Single-Atom Catalyst of Platinum Supported on Titanium Nitride for Selective Electrochemical Reactions

As a catalyst, single‐atom platinum may provide an ideal structure for platinum minimization. Herein, a single‐atom catalyst of platinum supported on titanium nitride nanoparticles were successfully prepared with the aid of chlorine ligands. Unlike platinum nanoparticles, the single‐atom active site...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Angewandte Chemie 2016-02, Vol.128 (6), p.2098-2102
Hauptverfasser: Yang, Sungeun, Kim, Jiwhan, Tak, Young Joo, Soon, Aloysius, Lee, Hyunjoo
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:As a catalyst, single‐atom platinum may provide an ideal structure for platinum minimization. Herein, a single‐atom catalyst of platinum supported on titanium nitride nanoparticles were successfully prepared with the aid of chlorine ligands. Unlike platinum nanoparticles, the single‐atom active sites predominantly produced hydrogen peroxide in the electrochemical oxygen reduction with the highest mass activity reported so far. The electrocatalytic oxidation of small organic molecules, such as formic acid and methanol, also exhibited unique selectivity on the single‐atom platinum catalyst. A lack of platinum ensemble sites changed the reaction pathway for the oxygen‐reduction reaction toward a two‐electron pathway and formic acid oxidation toward direct dehydrogenation, and also induced no activity for the methanol oxidation. This work demonstrates that single‐atom platinum can be an efficient electrocatalyst with high mass activity and unique selectivity. Nanokatalyse: Ein Einzelatom‐Platinkatalysator auf Titannitrid wurde mithilfe von Chlorliganden hergestellt und als Elektrokatalysator verwendet. Die Abwesenheit von Platin‐Ensembles sorgt für einzigartige Selektivitäten in der Sauerstoffreduktion sowie der Ameisensäure‐ und Methanoloxidation.
ISSN:0044-8249
1521-3757
DOI:10.1002/ange.201509241