Fluorescence and Spin Properties of Defects in Single Digit Nanodiamonds
Source abstract
Abstract
This article reports stable photoluminescence and high-contrast optically detected electron spin resonance (ODESR) from single nitrogen-vacancy (NV) defect centers created within ultrasmall, disperse nanodiamonds of radius less than 4 nm. Unexpectedly, the efficiency for the production of NV fluorescent defects by electron irradiation is found to be independent of the size of the nanocrystals. Fluorescence lifetime imaging shows lifetimes with a mean value of around 17 ns, only slightly longer than the bulk value of the defects. After proper surface cleaning, the dephasing times of the electron spin resonance in the nanocrystals approach values of some microseconds, which is typical for the type Ib diamond from which the nanoparticle is made. We conclude that despite the tiny size of these nanodiamonds the photoactive nitrogen-vacancy color centers retain their bulk properties to the benefit of numerous exciting potential applications in photonics, biomedical labeling, and imaging.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Diamond and Carbon-based Materials Research · Metal and Thin Film Mechanics · Electronic and Structural Properties of Oxides
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Physics, University of Stuttgart, Stuttgart, Germany
Structure and Activity of Normal and Pathological Biomolecules, INSERM/UEVE U829, Bat. Maupertuis, rue du père Jarlan 91025 Evry, France
Centre des Matériaux, Mines-ParisTech, UMR7633 BP 87, 91003 Evry Cedex, France
Johannes Gutenberg-Universität Mainz, Johann-Joachim-Becher-Weg 45, D-55099 Mainz, Germany
PicoQuant GmbH, Rudower Chaussee 29, D-12489 Berlin, Germany
Texas A&M University, College Station, Texas 77843
References (30)
Show source-provided references
1. Chang Y. R. · Nat. Nanotechnol. · 2008 · 3 · 28410.1038/nnano.2008.99 ↗
2. Fu C. C. · Proc. Natl. Acad. Sci. U.S.A. · 2007 · 104 · 72710.1073/pnas.0605409104 ↗
3. Krueger A. · Adv. Mater. · 2008 · 20 · 244510.1002/adma.200701856 ↗
4. Huang H. J. · ACS Nano · 2008 · 2 · 20310.1021/nn7000867 ↗
5. Park Y. S. · Nano Lett. · 2006 · 6 · 207510.1021/nl061342r ↗
6. Schietinger S. · Nano Lett. · 2008 · 8 · 391110.1021/nl8023627 ↗
7. Schrand A. M. · J. Phys. Chem. B · 2007 · 111 · 210.1021/jp066387v ↗
8. Lam R. · ACS Nano · 2008 · 2 · 209510.1021/nn800465x ↗
9. Michalet X. · Science · 2005 · 307 · 53810.1126/science.1104274 ↗
10. Cao L. · J. Am. Chem. Soc. · 2007 · 129 · 1131810.1021/ja073527l ↗
11. Beveratos A. · Phys. Rev. A · 2001 · 64 · 6180210.1103/PhysRevA.64.061802 ↗
12. Kurtsiefer C. · Phys. Rev. Lett. · 2000 · 85 · 29010.1103/PhysRevLett.85.290 ↗
13. Wu E. · Opt. Express · 2006 · 14 · 129610.1364/OE.14.001296 ↗
14. Balasubramanian G. · Nature · 2008 · 455 · 64810.1038/nature07278 ↗
15. Hartl A. · Nat. Mater. · 2004 · 3 · 73610.1038/nmat1204 ↗
16. Rubio-Retama J. · Langmuir · 2006 · 22 · 583710.1021/la060167r ↗
17. Yang W. S. · Nat. Mater. · 2003 · 2 · 6310.1038/nmat809 ↗
18. Wu E. · New J. Phys. · 2007 · 9 · 43410.1088/1367-2630/9/12/434 ↗
19. Osawa E. · Pure Appl. Chem. · 2008 · 80 · 136510.1351/pac200880071365 ↗
20. 10.1002/smll.20080180210.1002/smll.200801802 ↗
21. Wrachtrup J. · J. Phys.: Condens. Matter · 2006 · 18 · S807
22. Campbell B. · Phys. Status Solidi A · 2000 · 181 · 9910.1002/1521-396X(200009)181:1<99::AID-PSSA99>3.0.CO;2-5 ↗
23. Batalov A. · Phys. Rev. Lett. · 2008 · 100 · 7740110.1103/PhysRevLett.100.077401 ↗
24. Lukosz W. · Opt. Commun. · 1977 · 20 · 19510.1016/0030-4018(77)90331-5 ↗
25. Maze J. R. · Nature · 2008 · 455 · 64410.1038/nature07279 ↗
26. Jelezko F. · Phys. Rev. Lett. · 2004 · 92 · 7640110.1103/PhysRevLett.92.076401 ↗
27. Hanson R. · Science · 2008 · 320 · 35210.1126/science.1155400 ↗
28. Maze J. R. · Phys. Rev. B · 2008 · 78 · 9430310.1103/PhysRevB.78.094303 ↗
29. Balasubramanian G. · Nat. Mater. · 2009 · 8 · 38310.1038/nmat2420 ↗
30. Mims W. B. · 1972