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dc.contributor.authorGriffin, Robert Guy
dc.contributor.authorPrisner, T. F.
dc.date.accessioned2013-01-08T15:03:36Z
dc.date.available2013-01-08T15:03:36Z
dc.date.issued2010-05
dc.identifier.issn1463-9076
dc.identifier.issn1463-9084
dc.identifier.urihttp://hdl.handle.net/1721.1/76185
dc.description.abstractSensitivity is a critical issue in NMR spectroscopy, microscopy and imaging, and the factor that often limits the success of various applications. The origin of low sensitivity in NMR is well known to be due to the small magnetic moment of nuclear spins, which yields small Boltzmann polarizations and weak absorption signals. Historically, each advance in technology and methodology that has increased the signal-to-noise in NMR has shifted the boundary of what is achievable, often opening new areas of application and directions of research. The archetypal example of this phenomenon was the introduction of Fourier transform spectroscopy which led to increases of ~10[superscript 2]-fold in signal-to-noise, revolutionizing NMR and many other forms of spectroscopy. More recent technological developments of note include the continuing development of higher field superconducting magnets which increases polarization, and cryoprobes in which the excitation/detection coil is maintained at low temperatures increasing sensitivity through a higher probe Q and decreasing receiver noise. In addition, innovations in NMR methodology have improved sensitivity, classic examples being Hartmann–Hahn cross polarization, and J-coupling meditated transfer methods, and the introduction of 1H detection of [superscript 13]C/[superscript 15]N resonances. Furthermore, techniques for non-inductive detection of resonance, such as the AFM-based technique of magnetic resonance force microscopy (MRFM), have recently allowed observation of a single electron spin, and ~100 nuclear spins/√Hz[superscript 8].en_US
dc.language.isoen_US
dc.publisherRoyal Society of Chemistry, Theen_US
dc.relation.isversionofhttp://dx.doi.org/10.1039/c0cp90019ben_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourceGriffin via Erja Kajosaloen_US
dc.titleHigh field dynamic nuclear polarization—the renaissanceen_US
dc.typeArticleen_US
dc.identifier.citationGriffin, R. G., and T. F. Prisner. “High Field Dynamic Nuclear Polarization—the Renaissance.” Physical Chemistry Chemical Physics 12.22 (2010): 5737.en_US
dc.contributor.departmentFrancis Bitter Magnet Laboratory (Massachusetts Institute of Technology)en_US
dc.contributor.approverGriffin, Robert G.
dc.contributor.mitauthorGriffin, Robert Guy
dc.relation.journalPhysical Chemistry Chemical Physicsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
dspace.orderedauthorsGriffin, R. G.; Prisner, T. F.en
dc.identifier.orcidhttps://orcid.org/0000-0003-1589-832X
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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