Single‐Molecule Mechanoresistivity by Intermetallic Bonding

Abstract: The metal‐electrode interface is key to unlocking emergent behaviour in all organic electrified systems, from battery technology to molecular electronics. In the latter, interfacial engineering has enabled efficient transport, higher device stability, and novel functionality. Mechanoresistivity – the change in electrical behaviour in response to a mechanical stimulus and a pathway to extremely sensitive force sensors – is amongst the most studied phenomena in molecular electronics, and the molecule‐electrode interface plays a pivotal role in its emergence, reproducibility, and magnitude. In this contribution, we show that organometallic molecular wires incorporating a Pt (II) cation show mechanoresistive behaviour of exceptional magnitude, with conductance modulations of more than three orders of magnitude upon compression by as little as 1 nm. We synthesised series of cyclometalated Pt (II) molecular wires, and used scanning tunnelling microscopy – break junction techniques to characterise their electromechanical behaviour. Mechanoresistivity arises from an interaction between the Pt (II) cation and the Au electrode triggered by mechanical compression of the single‐molecule device, and theoretical modelling confirms this hypothesis. Our study provides a new tool for the design of functional molecular wires by exploiting previously unreported ion‐metal interactions in single‐molecule devices, and develops a new framework for the development of mechanoresistive molecular junctions.

Angaben zum Objekt

• Standort: Deutsche Nationalbibliothek Frankfurt am Main
• Umfang: Online-Ressource
• Sprache: Englisch

Verweise und Beziehungen

• Erschienen in: Single‐Molecule Mechanoresistivity by Intermetallic Bonding ; day:06 ; month:11 ; year:2024 ; extent:8 ; Angewandte Chemie / International edition. International edition ; (06.11.2024) (gesamt 8)

Beteiligte, Orts- und Zeitangaben

• Urheber: Sil, Amit ; Spano, Chiara E. ; Chelli, Yahia ; Higgins, Simon J. ; Sangtarash, Sara ; Piccinini, Gianluca ; Graziano, Mariagrazia ; Nichols, Richard J. ; Sadeghi, Hatef ; Vezzoli, Andrea

Weitere Informationen

• DOI: 10.1002/anie.202418062
• URN: urn:nbn:de:101:1-2411061410487.023136781003
• Rechteinformation: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
• Letzte Aktualisierung: 15.08.2025, 07:22 MESZ