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Philipp Gutfreund

Publications and source records attributed to Philipp Gutfreund.

14 recordsLinked to original sources

Towards real-time surrogate-free Bayesian inversion for neutron reflectometry

Neutron reflectometry (NR) is a key enabling technology for many areas of scientific development. Although the forward reflectivity model is well-known, inferring the physical properties of a sample from NR data requires the solution of an inverse problem. Increasingly, beamline scientists are using NR in fast kinetic configurations and probing highly-complex structures and interfaces, introducing significant uncertainty. Existing uncertainty quantification (UQ) approaches in NR, such as Markov-Chain Monte-Carlo (MCMC), suffer from poor sample efficiency and slow convergence times. Recently, surrogate machine learning models have been proposed as an alternative. However, physical intuition is lost when replacing governing equations with fast surrogates. Instead, we propose a rapid, surrogate-free Bayesian inversion for NR. Our approach offers a step-change in inference speed and efficiency. For the first time in NR, exact gradients through the reflectivity are computed, enabling highly performant gradient-based inference schemes: Hamiltonian Monte-Carlo offers significant advances in sample efficiency compared to MCMC. Variational inference enables approximate UQ on the order of seconds rather than hours. We demonstrate state-of-the-art performance on a thick oxide quartz film, and robust co-fitting performance in the high complexity regime of organic LED multilayer devices. Additionally, we provide an open-source library of reflectometry kernels in the python language.

cs.LG

Neutron reflectometry on superspreading and non-superspreading trisiloxane surfactants

Certain trisiloxane surfactants have the remarkable property of being able to superspread: Small volumes of water rapidly wet large areas of hydrophobic surfaces. The molecular properties of the surfactants which govern this technologically relevant effect are still under debate. To gain a deeper understanding, the surfactant behaviour during the spreading process needs to be studied at molecular length scales. Here, we present neutron reflectivity analyses of two trisiloxane surfactants of similar chemical structure, of which only one exhibits superspreading properties. We present an approach to determining the composition of the adsorbed surfactant layer in spread surfactant films at the solid-liquid interface, accounting for contributions from attenuated back-reflections of the neutron beam in films with thicknesses in the range of several tens to hundreds of micrometers. Differences between superspreading and non-superspreading surfactants with regard to their volume fraction profiles at the solid/liquid interface obtained in the self-consistent analysis of the reflectivity curves are in agreement with a simple explanation of the difference in spreading behaviour based on thermodynamics.

cond-mat.soft

Near surface concentration profile of sheared semi-dilute polymer solutions

Controlling the structure of polymer solutions near a solid surface is crucial for many industrial processes, as it significantly impacts solution flow and influences slip at the interface. To date, only a few techniques have been developed to experimentally investigate this type of interface at the nanometric scale of solid/liquid interaction. In this study, we probe the interface between a smooth sapphire surface and a semi-diluted polystyrene solution, using neutron reflectivity. A special setup for flow measurements under shear has been designed and optimized. Our results show that, at rest, polymer chains are globally depleted from the solid surface. Contrary to common assumptions, some polystyrene chains do adsorb onto the wall. Under flow conditions, we experimentally demonstrate that the depletion layer remains stable, a finding that has been hypothesized but only vaguely confirmed in the literature.

cond-mat.soft

Photo-Switchable Surfactants for Responsive Air-Water Interfaces: Azo vs. Arylazopyrazole Amphiphiles

