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Long spin coherence times on C$_{59}$N-C$_{60}$ heterodimer radicals entrapped in cycloparaphenylene rings
ID
Tanuma, Yuri
(
Author
),
ID
Knaflič, Tilen
(
Author
),
ID
Anézo, Bastien
(
Author
),
ID
Stangel, Christina
(
Author
),
ID
Volkmann, Jannis
(
Author
),
ID
Tagmatarchis, Nikos
(
Author
),
ID
Wegner, Hermann A.
(
Author
),
ID
Arčon, Denis
(
Author
),
ID
Ewels, Christopher Paul
(
Author
)
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https://pubs.acs.org/doi/10.1021/acs.jpcc.2c09049
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Abstract
We investigate the effect of introducing C$_{60}$ to (C$_{59}$N)$_2$ and the molecular ring, [10]cycloparaphenylene ([10]CPP), using electron paramagnetic resonance (EPR) measurements supported by density functional theory (DFT) calculations. Incorporating C$_{60}$ into the system results in the formation of novel stable [10]CPP ⊃ C$_{59}$N-C$_{60}$$^•$ ⊂ [10]CPP encapsulated heterodimer radicals whose spin is localized on C$_{60}$ and manifests in EPR measurements as a signal at g = 2.0022 without any discernable hyperfine structure. This signal has an exceptionally long spin coherence lifetime of 440 μs at room temperature, far longer than any of the radical fullerene species reported in the literature and over twice that of the C$_{59}$N$^•$ ⊂ [10]CPP radical. The radicals are long-lived, with EPR signal still strong over a year after thermal activation. The [10]CPP ⊃ C$_{59}$N-C$_{60}$$^•$ ⊂ [10]CPP oligomer is more stable than C$_{59}$N$^•$ ⊂ [10]CPP radicals and becomes the predominant species at room temperature after annealing. Its formation is thermally activated with an experimental activation energy of only 0.189 eV, as compared to 0.485 eV for the pure azafullerene-[10]CPP case. The [10]CPP ⊃ C$_{59}$N-C$_{60}$$^•$ ⊂ [10]CPP radicals discovered here could be used to bridge C$_{59}$N$^•$ ⊂ [10]CPPs acting as qubits, providing effective coupling between them.
Language:
English
Keywords:
physical chemistry
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
FMF - Faculty of Mathematics and Physics
Publication status:
Published
Publication version:
Version of Record
Year:
2023
Number of pages:
Str. 6552-6561
Numbering:
Vol. 127, iss. 13
PID:
20.500.12556/RUL-147226
UDC:
544
ISSN on article:
1932-7447
DOI:
10.1021/acs.jpcc.2c09049
COBISS.SI-ID:
148195843
Publication date in RUL:
27.06.2023
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1352
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68
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Record is a part of a journal
Title:
The journal of physical chemistry. C
Publisher:
American Chemical Society
ISSN:
1932-7447
COBISS.SI-ID:
28455429
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Secondary language
Language:
Slovenian
Keywords:
fizikalna kemija
Projects
Funder:
Other - Other funder or multiple funders
Funding programme:
Hokkaido University, CAREM, Research Grants for Young Researchers
Funder:
Other - Other funder or multiple funders
Funding programme:
France, Government Scholarships
Funder:
Other - Other funder or multiple funders
Funding programme:
Japan, JSPS Overseas Research Fellowships
Funder:
ARRS - Slovenian Research Agency
Project number:
P1-0125
Name:
Fizika kvantnih in funkcionalnih materialov
Funder:
ARRS - Slovenian Research Agency
Project number:
J1-3007
Name:
Kvantno procesiranje fulerenskih kubitov z diamantnimi senzorji
Funder:
ARRS - Slovenian Research Agency
Project number:
N1-0220
Name:
Napredna optična magnetometrija vrtinčnih niti v nekonvencionalnih superprevodnikih
Funder:
Other - Other funder or multiple funders
Funding programme:
Ministry of Europe and Foreign Affairs (MEAE), PHC Proteus, Exchange funding
Project number:
46151XJ
Funder:
Other - Other funder or multiple funders
Funding programme:
Ministry Higher Education and Research (MESR), PHC Proteus, Exchange funding
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