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 µmol/m²); for Azo-TB the change was only moderate (maximum change of Γ: 1.02 µmol/m²). 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.

A new light-switchable azo-surfactant arylazopyrazole tetraethylene glycol carboxylic acid (AAP-E4) was used as a molecular building block to functionalize macroscopic foams. AAP-E4 was studied in the bulk solution with UV/vis spectroscopy and at the interface with sum-frequency generation (SFG) as well as tensiometry. Additional foaming experiments were performed with a dynamic foam analyzer to study the role of AAP-E4 surfactants at the ubiquitous air–water interface as well as within macroscopic foam. In the bulk, it is possible to switch the AAP-E4 surfactant reversibly from trans to cis configurations and vice versa using 380 nm UV and 520 nm green light, respectively. At the interface, we demonstrate the excellent switching ability of AAP-E4 surfactants and a substantial modification of the surface tension. In addition, we show that the response of the interface is strongly influenced by lateral electrostatic interactions, which can be tuned by the charging state of AAP-E4. Consequently, the electrostatic disjoining pressure and thus the foam stability are highly dependent on the bulk pH and the charging state of the interface. For that reason, we have studied both the surface net charge (SFG) and the surface excess (tensiometry) as important parameters that determine foam stability in this system and show that neutral pH conditions lead to the optimal compromise between switching ability, surface excess, and surface charging. Measurements on the foam stability demonstrated that foams under irradiation with green light are more stable than foams irradiated with UV light.

Responsive foams and interfaces, are interesting building blocks for active materials that respond and adapt to external stimuli. We have used the photochromic reaction of a spiropyran sulfonate surfactant to render interfacial, rising bubble as well as foaming properties active to light stimuli.In order to address the air-water interface on a molecular level, we have applied sum-frequency generation (SFG) spectroscopy which has provided qualitative information on the surface excess and the interfacial charging state as a function of light irradiation and solution pH. Under blue light irradiation, the surfactant forms a closed ring spiro form (SP), whereas under dark conditions the ring opens and the merocyanine (MC) form is generated. Using SFG spectroscopy, we show that at the interface, different pH conditions of the bulk solution lead to changes in the interfacial charging state. We have exploited the fact that the MC surfactant's O-H group can be deprotonated as a function of pH, and used that to tune the molecules net charge at the interface. In fact, SFG spectroscopy shows that with increasing pH the intensity of the O-H stretching band from interfacial water molecules increases which we associate to an increase in surface net charge. At a pH of 5.3, irradiation with blue light leads to a reversible decrease of O-H intensities, whereas the C-H intensities were unchanged compared to the corresponding intensities under dark conditions. These results are indicative of changes in the surface net charge with light irradiation, which are also expected to influence the foam stability via changes in the electrostatic disjoining pressure. In fact, measurements of the foam stabilities are consistent with this hypothesis with higher foam stability under dark conditions. At pH 2.7 this behavior is reversed as far as the surface tension and surface charging as well as the foam stability are concerned. This is corroborated by rising bubble experiments, which demonstrated an unprecedented reduction of ~30 % in bubble velocity when the bubbles were irradiated with blue light compared to the velocity of bubbles with the

Polyelectrolyte/surfactant (P/S) mixtures find many applications but are static in nature and cannot be reversibly reconfigured through the application of external stimuli. Using a new type of photoswitchable surfactants, we use light to trigger property changes in mixtures of an anionic polyelectrolyte with a cationic photoswitch such as electrophoretic mobilities, particle size, as well as their interfacial structure and their ability to stabilize aqueous foam. For that, we show that prevailing hydrophobic intermolecular interactions can be remotely controlled between poly(sodium styrene sulfonate) (PSS) and arylazopyrazole tetraethylammonium bromide (AAP-TB). Shifting the chemical potential for P/S binding with E/Z photoisomerization of the surfactants can reversibly disintegrate even large aggregates (>4 μm) and is accompanied by a substantial change in the net charging state of PSS/AAP-TB complexes, e.g., from negative to positive excess charges upon light irradiation. In addition to the drastic changes in the bulk solution, also at air−water interfaces, the interfacial stoichiometry and structure change drastically on the molecular level with E/Z photoisomerization, which can also drive the stability of aqueous foam on a macroscopic level.