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Volume 84A, number 9 PHYSICS LETTERS 31 August 1981 MAGNETIZATION OF CeAg AT HIGH PRESSURE Makio KURISU, Hideoki KADOMATSU and Hiroshi FUJ1WARA Department of Materials Science, Faculty of Science, Hiroshima University, Hiroshima 730, Japan Received 21 May 1981 Magnetization measurements for CeAg under hydrostatic pressures up to 4.0 kbar and CeAg 1_~ln~ compounds (0.01 ‘~ x~ 0.20) at normal pressure were made at 4.2 K in magnetic fields up to 50 kOe. It was found that the magnetization of CeAg under pressure and of CeAg .~ mx were larger than that of CeAg at normal pressure. The intermetallic compound CeAg shows a struc- plied magnetic fields up to 50 kOe generated with a tural distortion from cubic to tetragonal at TM = 16 K superconducting magnet. The pressures were generated as the temperature is lowered, and becomes ferromag- in a miniature piston—cylinder clamp press~1re cell of netic below the Curie temperature Tc = 5.5 K [1]. Be—Cu, where the pressure transmitting medium was a Therefore, it is to be expected that the magnetic char- mixture of 1 : 1 n-pentane and isoamyl alcohol, and acter of CeAg is not independent of the distortion due the hydrostatic pressure could be retained by cooling to the closeness of TM and Tc. The purpose of our in- the cell and sample slowly down to the liquid helium vestigation is to elucidate the above-mentioned situa- temperature range. The pressure near 4.2 K was deter- tion from both the pressure effect and the alloying ef- mined from the pressure dependence of the supercon- fect by substituting In for Ag, since we believe that the ducting transition temperature of Sn by measuring the pressure and alloying effects are complementary to each ac susceptibility with a Hartshorn bridge circuit. It was other. found that the pressures at 4.2 K were reduced by 2.4 In a previous paper [1], we reported the pressure ef- kbar from those at room temperature. In order to re- fect on TC and TM determined from an electrical resis- duce the magnetization of the pressure cell itself, tivity measurement from 4.2 K to 300 K under hydro- dummy Be—Cu cells were connected to both ends of static pressures up to 5 kbar, and both TC and TM in- the pressure cell and other contrivances with respect creased with increasing pressure. Quite recently, Eiling to the smooth setting of the whole cell assembly were and Schilling [2] have extended the resistivity measure- made. Details of the pressure and dummy cells will be ment up to 40 kbar and found a maximum at a pres- described in a separate paper [3] together with a de- sure p 7 kbar in the pressure dependence of Tc. The scription of the magnetometer. present paper gives the results of the magnetization Fig. 1 shows magnetization curves of CeAg at var- measurement of CeAg at 4.2 K under pressures up to 4 ious pressures as a function of the effective magnetic kbar and that of CeAg1_~In~ withx in the range be- field Heff; the closed and open circles indicate the ex- tween 0.01 and 0.20 at normal pressure. perimental points in the initial magnetization process Polycrystals of CeAg and CeAg1 ~In~ (x = 0.01, and with decreasing magnetic field, respectively. The 0.02, 0.03, 0.05, 0.10 and 0.20) were prepared in ac- magnetization subsequent to the demagnetization was cordance with the prescription of ref. [1] and the found to be reversible. It is noted that the same mag- samples were of spherical form, 3—5 mm in diameter. netization curves as shown in fig. 1 were obtained af- Magnetization curves were measured by a vibrating ter the sample was warmed up to room temperature sample magnetometer with a frequency of 2 Hz in ap- and cooled down again to 4.2 K. The results are ar- ranged as follows. 496 0 031—9163/81/0000—0000/s 02.50 © North-Holland Publishing Company

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Page 1: Magnetization of CeAg at high pressure

Volume84A, number9 PHYSICSLETTERS 31 August1981

MAGNETIZATION OF CeAgAT HIGH PRESSURE

Makio KURISU, Hideoki KADOMATSU andHiroshi FUJ1WARADepartmentofMaterials Science,Facultyof Science,HiroshimaUniversity,Hiroshima 730,Japan

Received21 May 1981

Magnetizationmeasurementsfor CeAgunderhydrostaticpressuresup to 4.0 kbar andCeAg1_~ln~compounds(0.01

‘~ x ~ 0.20)at normalpressureweremadeat4.2 K in magneticfields up to 50 kOe. It wasfound thatthe magnetizationof CeAgunderpressureandof CeAg .~ mx werelarger thanthatof CeAgat normalpressure.

