Responsive Materialien und Grenzflächen

Fluide Grenzflächen sind eine einzigartige Plattform sind, um schaltbare Bausteine auf molekularer Ebene und in kompakten Geometrien d.h. mit starken lateralen Wechselwirkungen zu untersuchen. Beispielsweise können wir Grenzflächen durch Adsorption und anschließende Selbstorganisation von Molekülen leicht mit maßgeschneiderten molekularen Bausteinen modifizieren und so die molekularen Eigenschaften auf die der Grenzfläche übertragen. Darüber hinaus haben wir mehrere Beispiele dafür, wie Grenzflächeneigenschaften auf größeren makroskopischen Längenskalen das Verhalten weicher Materialien wie Schäume oder Emulsionen dominieren können. Unser Ansatz ermöglicht es Materialeigenschaften durch das molekulare Design vorhandenen Grenzflächen zu prägen, wodurch wir zum Beispiel mit der Verwendung von molekularen Schaltern an Grenzflächen sowohl die Grenzflächen- als auch Materialeigenschaften durch externe Stimuli wie Temperatur oder Licht gezielt manipulieren können.

Dazu verwenden wir photoschaltbare Amphiphile mit deren Hilfe wir insbesondere durch die Beleuchtung mit Licht zeitlich und räumlich lokalisierte Reaktionen auslösen die auch eine Steuerung von Materialeigenschaften ermöglichen. In zukünftigen Arbeiten schlagen wir vor, amphiphile molekulare Schalter wie Arylazopyrazol-Derivate zu verwenden, um diese mit unterschiedlichen elektrostatischen sowie zusätzlichen dispersen Wechselwirkungen an der Grenzfläche auszustatten und so deren Fähigkeit Grenzflächeneigenschaften mit Licht zu verändern massiv zu verbessern.

Neben den schaltbaren Tensiden verwenden werden als weitere Bausteine Makromoleküle wie thermoresponsive Polymere z.B. Hydroxypropylcellulose von uns untersucht. Wir setzen diese Arbeit derzeit fort, indem wir Polymer-Mischungen mit Arylazopyrazol-Tensiden untersuchen, um multiresponsive sowie adaptive Eigenschaften an Grenzflächen und in Schäumen zu erreichen.

Molekulare Selbstorganisation an festen Oberflächen und Struktur-Eigenschafts-Beziehungen und Benetzungsdynamik organischer Dünnfilme mit Photoschaltern

In diesem Projekt untersuchen wir das dynamische Benetzungsverhalten von photoschaltbaren Oberflächen. Dazu werden Festkörperoberflächen mit Photoschaltern funktionalisiert, um die Benetzungseigenschaften des Festkörpers reversibel verändern können. Solche Prozesse sind von großem Interesse in Anwendungen z.B. für selbstreinigende Oberflächen, in der Mikrofluidik oder für abstimmbare Linsen.

Aber selbst für passive Oberflächen, die ihre molekularen Eigenschaften nicht mehr ändern können, wenn sie mit einer Flüssigkeit in Kontakt kommen, ist eine quantitative Beschreibung der Benetzungsdynamik noch immer eine große Herausforderung. Dies gilt insbesondere dann, wenn auch Änderungen auf molekularer Ebene durch Anpassung des Substrats an unterschiedliche chemische Umgebungen oder das (von uns) gewünschte Schalten der Moleküle in der Oberfläche mit Licht berücksichtigt werden müssen. Wir konnten zeigen, dass selbst sehr einfache selbstorganisierte Monoschichten, welche Moleküle mit langen Alkylketten (z. B. C12 oder C18) aufweisen, eine andere Struktur aufweisen, wenn sie von einem polaren Lösungsmittel benetzt werden. Aus diesem Grund glauben wir, dass ein Verständnis der Benetzungsdynamik von photoschaltbaren Substraten Informationen auf molekularer Ebene über die Substratdynamik und Strukturänderungen unter verschiedenen Lichtbedingungen sowie verschiedenen chemischen Umgebungen erfordert. Zur Aufklärung dieser Prozesse auf der molekularen Ebene wird nichtlineare optische Spektroskopie eingesetzt.

