Cargando…

Biomimetic versus enzymatic high-potential electrocatalytic reduction of hydrogen peroxide on a functionalized carbon nanotube electrode

We report the non-covalent functionalization of a multi-walled carbon nanotube (MWCNT) electrode with a biomimetic model of the horseradish peroxidase (HRP) active site. By modifying the MWCNT electrode surface with imidazole-modified polypyrrole, a new biomimetic complex of HRP was synthesized on t...

Descripción completa

Detalles Bibliográficos
Autores principales: Reuillard, Bertrand, Gentil, Solène, Carrière, Marie, Le Goff, Alan, Cosnier, Serge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666682/
https://www.ncbi.nlm.nih.gov/pubmed/29142732
http://dx.doi.org/10.1039/c5sc01473e
Descripción
Sumario:We report the non-covalent functionalization of a multi-walled carbon nanotube (MWCNT) electrode with a biomimetic model of the horseradish peroxidase (HRP) active site. By modifying the MWCNT electrode surface with imidazole-modified polypyrrole, a new biomimetic complex of HRP was synthesized on the MWCNT sidewalls via the coordination of imidazole (Im) to the metal centre of iron protoporphyrin IX, affording (Im)(PP)Fe(III) . Compared to the pi-stacking of non-coordinated (PP)Fe(III) on a MWCNT electrode, the (Im)(PP)Fe(III) -modified MWCNT electrode exhibits higher electrocatalytic activity with an I (max) = 0.52 mA cm(–2) for the reduction of H(2)O(2), accompanied by a high onset potential of 0.43 V vs. Ag/AgCl. The performances of these novel surface-confined HRP mimics were compared to those of a MWCNT electrode modified by HRP. Although the enzyme electrode displays a higher electrocatalytic activity towards H(2)O(2) reduction, the (Im)(PP)Fe(III) -modified MWCNT electrode exhibits a markedly higher operational stability, retaining 63% of its initial activity after one month.