Abrasively Immobilised Multiwalled Carbon Nanotube Agglomerates: A Novel Electrode Material Approach for the Analytical Sensing of pH

We demonstrate for the first time that agglomerates of multiwalled carbon nanotubes (MWCNTs) can be formed in which the binder in the agglomerate is itself a redox‐active molecular solid. Two separate agglomerates were formed by dissolving 9,10‐phenanthraquinone (PAQ) or 1,2‐napthaquinone (NQ) in ac...

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Published in:Chemphyschem Vol. 5; no. 5; pp. 669 - 677
Main Authors: Wildgoose, Gregory G., Leventis, Henry C., Streeter, Ian, Lawrence, Nathan S., Wilkins, Shelley J., Jiang, Li, Jones, Timothy G. J., Compton, Richard G.
Format: Journal Article
Language:English
Published: Weinheim WILEY-VCH Verlag 17-05-2004
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Abstract We demonstrate for the first time that agglomerates of multiwalled carbon nanotubes (MWCNTs) can be formed in which the binder in the agglomerate is itself a redox‐active molecular solid. Two separate agglomerates were formed by dissolving 9,10‐phenanthraquinone (PAQ) or 1,2‐napthaquinone (NQ) in acetone together with MWCNTs and adding an excess of aqueous solution to cause precipitation of agglomerates, approximately 10 µ;m in dimension, which consist of bundles of nanotubes running into and throughout the amorphous molecular solid that binds the agglomerate together. The nature of this structure, when immobilised on a substrate electrode and in contact with aqueous electrolyte solutions, gives rise to many three‐phase boundaries, electrolyte|agglomerate|conductor, which is advantageous to the solid‐state analytical electrochemistry of such a material as it imparts a larger electroactive surface area than other modified carbon electrodes. The two agglomerates each gave a voltammetrically measurable response to changes in pH; when abrasively immobilised on a basal plane pyrolitic graphite electrode a plot of peak potential against pH produced a linear response for both MWCNT–PAQ and MWCNT–NQ agglomerates over the pH range pH 1–12 and over the temperature range 20–70 °C. Many three‐phase boundaries: The authors demonstrate for the first time that agglomerates of multiwalled carbon nanotubes can be formed in which the binder in the agglomerate is itself a redox‐active molecular solid (see picture). The nature of this structure, when immobilised on a substrate electrode and in contact with aqueous electrolyte solutions, gives rise to many three‐phase boundaries, which imparts a larger electroactive surface area than other modified carbon electrodes.
AbstractList We demonstrate for the first time that agglomerates of multiwalled carbon nanotubes (MWCNTs) can be formed in which the binder in the agglomerate is itself a redox‐active molecular solid. Two separate agglomerates were formed by dissolving 9,10‐phenanthraquinone (PAQ) or 1,2‐napthaquinone (NQ) in acetone together with MWCNTs and adding an excess of aqueous solution to cause precipitation of agglomerates, approximately 10 µ;m in dimension, which consist of bundles of nanotubes running into and throughout the amorphous molecular solid that binds the agglomerate together. The nature of this structure, when immobilised on a substrate electrode and in contact with aqueous electrolyte solutions, gives rise to many three‐phase boundaries, electrolyte|agglomerate|conductor, which is advantageous to the solid‐state analytical electrochemistry of such a material as it imparts a larger electroactive surface area than other modified carbon electrodes. The two agglomerates each gave a voltammetrically measurable response to changes in pH; when abrasively immobilised on a basal plane pyrolitic graphite electrode a plot of peak potential against pH produced a linear response for both MWCNT–PAQ and MWCNT–NQ agglomerates over the pH range pH 1–12 and over the temperature range 20–70 °C. Many three‐phase boundaries: The authors demonstrate for the first time that agglomerates of multiwalled carbon nanotubes can be formed in which the binder in the agglomerate is itself a redox‐active molecular solid (see picture). The nature of this structure, when immobilised on a substrate electrode and in contact with aqueous electrolyte solutions, gives rise to many three‐phase boundaries, which imparts a larger electroactive surface area than other modified carbon electrodes.
We demonstrate for the first time that agglomerates of multiwalled carbon nanotubes (MWCNTs) can be formed in which the binder in the agglomerate is itself a redox-active molecular solid. Two separate agglomerates were formed by dissolving 9,10-phenanthraquinone (PAQ) or 1,2-napthaquinone (NQ) in acetone together with MWCNTs and adding an excess of aqueous solution to cause precipitation of agglomerates, approximately 10 microns in dimension, which consist of bundles of nanotubes running into and throughout the amorphous molecular solid that binds the agglomerate together. The nature of this structure, when immobilised on a substrate electrode and in contact with aqueous electrolyte solutions, gives rise to many three-phase boundaries, electrolyte|agglomerate|conductor, which is advantageous to the solid-state analytical electrochemistry of such a material as it imparts a larger electroactive surface area than other modified carbon electrodes. The two agglomerates each gave a voltammetrically measurable response to changes in pH; when abrasively immobilised on a basal plane pyrolitic graphite electrode a plot of peak potential against pH produced a linear response for both MWCNT-PAQ and MWCNT-NQ agglomerates over the pH range pH 1-12 and over the temperature range 20-70 degrees C.
