Magnetocaloric Effect In Gd5(SixGe1-x)4 Alloys

dc.contributor
Universitat de Barcelona. Departament de Física Fonamental
dc.contributor.author
Casanova i Fernàndez, Fèlix
dc.date.accessioned
2011-04-12T13:41:55Z
dc.date.available
2004-10-13
dc.date.issued
2004-03-09
dc.date.submitted
2004-10-13
dc.identifier.isbn
8468889024
dc.identifier.uri
http://www.tdx.cat/TDX-1013104-132902
dc.identifier.uri
http://hdl.handle.net/10803/1789
dc.description.abstract
This Ph.D. Thesis has been devoted to the preparation and characterisation of bulk Gd5(SixGe1-x)4 alloys and to the study of the magnetocaloric effect at the first-order magnetostructural transition appearing in these compounds. We summarise the most relevant results from this research:<br/><br/>- Bulk Gd5(SixGe1-x)4 samples with 0¡Âx ¡Â0.5 have been prepared by using our home-made arc-melting furnace. Characterisation techniques (SEM, microprobe, XRD, DSC, magnetisation, ac susceptibility) show that the 5:4 phase with the desired x is obtained. Some spread around the nominal value and secondary 5:3 and 1:1 phases are detected. Heat treatment favour the segregation of these secondary phases, but also reduce the spread in the x value. A treatment at 920 ¨¬C for 4 hours in a 10-5 mb vacuum furnace enables a trade-off between phase segregation and removal of x spread.<br/><br/>- A new differential scanning calorimeter (DSC), which operates under applied magnetic fields of up to 5 T and within the temperature range 10-300 K, has been developed. This calorimeter enables an accurate determination of the entropy change associated with a magnetostructural phase transition. The transition can be induced by sweeping either T or H. <br/><br/>- It has been shown that the Clausius-Clapeyron equation and DSC measurements yield the entropy change associated with the first-order magnetostructural transition, &#8710;S. If the Maxwell relation is evaluated only within the field range over which the transition takes place, the same value is obtained. When the Maxwell relation is evaluated over the whole field range, the T and H dependences of the magnetisation in each phase outside the transition region yield an additional entropy change to that associated with that of the actual first-order transition. The transition temperature Tt must significantly shift with the applied field, in order to achieve a large MCE taking advantage of &#8710;S.<br/><br/>- DSC under H has been used to measure &#8710;S for Gd5(SixGe1-x)4, x ¡Â0.5. &#8710;S scales with Tt, which is a direct consequence of the fact that Tt is tuned by x and H and it is thus expected to be universal for any material showing a field-induced transition. The specific shape of &#8710;S vs. Tt will depend on the details of the phase diagram, Tt(x). The scaling of &#8710;S shows the equivalence of magnetovolume and substitution-related effects in Gd5(SixGe1-x)4 alloys.<br/><br/>- The variation of the transition field with the transition temperature, dHt/dTt, has been studied in Gd5(SixGe1-x)4 for 0¡Âx ¡Â0.5. It is shown that dHt/dTt governs the scaling of &#8710;S with Tt. Two distinct behaviours for dHt/dTt have been found on the two compositional ranges where the magnetostructural transition occurs, showing the difference in the strength of the magnetoelastic coupling in this system.<br/><br/>- It has been shown that an unreported field-induced magnetic phase transition exists from the AFM phase to a phase which presents short-range correlations (SRAFM). The results suggest that the transition results from the breaking of the long-range AFM correlations when a magnetic field is applied, which leads to competing FM and AFM short-range correlations. FM correlations are also relevant in the whole long-range AFM phase. The expected transition from the SRAFM to the PM phase takes place at ~240 K at zero field, being widened and smoothed under applied field. This finding in the Ge-rich Gd5(SixGe1-x)4 alloys arises from the competition between the intraslab FM interactions and the interslab AFM interactions.<br/><br/>- The dynamics of the first-order transition in Gd5(SixGe1-x)4 alloys has been studied by cycling virgin samples. The field-induced entropy change increases during the first cycles, then reaching a stationary value. This behaviour is related to the avalanche distribution, which also evolves with cycling. The structure of avalanches becomes repetitive after a few cycles tending towards a power-law distribution, unveiling the athermal character of the transition.
cat
dc.format.mimetype
application/pdf
dc.language.iso
eng
dc.publisher
Universitat de Barcelona
dc.rights.license
ADVERTIMENT. L'accés als continguts d'aquesta tesi doctoral i la seva utilització ha de respectar els drets de la persona autora. Pot ser utilitzada per a consulta o estudi personal, així com en activitats o materials d'investigació i docència en els termes establerts a l'art. 32 del Text Refós de la Llei de Propietat Intel·lectual (RDL 1/1996). Per altres utilitzacions es requereix l'autorització prèvia i expressa de la persona autora. En qualsevol cas, en la utilització dels seus continguts caldrà indicar de forma clara el nom i cognoms de la persona autora i el títol de la tesi doctoral. No s'autoritza la seva reproducció o altres formes d'explotació efectuades amb finalitats de lucre ni la seva comunicació pública des d'un lloc aliè al servei TDX. Tampoc s'autoritza la presentació del seu contingut en una finestra o marc aliè a TDX (framing). Aquesta reserva de drets afecta tant als continguts de la tesi com als seus resums i índexs.
dc.source
TDX (Tesis Doctorals en Xarxa)
dc.subject
Aliatges
dc.subject
Magnetisme
dc.subject
Efecte magnetocalòric
dc.subject.other
Ciències Experimentals i Matemàtiques
dc.title
Magnetocaloric Effect In Gd5(SixGe1-x)4 Alloys
dc.type
info:eu-repo/semantics/doctoralThesis
dc.type
info:eu-repo/semantics/publishedVersion
dc.subject.udc
53
cat
dc.contributor.director
Batlle Gelabert, Xavier
dc.rights.accessLevel
info:eu-repo/semantics/openAccess
cat
dc.identifier.dl
B.46763-2004


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1.CHAPTER_1.pdf

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10.CONCLUSIONS.pdf

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11.LIST_OF_PUBLICATIONS.pdf

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13.BIBLIOGRAFIA.pdf

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