Magnetic-Semiconductors in Fe-Ti
Transcription
Magnetic-Semiconductors in Fe-Ti
Magnetic-Semiconductors in Fe-Ti-Oxide Series and Their Potential Applications R .K. Pandey*1,2, P. Padmini1, L. F. Deravi3, N.N. Patil4, P. Kale1, J. Zhong1, J. Dou2, L. Navarrete2, R. Schad2, and M. Shamsuzzoha5 1 2 Electrical and Computer Engineering, Physics and Astronomy, 3 Chemistry, 4 Computer Science, 5 Central Analytical Facilities (CAF) The University of Alabama, Tuscaloosa, AL, USA C. O’Brien6 and W. J. Geerts6 6 Department of Physics Texas State University, San Marcos, TX, USA *Email: rpandey@bama.ua.edu and pandeyrk@att.net Abstract Multifunctional nature of the Fe-Ti-oxides make them attractive candidates for novel applications in which their coupled semiconductor, magnetic, dielectric and optical properties can be exploited. In particular, they appear to be good candidates for the emerging technologies such as spintronics, magneto-electronics, and radhard electronics. In this paper we deal mostly with pseudobrookite (Fe2TiO5), both pure and Mn-substituted variety. Materials processing, structural, magnetic and semiconducting properties have been discussed in-depth. The temperature and magnetic field dependence on the non-liner I-V characteristics are established opening the possibilities for fabricating magnetically switched devices. 1. Introduction Iron titanates, Fe-Ti-oxides, are well known to geophysicists and geologists and their unusual magnetic properties have been of great interest to geophysicists for a very long time. But they have rarely been studied for their unique electrical, dielectric and magnetic properties with potential applications in microelectronics and its related technologies. The multifunctional nature (wide band-gap semiconductor, magnetic and dielectric properties) of some members of this family has been recognized only recently resulting in interest of a large group of researchers to study this system. Particularly the coupled magnetic and semiconductor properties of some members of the ilmenite-hematite solid solutions (IH) and Mn-doped pseudobrookite (Mn-PsB) are of special interest both from the fundamental materials science point of view and their potential impact to such emerging technologies as spintronics, magneto-electronics and radhard electronics. Nature produces three stable compounds in the irontitanate system, namely, ilmenite (FeTiO3), pseudobrookite (Fe2TiO5) and ulv spinel (Fe2TiO4). Ilmenite is the lead member of the group and most viable as a source of TiO2 pigment. Its very interesting geomagnetism has been extensively studied by geologists. In the recent past, after its discovery on the moon in one of the earlier space explorations, it drew attention of space scientists because of the possibility (or, dream) of colonizing the moon some day and setup civilization there. It is also a very prominent raw material on earth and is used in shielding nuclear radiation. When mixed with hematite, it assumes the character of solid solutions with interesting electrical and magnetic properties [1,2]. Many members of this series are wide band gap semiconductors with band gap greater than 2.0 eV as well as ferromagnetic with the Curie point well above the room temperature. This uniqueness of properties makes them extremely attractive candidates for research leading to some novel applications in microelectronics and perhaps also spintronics. In the last few years this system has been extensively studied by our group leading to some pioneering publications. The interested readers are referred to references [3-8]. The focus of this paper is not IH rather the lesser known member of the Fe-Ti-oxide, namely, pseudobrookite (PsB) and Mn-doped pseudobrookite (Mn-PsB). Like the IH solid solution it is also a potential candidate for spintronics, magneto-electronics and radhard electronics and microelectronics in general. Compared to the IH this material is less complicated, very stable even at high temperatures and can be processed with greater ease and reliability in air as ceramic, epitaxial and high quality thin films and most importantly as bulk single crystals. In comparison, it is almost impossible to grow single crystals of IH by any known single crystal growth method. The phase diagrams [9,10] point to the possibility of dissociation of IH at high temperatures at which the crystals must be grown. From the phase diagram [11] one infers that PsB melts congruently at about 1550 C. This advantage makes Mn-PsB perhaps