We demonstrate for the first time that agglomerates of multiwalled carbon nanotubes (MWCNTs) can be formed in which the binder in the agglomerate is itself a redox‐active molecular solid. Two separate agglomerates were formed by dissolving 9,10‐phenanthraquinone (PAQ) or 1,2‐napthaquinone (NQ) in acetone together with MWCNTs and adding an excess of aqueous solution to cause precipitation of agglomerates, approximately 10 µ;m in dimension, which consist of bundles of nanotubes running into and throughout the amorphous molecular solid that binds the agglomerate together. The nature of this structure, when immobilised on a substrate electrode and in contact with aqueous electrolyte solutions, gives rise to many three‐phase boundaries, electrolyte|agglomerate|conductor, which is advantageous to the solid‐state analytical electrochemistry of such a material as it imparts a larger electroactive surface area than other modified carbon electrodes. The two agglomerates each gave a voltammetrically measurable response to changes in pH; when abrasively immobilised on a basal plane pyrolitic graphite electrode a plot of peak potential against pH produced a linear response for both MWCNT–PAQ and MWCNT–NQ agglomerates over the pH range pH 1–12 and over the temperature range 20–70  ° C.
Author Leventis, Henry C.
Compton, Richard G.
Jiang, Li
Lawrence, Nathan S.
Wilkins, Shelley J.
Jones, Timothy G. J.
Streeter, Ian
Wildgoose, Gregory G.
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  givenname: Henry C.
  surname: Leventis
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  organization: Physical and Theoretical Chemistry Laboratory, University of Oxford, South Parks Road, Oxford, OX1 3QZ, U.K., Fax:(+44) 1865-275410
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  givenname: Ian
  surname: Streeter
  fullname: Streeter, Ian
  organization: Physical and Theoretical Chemistry Laboratory, University of Oxford, South Parks Road, Oxford, OX1 3QZ, U.K., Fax:(+44) 1865-275410
– sequence: 4
  givenname: Nathan S.
  surname: Lawrence
  fullname: Lawrence, Nathan S.
  organization: Physical and Theoretical Chemistry Laboratory, University of Oxford, South Parks Road, Oxford, OX1 3QZ, U.K., Fax:(+44) 1865-275410
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  givenname: Shelley J.
  surname: Wilkins
  fullname: Wilkins, Shelley J.
  organization: Department of Materials, University of Oxford, Parks Road, Oxford, OX1 3PH, U.K
– sequence: 6
  givenname: Li
  surname: Jiang
  fullname: Jiang, Li
  organization: Schlumberger Cambridge Research, High Cross, Madingley Road, Cambridge, CB3 0EL, U.K
– sequence: 7
  givenname: Timothy G. J.
  surname: Jones
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  givenname: Richard G.
  surname: Compton
  fullname: Compton, Richard G.
  email: richard.compton@chem.ox.ac.uk
  organization: Physical and Theoretical Chemistry Laboratory, University of Oxford, South Parks Road, Oxford, OX1 3QZ, U.K., Fax:(+44) 1865-275410
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Issue 5
Keywords Scanning electron microscopy
electrochemistry
Quinone
Carbon nanotubes
modified carbon electrodes
Electrode material
Chemical sensor
nanostructures
Surface structure
Electrodes
multiwalled carbon nanotubes
sensors
Morphology
pH
Naphthoquinone
Modified material
Language English
License CC BY 4.0
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Snippet We demonstrate for the first time that agglomerates of multiwalled carbon nanotubes (MWCNTs) can be formed in which the binder in the agglomerate is itself a...
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SubjectTerms Analytical chemistry
Chemistry
Chemistry, Physical - methods
Electrochemistry
Electrons
Exact sciences and technology
General, instrumentation
Hydrogen-Ion Concentration
Microscopy, Electron, Scanning
Models, Molecular
modified carbon electrodes
multiwalled carbon nanotubes
nanostructures
Nanotubes, Carbon - chemistry
Nanotubes, Carbon - ultrastructure
Naphthoquinones - chemistry
Oxidation-Reduction
Phenanthrenes - chemistry
sensors
Temperature
Title Abrasively Immobilised Multiwalled Carbon Nanotube Agglomerates: A Novel Electrode Material Approach for the Analytical Sensing of pH
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https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcphc.200400030
https://www.ncbi.nlm.nih.gov/pubmed/15179719
Volume 5
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