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dc.contributor.author
Sotoma, Shingo
dc.contributor.author
Terada, Daiki
dc.contributor.author
Segawa, Takuya F.
dc.contributor.author
Igarashi, Ryuji
dc.contributor.author
Harada, Yoshie
dc.contributor.author
Shirakawa, Masahiro
dc.date.accessioned
2018-05-15T12:23:21Z
dc.date.available
2018-04-08T04:53:54Z
dc.date.available
2018-04-09T05:44:48Z
dc.date.available
2018-05-15T12:23:21Z
dc.date.issued
2018-04-03
dc.identifier.issn
2045-2322
dc.identifier.other
10.1038/s41598-018-23635-5
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/256165
dc.identifier.doi
10.3929/ethz-b-000256165
dc.description.abstract
The development of sensors to estimate physical properties, and their temporal and spatial variation, has been a central driving force in scientific breakthroughs. In recent years, nanosensors based on quantum measurements, such as nitrogen-vacancy centres (NVCs) in nanodiamonds, have been attracting much attention as ultrastable, sensitive, accurate and versatile physical sensors for quantitative cellular measurements. However, the nanodiamonds currently available for use as sensors have diameters of several tens of nanometres, much larger than the usual size of a protein. Therefore, their actual applications remain limited. Here we show that NVCs in an aggregation of 5-nm-sized detonation-synthesized nanodiamond treated by Krüger’s surface reduction (termed DND-OH) retains the same characteristics as observed in larger diamonds. We show that the negative charge at the NVC are stabilized, have a relatively long T2 spin relaxation time of up to 4 μs, and are applicable to thermosensing, one-degree orientation determination and nanometric super-resolution imaging. Our results clearly demonstrate the significant potential of DND-OH as a physical sensor. Thus, DND-OH will raise new possibilities for spatiotemporal monitoring of live cells and dynamic biomolecules in individual cells at single-molecule resolution.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
Nature
en_US
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
Nanoparticles
en_US
dc.subject
Nanosensors
en_US
dc.subject
Physical Chemistry
en_US
dc.title
Enrichment of ODMR-active nitrogen-vacancy centres in five-nanometre-sized detonation-synthesized nanodiamonds: Nanoprobes for temperature, angle and position
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 4.0 International
ethz.journal.title
Scientific Reports
ethz.journal.volume
8
en_US
ethz.journal.issue
1
en_US
ethz.journal.abbreviated
Sci Rep
ethz.pages.start
5463
en_US
ethz.size
8 p.; supplementary information 9 p.
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.scopus
ethz.publication.place
London
en_US
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02010 - Dep. Physik / Dep. of Physics::02505 - Laboratorium für Festkörperphysik / Laboratory for Solid State Physics::03906 - Degen, Christian / Degen, Christian
en_US
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02010 - Dep. Physik / Dep. of Physics::02505 - Laboratorium für Festkörperphysik / Laboratory for Solid State Physics::03906 - Degen, Christian / Degen, Christian
ethz.date.deposited
2018-04-08T04:53:57Z
ethz.source
FORM
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2018-04-09T05:44:56Z
ethz.rosetta.lastUpdated
2024-02-02T04:46:46Z
ethz.rosetta.versionExported
true
ethz.COinS
ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.atitle=Enrichment%20of%20ODMR-active%20nitrogen-vacancy%20centres%20in%20five-nanometre-sized%20detonation-synthesized%20nanodiamonds:%20Nanoprobes%20for%20temperature,%20angle&rft.jtitle=Scientific%20Reports&rft.date=2018-04-03&rft.volume=8&rft.issue=1&rft.spage=5463&rft.issn=2045-2322&rft.au=Sotoma,%20Shingo&Terada,%20Daiki&Segawa,%20Takuya%20F.&Igarashi,%20Ryuji&Harada,%20Yoshie&rft.genre=article&rft_id=info:doi/10.1038/s41598-018-23635-5&
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