in their volume. Confinement can induce a shift in the balance of phases (eg the liquid-vapor transition, also called capillary condensation), it can change the glass transition temperature of the polymer, or impose order on the molecular arrangement of fluid. The changes in the mechanical properties of liquid interfaces are particularly important in applications. However the level of understanding, the simple case of Newtonian liquids is still controversial, with one hand, numerical simulations show that the viscosity should not be changed for some higher molecular sizes containment, and secondly non-unanimous experiences, sometimes showing qualitative changes in rheological properties under confinement. Recently we have shown that the methods of hydrodynamic impedance sphere-plane geometry is a privileged, non-intrusive method and unambiguous, to discuss the mechanics of nano-liquid interfaces (1,2). As interphase, ie fluid layers whose properties are modified by the proximity of a solid, it is possible to accede their contactless module, so without the disturbance caused by a second surface.S As regards the effect of confinement on the rheology, we have shown that the elastic deformation across the pico meter of confining surfaces, gives a strong modification beyond apparent rheology of the fluid, even in the absence of any intrinsic effect. The thesis aims to implement the hydrodynamic impedance methods to study the rheology of polymer solutions confined. We specifically consider two models of fundamental importance as well as practical systems: brushes grafted polymer whose mechanical properties are an issue in lubrication applications as well as for biological flows and solutions of water-soluble polymers interest in enhanced oil recovery, in order to understand the effects of thinning containment and to distinguish between changes in viscosity and depletion layer induced by the flow. At the instrumental level, one of the challenges of the thesis is to implement the hydrodynamic impedance measurements on two complementary instruments at the level of the probe: the measuring dynamic power (SFA) of Liphy, and AFM interferometric detection developed at the Institut Néel. These different scales of investigation will help to clarify the medium average mechanical properties of liquids confined and their gradients near the wall. A view of work will be to look mechanical and rheological properties of polymer brushes intrinsic determined directly on SFA or AFM with their functional properties: lubricating properties of sliding contacts, or modification of the flow in microchannels. This will continue on the implementation by Lionel Bureau Liphy experimental platform: SFA friction advised biomimetic micro-fluidic systems (walls functionalized polymer brushes). The challenge will be to understand how the mechanical and rheological properties of brushes determine those systems in which they operate.