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Solid State Communications, Vol. 18, Pp. 889—891, 1976. Pergamon Press. Printed in Great Britain OPTICAL SPIN ORIENTATION OF EXCITONS IN GaSe UNDER LONGITUDINAL MAGNETIC FIELD F. Minami, Y. Oka and T. Kushida The Institute for Solid State Physics, The University of Tokyo, Roppongi, Mmato-ku, Tokyo 106, Japan (Received 21 October 1975 by Y. Toyozawa) The degree of circular polarization of the free-exciton luminescence line has been measured in GaSe excited by circularly polarized light at 4.2 K under longitudinal magnetic field. The result shows that the spin relaxation time of exciton is field-dependent but the spin memory before reaching the exciton ground state is almost unaffected by the applied longitudinal mag- netic field. THE OPTICAL orientation of spins of free carriers and where L~ (or L) is the intensity of the luminescence excitons has recently been studied in various semicon- component with the photon spin parallel (or anti-parallel) ductors. 13 It has been found that valuable information to that of the exciting light. In order to measure this on the relaxation kinetics of these excited particles can quantity, a X/4 plate rotating~ at 33 Hz and a linear polar- be obtained by this technique. Especially, the study of izer was placed between the sample and the spectrometer. the degree of polarization of luminescence with varying Then, the outputs of the two lock-in amplifiers set at transverse magnetic field is a powerful method to deter- 750 and 66 Hz represent the average intensity (L’ + L )/2 mine the lifetime as well as the spin relaxation time, and and the difference (L~ —L)/2, respectively. These out- a number of experiments have been carried out by this puts were processed by a computer and the degree of method on various materials. As to the effect of applied polarization p was displayed on a chart recorder simul- longitudinal magnetic field, however, only a few works taneously with the ordinary emission spectra and dif- have been reported on the optical orientations of free- ference signal spectra. Although the measurement was electron spins and nuclear spins.46 In the present made on the whole spectral region of luminescence, in communication, we report the measurement of the de- the present communication we confine ourselves to the gree of polarization of exciton luminescence in GaSe free-exciton line (cf. Fig. 1). under longitudinal magnetic field. In addition to the In a magnetic field H 1 applied parallel to the c-axis, first observation of the effect of the longitudinal field on the degree of polarization of luminescence is given by the the optical spin orientation of excitons, the field following expression: 4 dependences of the spin relaxation time and the spin T r / H memory before reaching the emitting state have been p(H,) = G + tanh 1~11~ ‘J , (2) obtained separately. T1 + T T1 + T \ 2kT The GaSe crystal grown by Bridgman method was where r and T1 are the lifetime and the spin relaxation directly immersed in liquid He and excited by circularly time of the emitting state, G is a phenomenological para- polarized light (A = 570 nm) incident parallel to the meter which characterizes the spin memory before reach- crystal c-axis. The excitation source employed was a c.w. ing the luminescent level, g11 is the g-value of the emitting tunable dye laser (Spectra Physics model 370) pumped state in the parallel configuration, PB is the Bohr mag- by an argon ion laser. The exciting beam was chopped neton, k is the Boltzmann constant and T is the absolute at 750 Hz, passed through a circular polarizer (Polaroid temperature of the crystal. In case that the spin memory HNCP 37), and then focused into the sample. The back- is completely lost, we obtain only the second term in ward-directed luminescence was analysed by a 0.75 m the right-hand side of equation (2). We shall call the first single grating spectrometer (Spex model 1700). The and the second terms of this equation the spin memory signal was detected by an S-20 type photomultiplier term and the thermalization term. Because they are even (Hamamatsu TV model R453) and fed into two lock-in and odd functions of H1, respectively, we can obtain amplifiers (PAR model 121). The degree of circular these two terms separately by making ~ {p(H,) + p (— H1)} polarization of luminescence is defined as and ~ {p (H,) p (— H1)}. L~ —L Figure 1 shows the magnitudes.of these two terms = L~ + L - , (1) thus obtained for the exciton line as a function of the applied longitudinal magnetic field. We see that both 889

Optical spin orientation of excitons in GaSe under longitudinal magnetic field

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Solid StateCommunications,Vol. 18,Pp. 889—891,1976. PergamonPress. Printedin GreatBritain

OPTICAL SPINORIENTATIONOFEXCITONS IN GaSeUNDER LONGITUDINAL MAGNETIC FIELD

F. Minami,Y. OkaandT. Kushida

TheInstitutefor Solid StatePhysics,TheUniversityof Tokyo, Roppongi,Mmato-ku,Tokyo 106, Japan

(Received21 October1975by Y. Toyozawa)

The degreeof circularpolarizationof the free-excitonluminescencelinehasbeenmeasuredin GaSeexcitedby circularly polarizedlight at 4.2Kunderlongitudinalmagneticfield. The resultshowsthat the spinrelaxationtime of excitonis field-dependentbutthe spinmemorybeforereachingtheexcitongroundstateis almostunaffectedby the appliedlongitudinalmag-neticfield.

