Journal article

Iron oxide particles are the active sites for hydrogen peroxide sensing at multiwalled carbon nanotube modified electrodes.

Abstract:: We demonstrate that the "electrocatalytic" hydrogen peroxide detection reported at multiwalled carbon nanotube modified electrodes is due to iron oxide particles arising from the chemical vapor deposition nanotube fabrication process rather than due to intrinsic catalysis attributable to the carbon nanotubes arising, for example, from edge plane-like sites/defects.

Publication status:: Published

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APA Style

Sljukić, B., Banks, C., & Compton, R. (2006). Iron oxide particles are the active sites for hydrogen peroxide sensing at multiwalled carbon nanotube modified electrodes. Nano Letters, 6(7), 1556–1558.

MLA Style

Sljukić, B., et al. “Iron Oxide Particles Are the Active Sites for Hydrogen Peroxide Sensing at Multiwalled Carbon Nanotube Modified Electrodes.” Nano Letters, vol. 6, no. 7, 2006, pp. 1556–58.

Chicago Style

Sljukić, B, C Banks, and R Compton. 2006. “Iron Oxide Particles Are the Active Sites for Hydrogen Peroxide Sensing at Multiwalled Carbon Nanotube Modified Electrodes.” Nano Letters 6 (7): 1556–58.
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Publisher copy:: 10.1021/nl060366v

Authors

+ Sljukić, B More by this author

Role:: Author

+ Banks, C More by this author

Role:: Author

+ Compton, R More by this author

Institution:: University of Oxford
Division:: MPLS
Department:: Chemistry
Sub department:: Physical & Theoretical Chem
Role:: Author

Journal:: Nano letters More from this journal
Volume:: 6
Issue:: 7
Pages:: 1556-1558
Publication date:: 2006-07-01
DOI:: 10.1021/nl060366v
EISSN:: 1530-6992
ISSN:: 1530-6984

Language:: English
Keywords:: Electrodes

Electrochemistry

Ferric Compounds

Hydrogen Peroxide

Nanotubes, Carbon

Binding Sites

Oxidation-Reduction

Surface Properties
UUID:: uuid:1a30199c-236d-4ae1-8fcc-55fba15084c0
Local pid:: pubs:33539
Source identifiers:: 33539
Deposit date:: 2012-12-19

Terms of use

Copyright date:: 2006

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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