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.
Authors
- Jessem Landoulsi (ORCID: https://orcid.org/0000-0003-2394-4437)
- Christophe Méthivier (ORCID: https://orcid.org/0000-0003-3296-8430)
- Laetitia Valentin
- H Bouloussa
- Dominique Costa (ORCID: https://orcid.org/0000-0002-3781-9867)
- Antoine Miche (ORCID: https://orcid.org/0000-0002-8006-1123)
- Pauline Cornette
- Joanne Lê-Chesnais (ORCID: https://orcid.org/0009-0001-6562-0580)
- Fatima E. Bouatir
Institutions
- 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)
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
Funders
- Grand Équipement National De Calcul Intensif