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Arzhang's natural habitat

Prof Arzhang Ardavan

Professor of Physics

Research theme

  • Quantum materials

Sub department

  • Condensed Matter Physics

Research groups

  • Quantum spin dynamics
arzhang.ardavan@physics.ox.ac.uk
Telephone: 01865 (2)72366
Clarendon Laboratory, room 267
Personal website
  • About
  • Publications

Morphology of the nonspherically decaying radiation beam generated by a rotating superluminal source

(2006)

Authors:

Houshang Ardavan, Arzhang Ardavan, John Singleton, Joseph Fasel, Andrea Schmidt
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Multifrequency millimeter wave study of excited energy states in the high-spin molecule Cr10 (OMe) 20 (O2 CCMe3) 10

Physical Review B - Condensed Matter and Materials Physics 73:21 (2006)

Authors:

S Sharmin, A Ardavan, SJ Blundell, O Rival, P Goy, EJL McInnes, DM Low

Abstract:

We report multifrequency high-field millimeter-wave magneto-optical measurements on the high-spin molecule, Cr10 (OMe) 20 (O2 CCMe3) 10. We find that at temperatures above 15 K and at magnetic fields above 6 T, the simple ESR spectrum expected for a single molecule magnet is markedly altered. Our data strongly suggest the presence of a higher spin excited state multiplet lying only about 10 K above the ground state. © 2006 The American Physical Society.
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Davies electron-nuclear double resonance revisited: enhanced sensitivity and nuclear spin relaxation.

J Chem Phys 124:23 (2006) 234508

Authors:

Alexei M Tyryshkin, John JL Morton, Arzhang Ardavan, SA Lyon

Abstract:

Over the past 50 years, electron-nuclear double resonance (ENDOR) has become a fairly ubiquitous spectroscopic technique, allowing the study of spin transitions for nuclei which are coupled to electron spins. However, the low spin number sensitivity of the technique continues to pose serious limitations. Here we demonstrate that signal intensity in a pulsed Davies ENDOR experiment depends strongly on the nuclear relaxation time T(1n), and can be severely reduced for long T(1n). We suggest a development of the original Davies ENDOR sequence that overcomes this limitation, thus offering dramatically enhanced signal intensity and spectral resolution. Finally, we observe that the sensitivity of the original Davies method to T(1n) can be exploited to measure nuclear relaxation, as we demonstrate for phosphorous donors in silicon and for endohedral fullerenes N@C(60) in CS(2).
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Davies electron-nuclear double resonance revisited: Enhanced sensitivity and nuclear spin relaxation

Journal of Chemical Physics 124:23 (2006)

Authors:

AM Tyryshkin, JJL Morton, A Ardavan, SA Lyon

Abstract:

Over the past 50 years, electron-nuclear double resonance (ENDOR) has become a fairly ubiquitous spectroscopic technique, allowing the study of spin transitions for nuclei which are coupled to electron spins. However, the low spin number sensitivity of the technique continues to pose serious limitations. Here we demonstrate that signal intensity in a pulsed Davies ENDOR experiment depends strongly on the nuclear relaxation time T1n, and can be severely reduced for long T1n. We suggest a development of the original Davies ENDOR sequence that overcomes this limitation, thus offering dramatically enhanced signal intensity and spectral resolution. Finally, we observe that the sensitivity of the original Davies method to T1n can be exploited to measure nuclear relaxation, as we demonstrate for phosphorous donors in silicon and for endohedral fullerenes N@ C60 in C S2. © 2006 American Institute of Physics.
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Synthesis and reactivity of N@C60O

Physical Chemistry Chemical Physics 8:17 (2006) 2083-2088

Authors:

MAG Jones, DA Britz, JJL Morton, AN Khlobystov, K Porfyrakis, A Ardavan, GAD Briggs

Abstract:

The endohedral fullerene epoxide N@C60O was synthesised, isolated by High Performance Liquid Chromatography (HPLC), and characterised by Electron Spin Resonance (ESR). This nitrogen radical displays predominantly axial symmetry characteristics as expected for a monoadduct, evidenced by a zero-field splitting D parameter of 6.6 MHz and an E parameter of 0.5 MHz in powder at 77 K. Photo- and thermally-activated silencing of the nitrogen radical were observed, the latter showing the evolution of a new spin signal during heating at 100°C. We suggest that loss of nitrogen spin is due to coupling with a radical formed by opening of the epoxide ring. This implies that the reaction of C60O with C60 in the solid state proceeds via a radical, rather than ionic, intermediate. © the Owner Societies 2006.
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