THE OPTICAL orientationof spinsof freecarriersand whereL~(orL) is the intensityof the luminescenceexcitonshasrecentlybeenstudiedin varioussemicon- componentwith thephotonspin parallel(oranti-parallel)ductors.13It hasbeenfoundthatvaluableinformation to thatof the exciting light. In orderto measurethisonthe relaxationkineticsof theseexcitedparticlescan quantity,a X/4 platerotating~at 33 Hz anda linearpolar-beobtainedby this technique.Especially,the studyof izer wasplacedbetweenthesampleand thespectrometer.the degreeof polarizationof luminescencewithvarying Then,the outputsof the two lock-in amplifierssetattransversemagneticfield is a powerfulmethodto deter- 750and66Hz representthe averageintensity(L’ + L )/2mine thelifetime as well asthe spinrelaxationtime,and andthe difference(L~—L)/2, respectively.Theseout-a numberof experimentshavebeencarriedoutby this putswereprocessedby acomputerandthe degreeofmethodon variousmaterials.As to the effectof applied polarizationp was displayedon a chartrecordersimul-longitudinalmagneticfield, however,onlya few works taneouslywith the ordinaryemissionspectraanddif-havebeenreportedon the opticalorientationsof free- ferencesignalspectra.Althoughthemeasurementwaselectronspinsandnuclearspins.46In the present madeon thewholespectralregionof luminescence,incommunication,we reportthe measurementof the de- thepresentcommunicationwe confineourselvesto thegreeof polarizationof excitonluminescencein GaSe free-excitonline (cf. Fig. 1).underlongitudinalmagneticfield. In additionto the In a magneticfield H

1 appliedparallelto thec-axis,first observationof theeffect of the longitudinal field on thedegreeof polarizationof luminescenceis givenby thethe opticalspinorientationof excitons,thefield following expression:

4dependencesof the spinrelaxationtime andthe spin T r / Hmemorybeforereachingtheemitting statehavebeen p(H,) = G + tanh

1~11~‘J , (2)obtainedseparately. T1 + T T1 + T \ 2kT

TheGaSecrystalgrownby Bridgmanmethodwas wherer andT1 arethe lifetime andthespinrelaxationdirectly immersedin liquid He andexcitedby circularly time of theemittingstate,G is a phenomenologicalpara-polarizedlight (A = 570nm) incidentparallelto the meterwhich characterizesthe spinmemorybeforereach-crystalc-axis. Theexcitationsourceemployedwasa c.w. ing the luminescentlevel,g11 is theg-valueof the emittingtunabledyelaser(SpectraPhysicsmodel 370)pumped statein theparallelconfiguration,PB isthe Bohr mag-by anargonion laser.The excitingbeamwaschopped neton,k is the BoltzmannconstantandT is theabsoluteat 750Hz, passedthrougha circular polarizer(Polaroid temperatureof the crystal. In casethat thespinmemoryHNCP37),andthen focusedinto the sample.Theback- is completelylost,we obtainonly the secondterminward-directedluminescencewasanalysedby a 0.75m the right-handside of equation(2). We shallcall the firstsinglegratingspectrometer(Spexmodel 1700).The andthe secondtermsof this equationthespinmemorysignalwasdetectedby an S-20type photomultiplier termand thethermalizationterm.Becausetheyare even(HamamatsuTV modelR453)andfed into two lock-in andodd functionsof H1, respectively,we canobtainamplifiers(PARmodel 121).The degreeof circular thesetwo termsseparatelyby making~ {p (H,) + p(— H1)}polarizationof luminescenceis definedas and~{p (H,) — p(— H1)}.

