Development
The OSTE polymer resins were originally developed by Tommy Haraldsson and Fredrik Carlborg at the group of Micro and Nanosystems at theReaction mechanism
The OSTE resins are cured via a rapid thiol-ene “Click” reaction between thiols and allyls. The thiols and allyls react in a perfectly alternating fashion and has a very high conversion rate (up to 99%), the initial off-stoichiometry of the monomers will exactly define the number off unreacted groups left after the polymerization. With the right choice of monomers very high off-stoichiometry ratios can be attained while maintaining good mechanical properties. The off-stoichiometry thiol-ene-epoxies, or OSTE+ polymers, are created in a two-step curing process where a first rapid thiol-ene reaction defines the geometric shape of the polymer while leaving an excess of thiols and all the epoxy unreacted. In a second step all the remaining thiol groups and the epoxy groups are reacted to form an inert polymer.Properties
OSTE polymers
The main advantages put forward of the UV-cured OSTE polymers in microsystems have been their i) dry bonding capacity by reacting a polymer with thiol excess to a second polymer with allyl excess at room-temperature using only UV-light, ii) their well-defined and tunable number of surface anchors (thiols or allyls) present on the surface that can be used for direct surface modification and iii) their wide tuning range of mechanical properties from rubbery to thermoplastic-like depending only on the choice of off-stoichiometry. The glass transition temperature typically varies from below room-temperature for high off-stoichiometric ratios to 75 °C for a stoichiometric blend of tetrathiol and triallyl. They are typically transparent in the visible range. A disadvantage put forward with the OSTE-polymers is the leaching out of unreacted monomers at very high off-stoichiometric ratios which may affect cells and proteins in lab-on-chips, although cell viability has been observed for cell cultures on low off-stoichiometric OSTE.OSTE+ polymers
The dual-cure thiol-ene-epoxies, or OSTE+ polymers, differ from the OSTE-polymers in that they have two separated curing steps. After the first UV-initiated step, the polymer is rubbery and can easily be deformedFabrication
OSTE polymers
The OSTE resins can be cast and cured in a structured silicone molds or coated permanent photoresist. OSTE polymers have also shown excellent photostructuring capability using photomasks, enabling for example powerful and flexible capillary pumps.OSTE+ polymers
The OSTE+ resins are first UV-cured in the same way as the OSTE-polymers but are later thermally cured to stiffen and bond to a substrate.Applications
Lab-on-a-chip
OSTE+ allows for soft lithography microstructuring, strong biocompatible dry bonding to almost any substrate duringBio packaging
Biosensors are used for a range of biological measurements. OSTE packaging for biosensing has been demonstrated for QCM, and photonic ring resonator sensors.Wafer bonding
Adhesive wafer bonding has become an established technology in microelectromechanical systems (MEMS) integration and packaging applications. OSTE is suitable for heterogeneous silicon wafer level integration depending on its application in low temperature processes due to its ability to cure even in room temperatures.Microarray imprinting and surface energy patterning
Imprinting of arrays with hydrophilic-in-hydrophobic microwells is made possible using an innovative surface energy replication approach by means of a hydrophobic thiol-ene polymer formulation. In this polymer, hydrophobic-moiety-containing monomers self-assemble at the hydrophobic surface of the imprinting stamp, which results in a hydrophobic replica surface after polymerization. After removing the stamp, microwells with hydrophobic walls and a hydrophilic bottom are obtained. Such fast and inexpensive procedure can be utilised in digital microwell array technology toward diagnostic applications.OSTE e-beam resist
OSTE resin can also be used as e-beam resist, resulting in nanostructures that allow direct protein functionalization.References
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