Streamlined approach for covalently anchoring end-functionalised cationic monolayers onto silver substrates for surface coatings

The successful fabrication of high-quality, functionalised monolayers demands a meticulous understanding of the intricate interplay between solvent properties and deposition time. This study introduces a streamlined method for covalently anchoring end-functionalised cationic self-assembled monolayers (SAMs) onto silver (Ag) substrates, achieving enhanced surface coverage, uniformity, and electrochemical performance. The ammonium-terminated SAM, dibromo-10,10’-bis(triethylammoniumdecyl)disulfide (C10-TEA-SAM), was synthesised and its structure confirmed via ¹H NMR spectroscopy. Optimised C10-TEA-SAM immobilisation onto Ag surfaces, employing ethanol as the solvent due to its superior solvating ability for the ionic C10-TEA-SAM molecules, yielded a well-covered, hydrophilic surface. Contact angle (CA) measurements revealed a progressive decrease in CA with increasing immersion time, reaching a minimum of 5.85° after 5 days, indicative of enhanced hydrophilicity. Furthermore, atomic force microscopy revealed a concomitant reduction in surface roughness with prolonged immersion, suggesting the formation of a smoother and more uniform monolayer. Attenuated Total Reflectance Fourier Transform Infrared (ATR-FTIR) spectroscopy confirmed the presence of the C10-TEA-SAM on the Ag surface, while electrochemical impedance spectroscopy (EIS) revealed the insulating nature of the Ag/C10-TEA-SAM interface. This insulating behaviour, characterised by a larger semi-circle impedance and increased bulk resistance, is indicative of a highly ordered, defect-free structure with minimal electron transfer, analogous to long-chain alkanethiol monolayers. These findings collectively demonstrate the efficacy of this optimised approach in creating high-quality cationic SAMs on Ag substrates, offering strong potential for sensor and surface-coating applications. • Developed a stable, uniform method to anchor triethylammonium-functionalised self-assembled monolayers on silver surfaces Ag. • Identified ethanol as the optimal solvent, achieving a contact angle reduction to 5.85° for hydrophilic surfaces. • Produced defect-free monolayer coatings for sensors and surface applications. • Established a robust streamlined approach for applications in sensors and surface coatings.

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Publication Details

Journal
Next Materials
Published
2026-02-09
DOI
https://doi.org/10.1016/j.nxmate.2026.101706
Primary Topic
Molecular Junctions and Nanostructures
Type
article
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article

Streamlined approach for covalently anchoring end-functionalised cationic monolayers onto silver substrates for surface coatings

A.A. Bakar, S. Hisham, M.Z. Sahdan, H.A. Tajuddin et al.
Next Materials
Molecular Junctions and Nanostructures
article

Streamlined approach for covalently anchoring end-functionalised cationic monolayers onto silver substrates for surface coatings

A.A. Bakar, S. Hisham, M.Z. Sahdan, H.A. Tajuddin, N.H. Hashim, Z.H. Z. Abidin
article en

Abstract

The successful fabrication of high-quality, functionalised monolayers demands a meticulous understanding of the intricate interplay between solvent properties and deposition time. This study introduces a streamlined method for covalently anchoring end-functionalised cationic self-assembled monolayers (SAMs) onto silver (Ag) substrates, achieving enhanced surface coverage, uniformity, and electrochemical performance. The ammonium-terminated SAM, dibromo-10,10’-bis(triethylammoniumdecyl)disulfide (C10-TEA-SAM), was synthesised and its structure confirmed via ¹H NMR spectroscopy. Optimised C10-TEA-SAM immobilisation onto Ag surfaces, employing ethanol as the solvent due to its superior solvating ability for the ionic C10-TEA-SAM molecules, yielded a well-covered, hydrophilic surface. Contact angle (CA) measurements revealed a progressive decrease in CA with increasing immersion time, reaching a minimum of 5.85° after 5 days, indicative of enhanced hydrophilicity. Furthermore, atomic force microscopy revealed a concomitant reduction in surface roughness with prolonged immersion, suggesting the formation of a smoother and more uniform monolayer. Attenuated Total Reflectance Fourier Transform Infrared (ATR-FTIR) spectroscopy confirmed the presence of the C10-TEA-SAM on the Ag surface, while electrochemical impedance spectroscopy (EIS) revealed the insulating nature of the Ag/C10-TEA-SAM interface. This insulating behaviour, characterised by a larger semi-circle impedance and increased bulk resistance, is indicative of a highly ordered, defect-free structure with minimal electron transfer, analogous to long-chain alkanethiol monolayers. These findings collectively demonstrate the efficacy of this optimised approach in creating high-quality cationic SAMs on Ag substrates, offering strong potential for sensor and surface-coating applications. • Developed a stable, uniform method to anchor triethylammonium-functionalised self-assembled monolayers on silver surfaces Ag. • Identified ethanol as the optimal solvent, achieving a contact angle reduction to 5.85° for hydrophilic surfaces. • Produced defect-free monolayer coatings for sensors and surface applications. • Established a robust streamlined approach for applications in sensors and surface coatings.

Next MaterialsVol. 11
University of Malaya (MY), Tun Hussein Onn University of Malaysia (MY)
Openalex Percentile: Top 62%
Molecular Junctions and Nanostructures
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