L~—L Figure 1 showsthemagnitudes.ofthesetwo terms= L~+ L - , (1) thusobtainedfor the exciton line asa function of the

appliedlongitudinal magneticfield. We seethatboth

889

Page 2: Optical spin orientation of excitons in GaSe under longitudinal magnetic field

890 OPTICAL SPINORIENTATION OFEXCITONS IN GaSe Vol. 18,No. 7

---

GaSe 4.2K20 / Excitation 570nm -~

FE 2 10 - S

10 0.5 /600 595 590

7 A(nm)

0 I

0 5 10 15 ‘~0 5 10 15H

3 (kG) H, (kG)Fig. 1. Longitudinalmagnetic-fielddependenceof the . .

magnitudesof~{p(H,)+ p(— H,)) (uppercurvea)and Fig. 2. The ratio of the spinrelaxationtime T1 and the~{p(H,) — p (— H,)} (lower curveb) measuredat the lifetime r of exciton,andthe spinmemoryG beforefree-excitonline center(587.8nm) of GaSeat 4.2K. The reachingthe excitongroundstateasa function of theemissionspectrumof thestudiedsampleis alsoshownin appliedlongitudinalmagneticfield.the inset,wherethe free excitonline is denotedby anarrow. of the intermediateexcitonstatesdiscussedby Bonnot

eta!.8 Sincethedensityof thefreeexciton luminescencevaluesincreasewithH,. The field dependenceof line did not changeby theapplicationof an external~{p (H,) — p (— H,))was foundto coincidewell with magneticfield, theexciton lifetime r is consideredto bethatmeasuredunderthe excitationby linearly polarized independentof H,. Therefore,themagnetic-fielddepend-light. This factconfirmsthat this quantityis dueto the enceof T1/r is ascribedto that of T1. The increaseofthermalizationtermwhich is irrelevantto thespinmem- thespinrelaxationtimewithH1 is explainedby amech-ory. From this thermalizationterm we candetermine anismanalogousto the motionalnarrowingeffect. Whenthefield dependenceof T1 /r by theuseof equation(2). the Larmorfrequencyof excitonspinexceedstherateThe resultis shown in Fig. 2. The valueof g11 —~2.7~was of the modulationof randomlocal field which isusedin this analysis.It is notedthat thespin relaxation responsiblefor the spinrelaxation,the effectivetimeoftime T1 is of thesameorderof magnitudeas the life- interactionbetweentherandomfield and theexcitontime i-. As H, is increased,T1 /r first increases,then is spinis not determinedby themodulationratebut issaturatedaroundH, of 8 KG. Thefield dependenceof reducedbecauseof therapidmotionof the magneticG is alsoplottedin Fig .2. Thiswasobtainedfrom the moment.Thus,the spinrelaxationtimebeginsto slowspinmemoryterm by usingtheH,-dependenceof T1/r. downwhentheLarmor frequencybecomescomparableWe notice that G is almostindependentofH, andabout to themodulationrateof therandomlocal field. From0.4—0.5. theresult of Fig. 2, the lattermodulationrateis estimated

Theflat dependenceof G on H, may bereasonable to beof the order of 1010 sec* The saturationof T11rbecausetime requiredfor the exciton to reachthe lowest at largevaluesof H, may indicatethepresenceof anotherstateafter theoptical generationis consideredto bevery spinrelaxationmechanismwith muchhighermodulationshortcomparedwith T1 (— r). That theabsolutevalue rate.More detaileddiscussionof theH,-dependenceofof G is lessthan unity may bedue to theL—Tsplitting T1/r will be given in a separatepaper.

9

REFERENCES

1. LAMPEL G.,Phys.Rev.Lett. 20,491(1968).

2. ZAKHARCHENYA B.P.,Proc. mt. ConfSemicond.Phys.,Warsaw,p. 1327.Polish Scientific,Warsaw(1972).

3. LAMPEL G.,Proc. mt. ConfSemicond.Phys.,Stuttgart,p. 743. Teubner,Stuttgart(1974).

4. PARSONSR.R.,Can. J.Phys.49, 1850(1971).

5. DZHIOEV R.I., ZAKHARCHENYA B.P.,FLEISHERV.G. & VEKUA V.L., Soy.Phys.Semicond.7, 1237(1974).

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Vol. 18,No. 7 OPTICAL SPINORIENTATIONOF EXCITONS IN GaSe 89i

6. BERKOVITS V.L., EKIMOV A.I. & SAFAROVV.1.,Soy.Phys.JETP38, 169 (1974).

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