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Using Neutron Spin Echo Resolved Grazing Incidence Scattering to Investigate Organic Solar Cell Materials

The spin echo resolved grazing incidence scattering (SERGIS) technique has been used to probe the length-scales associated with irregularly shaped ...

Rutherford Appleton Laboratory

We report the first dynamic in situ electrochemical neutron reflectivity (NR) measurements on electroactive films. By using a boxcar integration strategy within a cyclic voltammetric experiment, it is possible to acquire neutron reflectivity data associated with narrow, defined windows of potential. Accumulation of data from repetitive cycles allows one to build up potential- (time-) resolved profiles. The effective time resolution is now on the order of seconds, as compared to ca. 1 h using conventional methodology, making in situ NR a practical technique for dynamic electrochemical studies. Illustrative data for polyvinylferrocene films reveal hysteresis in (de)swelling, incomplete desolvation upon reduction, and transient salt retention, all of which respond to time-scale variations.

Dynamic in situ electrochemical neutron reflectivity measurements.

Adsorption and interfacial properties of model methyl-capped nonionic surfactants C8E4OMe [C8H17O(C2H4O)4CH3] and C10E4OMe [C10H21O(C2H4O)4CH3] were studied in water and water/ethylene glycol mixtures as well as pure ethylene glycol. Critical micellar concentrations (cmc's), surface tensions, and surface excess were determined using surface tension (ST) and neutron reflection (NR) as a function of solvent type and surfactant tail length. The ST results show a strong dependence on solvent type in terms of cmc. The NR data were analyzed using a single-layer model for the adsorbed surfactant films. Surprisingly, the adsorption parameters obtained in both water and pure ethylene glycol were very similar, and variations in film thickness or area per molecule are negligible in respect of the uncertainties. Similarly, for C10E4OMe, estimates for the free energies of adsorption and micellization show only a weak solvent dependence. These results suggest that for such model nonionic surfactants dilute solution properties are dictated by solvophobicity, which is quite similar for this class of water, glycol, and water-glycol mixtures. More specifically, the nature of the adsorption layer appears to be hardly affected by the type of solvent subphase. The findings highlight the significance of solvophobicity and show that model nonionic surfactants can behave very similarly in hydrogen-bonding glycol solvents and water.

Unexpected adsorption behavior of nonionic surfactants from glycol solvents.

A combination of XPS, reflectance infrared spectroscopy, and neutron reflectivity measurements has been used to probe the spatial and global extents to which carboxylic acid motifs in electrodeposited conducting polymer films can be functionalized by reaction with vapor phase reagents (a carbodiimide together with trifluoroethanol) with the goal of controlling hydrophobicity. Across a range of polymer deposition and reaction temperatures, neutron reflectivity showed that, surprisingly, functionalization of the polymer matrix at depths >5-10 nm into the polymer film was always significantly lower than at the exposed surface. The most efficient functionalization was found to occur when a low-density polymer matrix was prepared by elution of motifs cleaved from the polymer by base hydrolysis. Finally, when trifluoroethanol functionalization was performed, the macroscopic property of hydrophobicity was related to the surface, internal microstructure, and composition of the reacted films as elucidated by the above combination of probes.

Determining compositional profiles within conducting polymer films following reaction with vapor phase reagents.

A new approach to promoting and controlling polymer surface functionalization with acidic or basic polar functional groups is demonstrated and evaluated. Blended polymer films were annealed under pH-buffered conditions, and polar end-functional groups were found to promote surface segregation of the functional polymers. Surface segregation of carboxylic acid (COOH)-functionalized polystyrene increases dramatically with increasing pH from 1.9 to 9.4, whereas the opposite behavior is seen for amine (NH2)-functionalized polystyrene. Neutron reflectometry and nuclear reaction analysis were used to obtain surface excess values for the functional polymers. Subsequent SCFT analysis of the composition versus depth profiles indicates that the affinity of each functional group for the polymer surface changes by about 3k(B)T over this pH range.

pH-controlled polymer surface segregation.

The Goos-Hänchen effect is a spatial shift along an interface resulting from an interference effect that occurs for total internal reflection. This phenomenon was suggested by Sir Isaac Newton, but it was not until 1947 that the effect was experimentally observed by Goos and Hänchen. We provide the first direct, absolute, experimental determination of the Goos-Hänchen shift for a particle experiencing a potential well as required by quantum mechanics: namely, wave-particle duality. Here, the particle is a spin-polarized neutron reflecting from a film of magnetized material. We detect the effect through a subtle change in polarization of the neutron. Here, we demonstrate, through experiment and theory, that neutrons do exhibit the Goos-Hänchen effect and postulate that the associated time shift should also be observable.

Observation of the Goos-Hänchen shift with neutrons.

