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Crystal structure inside calcium fluoride with an implanted muon
Credit: SJB

Professor Stephen Blundell

Professor of Physics

Research theme

  • Quantum materials

Sub department

  • Condensed Matter Physics

Research groups

  • Muons and magnets
Stephen.Blundell@physics.ox.ac.uk
Telephone: 01865 (2)72347
Clarendon Laboratory, room 108
  • About
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  • Research
  • Publications

Two-dimensional XY behavior observed in quasi-two-dimensional quantum Heisenberg antiferromagnets

Physical Review B - Condensed Matter and Materials Physics 79:13 (2009)

Authors:

F Xiao, FM Woodward, CP Landee, MM Turnbull, C Mielke, N Harrison, T Lancaster, SJ Blundell, PJ Baker, P Babkevich, FL Pratt

Abstract:

The magnetic properties of a family of molecular-based quasi-two- dimensional S=1/2 Heisenberg antiferromagnets are reported. Three compounds, [Cu (pz) 2 (ClO4) 2, Cu (pz) 2 (BF4) 2, and [Cu (pz) 2 (NO3)] (PF6)] contain similar planes of Cu2+ ions linked into magnetically square lattices by bridging pyrazine molecules (pz= C4 H4 N2). The anions provide charge balance as well as isolation between the layers. Single crystal measurements of susceptibility and magnetization, as well as muon-spin-relaxation studies, reveal low ratios of Néel temperatures to exchange strengths (4.25/17.5=0.243, 3.80/15.3=0.248, and 3.05/10.8=0.282, respectively) while the ratio of the anisotropy fields HA (kOe) to the saturation field HSAT (kOe) are small (2.6/490=5.3× 10-3, 2.4/430=5.5× 10-3, and 0.07/300=2.3× 10-4, respectively), demonstrating close approximations to a two-dimensional Heisenberg model. The susceptibilities of ClO4 and BF4 show evidence of an exchange-anisotropy crossover (Heisenberg to XY) at low temperatures; their ordering transitions are primarily driven by the XY behavior with the ultimate three-dimensional transition appearing parasitically. The PF6 compound remains Heisenberg type at all temperatures, with its transition to the Néel state due to the interlayer interactions. Effects of field-induced anisotropy have been observed. © 2009 The American Physical Society.
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Coexistence of static magnetism and superconductivity in SmFeAsO(1-x)F(x) as revealed by muon spin rotation.

Nat Mater 8:4 (2009) 310-314

Authors:

AJ Drew, Ch Niedermayer, PJ Baker, FL Pratt, SJ Blundell, T Lancaster, RH Liu, G Wu, XH Chen, I Watanabe, VK Malik, A Dubroka, M Rössle, KW Kim, C Baines, C Bernhard

Abstract:

The recent observation of superconductivity with critical temperatures (Tc) up to 55 K in the pnictide RFeAsO(1-x)F(x), where R is a lanthanide, marks the first discovery of a non-copper-oxide-based layered high-Tc superconductor. It has raised the suspicion that these new materials share a similar pairing mechanism to the cuprate superconductors, as both families exhibit superconductivity following charge doping of a magnetic parent material. In this context, it is important to follow the evolution of the microscopic magnetic properties of the pnictides with doping and hence to determine whether magnetic correlations coexist with superconductivity. Here, we present a muon spin rotation study on SmFeAsO(1-x)F(x), with x=0-0.30 that shows that, as in the cuprates, static magnetism persists well into the superconducting regime. This analogy is quite surprising as the parent compounds of the two families have rather different magnetic ground states: itinerant spin density wave for the pnictides contrasted with the Mott-Hubbard insulator in the cuprates. Our findings therefore suggest that the proximity to magnetic order and associated soft magnetic fluctuations, rather than strong electronic correlations in the vicinity of a Mott-Hubbard transition, may be the key ingredients of high-Tc superconductors.
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Muon spin relaxation studies of critical fluctuations and diffusive spin dynamics in molecular magnets

Physica B Condensed Matter Elsevier 404:5-7 (2009) 585-589

Authors:

Francis Pratt, Tom Lancaster, Peter Baker, Stephen Blundell, Wakako Kaneko, Masaaki Ohba, Susumu Kitagawa, Seiko Ohira-Kawamura, Seishi Takagi
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Storing quantum information in chemically engineered nanoscale magnets

Journal of Materials Chemistry 19:12 (2009) 1754-1760

Authors:

A Ardavan, SJ Blundell

Abstract:

We review the implementation of quantum information processing using quantum spins and pulsed spin resonance techniques. Molecular magnets, nanoscale clusters of coupled transition metal ions, offer various potential advantages over other spin systems as the building blocks of a quantum computer. We describe the strategies which must be employed in order to implement quantum algorithms in such nanoscale magnets and explain why, when evaluating the suitability of any physical system for embodying a qubit, it is essential to determine the phase relaxation time appropriate for an individual molecular spin. Experiments utilising pulsed spin resonance techniques show that the phase relaxation times in at least some molecular magnets are long enough to permit multiple qubit operations to be performed. © The Royal Society of Chemistry 2009.
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2D XY Behavior observed in quasi-2D quantum Heisenberg antiferromagnets

(2009)

Authors:

F Xiao, FM Woodward, CP Landee, MM Turnbull, C Mielke, N Harrison, T Lancaster, SJ Blundell, PJ Baker, P Babkevich, FL Pratt
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