54 research outputs found
Magnetocaloric effect in itinerant electron metamagnetic systems La(Fe1-xCox)11.9Si1.1
The NaZn13-type compounds La(Fe1–xCox)11.9Si1.1 (x=0.04, 0.06, 0.08) were successfully synthesized, in which the Si content is the limit that can be reached by arc-melting technique. TC is tunable from 243 to 301 K with Co doping from x=0.04 to 0.08. Great magnetic entropy change S in a wide temperature range from ~230 to ~320 K has been observed. The adiabatic temperature change Tad upon changing magnetic field was also directly measured. Tad of sample x=0.06 reaches ~2.4 K upon a field change from 0 to 1.1 T. The temperature hysteresis upon phase transition is small, ~1 K, for all samples. The influence of Co doping on itinerant electron metamagnetic transition and magnetic entropy change is discussed. ©2005 American Institute of Physics.published_or_final_versio
Inverse magnetocaloric effect in ferromagnetic Ni-Mn-Sn alloys
The magnetocaloric effect (MCE) in paramagnetic materials has been widely
used for attaining very low temperatures by applying a magnetic field
isothermally and removing it adiabatically. The effect can be exploited also
for room temperature refrigeration by using recently discovered giant MCE
materials. In this letter, we report on an inverse situation in Ni-Mn-Sn
alloys, whereby applying a magnetic field adiabatically, rather than removing
it, causes the sample to cool. This has been known to occur in some
intermetallic compounds, for which a moderate entropy increase can be induced
when a field is applied, thus giving rise to an inverse magnetocaloric effect.
However, the entropy change found for some ferromagnetic Ni-Mn-Sn alloys is
just as large as that reported for giant MCE materials, but with opposite sign.
The giant inverse MCE has its origin in a martensitic phase transformation that
modifies the magnetic exchange interactions due to the change in the lattice
parameters.Comment: 12 pages, 4 figures, to appear in Nature Materials (online published,
15 May 2005
Magnetism, FeS colloids, and Origins of Life
A number of features of living systems: reversible interactions and weak
bonds underlying motor-dynamics; gel-sol transitions; cellular connected
fractal organization; asymmetry in interactions and organization; quantum
coherent phenomena; to name some, can have a natural accounting via
interactions, which we therefore seek to incorporate by expanding the horizons
of `chemistry-only' approaches to the origins of life. It is suggested that the
magnetic 'face' of the minerals from the inorganic world, recognized to have
played a pivotal role in initiating Life, may throw light on some of these
issues. A magnetic environment in the form of rocks in the Hadean Ocean could
have enabled the accretion and therefore an ordered confinement of
super-paramagnetic colloids within a structured phase. A moderate H-field can
help magnetic nano-particles to not only overcome thermal fluctuations but also
harness them. Such controlled dynamics brings in the possibility of accessing
quantum effects, which together with frustrations in magnetic ordering and
hysteresis (a natural mechanism for a primitive memory) could throw light on
the birth of biological information which, as Abel argues, requires a
combination of order and complexity. This scenario gains strength from
observations of scale-free framboidal forms of the greigite mineral, with a
magnetic basis of assembly. And greigite's metabolic potential plays a key role
in the mound scenario of Russell and coworkers-an expansion of which is
suggested for including magnetism.Comment: 42 pages, 5 figures, to be published in A.R. Memorial volume, Ed
Krishnaswami Alladi, Springer 201
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