a superior class of material than IH solid solutions for developing applications on large scale. PsB crystallizes in orthorhombic structure with the lattice constant of a = 0.97, b = 0.99 and c = 0.37 nm [11]. Its crystal structure has been extensively studied and the general agreement is that it is the most stable member of the Fe-titanate family and is in equilibrium with atmospheric oxygen [12-14]. In 1981, however, its monoclinic phase was discovered which converts to the orthorhombic phase at about 927 ºC [15]. For the growth of the monoclinic phase a relatively fast cooling rate of 10 ºCh-1 was used. The flux contained a small amount of SrO. It is not clear whether the growth of monoclinic phase was promoted by the presence of alkaline earth oxide or was the result of fast cooling. It was found that the monoclinic crystals were magnetic, more precisely perhaps parasitic magnetism instead of intrinsic ferromagnetism. In contrast, pure PsB crystals are paramagnetic, or at best weakly magnetic, at room temperature. They show strong anisotropic uniaxial “spin-freezing” behavior [16,17]. The spin-glass transition occurs between at 53 and 55 K. In PsB iron ions exist predominately in 3+ state and are believed to be the contributor to spin-glass freezing. From M ssbauer-effect it was concluded that the spins of the Fe3+ ions are parallel to the crystallographic c-axis [16]. Later in this paper we will show that Mn-doping enhances its ferromagnetic property while still retaining its semiconductor property. Both pure PsB and Mndoped PsB are n-type semiconductors. Because of the coupled semiconductor-magnetic properties Mn-PsB is an attractive material for spintronics, and magnetoelectronics. It is believed to have strong radiation immunity like IH [5,7] which makes it also a suitable candidate for radhard electronics. 2. Materials Processing (a) Sample Processing: Three types of samples were processed for this study – ceramic, films and bulk single crystals. Ceramic: In order to first understand the basic nature of physical properties and processing chemistry dense, homogeneous ceramic samples were processed using the standard procedure [18]. Another reason for making high quality ceramic discs is that we need targets for the growth of films by the laser ablation method which will be described later in this paper. The samples were mostly 1 inch diameter discs having the thickness between 3 to 4 mm. High purity powder of pseudobrookite was used to press disks at 10,000 psi using an automatic uniaxial press. All the initial pressing was done at room temperature in the presence of air. These green ceramic were sintered multiple times and finally annealed in Aratmosphere to obtain dense, and chemically homogeneous disks showing the desired x-ray diffraction patterns and low resistance.. The details for making highly dense and homogenous ceramic samples of IH have been recently reported in reference [19]. Because of the chemical similarities with IH we adopted the same processing protocol for making PsB and Mn-PsB ceramic as for IH ceramic. Since pure PsB is not magnetic it was decided to dope it with Mn3+ ions (source being Mn2O3) to make it ferromagnetic. First ceramic of PsB with varying percentage of Mn was processed and characterized. Samples having Mn-doping from 4 to 40 atomic percent showed both n-type as well as ferromagnetic behavior at room temperature. The highest magnetic moment was obtained when a doping level of 40 percent was used. Bulk single crystal: Growth of single crystals of PsB was undertaken because of the limited literature available that deal with the magnetic and electrical properties of PsB as well as for studying the feasibility of potential applications. High temperature solution growth method was used for crystal growth using PbO⋅V2O5 flux. The charge to flux ratio was maintained at 7.5:92.5 by weight for all growth experiments as originally reported in [20]. Czochralski growth was reported in [21]. Our first few runs produced high quality crystals but small in size. Larger crystals, 812 mm × 2-3 mm × 3-5 mm, were grown by seeding the melt and introducing the growth procedure as shown in Figure 1. Once the growth runs were over, crystals were harvested by dissolving the flux in 25% HNO3 acid. Platinum crucibles were used because of the very aggressive nature of molten flux and growth taking place in air at high temperatures. For the growth of Mn-PsB crystals, the charge was prepared with 40% Mn. The growth was