4.7 Article

Probing charge transfer through antifouling polymer brushes by electrochemical methods: The impact of supporting self-assembled monolayer chain length

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ANALYTICA CHIMICA ACTA
卷 1276, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.aca.2023.341640

关键词

Polymer brushes; Self-assembled monolayers; Antifouling; Cyclic voltammetry; Electrochemical impedance spectroscopy; 3D printed electrochemical cell

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Ultrathin surface-tethered polymer brushes, particularly the zwitterionic poly(carboxybetaine) (pCB) brushes, show great potentials in sensing applications. Experimental studies were conducted to investigate the influence of the alkanethiolate self-assembled monolayers (SAMs) chain length on the properties of the antifouling poly(carboxybetaine methacrylamide) (pCBMAA) brushes. The results showed that the SAM length has a significant impact on the characteristics of the brushes, with longer-chain SAMs exhibiting better biofouling resistance.
Ultrathin surface-tethered polymer brushes represent attractive platforms for a wide range of sensing applications in strategically vital areas such as medicine, forensics, or security. The recent trends in such developments towards real world conditions highlighted the role of zwitterionic poly(carboxybetaine) (pCB) brushes which provide excellent antifouling properties combined with bio-functionalization capacity. Highly dense pCB brushes are usually prepared by the grafting from polymerization triggered by initiators on self-assembled monolayers (SAMs). Here, multi-methodological experimental studies are pursued to elucidate the impact of the alkanethiolate SAM chain length (C6, C8 and C11) on structural and functional properties of antifouling poly(carboxybetaine methacrylamide) (pCBMAA) brush. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) in a custom-made 3D printed cell employing [Ru(NH3)6]3+/2+ redox probe were used to investigate penetrability of SAM/pCBMAA bilayers for small molecules and interfacial charge transfer characteristics. The biofouling resistance of pCBMAA brushes was characterized by surface plasmon resonance; ellipsometry and FT-IRRAS spectroscopy were used to determine swelling and relative density of the brushes synthesized from initiator-bearing SAMs with varied carbon chain length. The SAM length was found to have a substantial impact on all studied characteristics; the highest value of charge transfer resistance (Rct) was observed for denser pCBMAA on longer-chain (C11) SAM when compared to shorter (C8/C6) SAMs. The observed high value of Rct for C11 implies a limitation for the analytical performance of electrochemical sensing methods. At the same time, the pCBMAA brushes on C11 SAM exhibited the best bio-fouling resistance among inspected systems. This demonstrates that proper selection of supporting structures for brushes is critical in the design of these assemblies for biosensing applications.

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