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Quantum signatures of a molecular nanomagnet in direct magnetocaloric measurements.


ABSTRACT: Geometric spin frustration in low-dimensional materials, such as the two-dimensional kagome or triangular antiferromagnetic nets, can significantly enhance the change of the magnetic entropy and adiabatic temperature following a change in the applied magnetic field, that is, the magnetocaloric effect. In principle, an equivalent outcome should also be observable in certain high-symmetry zero-dimensional, that is, molecular, structures with frustrated topologies. Here we report experimental realization of this in a heptametallic gadolinium molecule. Adiabatic demagnetization experiments reach ~200?mK, the first sub-Kelvin cooling with any molecular nanomagnet, and reveal isentropes (the constant entropy paths followed in the temperature-field plane) with a rich structure. The latter is shown to be a direct manifestation of the trigonal antiferromagnetic net structure, allowing study of frustration-enhanced magnetocaloric effects in a finite system.

SUBMITTER: Sharples JW 

PROVIDER: S-EPMC4220460 | biostudies-literature | 2014

REPOSITORIES: biostudies-literature

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Quantum signatures of a molecular nanomagnet in direct magnetocaloric measurements.

Sharples Joseph W JW   Collison David D   McInnes Eric J L EJ   Schnack Jürgen J   Palacios Elias E   Evangelisti Marco M  

Nature communications 20141022


Geometric spin frustration in low-dimensional materials, such as the two-dimensional kagome or triangular antiferromagnetic nets, can significantly enhance the change of the magnetic entropy and adiabatic temperature following a change in the applied magnetic field, that is, the magnetocaloric effect. In principle, an equivalent outcome should also be observable in certain high-symmetry zero-dimensional, that is, molecular, structures with frustrated topologies. Here we report experimental reali  ...[more]

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