Arylazopyrazoles (AAPs) as substitutes for azo derivatives have gained considerable attention due to their superior properties offering E/Z photo-isomerization with high yield. In order to compare and quantify their performance, azobenzene tetraethylammonium (Azo-TB) and arylazopyrazole tetraethylammonium (AAP-TB) bromides were synthesized and characterized in the bulk (water) using NMR spectroscopy. At the air-water interface complementary information from vibrational sum-frequency generation (SFG) spectroscopy and neutron reflectometry (NR) has revealed the effects of E/Z isomerization in great detail. In bulk water the photostationary states of >89% for E/Z switching in both directions were very similar for the surfactants, while their interfacial behavior was substantially different. In particular, the surface excess $Γ$ of the surfactants changed drastically between E/Z isomers for AAP-TB (maximum change of $Γ$: 2.15 $μ$mol/m$^2$); for Azo-TB the change was only moderate (maximum change of $Γ$: 1.02 $μ$mol/m$^2$). Analysis of SFG spectra revealed that strong non-resonant contributions that heterodyned the resonant vibrational bands were proportional to $Γ$, enabling the aromatic C-H band to be interpreted as an indicator for changes in interfacial molecular order. Close comparison of $Γ$ from NR with the SFG amplitude from the aromatic C-H stretch as a function of concentrations and E/Z conformation revealed substantial molecular order changes for AAP-TB. In contrast, only $Γ$ and not the molecular order varied for Azo-TB. These differences in interfacial properties are attributed to the molecular structure of the AAP center that enables favorable lateral interactions at the air-water interface, causing closed-packed interfacial layers and substantial changes during E/Z photo-isomerization.

cond-mat.soft

The viscoelastic signature underpinning polymer deformation under shear flow

Entangled polymers are deformed by a strong shear flow. The shape of the polymer, called the form factor, is measured by small angle neutron scattering. However, the real-space molecular structure is not directly available from the reciprocal-space data, due to the phase problem. Instead, the data has to be fitted with a theoretical model of the molecule. We approximate the unknown structure using piecewise straight segments, from which we derive an analytical form factor. We fit it to our data on a semi-dilute entangled polystyrene solution under in situ shear flow. The character of the deformation is shown to lie between that of a single ideal chain (viscous) and a cross-linked network (elastic rubber). Furthermore, we use the fitted structure to estimate the mechanical stress, and find a fairly good agreement with rheology literature.

cond-mat.soft

Shear deformation of low-density polymer brushes in a good solvent

Self-consistent field approach is used to model a single end-tethered polymer chain on a substrate subject to various forces in three dimensions. Starting from a continuous Gaussian chain model, the following perturbations are considered: (i) hydrodynamic interaction with an externally imposed shear flow for which a new theoretical framework is formulated; (ii) excluded volume effect in a good solvent, treated in a mean field approximation; (iii) monomer-substrate repulsion. While the chain stretches along the flow, the change of the density profile perpendicular to the substrate is negligible for any reasonable simulation parameters. This null effect is in agreement with multiple neutron scattering studies.

physics.comp-ph

Dynamical structure of entangled polymers simulated under shear flow

The non-linear response of entangled polymers to shear flow is complicated. Its current understanding is framed mainly as a rheological description in terms of the complex viscosity. However, the full picture requires an assessment of the dynamical structure of individual polymer chains which give rise to the macroscopic observables. Here we shed new light on this problem, using a computer simulation based on a blob model, extended to describe shear flow in polymer melts and semi-dilute solutions. We examine the diffusion and the intermediate scattering spectra during a steady shear flow. The relaxation dynamics are found to speed up along the flow direction, but slow down along the shear gradient direction. The third axis, vorticity, shows a slowdown at the short scale of a tube, but reaches a net speedup at the large scale of the chain radius of gyration.

physics.comp-ph

Towards generalized data reduction on a chopper-based time-of-flight neutron reflectometer

The calculation of neutron reflectivity from raw time-of-flight data including instrumental corrections as well as improved resolution calculation is presented. The theoretical calculations are compared to experimental data measured on the vertical sample plane reflectometer D17 and the horizontal sample plane reflectometer FIGARO at the Institut Laue-Langevin, Grenoble, France (ILL). This article comprises the mathematical body of the time-of-flight reflectivity data reduction software COSMOS which is used on D17 and FIGARO.

physics.ins-det

The search for Nanobubbles by using specular and off-specular Neutron Reflectometry

