Kagome staircase compounds Ni3 V2 O8 and Co3 V2 O8 studied with implanted muons

Physical Review B - Condensed Matter and Materials Physics 75:6 (2007)

Authors:

T Lancaster, SJ Blundell, PJ Baker, D Prabhakaran, W Hayes, FL Pratt

Abstract:

We present the results of muon-spin relaxation (μ+ SR) measurements on the kagome staircase compounds Ni3 V2 O8 and Co3 V2 O8. The magnetic behavior of these materials may be described in terms of two inequivalent magnetic ion sites, known as spine sites and cross-tie sites. Our μ+ SR results allow us to probe each of these sites individually, revealing the distribution of the local magnetic fields near these positions. We are able not only to confirm the magnetic structures of the various phases proposed on the basis of bulk measurements but also to give an insight into the temperature evolution of the local field distribution in each phase. © 2007 The American Physical Society.

Angle-dependent magnetoresistance oscillations due to magnetic breakdown orbits

(2007)

Authors:

AF Bangura, PA Goddard, J Singleton, SW Tozer, AI Coldea, A Ardavan, RD McDonald, SJ Blundell, JA Schlueter

Will spin-relaxation times in molecular magnets permit quantum information processing?

Physical Review Letters 98:5 (2007)

Authors:

A Ardavan, O Rival, JJL Morton, SJ Blundell, AM Tyryshkin, GA Timco, REP Winpenny

Abstract:

Using X-band pulsed electron-spin resonance, we report the intrinsic spin-lattice (T1) and phase-coherence (T2) relaxation times in molecular nanomagnets for the first time. In Cr7M heterometallic wheels, with M=Ni and Mn, phase-coherence relaxation is dominated by the coupling of the electron spin to protons within the molecule. In deuterated samples T2 reaches 3μs at low temperatures, which is several orders of magnitude longer than the duration of spin manipulations, satisfying a prerequisite for the deployment of molecular nanomagnets in quantum information applications. © 2007 The American Physical Society.

Will Spin-Relaxation Times in Molecular Magnets Permit Quantum Information Processing?

Physical Review Letters 98 (2007) 057201 4pp

Authors:

A Ardavan, John J.L. Morton, Olivier Rival, Stephen J. Blundell

Characterization of the crystal and magnetic structures of the mixed-anion coordination polymer Cu(HCO2)(NO3)(pyz) {pyz = Pyrazine} by X-ray diffraction, ac magnetic susceptibility, dc magnetization, muon-spin relaxation, and spin dimer analysis.

Inorg Chem 46:1 (2007) 213-220

Authors:

JL Manson, T Lancaster, JA Schlueter, SJ Blundell, ML Brooks, FL Pratt, CL Nygren, H-J Koo, D Dai, M-H Whangbo

Abstract:

The mixed-anion coordination polymer Cu(HCO2)(NO3)(pyz) was synthesized, its crystal structure was determined by X-ray diffraction, and its magnetic structure was characterized by ac susceptibility, dc magnetization, muon-spin relaxation, and spin dimer analysis. The crystal structure consists of five-coordinate Cu2+ ions that are connected through syn-anti bridging mu-HCO2- and mu-pyz ligands to form a highly corrugated two-dimensional layered network. Bulk magnetic measurements show a broad maximum in chi(T) at 6.6 K. The HCO2- and pyz ligands mediate ferromagnetic and antiferromagnetic spin exchange interactions between adjacent Cu2+ ions with the spin exchange parameters J/kB = 8.17 and -5.4 K, respectively (H = -JSigmaSi x Sj). The muon-spin relaxation data show a transition to a long-range magnetic ordering below TN = 3.66(3) K. For T < TN, the M(H) and chi'ac measurements provide evidence for a field-induced spin-flop transition at 15.2 kOe. That Cu(HCO2)(NO3)(pyz) undergoes a long-range magnetic ordering is an unexpected result because the one-dimensional Cu(NO3)2(pyz) and three-dimensional Cu(HCO2)2(pyz) compounds display linear chain antiferromagnetism with no long-range magnetic ordering down to 2 K.