Reactions at Electrode/Electrolyte Interfaces

In this project, we use our expertise in nonlinear optical scattering to study electrocatalytic reactions in situ and partly also in operando. Currently we have a strong focus on the catalysis of CO₂ in room temperature ionic liquids (ILs). In CO₂ catalysis, ILs have been shown to yield low overpotentials and reduction reactions that can occur at potentials close to the theoretical thermodynamic potential. This makes ionic liquids highly interesting electrolytes for CO₂ catalysis. However, in comparison to aqueous electrolytes, where extensive studies exist, we have just started to understand CO₂ reduction reactions (CO₂RR) on catalyst surfaces in contact with ionic liquids. For that, our group has established new in situ and in operando spectroscopies that can provide detailed molecular level information on CO₂RR. So far, our work was focused mostly on Pt electrode surfaces which were the ideal choice to understand the molecular origin of the low overpotentials for CO₂RR. In the future, we want to go beyond the fundamentally useful but for real world applications irrelevant Pt catalysts to new and much more relevant Cu and Cu/Au surface alloys have not been studied in ionic liquids in detail yet, but are expected to yield C₁ products like HCOOH and possibly also C₂ products. Several work packages will concentrate on delivering molecular level information from in situ/in operando spectroscopy of CO₂ reaction pathways for Cu electrodes, while we also plan to extract the products from CO₂RR in a continuous process. This will be done in a separate working package that is run parallel to the other addressing more fundamental aspects of CO₂RR in ionic liquids.

• A. Kemna and B. Braunschweig, Potential-Induced Adsorption and Structuring of Water at Pt(111) Electrode Surfaces in Contact with an Ionic Liquid, J. Phys. Chem. Lett. 11, 7116-7121 (2020)
• B. Ratschmeier, A. Kemna, B. Braunschweig, Role of H₂O for CO₂ Reduction Reactions at Plati-num/Electrolyte Interfaces in Imidazolium Room-Temperature Ionic Liquids, ChemElectroChem 7, 1765-1774 (2020)
• A. Kemna, N. García Rey and B. Braunschweig, Mechanistic Insights on CO₂ Reduction Reactions at Platinum/[BMIM][BF₄] Interfaces from In Operando Spectroscopy, ACS Catalysis 8, 6284-6292 (2019)
• B. Braunschweig, P. Mukherjee, J. L. Haan and D. D. Dlott, Vibrational sum-frequency generation study of the CO₂ electrochemical reduction at Pt/EMIM-BF₄ solid/liquid interfaces, J. Electroanalytical Chem. 800, 144-150 (2017)
• B. Braunschweig and Andrzej Wieckowski, Surface Spectroscopy of Pt(111) Single-Crystal Electro-lyte Interfaces with Broadband Sum-Frequency Generation, J. Electroanal. Chem. 716, 136-144 (2014)
• B. Braunschweig, D. Hibbitts, M. Neurockand, A. Wieckowski, Electrocatalysis: a Fuel Cell and Sur-face Science Perspective, Catalysis Today 202, 197-209 (2013)

Surfactants and Macromolecules at Electrified Interfaces

Particularly, ions are of great importance as they can specifically bind to charge determining groups of proteins such as carboxylates or in analogous way bind to surfactants or polyelectrolytes. In addition, ions within the electric double layer of a charged interface can screen the interfacial electric field that is produced by the presence of e.g. proteins or surfactants and their net charge. Ion partitioning at interfaces can also directly inhibit bubble coalescence. Thus, specific ion adsorption due to ion pairing and ion partitioning can be applied to tune interfacial intermolecular interactions by either screening the interfacial electric field but also by enforcing a charge reversal upon the interface. The effects of ions on the molecular structure of neat water surfaces are equally im-portant and will be addressed in a similar way. In general, the issue of ions at aqueous interfaces impacts a long-standing problem on the origin of salt effects on the solubility of proteins and other macromolecules or colloidal particles which was originally invoked by Hofmeister. A particular focus is on the effects of ions on surface charge, molecular order and structure of surface adsorbates (proteins, polyelectrolytes, surfactants and their mixtures) since the presence of ions can significantly change intermolecular interactions at the interface from attractive to repulsive.

