par Lenne, Quentin;Mattiuzzi, Alice
;Jabin, Ivan
;Le Poul, Nicolas;Leroux, Yann;Lagrost, Corinne
Référence Advanced Materials Interfaces, 7, 23, 2001557
Publication Publié, 2020-12-01


Référence Advanced Materials Interfaces, 7, 23, 2001557
Publication Publié, 2020-12-01
Article révisé par les pairs
Résumé : | The deliberate surface modification of nanocatalysts with organic ligands has recently emerged as a promising strategy to boost their efficiency, durability, and/or selectivity in key electrocatalytic processes. The interface between the metallic interface and the immobilized ligands promotes high electrocatalytic activity. Herein, the oxygen reduction reaction activity of gold nanoparticles functionalized with a covalently bound monolayer of calix[4]arenes is compared with commercially available gold nanoparticles, classically stabilized through electrostatic adsorption of citrates onto the gold surfaces. Nanocatalysts coated by calix[4]arenes show enhanced selectivity and stability compared to their citrate-stabilized counterparts. These nanohybrids exhibit excellent activity with a dominant 4-electron reduction of O2 with good electrocatalytic performances along with a high robustness under operation as revealed by X-ray photoelectron spectroscopy analyses. |