We have studied the pH-dependent interaction between mycolic acid (MA) monolayers and hydrophobic and hydrophilic surfaces using molecular (colloidal probe) force spectroscopy. In both cases, hydrophobic and hydrophilic monolayers (prepared by Langmuir-Blodgett and Langmuir-Schaefer deposition on silicon or hydrophobized silicon substrates, respectively) were studied. The force spectroscopy data, fitted with classical DLVO (Derjaguin, Landau, Verwey, and Overbeek) theory to examine the contribution of electrostatic and van der Waals forces, revealed that electrostatic forces are the dominant contribution to the repulsive force between the approaching colloidal probe and MA monolayers. The good agreement between data and the DLVO model suggest that beyond a few nm away from the surface, hydrophobic, hydration, and specific chemical bonding are unlikely to contribute to any significant extent to the interaction energy between the probe and the surface. The pH-dependent conformation of MA molecules in the monolayer at the solid-liquid interface was studied by ellipsometry, neutron reflectometry, and with a quartz crystal microbalance. Monolayers prepared by the Langmuir-Blodgett method demonstrated a distinct pH-responsive behaviour, while monolayers prepared by the Langmuir-Schaefer method were less sensitive to pH variation. It was found that the attachment of water molecules plays a vital role in determining the conformation of the MA monolayers.

Adhesive and conformational behaviour of mycolic acid monolayers.

Understanding the gelation of liquids by low molecular weight solutes at low concentrations gives an insight into many molecular recognition phenomena and also offers a simple route to modifying the physical properties of the liquid. Bis-(α,β-dihydroxy ester)s are shown here to gel thermoreversibly a wide range of solvents, raising interesting questions as to the mechanism of gelation. At gelator concentrations of 5-50 mg ml⁻¹, gels were successfully formed in acetone, ethanol/water mixtures, toluene, cyclohexane and chloroform (the latter, albeit at a higher gelator concentration). A range of neutron techniques - in particular small-angle neutron scattering (SANS) - have been employed to probe the structure of a selection of these gels. The universality of gelation in a range of solvent types suggests the gelation mechanism is a feature of the bis-(α,β-dihydroxy ester) motif, with SANS demonstrating the presence of regular structures in the 30-40 Å range. A correlation between the apparent rodlike character of the structures formed and the polarity of the solvent is evident. Preliminary spin-echo neutron scattering studies (SESANS) indicated the absence of any larger scale structures. Inelastic neutron spectroscopy (INS) studies demonstrated that the solvent is largely unaffected by gelation, but does reveal insights into the thermal history of the samples. Further neutron studies of this kind (particularly SESANS and INS) are warranted, and it is hoped that this work will stimulate others to pursue this line of research.

Gelation or molecular recognition; is the bis-(α,β-dihydroxy ester)s motif an omnigelator?

A unique surface force type apparatus that allows the investigation of a confined thin film using neutron reflection is described. The central feature of the setup consists of a solid substrate (silicon) and a flexible polymer membrane (Melinex(®)). We show that inflation of the membrane against the solid surface provides close and even contact between the interfaces over a large surface area. Both heavy water and air can be completely squeezed out from between the flexible film and the solid substrate, leaving them in molecular contact. The strength of confinement is controlled by the pressure used to inflate the membrane. Dust provides a small problem for this approach as it can get trapped between membrane and substrate to prevent a small part of the membrane from making good contact with the substrate. This results in the measured neutron reflectivity containing a small component of an unwanted reflection, between 10% and 20% at low confining pressures (1 bar) and between 1% and 5% at high confining pressures (5 bar). However, we show that this extra signal does not prevent good and clear information on the structure of thin films being extracted from the neutron reflectivity. The effects of confinement are illustrated with data from a poly(vinyl pyrollidone) gel layer in water, a polyelectrolyte multilayer in water, and with data from a stack of supported lipid-bilayers swollen with D(2)O vapor. The data demonstrates the potential of this apparatus to provide information on the structure of thin films under confinement for a known confining pressure.

Measuring the structure of thin soft matter films under confinement: a surface-force type apparatus for neutron reflection, based on a flexible membrane approach.

Article	Year
Dynamic in situ electrochemical neutron reflectivity measurements. Journal of the American Chemical Society\| PubMed ID: 15563146	2004
Unexpected adsorption behavior of nonionic surfactants from glycol solvents. Langmuir : the ACS journal of surfaces and colloids\| PubMed ID: 17154601	2006
Determining compositional profiles within conducting polymer films following reaction with vapor phase reagents. The journal of physical chemistry. B\| PubMed ID: 17402770	2007
pH-controlled polymer surface segregation. Langmuir : the ACS journal of surfaces and colloids\| PubMed ID: 19437721	2009
Observation of the Goos-Hänchen shift with neutrons. Physical review letters\| PubMed ID: 20366352	2010
Adhesive and conformational behaviour of mycolic acid monolayers. Biochimica et biophysica acta\| PubMed ID: 20529662	2010
Gelation or molecular recognition; is the bis-(α,β-dihydroxy ester)s motif an omnigelator? Beilstein journal of organic chemistry\| PubMed ID: 21160568	2010
Measuring the structure of thin soft matter films under confinement: a surface-force type apparatus for neutron reflection, based on a flexible membrane approach. The Review of scientific instruments\| PubMed ID: 23206072	2012

Robert M. Dalgliesh

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