Field effects can lead to substantial changes in the SFG spectrum of interfacial water molecules and can be used to track changes that are associated with different surface charging conditions. For these studies, we will systematically vary the salt and its concentration in the electrolyte so that we can compare series of SHG/SFG experiments from hard ions to soft ions. As we perform these studies with different molecules, that have quite different charge determining groups e.g. amines, carboxylate or sulfates, we can also address ion pairing at these groups as well as ion partitioning at hydrophobic parts of modified liquid interfaces. Here, we combine SFG spectroscopy with measurements in a thin-film pressure balance were the disjoining pressure in foam films can be determined. In fact, we could very recently demonstrate that these two methods provide complementary information (see García Rey et al. in JPCC (2019) below).

• M. E. Richert, G. Gochev and B. Braunschweig, Specific Ion Effects of Trivalent Cations on the Struc-ture and Charging State of β-Lactoglobulin Adsorption Layers, Langmuir (under review in revised form)
• M. García Rey, E. Weißenborn, F. Schulze-Zachau, G. Gochev, B. Braunschweig, Quantifying Dou-ble-Layer Potentials at Liquid-Gas Interfaces from Vibrational Sum-Frequency Generation, J. Phys. Chem C 123, 1279-1286 (2019)
• F. Schulze-Zachau, S. Bachmann, B. Braunschweig, Effects of Ca²⁺ Ion Condensation on the Mo-lecular Structure of Polystyrene Sulfonate at Air-Water Interfaces, Langmuir 34, 11714-11722 (2018)
• S. Streubel, F. Schulze-Zachau, E. Weißenborn, B. Braunschweig, Ion Pairing and Adsorption of Azo Dye/C₁₆TAB Surfactants at the Air−Water Interface, J. Phys. Chem. C 121, 27992−28000 (2017)
• B. Braunschweig, F. Schulze-Zachau, E. Nagel, K. Engelhardt, S. Stoyanov, G. Gochev, Khr.Khristov, E. Mileva, D. Exerowa, R. Miller and W. Peukert, Specific effects of Ca²⁺ ions and molecular structure of β-lactoglobulin interfacial layers that drive macroscopic foam stability, Soft Matter 12, 5995 (2016)
• F. R. Beierlein, T. Clark, B. Braunschweig, K. Engelhardt, L. Glas, W. Peukert, Carboxylate Ion Pair-ing with Alkali-Metal Ions for β-Lactoglobulin and Its Role on Aggregation and Interfacial Adsorption, J. Phys. Chem. B 119, 5505 (2015)

Interface Characterization in Colloids with Nonlinear Optical Scattering Methods

A molecular understanding of nanoparticle surfaces and their functionalization is of great importance not only from fundamental aspects but is also highly demanded in specific applications. However, the mechanism and the kinetics of nanoparticle surface modification are still widely unknown on a molecular level, which is due to a lack of in situ techniques with high temporal resolution. In our present work we were able to follow the adsorption kinetics e.g. of thiolates on citrate stabilized Au nanoparticles by applying second-harmonic light scattering (SHS) and have separated in situ adsorption on defect and terrace sites which was hitherto not accessible.

We expect that our research will help to optimize functionalization of Au nanoparticle surfaces and that the mechanistic understanding which we provide can be transferred also to other nanoparticle systems. Furthermore, we have applied SHS to study double layer charging and the orientation of water molecules at surfaces of polymer particles. Changing the pH has a dramatic effect on the surface potential which can be in many cases tuned from positive to negative values and has allowed us to record changes in SHS signals while the isoelectric point of the particles is being crossed. The SHS signal is a function of two contributions which are directly related to the first molecular layer, its orientation, and to a second electric field induced contribution of the unidirectional field within the interfacial electric double layer. Through additional charge screening experiments we measured the surface charge density for positively as well as for negatively charged particle surfaces and confirmed the isoelectric point, where an increase in ionic strength had little effect on the SHS intensity. Furthermore, we have determined the net orientation of water molecules directly adsorbed to the particle surface from pH-dependent changes in the relative phase of the two SHS contributions. Using SHS we can also identify morphology changes where we could provide new information on the growth of Au nanoshells with an in situ study that has used a combination of in situ SHS and UV-Vis spectroscopy and ex situ scanning electron microscopy.

