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 - Funding Information:
This research is based upon work supported by InnoSuisse through the Swiss Competence Center for Energy Research (SCCER) Heat & Electricity Storage and by the National Science Foundation, Division of Chemistry CHE-1900476 (Y.P.). The use of the Advanced Photon Source, an Office of Science User Facility operated by the U.S. Department of Energy (DOE) Office of Science by Argonne National Laboratory, was supported by the U.S. DOE under Contract DE-AC02-06CH11357. The PNC/XSD (Sector 20) facilities at the Advanced Photon Source and research at these facilities were supported by the U.S. Department of Energy?Basic Energy Science the Canadian Light Source and its funding partners, the University of Washington, and the Advanced Photon Source. J. H.-D. and X.S.-M. acknowledge financial support from MINECO (CTQ2017-89132-P) and Generalitat de Catalunya (2017SGR1320). A.C.-V. acknowledges the financial support from the ?Ramon y Cajal? Fellowship, funded by Spanish MEC and the European Social Fund (RyC-2016-19930) and and the Spanish ?Ministerio de Ciencia, Innovacion y Universidades? (PGC2018-100818-A-I00).
Funding Information:
This research is based upon work supported by InnoSuisse through the Swiss Competence Center for Energy Research (SCCER) Heat & Electricity Storage and by the National Science Foundation, Division of Chemistry CHE-1900476 (Y.P.). The use of the Advanced Photon Source, an Office of Science User Facility operated by the U.S. Department of Energy (DOE) Office of Science by Argonne National Laboratory, was supported by the U.S. DOE under Contract DE-AC02-06CH11357. The PNC/XSD (Sector 20) facilities at the Advanced Photon Source and research at these facilities were supported by the U.S. Department of Energy—Basic Energy Science, the Canadian Light Source and its funding partners, the University of Washington, and the Advanced Photon Source. J. H.-D. and X.S.-M. acknowledge financial support from MINECO (CTQ2017-89132-P) and Generalitat de Catalunya (2017SGR1320). A.C.-V. acknowledges the financial support from the “Ramon y Cajal” Fellowship, funded by Spanish MEC and the European Social Fund (RyC-2016-19930) and and the Spanish “Ministerio de Ciencia, Innovación y Universidades” (PGC2018-100818-A-I00).
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 - https://www.scopus.com/pages/publications/85087677021
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 -