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dc.contributor.author
Chaudhari, Sachin R.
dc.contributor.author
Berruyer, Pierrick
dc.contributor.author
Gajan, David
dc.contributor.author
Reiter, Christian
dc.contributor.author
Engelke, Frank
dc.contributor.author
Silverio, Daniel L.
dc.contributor.author
Copéret, Christophe
dc.contributor.author
Lelli, Moreno
dc.contributor.author
Lesage, Anne
dc.contributor.author
Emsley, Lyndon
dc.date.accessioned
2023-07-15T11:33:10Z
dc.date.available
2017-06-12T05:32:00Z
dc.date.available
2023-07-15T11:33:10Z
dc.date.issued
2016
dc.identifier.issn
1463-9084
dc.identifier.issn
1463-9076
dc.identifier.other
10.1039/c6cp00839a
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/116095
dc.identifier.doi
10.3929/ethz-b-000116095
dc.description.abstract
DNP-enhanced solid-state NMR spectroscopy under magic angle spinning (MAS) is rapidly developing into a powerful analytical tool to investigate the structure of a wide range of solid materials, because it provides unsurpassed sensitivity gains. Most developments and applications of DNP MAS NMR were so far reported at moderate spinning frequencies (up to 14 kHz using 3.2 mm rotors). Here, using a 1.3 mm MAS DNP probe operating at 18.8 T and ∼100 K, we show that signal amplification factors can be increased by up to a factor two when using smaller volume rotors as compared to 3.2 mm rotors, and report enhancements of around 60 over a range of sample spinning rates from 10 to 40 kHz. Spinning at 40 kHz is also shown to increase 29Si coherence lifetimes by a factor three as compared to 10 kHz, substantially increasing sensitivity in CPMG type experiments. The contribution of quenching effects to the overall sensitivity gain at very fast MAS is evaluated, and applications are reported on a functionalised mesostructured organic–inorganic material.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
Royal Society of Chemistry
en_US
dc.rights.uri
http://creativecommons.org/licenses/by/3.0/
dc.title
Dynamic nuclear polarization at 40 kHz magic angle spinning
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 3.0 Unported
dc.date.published
2016-03-14
ethz.journal.title
Physical Chemistry Chemical Physics
ethz.journal.volume
18
en_US
ethz.journal.issue
15
en_US
ethz.journal.abbreviated
Phys. Chem. Chem. Phys.
ethz.pages.start
10616
en_US
ethz.pages.end
10622
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.identifier.scopus
ethz.identifier.nebis
002005974
ethz.publication.place
Cambridge
en_US
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02020 - Dep. Chemie und Angewandte Biowiss. / Dep. of Chemistry and Applied Biosc.::02513 - Laboratorium für Anorganische Chemie / Laboratory of Inorganic Chemistry::03872 - Copéret, Christophe / Copéret, Christophe
en_US
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02020 - Dep. Chemie und Angewandte Biowiss. / Dep. of Chemistry and Applied Biosc.::02513 - Laboratorium für Anorganische Chemie / Laboratory of Inorganic Chemistry::03872 - Copéret, Christophe / Copéret, Christophe
ethz.date.deposited
2017-06-12T05:34:08Z
ethz.source
ECIT
ethz.identifier.importid
imp5936545fe926246091
ethz.ecitpid
pub:177949
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2017-07-13T19:03:47Z
ethz.rosetta.lastUpdated
2024-02-03T01:42:23Z
ethz.rosetta.versionExported
true
ethz.COinS
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