• R. Dinkel, J. Jakobi, A.R. Ziefuß, S. Barcikowski, B. Braunschweig, W. Peukert, Role of Citrate and NaBr at the Surface of Colloidal Gold Nanoparticles during Functionalization, J. Phys. Chem. C 122, 27383-27391 (2018)
• R. Dinkel, W. Peukert and B. Braunschweig, In situ spectroscopy of ligand exchange reactions at the surface of colloidal gold and silver nanoparticles, J. Phys.: Cond. Mat. 29, 133002 (2017) Invited Re-view
• R. Dinkel, B. Braunschweig, W. Peukert, Fast and slow ligand exchange at the surface of colloidal gold nanoparticles, J. Phys. Chem. C 120, 1673 – 1682 (2016)
• C. Sauerbeck, B. Braunschweig and W. Peukert, Surface charging and interfacial water structure of amphoteric colloidal particles, J. Phys. Chem. C 118, 10033-10042 (2014)
• C. Sauerbeck, M. Haderlein, B. Schürer, B. Braunschweig, W. Peukert and R.N. Klupp Taylor, Shed-ding Light on the Growth of Au Nanoshells, ACS Nano 8, 3088-3096 (2014)

ERC Grant SUPERFOAM

ERC Grant SUPERFOAM

Foams are ubiquitous in our daily lives be it as milk foam on our cappuccino or as heat insulation of the building we live in.
The various important technological applications range from lightweight materials, waste water treatment to recycling of rare earth metals via ion flotation just to mention a few.
The vast number of possibilities to use foam in industrial processes and products originate from a unique tunability of optical, mechanical as well as chemical properties. This makes foams to an exciting object of current interdisciplinary research.

Although making aqueous foam is surprisingly easy as one “simply” has to lower the water’s surface tension by additions of surface active molecules, the foam is in most cases inherently unstable. Furthermore, foam formulation is usually performed purely empirically because the actual driving forces must be controlled on several length scales that reach down to the molecular level. For that reason understanding and controlling foam properties with a bottom-up approach is a major challenge in current research.

Structure-Property Relationship

Foams are hierarchical materials and as such they are greatly affected by the arrangement and distribution of gas bubbles on a macroscopic scale as well as on thickness and composition of lamella on a mesoscopic scale.
Although they are hidden in the bulk, liquid-gas interfaces are a building block of foams with overwhelming importance.
Thus composition, conformation and intermolecular interactions of a few molecular layers at liquid-gas interfaces – that are ubiquitous in aqueous foam – determine properties throughout the entire hierarchical chain.

Methodology of the SUPERFOAM project

In order, to put foam formulation and also our knowledge on foams on a molecular basis we need to characterize the latter in situ and on a molecular level. For that reason, our goal is to identify molecular building blocks which are comprised of solutes, ions and solvents at interfaces and their interactions that make the most stable foams or drive other foam properties. Once identified, we can use these building blocks to break the ground for new ways in foam formulation and related fields. Specifically, from this project we will get a library of structure-property relationships (SUPER) from which we can select molecular ingredients, tailor their interactions and thus generate FOAM based on molecular control.

Experimental Approach

The main focus of the ERC Starting Grant project SUPERFOAM will be on the molecular structure of interfaces and in situ charac-terization of interfaces. These experiments are a nucleation point for further studies on larger length scales - lamella, bubbles and macroscopic foam - which will be performed with solutions of identical composition. The approach will enable us to trace foam properties, bubble coalescence and lamella properties back to the actual molecular structures defining them. For that reason, we will divide the project into small work packages, which we can handle experimentally. At the conclusion of this project, we can unite the individual parts into a single concept on how molecular structures at gas-water interfaces should look like in order to make foam with the desired properties.

Interfaces

• Structure
• Composition
• Charging
• Adsorption kinetics of surface active molecules

Foam films and rising bubbles

• Composition
• Disjoining Pressure

Macroscopic Foam

• Bubble size distribution
• Stability & more