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dc.contributor.authorNocera, Daniel G.
dc.date.accessioned2013-11-25T20:30:27Z
dc.date.available2013-11-25T20:30:27Z
dc.date.issued2009-09
dc.date.submitted2009-07
dc.identifier.issn0020-1669
dc.identifier.issn1520-510X
dc.identifier.urihttp://hdl.handle.net/1721.1/82591
dc.description.abstractPersonalized energy (PE) is a transformative idea that provides a new modality for the planet’s energy future. By providing solar energy to the individual, an energy supply becomes secure and available to people of both legacy and nonlegacy worlds and minimally contributes to an increase in the anthropogenic level of carbon dioxide. Because PE will be possible only if solar energy is available 24 h a day, 7 days a week, the key enabler for solar PE is an inexpensive storage mechanism. HY (Y = halide or OH[superscript −]) splitting is a fuel-forming reaction of sufficient energy density for large-scale solar storage, but the reaction relies on chemical transformations that are not understood at the most basic science level. Critical among these are multielectron transfers that are proton-coupled and involve the activation of bonds in energy-poor substrates. The chemistry of these three italicized areas is developed, and from this platform, discovery paths leading to new hydrohalic acid- and water-splitting catalysts are delineated. The latter water-splitting catalyst captures many of the functional elements of photosynthesis. In doing so, a highly manufacturable and inexpensive method for solar PE storage has been discovered.en_US
dc.description.sponsorshipNational Science Foundation (U.S.)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.)en_US
dc.description.sponsorshipUnited States. Air Force Office of Scientific Researchen_US
dc.description.sponsorshipUnited States. Army Research Officeen_US
dc.description.sponsorshipUnited States. Dept. of Energyen_US
dc.description.sponsorshipChesonis Family Foundationen_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/ic901328ven_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePMCen_US
dc.titleChemistry of Personalized Solar Energyen_US
dc.typeArticleen_US
dc.identifier.citationNocera, Daniel G. “Chemistry of Personalized Solar Energy.” Inorganic Chemistry 48, no. 21 (November 2, 2009): 10001-10017.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.mitauthorNocera, Daniel G.en_US
dc.relation.journalInorganic Chemistryen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsNocera, Daniel G.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-4507-1115
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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