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Updated: Feb 18, 2026

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
Biomimetic versus enzymatic high-potential electrocatalytic reduction of hydrogen peroxide on a functionalized carbon
Bertrand Reuillard1, Solène Gentil1, Marie Carrière1
1Univ. Grenoble Alpes , DCM UMR 5250 , F-38000 Grenoble , France and CNRS , DCM UMR 5250 , F-38000 Grenoble , France .
Abstract:
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 . Compared to the pi-stacking of non-coordinated (PP)Fe on a MWCNT electrode, the (Im)(PP)Fe -modified MWCNT electrode exhibits higher electrocatalytic activity with an Imax = 0.52 mA cm-2 for the reduction of H2O2, 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 H2O2 reduction, the (Im)(PP)Fe -modified MWCNT electrode exhibits a markedly higher operational stability, retaining 63% of its initial activity after one month.
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