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CMP
Credit: Jack Hobhouse

Junjie Liu

Academic Visitor

Sub department

  • Condensed Matter Physics

Research groups

  • Quantum spin dynamics
junjie.liu@physics.ox.ac.uk
Telephone: 01865 (2)72318
Clarendon Laboratory, room 252.1
  • About
  • Publications

EPR and magnetic quantum tunneling studies of the mixed valent [Mn4(anca)4(Hedea)2(edea)2]·2CHCl3, EtOH single-molecule magnet

Polyhedron Elsevier 30:18 (2011) 2965-2968

Authors:

Junjie Liu, Christopher C Beedle, Harjah M Quddusi, Enrique del Barco, David N Hendrickson, Stephen Hill
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Accidentally on purpose: construction of a ferromagnetic, oxime-based [Mn(III)2] dimer.

Dalton transactions (Cambridge, England : 2003) 40:39 (2011) 9999-10006

Authors:

Ross Inglis, Edel Houton, Junjie Liu, Alessandro Prescimone, Joan Cano, Stergios Piligkos, Stephen Hill, Leigh F Jones, Euan K Brechin

Abstract:

The serendipitous self-assembly of the complex [Mn(III)(2)Zn(II)(2)(Ph-sao)(2)(Ph-saoH)(4)(hmp)(2)] (1),whose magnetic core consists solely of two symmetry equivalent Mn(iii) ions linked by two symmetry equivalent -N-O- moieties, provides a relatively simple model complex with which to study the magneto-structural relationship in oxime-bridged Mn(III) cluster compounds. Dc magnetic susceptibility measurements reveal ferromagnetic (J = +2.2 cm(-1)) exchange resulting in an S = 4 ground state. Magnetisation measurements performed at low temperatures and high fields reveal the presence of significant anisotropy, with ac measurements confirming slow relaxation of the magnetisation and Single-Molecule Magnetism behaviour. Simulations of high field, high frequency EPR data reveal a single ion anisotropy, D((Mn(III))) = -3.83 cm(-1). DFT studies on a simplified model complex of 1 reveal a pronounced dependence of the exchange coupling on the relative twisting of the oxime moiety with respect to the metal ion positions, as suggested previously in more complicated [Mn(III)(3)] and [Mn(III)(6)] clusters.
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Relieving frustration: The case of antiferromagnetic Mn3 molecular triangles

Physical Review B American Physical Society (APS) 84:9 (2011) 094443

Authors:

J Liu, C Koo, A Amjad, PL Feng, E-S Choi, E del Barco, DN Hendrickson, S Hill
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Cationic Mn4 single-molecule magnet with a sterically isolated core.

Inorganic chemistry 50:16 (2011) 7367-7369

Authors:

Katie J Heroux, Hajrah M Quddusi, Junjie Liu, James R O'Brien, Motohiro Nakano, Enrique del Barco, Stephen Hill, David N Hendrickson

Abstract:

The synthesis, structure, and magnetic properties of a ligand-modified Mn(4) dicubane single-molecule magnet (SMM), [Mn(4)(Bet)(4)(mdea)(2)(mdeaH)(2)](BPh(4))(4), are presented, where the cationic SMM units are significantly separated from neighboring molecules in the crystal lattice. There are no cocrystallized solvate molecules, making it an ideal candidate for single-crystal magnetization hysteresis and high-frequency electron paramagnetic resonance studies. Increased control over intermolecular interactions in such materials is a crucial factor in the future application of SMMs.
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Asymmetric Berry-phase interference patterns in a single-molecule magnet.

Physical review letters 106:22 (2011) 227201

Authors:

HM Quddusi, J Liu, S Singh, KJ Heroux, E del Barco, S Hill, DN Hendrickson

Abstract:

A Mn(4) single-molecule magnet displays asymmetric Berry-phase interference patterns in the transverse-field (H(T)) dependence of the magnetization tunneling probability when a longitudinal field (H(L)) is present, contrary to symmetric patterns observed for H(L)=0. Reversal of H(L) results in a reflection of the transverse-field asymmetry about H(T)=0, as expected on the basis of the time-reversal invariance of the spin-orbit Hamiltonian which is responsible for the tunneling oscillations. A fascinating motion of Berry-phase minima within the transverse-field magnitude-direction phase space results from a competition between noncollinear magnetoanisotropy tensors at the two distinct Mn sites.
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