Reversible Adsorption and Interfacial Photoisomerization of Azobenzene Surfactants Studied by QCM
Year: 2025
Type: article
Abstract: High Resolution Image Download MS PowerPoint Slide Photoresponsive surfactants offer a versatile approach for remotely controlling interfacial properties through light-triggered isomerization. Among them, azobenzene-based surfactants are particularly attractive due to their structural reversibility and stability under repeated irradiation. In this study, we investigate the dynamic adsorption and desorption behavior of the azobenzene-containing surfactant AzoC 6 at a glass–water interface under controlled UV and blue-light illumination. Using quartz crystal microbalance (QCM) measurements, we show that the interfacial mass change is governed by the isomeric composition in the bulk solution: the trans isomer exhibits strong adsorption, while the cis isomer is significantly less surface-active. We further quantify the photoisomerization kinetics at the interface, revealing that the isomerization rate constant decreases with a lower trans isomer concentration due to a transition from a diffuse multilayer to a confined double-layer structure. At higher concentrations, the rapid exchange between trans and cis isomers sustains dynamic interfacial rearrangements, facilitating the formation of spatial isomer gradients. These gradients generate light-driven diffusio-osmotic flows, with a time evolution that reflects the interfacial photoresponse. Our findings provide mechanistic insight into light-induced interfacial processes and highlight the potential of azobenzene surfactants for designing stimuli-responsive systems and soft materials with remote, reversible control.
Source: Langmuir
Authors: Maren Umlandt, Philipp Ortner, Nino Lomadze, Marek Bekir, Svetlana Santer, Yulia D. Gordievskaya
Institution: University of Potsdam
Language: English
Subfield: Materials Chemistry
Field: Materials Science
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,500
Funder: Deutsche Forschungsgemeinschaft
Awards: G141869318, G314795287, G359507783
OpenAlex ID: W4415589569