The intermetalliccompoundCeAgshowsa struc- pliedmagneticfields up to 50 kOegeneratedwithatural distortion from cubicto tetragonalat TM = 16 K superconductingmagnet.Thepressureswere generatedasthe temperatureis lowered,andbecomesferromag- in a miniaturepiston—cylinderclamppress~1recell ofneticbelow theCurie temperatureTc = 5.5 K [1]. Be—Cu,wherethepressuretransmittingmediumwasaTherefore,it is to be expectedthat themagneticchar- mixtureof 1 : 1 n-pentaneandisoamylalcohol,andacterof CeAgis not independentof the distortiondue thehydrostaticpressurecouldberetainedby coolingto the closenessof TM andTc.The purposeof our in- thecell andsampleslowly down to the liquid heliumvestigationis to elucidatethe above-mentionedsitua- temperaturerange.Thepressurenear4.2K was deter-tion from both thepressureeffectandthealloying ef- minedfrom the pressuredependenceof thesupercon-fect by substitutingIn for Ag, sincewe believethat the ducting transitiontemperatureof Snby measuringthepressureandalloyingeffectsarecomplementaryto each acsusceptibilitywith a Hartshornbridgecircuit. It wasother. foundthat the pressuresat 4.2 K were reducedby 2.4

In a previouspaper[1], we reportedthepressureef- kbar from thoseat room temperature.In order to re-fect on TC andTM determinedfrom anelectricalresis- ducethe magnetizationof the pressurecell itself,tivity measurementfrom 4.2 K to 300 K underhydro- dummyBe—Cu cells wereconnectedto bothendsofstaticpressuresup to 5 kbar, andbothTC and TM in- thepressurecell andothercontrivanceswith respectcreasedwith increasingpressure.Quiterecently,Eiling to thesmoothsettingof thewhole cell assemblywereandSchilling [2] haveextendedtheresistivitymeasure- made.Detailsof the pressureanddummycellswill bementup to 40 kbar andfounda maximumat a pres- describedin a separatepaper[3] togetherwith ade-surep 7 kbarin the pressuredependenceof Tc. The scriptionof the magnetometer.presentpapergives theresultsof themagnetization Fig. 1 showsmagnetizationcurvesof CeAgatvar-measurementof CeAgat 4.2 K underpressuresup to 4 iouspressuresasa functionof the effectivemagnetickbarand that of CeAg1_~In~withx in therangebe- field Heff; the closedandopencirclesindicatetheex-tween0.01 and0.20at normalpressure. perimentalpoints in the initial magnetizationprocess

Polycrystalsof CeAg and CeAg1 ~In~ (x = 0.01, andwith decreasingmagneticfield, respectively.The0.02,0.03,0.05, 0.10and0.20)were preparedin ac- magnetizationsubsequenttothedemagnetizationwascordancewith theprescriptionof ref. [1] and the found to bereversible.It is notedthat thesamemag-sampleswereof sphericalform, 3—5 mm in diameter. netizationcurvesasshown in fig. 1 wereobtainedaf-Magnetizationcurveswere measuredby a vibrating ter thesamplewaswarmedup to roomtemperaturesamplemagnetometerwith a frequencyof 2 Hz in ap- andcooleddown againto 4.2K. Theresultsare ar-

rangedasfollows.

496 0 031—9163/81/0000—0000/s02.50© North-HollandPublishingCompany

Page 2: Magnetization of CeAg at high pressure

Volume84A,number9 PHYSICSLETTERS 31 August1981

o-(~/f.u.) which would be lockedalongthetetragonalaxis,oc-

0:~h1 .G curstowardsthefield directionand themagneticfieldintensitywasnot strongenoughto completethedo-= •Okbaj 1.0 main rearrangementat highpressures.Therefore,theexperimentalfact thataat 4 kbarislowerthanthatatnormalpressuredoesnotseemto beserious.3.1Ic bar As a complementaryresult tothe pressureeffect,1.0 the magnetizationcurvesof theCeAg1_~In~system— P~2.1kb~r for variousIn concentrationsaregiven in fig. 2. It0~

1.0 similar to thoseat highpressures.In this alloying ef-

0 _~7~P=1.bar~ shouldbe notedthat themagnetizationprocessesarefect, the rapidincreaseandits shift tohighermagnetic0 fieldsin the initial magnetizationcurvesarewell de-

1.0 fined. Theyprobablyoriginatefrom anincreasein the

inducedmagnetocrystallineanisotropywith pressure0 or In concentration.a ~ P1k bar The magneticpropertiesof CeAgat normalpressure

________3.50 CeAg and temperatureslower than TM havebeenconsidered

0 I so far [4,5] by takinginto accounttheeffect of the

structuraldistortionat TM from cubicto tetragonalonat 4.2KC——— 0

_________ the electronicstructure;that is, this distortionsplits0 10 20 30 40 50

H~f(kOe)

Fig. 1. Magnetizationcurvesof CeAgatvariouspressures a-( JiB /f.u.)andatemperatureof 4.2 K.

