Real-time insight into nanostructure evolution during the rapid formation of ultra-thin gold layers on polymers. 2021

Matthias Schwartzkopf, and Sven-Jannik Wöhnert, and Vivian Waclawek, and Niko Carstens, and André Rothkirch, and Jan Rubeck, and Marc Gensch, and Jonas Drewes, and Oleksandr Polonskyi, and Thomas Strunskus, and Alexander M Hinz, and Simon J Schaper, and Volker Körstgens, and Peter Müller-Buschbaum, and Franz Faupel, and Stephan V Roth
Photon Science, Deutsches Elektronen-Synchrotron (DESY), Notkestr. 85, D-22607 Hamburg, Germany. matthias.schwartzkopf@desy.de.

Ultra-thin metal layers on polymer thin films attract tremendous research interest for advanced flexible optoelectronic applications, including organic photovoltaics, light emitting diodes and sensors. To realize the large-scale production of such metal-polymer hybrid materials, high rate sputter deposition is of particular interest. Here, we witness the birth of a metal-polymer hybrid material by quantifying in situ with unprecedented time-resolution of 0.5 ms the temporal evolution of interfacial morphology during the rapid formation of ultra-thin gold layers on thin polystyrene films. We monitor average non-equilibrium cluster geometries, transient interface morphologies and the effective near-surface gold diffusion. At 1 s sputter deposition, the polymer matrix has already been enriched with 1% gold and an intermixing layer has formed with a depth of over 3.5 nm. Furthermore, we experimentally observe unexpected changes in aspect ratios of ultra-small gold clusters growing in the vicinity of polymer chains. For the first time, this approach enables four-dimensional insights at atomic scales during the gold growth under non-equilibrium conditions.

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