Jack W. Jordan
Electrochemistry of redox-active molecules confined within narrow carbon nanotubes
Jordan, Jack W.; Townsend, William J. V.; Johnson, Lee R.; Walsh, Darren A.; Newton, Graham N.; Khlobystov, Andrei N.
Authors
William J. V. Townsend
Professor LEE JOHNSON LEE.JOHNSON@NOTTINGHAM.AC.UK
PROFESSOR OF ELECTROCHEMISTRY
Professor DARREN WALSH DARREN.WALSH@NOTTINGHAM.AC.UK
PROFESSOR OF CHEMISTRY
Professor GRAHAM NEWTON GRAHAM.NEWTON@NOTTINGHAM.AC.UK
PROFESSOR OF CHEMISTRY
Professor Andrei Khlobystov ANDREI.KHLOBYSTOV@NOTTINGHAM.AC.UK
PROFESSOR OF CHEMICAL NANOSCIENCE
Abstract
Confinement of molecules within nanocontainers can be a powerful tool for controlling the states of guest-molecules, tuning properties of host-nanocontainers and triggering the emergence of synergistic properties within the host–guest systems. Among nanocontainers, single-walled carbon nanotubes – atomically thin cylinders of carbon, with typical diameters below 2 nm and lengths reaching macroscopic dimensions – are ideal hosts for a variety of materials, including inorganic crystals, and organic, inorganic and organometallic molecules. The extremely high aspect ratio of carbon nanotubes is complemented by their functional properties, such as exceptionally high electrical conductivity and thermal, chemical and electrochemical stability, making carbon nanotubes ideal connectors between guest-molecules and macroscopic electrodes. The idea of harnessing nanotubes both as nanocontainers and nanoelectrodes has led to the incorporation of redox-active species entrapped within nanotube cavities where the host-nanotubes may serve as conduits of electrons to/from the guest-molecules, whilst restricting the molecular positions, orientations, and local environment around the redox centres. This review gives a contemporary overview of the status of molecular redox chemistry within ultra-narrow carbon nanotubes (nanotubes with diameters approaching molecular dimensions) highlighting the opportunities, pitfalls, and gaps in understanding of electrochemistry in confinement, including the role of nanotube diameter, size and shape of guest-molecules, type of electrolyte, solvent and other experimental conditions.
Citation
Jordan, J. W., Townsend, W. J. V., Johnson, L. R., Walsh, D. A., Newton, G. N., & Khlobystov, A. N. (2021). Electrochemistry of redox-active molecules confined within narrow carbon nanotubes. Chemical Society Reviews, 50(19), 10895-10916. https://doi.org/10.1039/d1cs00478f
Journal Article Type | Article |
---|---|
Acceptance Date | Aug 1, 2021 |
Online Publication Date | Aug 16, 2021 |
Publication Date | Oct 7, 2021 |
Deposit Date | Oct 28, 2021 |
Publicly Available Date | Aug 17, 2022 |
Journal | Chemical Society Reviews |
Print ISSN | 0306-0012 |
Electronic ISSN | 1460-4744 |
Publisher | Royal Society of Chemistry |
Peer Reviewed | Peer Reviewed |
Volume | 50 |
Issue | 19 |
Pages | 10895-10916 |
DOI | https://doi.org/10.1039/d1cs00478f |
Keywords | General Chemistry |
Public URL | https://nottingham-repository.worktribe.com/output/6541583 |
Publisher URL | https://pubs.rsc.org/en/content/articlelanding/2021/CS/D1CS00478F |
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Jordan Et Al Electrochemistry Of Redox-active Molecules Confined Within Narrow Carbon Nanotubes
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