J
Jonas C. Peters
Researcher at California Institute of Technology
Publications - 232
Citations - 28779
Jonas C. Peters is an academic researcher from California Institute of Technology. The author has contributed to research in topics: Catalysis & Ligand. The author has an hindex of 79, co-authored 231 publications receiving 23468 citations. Previous affiliations of Jonas C. Peters include Massachusetts Institute of Technology.
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Journal ArticleDOI
Benchmarking Heterogeneous Electrocatalysts for the Oxygen Evolution Reaction
TL;DR: In this paper, the authors report a protocol for evaluating the activity, stability, and Faradaic efficiency of electrodeposited oxygen-evolving electrocatalysts for water oxidation.
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Benchmarking Hydrogen Evolving Reaction and Oxygen Evolving Reaction Electrocatalysts for Solar Water Splitting Devices
Charles C. L. McCrory,Suho Jung,Ivonne M. Ferrer,Shawn Chatman,Jonas C. Peters,Thomas F. Jaramillo +5 more
TL;DR: A standard protocol is used as a primary screen for evaluating the activity, short-term (2 h) stability, and electrochemically active surface area (ECSA) of 18 and 26 electrocatalysts for the hydrogen evolution reaction (HER and OER) under conditions relevant to an integrated solar water-splitting device in aqueous acidic or alkaline solution.
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Catalytic conversion of nitrogen to ammonia by an iron model complex
TL;DR: Results indicate that a single iron site may be capable of stabilizing the various NxHy intermediates generated during catalytic NH3 formation, and propose that the interstitial carbon atom recently assigned in the nitrogenase cofactor may have a similar role, perhaps by enabling a singleIron site to mediate the enzymatic catalysis through a flexible iron–carbon interaction.
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Synthetic control of excited-state properties in cyclometalated Ir(III) complexes using ancillary ligands.
Jian Li,Peter I. Djurovich,Bert Alleyne,Muhammed Yousufuddin,Nam Nhat Ho,J. Christopher Thomas,Jonas C. Peters,Robert Bau,Mark E. Thompson +8 more
TL;DR: Electrochemical analysis of the (tpy)2 Ir(LL') complexes shows that the reduction potentials are largely unaffected by variation in the ancillary ligand, whereas the oxidation potentials vary over a much wider range (as much as 400 mV between two different LL' ligands).
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Electrocatalytic hydrogen evolution at low overpotentials by cobalt macrocyclic glyoxime and tetraimine complexes.
TL;DR: Digital simulations of the electrochemical data were used to study the mechanism of H2 evolution catalysis, and these studies are discussed.