S
Steven Y. Reece
Researcher at Massachusetts Institute of Technology
Publications - 32
Citations - 6605
Steven Y. Reece is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Proton-coupled electron transfer & Electron transfer. The author has an hindex of 23, co-authored 32 publications receiving 6033 citations. Previous affiliations of Steven Y. Reece include California Institute for Quantitative Biosciences.
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Journal ArticleDOI
Solar Energy Supply and Storage for the Legacy and Nonlegacy Worlds
Timothy R. Cook,Dilek K. Dogutan,Steven Y. Reece,Yogesh Surendranath,Thomas S. Teets,Daniel G. Nocera +5 more
TL;DR: The Scope of Review: Large-Scale Centralized Energy Storage, Chemical Energy Storage: Solar Fuels, and Capacitors 6486 5.1.2.
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Wireless Solar Water Splitting Using Silicon-Based Semiconductors and Earth-Abundant Catalysts
Steven Y. Reece,Jonathan A. Hamel,Kimberly Sung,Thomas D. Jarvi,Arthur J. Esswein,Joep J. H. Pijpers,Joep J. H. Pijpers,Daniel G. Nocera +7 more
TL;DR: The development of solar water-splitting cells comprising earth-abundant elements that operate in near-neutral pH conditions, both with and without connecting wires are described, allowing for direct solar-to-fuels conversion that captures many of the basic functional elements of a leaf.
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Proton-Coupled Electron Transfer in Biology: Results from Synergistic Studies in Natural and Model Systems
Steven Y. Reece,Daniel G. Nocera +1 more
TL;DR: This review presents complementary biological and model systems that explore PCET in electron transfer (ET) through hydrogen bonds, the activation of C-H bonds, and the generation and transport of amino acid radicals.
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Highly active cobalt phosphate and borate based oxygen evolving catalysts operating in neutral and natural waters
TL;DR: In this paper, a high surface area electrode is functionalized with cobalt-based oxygen evolving catalysts (Co-OEC), which achieves a current density of 100 mA cm−2 for water oxidation at 442 and 363 mV overpotential, respectively.
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Proton-coupled electron transfer: the mechanistic underpinning for radical transport and catalysis in biology
TL;DR: This discussion will present model systems containing orthogonal ET and PT pathways, thereby allowing the proton and electron tunnelling events to be disentangled and a case study of radical-based quantum catalysis in a natural biological enzyme, class I Escherichia coli ribonucleotide reductase.