1.0

At normalpressurep = 0 kbar,the magnetization

0.5 xro.1o11

XO.20’

a,in unitsof the Bohr magnetonper formulaunit,p~/fu,increaseswith increasingHeff, indicatingaratherlargehigh field susceptibility,and themagni-tudeat 50 kOeis 0.94I.LB/fu. Thespontaneousmagnet- x~o.oizationobtainedby extrapolatingsmoothlybackto 0 — I

zerofield in the decreasingcurveis about0.7pBIfu. 0

Thisvaluealmostagreeswith0.7 ±0.15,1B/fu ob- —

tainedfrom a neutrondiffraction measurementat 4.2 0 —

0K [4]. At 1.2 kbar,themagnetizationat 50 kOeis1.0

1.15~B/fu, which is considerablylargerthanthatatnormalpressure;that is, themagnetizationincreases 0

0with increasingpressure._________ 0.5However,a commentwill bemadeon theinitial ________

magnetizationprocess.Theinitial magnetizationcurve 0 — CeA~..XInX0 I

at 1.2 kbartendsto increaserapidly around5 kOe; this at 4.2rapid changeof increaseislikely to shift to higher _________ 0

magneticfields andto becomevague,aspressurein- C0—1~——20—3040 50

creases,andthemagnetizationstopsincreasingwith H~ff(kOe)pressure.Theseresultsarepossiblydue to thecircum- Fig. 2. Magnetizationcurvesof CeAg1_~In~compoundsatstancesthat the rearrangementof magneticdomains, normal pressureanda temperatureof 4.2 K.

497

Page 3: Magnetization of CeAg at high pressure

Volume 84A,number 9 PHYSICS LETTERS 31 August1981

thegroundstater8 quartetinto two doublets(4f in- with pressureor alloyingmay alsobeattributedto thisducedJahn—Tellereffect [6]). Both experimentalfacts increaseof occupationin the above-mentionedsense.at normalpressure,thata sharpincreasein the temper- In this case,however,theexchange-splittedlevelswouldaturecoefficientof the resistivity wasfoundbelow TM be widenedby enhancement.of the s—f interactionre-[1,7], andthat the spontaneousmagnetizationat 4.2K sulting from thed bandsplittingwith pressureor alloy-in thepresentwork is 0.7~B’ mayalsobe understood ing (bandJahn—Tellereffect [8]).in this scheme,sincetheexpectedmagnetizationfrom A carefulexaminationof thediscriminationbe-r8 is about

2/.LB. tweenthe proposedtwo kinds of Jahn—TellereffectsForthepurposeof understandingthe resultsin the [6,81 shouldbethenextproblemto beconsidered.

presentwork, however,we mayproposetheadditionalassumptionsthat(i) thehigherandlower statesof the Referencesabove-mentionedtwo doubletsarethosecarrying highandlow magneticmoments,respectively,andthe split- [1] H. Kadomatsu, M. Kurisu andH. Fujiwara,Phys.Lett.

ting betweenthetwo doubletsis relativelysmall since 70A (1979)472.- . . .. [2] A. Eiling andJ.S.Schilling,Phys.Rev. Lett. 46 (1981)

thetetragonaldistortionis small(~2%)[4], and (n) 364.eachdoubletundergoesanexchangesplittingbelowTC. [3] H. Kadomatsuet al., to bepublished.Then,theseexchange-splittedlevelswill be widened [4] D. Schmitt, P. Morin and J. Pierre, J. Magn.Magn.Mater.

withappliedmagneticfield H. As a result,the levels 8 (1978)249.

with highandlow momentsof the respectivestates [5] H. Ihrig and S. Methfessel,Z. Phys.B24 (1976)385.- . . . [6] D.K. Ray and1. Sivardiere Solid StateCommun. 19would be mixed, sothatthe occupationrn the high- (1976) 1053.

momentlevelincreasesor themagnetizationmcreases, [7] H. Ihrig andW. Lohmann, 1. Phys. F7 (1977)1957.

with increasingH. The increaseof themagnetization [8] H. Ihrig andS. Methfessel,Z. Phys.B24 (1976) 381.

498