Skip to main content
Home
Department Of Physics text logo
  • Research
    • Our research
    • Our research groups
    • Our research in action
    • Research funding support
    • Summer internships for undergraduates
  • Study
    • Undergraduates
    • Postgraduates
  • Engage
    • For alumni
    • For business
    • For schools
    • For the public
Menu
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

Solid-state quantum memory using the 31P nuclear spin

Nature 455:7216 (2008) 1085-1088

Authors:

JJL Morton, AM Tyryshkin, RM Brown, S Shankar, BW Lovett, A Ardavan, T Schenkel, EE Haller, JW Ager, SA Lyon

Abstract:

The transfer of information between different physical forms - for example processing entities and memory - is a central theme in communication and computation. This is crucial in quantum computation, where great effort must be taken to protect the integrity of a fragile quantum bit (qubit). However, transfer of quantum information is particularly challenging, as the process must remain coherent at all times to preserve the quantum nature of the information. Here we demonstrate the coherent transfer of a superposition state in an electron-spin 'processing' qubit to a nuclear-spin 'memory' qubit, using a combination of microwave and radio-frequency pulses applied to 31P donors in an isotopically pure 28Si crystal. The state is left in the nuclear spin on a timescale that is long compared with the electron decoherence time, and is then coherently transferred back to the electron spin, thus demonstrating the 31P nuclear spin as a solid-state quantum memory. The overall store-readout fidelity is about 90 per cent, with the loss attributed to imperfect rotations, and can be improved through the use of composite pulses. The coherence lifetime of the quantum memory element at 5.5 K exceeds 1 s. ©2008 Macmillan Publishers Limited. All rights reserved.
More details from the publisher

Temperature-dependent photoluminescence study of ErSc2N@C 80 and Er2ScN@C80 fullerenes

Physica Status Solidi (B) Basic Research 245:10 (2008) 1998-2001

Authors:

A Tiwari, G Dantelle, K Porfyrakis, A Ardavan, GAD Briggs

Abstract:

The photoluminescence study of the Er3+ ion in ErSc 2N@C80 and Er2ScN@C80 fullerenes in the temperature range of 5 K to 80 K is presented. New emission peaks are observed for both fullerenes above 20 K. These peaks arise from thermally populated crystal-field levels of the excited state. An anomalous behaviour of the PL peak area is observed with an increasing temperature which reveals an internal rearrangement of the cluster ErSc2N in ErSc 2N@C80. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.
More details from the publisher

Hyperfine structure of Sc@C82 from ESR and DFT

(2008)

Authors:

GW Morley, BJ Herbert, SM Lee, K Porfyrakis, TJS Dennis, D Nguyen-Manh, R Scipioni, J van Tol, AP Horsfield, A Ardavan, DG Pettifor, JC Green, GAD Briggs
More details from the publisher

Morphology of the nonspherically decaying radiation generated by a rotating superluminal source: reply to comment.

J Opt Soc Am A Opt Image Sci Vis 25:9 (2008) 2167-2169

Authors:

H Ardavan, A Ardavan, J Singleton, J Fasel, A Schmidt

Abstract:

The fact that the formula used by Hannay in the preceding Comment [J. Opt. Soc. Am. A25, 2165 (2008)] is "from a standard text on electrodynamics" neither warrants that it is universally applicable nor that it is unequivocally correct. We have explicitly shown [J. Opt. Soc. Am. A25, 543 (2008)] that, since it does not include the boundary contribution toward the value of the field, the formula in question is not applicable when the source is extended and has a distribution pattern that rotates faster than light in vacuo. The neglected boundary term in the retarded solution to the wave equation governing the electromagnetic field forms the basis of diffraction theory. If this term were identically zero, for the reasons given by Hannay, the diffraction of electromagnetic waves through apertures on a surface enclosing a source would have been impossible.
More details from the publisher
More details

Dynamic nuclear polarization with simultaneous excitation of electronic and nuclear transitions

Applied Magnetic Resonance 34:3-4 (2008) 347-353

Authors:

GW Morley, K Porfyrakis, A Ardavan, J Van Tol

Abstract:

Dynamic nuclear polarization transfers spin polarization from electrons to nuclei. We have achieved this by a new method, simultaneously exciting transitions of electronic and nuclear spins. The efficiency of this technique improves with increasing magnetic field. Experimental results are shown for N@C 60 with continuous-wave microwaves, which can be expected to produce even higher polarization than the corresponding pulsed techniques for electron spins greater than 1/2. The degree of nuclear polarization in this case can be easily monitored through the intensities of the well-resolved hyperfine components in the electron paramagnetic resonance spectrum. The nuclear spin-lattice relaxation time is orders of magnitude longer than that of the electrons. © 2008 Springer-Verlag.
More details from the publisher

Pagination

  • First page First
  • Previous page Prev
  • …
  • Page 27
  • Page 28
  • Page 29
  • Page 30
  • Current page 31
  • Page 32
  • Page 33
  • Page 34
  • Page 35
  • …
  • Next page Next
  • Last page Last

Footer Menu

  • Contact us
  • Giving to the Dept of Physics
  • Work with us
  • Media

User account menu

  • Log in

Follow us

FIND US

Clarendon Laboratory,

Parks Road,

Oxford,

OX1 3PU

CONTACT US

Tel: +44(0)1865272200

University of Oxfrod logo Department Of Physics text logo
IOP Juno Champion logo Athena Swan Silver Award logo

© University of Oxford - Department of Physics

Cookies | Privacy policy | Accessibility statement

Built by: Versantus

  • Home
  • Research
  • Study
  • Engage
  • Our people
  • News & Comment
  • Events
  • Our facilities & services
  • About us
  • Current students
  • Staff intranet