We apply specular and off-specular neutron reflection at the hydrophobic silicon/water interface to check for evidence of nanoscopic air bubbles whose presence is claimed after an ad hoc procedure of solvent exchange. Nanobubbles and/or a depletion layer at the hydrophobic/water interface have long been discussed and generated a plethora of controversial scientific results. By combining neutron reflectometry (NR), off-specular reflectometry (OSS) and grazing incidence small angle neutron scattering (GISANS), we studied the interface between hydrophobized silicon and heavy water before and after saturation with nitrogen gas. Our specular reflectometry results can be interpreted by assuming a sub-molecular sized depletion layer and the off-specular measurements show no change with nitrogen super saturated water. This picture is consistent with the assumption that, following the solvent exchange, no additional nanobubbles are introduced at significant concentrations (if present at all). Furthermore, we discuss the results, in terms of the maximum surface coverage of nanobubbles that could be present on the hydrophobic surface compatibly with the sensitivity limit of these techniques.

cond-mat.soft

Polymer brush collapse under shear flow

Shear responsive surfaces offer potential advances in a number of applications. Surface functionalisation using polymer brushes is one route to such properties, particularly in the case of entangled polymers. We report on neutron reflectometry measurements of polymer brushes in entangled polymer solutions performed under controlled shear, as well as coarse-grained computer simulations corresponding to these interfaces. Here we show a reversible and reproducible collapse of the brushes, increasing with the shear rate. Using two brushes of greatly different chain lengths and grafting densities, we demonstrate that the dynamics responsible for the structural change of the brush are governed by the free chains in solution rather than the brush itself, within the range of parameters examined. The phenomenon of the brush collapse could find applications in the tailoring of nanosensors, and as a way to dynamically control surface friction and adhesion.

cond-mat.soft

Simulation of Entangled Polymer Solutions

We present a computer simulation of entangled polymer solutions at equilibrium. The chains repel each other via a soft Gaussian potential, appropriate for semi-dilute solutions at the scale of a correlation blob. The key innovation to suppress chain crossings is to use a pseudo-continuous model of a backbone which effectively leaves no gaps between consecutive points on the chain, unlike the usual bead-and-spring model. Our algorithm is sufficiently fast to observe the entangled regime using a standard desktop computer. The simulated structural and mechanical correlations are in fair agreement with the expected predictions for a semi-dilute solution of entangled chains.

physics.comp-ph

Combined neutron reflectometry and rheology

We have combined neutron reflectometry with rheology in order to investigate the solid boundary of liquids and polymers under shear deformation. Our approach allows one to apply a controlled stress to a material while resolving the structural arrangements on the sub nanometer length scale with neutron reflectivity, off-specular and small angle scattering at the same time. The specularly reflected neutron intensity of a 20 % by weight solution of the Pluronic F127 in deuterated water is evaluated. We find pronounced changes in the near interface structure under applied deformation for surfaces with different surface energies, which are correlated with changes in the storage and loss modulus.

cond-mat.soft

Depth resolved grazing incidence scattering from the solid-liquid interface

We have applied small angle scattering in grazing incidence beam geometry on a time-of-flight neutron instrument. Due to the broad wavelength distribution provided for a specific incident beam angle the penetration depth of the neutron beam is varied over a broad range in a single measurement. The near surface structure of polymer micelles close to silicon substrates with distinct surface energy is resolved. It is observed that the very near-surface structure strongly depends on the surface coating whereas further away from the surface bulk like ordering is found. A more pronounced ordering is found close to surfaces with high surface energy.

cond-mat.soft

Solid Surface Structure Affects Liquid Order at the Polystyrene/SAM Interface

We present a combined x-ray and neutron reflectivity study characterizing the interface between polystyrene (PS) and silanized surfaces. Motivated by the large difference in slip velocity of PS on top of dodecyl-trichlorosilane (DTS) and octadecyl-trichlorosilane (OTS) found in previous studies, these two systems were chosen for the present investigation. The results reveal the molecular conformation of PS on silanized silicon. Differences in the molecular tilt of OTS and DTS are replicated by the adjacent phenyl rings of the PS. We discuss our findings in terms of a potential link between the microscopic interfacial structure and dynamic properties of polymeric liquids at interfaces.

cond-mat.soft