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Why Doesn't It Stick? Revealing the Impact of Mobile Oligomers on Ecoflex Surface Functionality and Bonding
Gloria M D'Amaral1, Hannah R Jessop1, Rahaf Nafez Hussein1
1Department of Chemistry and Biochemistry, University of Windsor, Windsor, Ontario N9B 3P4, Canada.
Abstract:
Achieving stable interfacial performance in soft electronics requires a nuanced understanding of how the bulk elastomer composition affects surface functionality. This relationship is well-established in Sylgard 184, a polydimethylsiloxane (PDMS) elastomer that, upon oxidation, forms a cohesive SiOx surface supporting strong adhesion to vapor- and solution-deposited functional films. In contrast, Ecoflex, a widely used ultrasoft silicone elastomer, exhibits a long-recognized but poorly understood incompatibility with metal and solution-processed conductors. Here, we introduce layered PDMS/Ecoflex composites as a new experimental platform for systematically probing this limitation. We show that mobile low-molecular-weight siloxane oligomers in Ecoflex can migrate through a 100 μm thick PDMS membrane cross-linked directly to the Ecoflex substrate, significantly altering surface properties and undermining film deposition. By systematically removing and reintroducing these additives, we demonstrate their pivotal role in driving wetting failure, adhesion loss, and electrical degradation. While removing the additives enables the deposition of uniform, adherent, and conductive gold films, these species are also essential to Ecoflex's extreme softness, revealing an inherent trade-off between surface functionality and mechanical compliance. Upon reintroduction, the oligomers restore softness but reverse the interfacial improvements, even compromising previously well-adhered films. These findings clarify the origin of Ecoflex's surface instability and underscore the need to consider bulk formulation when designing elastomer interfaces for soft electronics.
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