1999
DOI: 10.1149/1.1390813
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Electrochemical Modification of Boron-Doped Chemical Vapor Deposited Diamond Surfaces with Covalently Bonded Monolayers

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Cited by 141 publications
(116 citation statements)
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“…Furthermore, the order and coverage of the molecules in the modification layer is also dependent on both the molecules to be used and the surface. This has been illustrated by McCreery and coworkers [90] where the diazonium salt of nitroazobenzene gave well ordered monolayers on glassy carbon but not on the basal places of HOPG or diamond where the coverage was only between 50 to 70% of a monolayer [91]. Furthermore, the reaction in Scheme 1 is only the dominant reaction as side reactions do occur; the nature of which depends on the R group and the surface being modified.…”
Section: Aryl Diazonium Salt Modified Carbon Electrodesmentioning
confidence: 91%
“…Furthermore, the order and coverage of the molecules in the modification layer is also dependent on both the molecules to be used and the surface. This has been illustrated by McCreery and coworkers [90] where the diazonium salt of nitroazobenzene gave well ordered monolayers on glassy carbon but not on the basal places of HOPG or diamond where the coverage was only between 50 to 70% of a monolayer [91]. Furthermore, the reaction in Scheme 1 is only the dominant reaction as side reactions do occur; the nature of which depends on the R group and the surface being modified.…”
Section: Aryl Diazonium Salt Modified Carbon Electrodesmentioning
confidence: 91%
“…Electrochemically modified diamond surfaces Kuo et al introduced aromatic groups onto the surface of B-doped diamond by the electrochemical reduction of phenyl diazonium salts on the surface [64]. Diamond powders exposed to NO 2 near RT were found to have stably adsorbed RNOx and ROx species (in which R stands for radical) on the surface by Azambre et al [65].…”
Section: 5mentioning
confidence: 99%
“…The order and coverage of the modifier molecules in the modification layer also depends on the type of modifier as well as the substrate surface. This has been illustrated by McCreery and co-workers [20] where the diazonium salt of nitroazobenzene gave well ordered monolayers on glassy carbon but not on the basal planes of HOPG or diamond where the coverage was only between 50 -70% of a monolayer [21]. Steven et.al.…”
Section: Electrochemically Assisted Covalent Modificationmentioning
confidence: 86%