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dc.contributor.authorRegier, Tom Z.
dc.contributor.authorPeak, Derek
dc.contributor.authorSayed, Sayed Youssef
dc.contributor.authorRisch, Marcel
dc.contributor.authorStoerzinger, Kelsey Ann
dc.contributor.authorShao-Horn, Yang
dc.date.accessioned2017-06-05T16:20:39Z
dc.date.available2017-06-05T16:20:39Z
dc.date.issued2015-07
dc.identifier.issn1932-7447
dc.identifier.issn1932-7455
dc.identifier.urihttp://hdl.handle.net/1721.1/109590
dc.description.abstractThe ferri-/ferrocyanide redox couple is ubiquitous in many fields of physical chemistry. We studied its photochemical response to intense synchrotron radiation by in situ X-ray absorption spectroscopy (XAS). For photon flux densities equal to and above 2 × 1011 s–1 mm–2, precipitation of ferric (hydr)oxide from both ferricyanide and ferrocyanide solutions was clearly detectable, despite flowing fast enough to replace the solution in the flow cell every 0.4 s (flow rate 1.5 mL/min). During cyclic voltammetry, precipitation of ferric (hydr)oxide was promoted at reducing voltages and observed below 1011 s–1 mm–2. This was accompanied by inhibition of the ferri-/ferrocyanide redox, which we probed by time-resolved operando XAS. Our study highlights the importance of considering both electrochemical and spectroscopic conditions when designing in situ experiments.en_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/acs.jpcc.5b04609en_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.sourceProf. Shao-Horn via Angie Locknaren_US
dc.titleReversibility of Ferri-/Ferrocyanide Redox during Operando Soft X-ray Spectroscopyen_US
dc.typeArticleen_US
dc.identifier.citationRisch, Marcel, Kelsey A. Stoerzinger, Tom Z. Regier, Derek Peak, Sayed Youssef Sayed, and Yang Shao-Horn. “Reversibility of Ferri-/Ferrocyanide Redox During Operando Soft X-Ray Spectroscopy.” The Journal of Physical Chemistry C 119, no. 33 (August 20, 2015): 18903–18910.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Research Laboratory of Electronicsen_US
dc.contributor.approverShao-Horn, Yangen_US
dc.contributor.mitauthorRisch, Marcel
dc.contributor.mitauthorStoerzinger, Kelsey Ann
dc.contributor.mitauthorShao-Horn, Yang
dc.relation.journalThe Journal of Physical Chemistry Cen_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.orderedauthorsRisch, Marcel; Stoerzinger, Kelsey A.; Regier, Tom Z.; Peak, Derek; Sayed, Sayed Youssef; Shao-Horn, Yangen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-2820-7006
mit.licensePUBLISHER_POLICYen_US


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