Show simple item record

dc.contributor.authorWolcott, Abraham
dc.contributor.authorSchiros, Theanne
dc.contributor.authorTrusheim, Matthew E
dc.contributor.authorChen, Edward H
dc.contributor.authorNordlund, Dennis
dc.contributor.authorDiaz, Rosa E
dc.contributor.authorGaathon, Ophir
dc.contributor.authorEnglund, Dirk
dc.contributor.authorOwen, Jonathan S
dc.date.accessioned2021-10-27T20:04:06Z
dc.date.available2021-10-27T20:04:06Z
dc.date.issued2014
dc.identifier.urihttps://hdl.handle.net/1721.1/134236
dc.description.abstract© 2014 American Chemical Society. We investigate the aerobic oxidation of high-pressure, high-temperature nanodiamonds (5-50 nm dimensions) using a combination of carbon and oxygen K-edge X-ray absorption, wavelength-dependent X-ray photoelectron, and vibrational spectroscopies. Oxidation at 575°C for 2 h eliminates graphitic carbon contamination (>98%) and produces nanocrystals with hydroxyl functionalized surfaces as well as a minor component (<5%) of carboxylic anhydrides. The low graphitic carbon content and the high crystallinity of HPHT are evident from Raman spectra acquired using visible wavelength excitation (λexcit = 633 nm) as well as carbon K-edge X-ray absorption spectra where the signature of a core-hole exciton is observed. Both spectroscopic features are similar to those of chemical vapor deposited (CVD) diamond but differ significantly from the spectra of detonation nanodiamond. The importance of these findings to the functionalization of nanodiamond surfaces for biological labeling applications is discussed. (Figure Presented).
dc.language.isoen
dc.publisherAmerican Chemical Society (ACS)
dc.relation.isversionof10.1021/JP506992C
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.
dc.sourceACS
dc.titleSurface Structure of Aerobically Oxidized Diamond Nanocrystals
dc.typeArticle
dc.identifier.citationWolcott, A., et al. "Surface Structure of Aerobically Oxidized Diamond Nanocrystals." J Phys Chem C Nanomater Interfaces 118 46 (2014): 26695-702.
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
dc.relation.journalJournal of Physical Chemistry C
dc.eprint.versionFinal published version
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2019-06-14T13:43:10Z
dspace.orderedauthorsWolcott, A; Schiros, T; Trusheim, ME; Chen, EH; Nordlund, D; Diaz, RE; Gaathon, O; Englund, D; Owen, JS
dspace.date.submission2019-06-14T13:43:12Z
mit.journal.volume118
mit.journal.issue46
mit.metadata.statusAuthority Work and Publication Information Needed


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record