Resolving Peptide-Based Supramolecular Architecture Emerging at Reactive Copper/Water Interface

Understanding how molecular interactions evolve into ordered architectures at reactive solid/liquid interfaces remains a major challenge because surface reactivity can profoundly influence adsorption mechanisms. In such systems, multiple interfacial processes, including redox reactions, adsorption/desorption, coordination, and supramolecular organization, may occur simultaneously, making both chemical and structural characterization particularly challenging. Here, we investigate the adsorption behavior of small peptides at the copper/water interface and reveal the complex interplay between surface reactivity, self-assembly, and (supra)molecular organization. Specifically, by combining surface-sensitive techniques with density functional theory (DFT) calculations, we provide converging experimental and computational evidence on the formation of CuI-peptide units generated through interfacial copper oxidation and assembled into an interconnected three-dimensional network driven by the formation of Cu-S coordinative bonds and stabilized by weaker electrostatic and hydrogen-bonding interactions. AFM force spectroscopy further reveals reproducible nanomechanical events associated with a characteristic structural length scale of approximately 1 nm, in agreement with DFT predictions, indicating the existence of an elementary structural motif within the CuI-peptide network. The resulting assembly forms a thick, hydrated, and mechanically soft multilayer extending several tens of nanometers beyond the molecular dimensions of the peptide. Time-lapse AFM reveals a growth mechanism driven by the local reorganization of colloidal building blocks, resulting in dynamic film porosity that sustains continued growth of the adlayer. The combined experimental and theoretical results support a coupled redox-coordination-assembly-transport-controlled growth mechanism describing how molecular adsorption evolves into a supramolecular architecture at a reactive copper/water interface.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2026-09-12
DOI
https://doi.org/10.1021/acsami.6c13753
Primary Topic
Surface Chemistry and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Resolving Peptide-Based Supramolecular Architecture Emerging at Reactive Copper/Water Interface

Jessem Landoulsi, Christophe Méthivier, Laetitia Valentin, H Bouloussa et al.
ACS Applied Materials & Interfaces
Surface Chemistry and Catalysis
article

Resolving Peptide-Based Supramolecular Architecture Emerging at Reactive Copper/Water Interface

Jessem Landoulsi, Christophe Méthivier, Laetitia Valentin, H Bouloussa, Dominique Costa, Antoine Miche, Pauline Cornette, Joanne Lê-Chesnais, Fatima E. Bouatir
article en

Abstract

Understanding how molecular interactions evolve into ordered architectures at reactive solid/liquid interfaces remains a major challenge because surface reactivity can profoundly influence adsorption mechanisms. In such systems, multiple interfacial processes, including redox reactions, adsorption/desorption, coordination, and supramolecular organization, may occur simultaneously, making both chemical and structural characterization particularly challenging. Here, we investigate the adsorption behavior of small peptides at the copper/water interface and reveal the complex interplay between surface reactivity, self-assembly, and (supra)molecular organization. Specifically, by combining surface-sensitive techniques with density functional theory (DFT) calculations, we provide converging experimental and computational evidence on the formation of CuI-peptide units generated through interfacial copper oxidation and assembled into an interconnected three-dimensional network driven by the formation of Cu-S coordinative bonds and stabilized by weaker electrostatic and hydrogen-bonding interactions. AFM force spectroscopy further reveals reproducible nanomechanical events associated with a characteristic structural length scale of approximately 1 nm, in agreement with DFT predictions, indicating the existence of an elementary structural motif within the CuI-peptide network. The resulting assembly forms a thick, hydrated, and mechanically soft multilayer extending several tens of nanometers beyond the molecular dimensions of the peptide. Time-lapse AFM reveals a growth mechanism driven by the local reorganization of colloidal building blocks, resulting in dynamic film porosity that sustains continued growth of the adlayer. The combined experimental and theoretical results support a coupled redox-coordination-assembly-transport-controlled growth mechanism describing how molecular adsorption evolves into a supramolecular architecture at a reactive copper/water interface.

ACS Applied Materials & Interfaces
Centre National de la Recherche Scientifique (FR), Université Paris Cité (FR), Sorbonne Université (FR), Université Sorbonne Paris Nord (FR), Sorbonne Paris Cité (FR), Institut de Recherche de Chimie Paris (FR), Sorbonne University Abu Dhabi (AE), Université Paris 1 Panthéon-Sorbonne (FR)
Grand Équipement National De Calcul Intensif
Openalex Percentile: Top 20%
Surface Chemistry and Catalysis
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