TY - JOUR
T1 - Atomically Dispersed Iridium on Indium Tin Oxide Efficiently Catalyzes Water Oxidation
AU - Lebedev, Dmitry
AU - Ezhov, Roman
AU - Heras-Domingo, Javier
AU - Comas-Vives, Aleix
AU - Kaeffer, Nicolas
AU - Willinger, Marc
AU - Solans-Monfort, Xavier
AU - Huang, Xing
AU - Pushkar, Yulia
AU - Copéret, Christophe
N1 - Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/7/22
Y1 - 2020/7/22
N2 - Heterogeneous catalysts in the form of atomically dispersed metals on a support provide the most efficient utilization of the active component, which is especially important for scarce and expensive late transition metals. These catalysts also enable unique opportunities to understand reaction pathways through detailed spectroscopic and computational studies. Here, we demonstrate that atomically dispersed iridium sites on indium tin oxide prepared via surface organometallic chemistry display exemplary catalytic activity in one of the most challenging electrochemical processes, the oxygen evolution reaction (OER). In situ X-ray absorption studies revealed the formation of IrV═O intermediate under OER conditions with an Ir-O distance of 1.83 Å. Modeling of the reaction mechanism indicates that IrV═O is likely a catalyst resting state, which is subsequently oxidized to IrVI enabling fast water nucleophilic attack and oxygen evolution. We anticipate that the applied strategy can be instrumental in preparing and studying a broad range of atomically dispersed transition metal catalysts on conductive oxides for (photo)electrochemical applications.
AB - Heterogeneous catalysts in the form of atomically dispersed metals on a support provide the most efficient utilization of the active component, which is especially important for scarce and expensive late transition metals. These catalysts also enable unique opportunities to understand reaction pathways through detailed spectroscopic and computational studies. Here, we demonstrate that atomically dispersed iridium sites on indium tin oxide prepared via surface organometallic chemistry display exemplary catalytic activity in one of the most challenging electrochemical processes, the oxygen evolution reaction (OER). In situ X-ray absorption studies revealed the formation of IrV═O intermediate under OER conditions with an Ir-O distance of 1.83 Å. Modeling of the reaction mechanism indicates that IrV═O is likely a catalyst resting state, which is subsequently oxidized to IrVI enabling fast water nucleophilic attack and oxygen evolution. We anticipate that the applied strategy can be instrumental in preparing and studying a broad range of atomically dispersed transition metal catalysts on conductive oxides for (photo)electrochemical applications.
UR - http://www.scopus.com/inward/record.url?scp=85087677021&partnerID=8YFLogxK
U2 - 10.1021/acscentsci.0c00604
DO - 10.1021/acscentsci.0c00604
M3 - Article
AN - SCOPUS:85087677021
SN - 2374-7943
VL - 6
SP - 1189
EP - 1198
JO - ACS Central Science
JF - ACS Central Science
IS - 7
ER -