dc.contributor.author | Crumlin, Ethan J. | |
dc.contributor.author | Bluhm, Hendrik | |
dc.contributor.author | Stoerzinger, Kelsey Ann | |
dc.contributor.author | Hong, Wesley Terrence | |
dc.contributor.author | Shao-Horn, Yang | |
dc.date.accessioned | 2017-06-08T14:40:03Z | |
dc.date.available | 2017-06-08T14:40:03Z | |
dc.date.issued | 2015-08 | |
dc.date.submitted | 2015-05 | |
dc.identifier.issn | 0001-4842 | |
dc.identifier.issn | 1520-4898 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/109738 | |
dc.description.abstract | The understanding of fundamental processes in the bulk and at the interfaces of electrochemical devices is a prerequisite for the development of new technologies with higher efficiency and improved performance. One energy storage scheme of great interest is splitting water to form hydrogen and oxygen gas and converting back to electrical energy by their subsequent recombination with only water as a byproduct. However, kinetic limitations to the rate of oxygen-based electrochemical reactions hamper the efficiency in technologies such as solar fuels, fuel cells, and electrolyzers. For these reactions, the use of metal oxides as electrocatalysts is prevalent due to their stability, low cost, and ability to store oxygen within the lattice. However, due to the inherently convoluted nature of electrochemical and chemical processes in electrochemical systems, it is difficult to isolate and study individual electrochemical processes in a complex system. Therefore, in situ characterization tools are required for observing related physical and chemical processes directly at the places where and while they occur and can help elucidate the mechanisms of charge separation and charge transfer at electrochemical interfaces. | en_US |
dc.description.sponsorship | National Science Foundation (U.S.). Materials Research Science and Engineering Centers (Program) | en_US |
dc.description.sponsorship | Skoltech-MIT Center for Electrochemical Energy Storage | en_US |
dc.description.sponsorship | United States. Department of Energy | en_US |
dc.description.sponsorship | National Energy Technology Laboratory (U.S.) | en_US |
dc.description.sponsorship | Solid State Energy Conversion Alliance. Core Technology Program (DEFE0009435) | en_US |
dc.language.iso | en_US | |
dc.publisher | American Chemical Society (ACS) | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1021/acs.accounts.5b00275 | en_US |
dc.rights | Article 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.source | Prof. Shao-Horn via Angie Locknar | en_US |
dc.title | Insights into Electrochemical Reactions from Ambient Pressure Photoelectron Spectroscopy | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Stoerzinger, Kelsey A. et al. “Insights into Electrochemical Reactions from Ambient Pressure Photoelectron Spectroscopy.” Accounts of Chemical Research 48.11 (2015): 2976–2983. | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Materials Science and Engineering | en_US |
dc.contributor.approver | Shao-Horn, Yang | en_US |
dc.contributor.mitauthor | Stoerzinger, Kelsey Ann | |
dc.contributor.mitauthor | Hong, Wesley Terrence | |
dc.contributor.mitauthor | Shao-Horn, Yang | |
dc.relation.journal | Accounts of Chemical Research | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dspace.orderedauthors | Stoerzinger, Kelsey A.; Hong, Wesley T.; Crumlin, Ethan J.; Bluhm, Hendrik; Shao-Horn, Yang | en_US |
dspace.embargo.terms | N | en_US |
dc.identifier.orcid | https://orcid.org/0000-0003-1560-0749 | |
mit.license | PUBLISHER_POLICY | en_US |
mit.metadata.status | Complete | |