par Lenne, Quentin;Mattiuzzi, Alice 
;Jabin, Ivan ;Hamon, Jonathan;Leroux, Yann;Lagrost, Corinne
Référence Advanced Materials Interfaces, 10, page (2202219)
Publication Publié, 2023-01-10
;Jabin, Ivan ;Hamon, Jonathan;Leroux, Yann;Lagrost, CorinneRéférence Advanced Materials Interfaces, 10, page (2202219)
Publication Publié, 2023-01-10
Article révisé par les pairs
| Résumé : | A series of surface-functionalized gold nanocatalysts are synthesized. Through diazonium chemistry, calix[4]arene molecules are grafted at the gold surface. Sharing the same anchoring function and a common backbone, the calix[4]arene ligands possess distinct terminal chemical functions where the length, hydrophobic nature, and oxygen affinity are varied. Thanks to the versatility of the calix[4]arene platform, this paper only focuses on the molecular tuning of the solid/liquid interface through the change of the tail groups while electronic effects that are regulated by the anchoring function will be similar for all catalysts. Electrocatalytic tests demonstrate the influence of the tails group on the oxygen reduction reaction performances, including efficiency, selectivity, and durability. Beyond a pure geometric steric effect, it is shown that chemical properties of the ligands can effectively tune the interactions between the metallic catalyst and the electrolyte and reactants. |
