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Reversible Redox‐Driven Crystallization in a Paracyclophane Monolayer at a Solid–Liquid Interface

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Reversible Redox‐Driven Crystallization in a Paracyclophane Monolayer at a Solid–Liquid Interface. / Li, Zhi; Mali, Kunal; Hapiot, Philippe et al.
In: Advanced Functional Materials, 15.04.2024.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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APA

Li, Z., Mali, K., Hapiot, P., De Feyter, S., Attias, AJ., & Mertens, S. F. L. (2024). Reversible Redox‐Driven Crystallization in a Paracyclophane Monolayer at a Solid–Liquid Interface. Advanced Functional Materials. Advance online publication. https://doi.org/10.1002/adfm.202315861

Vancouver

Li Z, Mali K, Hapiot P, De Feyter S, Attias AJ, Mertens SFL. Reversible Redox‐Driven Crystallization in a Paracyclophane Monolayer at a Solid–Liquid Interface. Advanced Functional Materials. 2024 Apr 15. Epub 2024 Apr 15. doi: 10.1002/adfm.202315861

Author

Li, Zhi ; Mali, Kunal ; Hapiot, Philippe et al. / Reversible Redox‐Driven Crystallization in a Paracyclophane Monolayer at a Solid–Liquid Interface. In: Advanced Functional Materials. 2024.

Bibtex

@article{c1792c2b999f40a3bc3c87eebd04e30b,
title = "Reversible Redox‐Driven Crystallization in a Paracyclophane Monolayer at a Solid–Liquid Interface",
abstract = "The development and integration of cyclophanes into future functional materials require a detailed understanding of the physicochemical principles that underlie their properties, phase behavior, and in particular the relationship between structure and function. Here, electrochemically switchable crystallization of a ferrocene‐bearing 3D Janus tecton (M‐Fc) at the interface between highly oriented pyrolytic graphite (HOPG) and an electrolyte solution is demonstrated. The M‐Fc adlayer is successfully visualized under both ambient and electrochemical conditions using scanning tunneling microscopy. Voltammetric measurements show a surface‐confined redox process for the M‐Fc modified surface that drives the phase transition between a visible 2D ordered linear phase (M‐Fc0, with ferrocene in the neutral state) and an invisible gas‐like adsorption layer with high mobility when ferrocene is oxidized, M‐Fc+, and a “square scheme” mechanism explains the data. Analogous experiments in a ferrocene‐free tecton adlayer show no phase transition and confirm that the dynamics in M‐Fc are redox‐driven. On‐surface 3D nanoarchitectures are also demonstrated by forming inclusion complexes between M‐Fc and β‐cyclodextrin and device behavior through electrochemical scanning tunneling spectroscopy (STS). These results showcase the functional potential of this class of cyclophanes, which can find use in actuators, optical crystals, and other smart materials.",
keywords = "electrochemical switching, scanning tunneling microscopy, supramolecular self‐assembly, graphite, cyclophanes",
author = "Zhi Li and Kunal Mali and Philippe Hapiot and {De Feyter}, Steven and Andr{\'e}‐Jean Attias and Mertens, {Stijn F. L.}",
year = "2024",
month = apr,
day = "15",
doi = "10.1002/adfm.202315861",
language = "English",
journal = "Advanced Functional Materials",
issn = "1616-301X",
publisher = "John Wiley & Sons, Ltd",

}

RIS

TY - JOUR

T1 - Reversible Redox‐Driven Crystallization in a Paracyclophane Monolayer at a Solid–Liquid Interface

AU - Li, Zhi

AU - Mali, Kunal

AU - Hapiot, Philippe

AU - De Feyter, Steven

AU - Attias, André‐Jean

AU - Mertens, Stijn F. L.

PY - 2024/4/15

Y1 - 2024/4/15

N2 - The development and integration of cyclophanes into future functional materials require a detailed understanding of the physicochemical principles that underlie their properties, phase behavior, and in particular the relationship between structure and function. Here, electrochemically switchable crystallization of a ferrocene‐bearing 3D Janus tecton (M‐Fc) at the interface between highly oriented pyrolytic graphite (HOPG) and an electrolyte solution is demonstrated. The M‐Fc adlayer is successfully visualized under both ambient and electrochemical conditions using scanning tunneling microscopy. Voltammetric measurements show a surface‐confined redox process for the M‐Fc modified surface that drives the phase transition between a visible 2D ordered linear phase (M‐Fc0, with ferrocene in the neutral state) and an invisible gas‐like adsorption layer with high mobility when ferrocene is oxidized, M‐Fc+, and a “square scheme” mechanism explains the data. Analogous experiments in a ferrocene‐free tecton adlayer show no phase transition and confirm that the dynamics in M‐Fc are redox‐driven. On‐surface 3D nanoarchitectures are also demonstrated by forming inclusion complexes between M‐Fc and β‐cyclodextrin and device behavior through electrochemical scanning tunneling spectroscopy (STS). These results showcase the functional potential of this class of cyclophanes, which can find use in actuators, optical crystals, and other smart materials.

AB - The development and integration of cyclophanes into future functional materials require a detailed understanding of the physicochemical principles that underlie their properties, phase behavior, and in particular the relationship between structure and function. Here, electrochemically switchable crystallization of a ferrocene‐bearing 3D Janus tecton (M‐Fc) at the interface between highly oriented pyrolytic graphite (HOPG) and an electrolyte solution is demonstrated. The M‐Fc adlayer is successfully visualized under both ambient and electrochemical conditions using scanning tunneling microscopy. Voltammetric measurements show a surface‐confined redox process for the M‐Fc modified surface that drives the phase transition between a visible 2D ordered linear phase (M‐Fc0, with ferrocene in the neutral state) and an invisible gas‐like adsorption layer with high mobility when ferrocene is oxidized, M‐Fc+, and a “square scheme” mechanism explains the data. Analogous experiments in a ferrocene‐free tecton adlayer show no phase transition and confirm that the dynamics in M‐Fc are redox‐driven. On‐surface 3D nanoarchitectures are also demonstrated by forming inclusion complexes between M‐Fc and β‐cyclodextrin and device behavior through electrochemical scanning tunneling spectroscopy (STS). These results showcase the functional potential of this class of cyclophanes, which can find use in actuators, optical crystals, and other smart materials.

KW - electrochemical switching

KW - scanning tunneling microscopy

KW - supramolecular self‐assembly

KW - graphite

KW - cyclophanes

U2 - 10.1002/adfm.202315861

DO - 10.1002/adfm.202315861

M3 - Journal article

JO - Advanced Functional Materials

JF - Advanced Functional Materials

SN - 1616-301X

ER -