Affiliation:
1. CNRS Univ. Rennes ISCR–UMR 6226 Rennes 35000 France
2. X4C 48 rue Auguste Piccard Gosselies 6041 Belgium
3. Laboratoire de Chimie Organique Université libre de Bruxelles (ULB) CP 160/06, Avenue F.D. Roosevelt 50 Brussels 1050 Belgium
4. Institut des Matériaux de Nantes Université de Nantes UMR 6502, 2 rue de la Houssinière Nantes 44000 France
Abstract
AbstractA 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.
Funder
Agence Nationale de la Recherche
Cited by
2 articles.
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