initiated under the same general protocol as for pure PsB. Good quality crystals were obtained and presence of Mn was confirmed by EDAX analysis. T max Initial Heating T First Soaking Cycle @ 1350 C for 12-15 hours Second Soak @ 1325 oC for 2-4 hours Range of Crystallization: 1325 – 850 oC Very slow cooling @ 0.5-1 C per hour 100000 Rapid Cooling Time Fig.1 Crystal growth protocol, T = Temperature ( C) Film Growth: Films were grown by the PLD method using the home-made ceramic targets. The growth parameters were established by growing multiple films under different conditions. The following parameters were found to produce smooth textured films on (100) MgO substrates varying in thickness between 50 to 150 nm (depending upon the duration of growth) with good semiconductor and magnetic properties: 248 nm wavelength (Lambda Physique Excimer Laser) with a maximum power rating of 500 mJ per pulse; substrate temperature between 625 and 675 ºC, laser power energy 500 mJ, chamber maintained at 10-5 Torr, and substrate rotation rate of 5.0 rpm. Films of PsB have also been grown using the solgel technology [22,23]. No published literature is available that deals with the growth of Mn-substituted PsB films. We might be the first group to grow highly textured films of Mn-PsB with high enough quality as to study multifunctional properties. 3. Properties and Discussion Film and crystal samples were characterized by x-ray diffraction (XRD) for crystal structure, energy dispersed x-ray diffraction (EDAX) for chemical composition and general surface morphology, and transmission electron microscopy (TEM) for atomic periodicity. All samples were orthorhombic with lattice parameters in good agreement with reported values [11]. Films had very smooth surfaces with well pronounced texturing and the 2000 18.15 (020) 80000 Instensity (cps) T < T max: Super saturation surface roughness varied from 2 to 5 nm as determined from atomic force microscopy (AFM). They were transparent with faint gold color. The bulk crystals, however, were invariably black and no amount of annealing would change their color. Figure 2 shows the characteristic x-ray diffraction peaks and the rocking curve of pure PsB crystals. The well pronounced n(010) peaks and rocking curve width of 0.040º confirm the high quality of the crystals. The WDS analysis showed no trace of impurities or the presence of second phase. The TEM diffraction pattern in Figure 3 showed perfect atomic periodicity confirming the excellent quality of the crystal. 1500 Intensity(cps) . 1000 60000 0.040 deg 40000 36.74 (040) 500 0 10 20000 56.41 (060) 20 30 40 50 60 2Θ(deg) 70 80 90 0 -0.10 -0.05 0.00 0.05 0.10 ω (deg) Fig.2 XRD pattern (left) and rocking curve (right) of PsB crystal. Fig.3 TEM micrograph of PsB crystal The Seebeck coefficient measurements confirmed that both the PsB and Mn-PsB crystals are n-type semiconductors and Mn-PsB crystals displayed magnetic hysteresis loops. No well defined loops were found for the PsB crystals. Table I summarizes some of the properties of bulk crystals of the two types grown by seeded high temperature solution growth method. It is to be noted that both the resistivity and the activation energy is remarkably smaller for Mn-doped samples than for pure PsB. Mn-doping, or more precisely substitution, makes PsB more conductive and reduces its activation energy. Consequently, this material should be appropriate for device fabrication. Because of these advantages, emphasis was put on the growth of highly textured thin film of Mn-PsB. Its physical properties should serve as the bench-mark for technologists and process engineers. Various combinations of temperature and argon pressure inside the growth chamber were tried to find the optimum conditions that would yield the best samples with maximum magnetic moment, saturated magnetic loop and electrical conductivity. In Figure 4 XRD spectrum is presented for the films grown at 450 C under different values of chamber pressure and atmosphere. We find that 50 mT of Ar pressure produces the best crystallinity and texturing with the MgO substrate. (g) MgO substrate (f) Vac (e) 50mT Ar (d) 100mT Ar (c) 200mT Ar (b) 450C Vac (a) 300mT Ar 2500 Intensity 2000 1500 (g) (cm2V-1s-1) Bandgap (eV) (f) 30 o 650 C vacuum o 650 C 50m τ Ar 20 o 650 C 100m τ Ar (d) o M em u/g (b) (a) 0 30 35 40 2 theta (deg) 45 50 Table I: Important Parameters for PsB and Mn-PsB Bulk Crystals Seebeck coefficient ( V⋅K-1) Mobility Mn-PsB n-type n-type 2.197 0.294 -35 ? 0.92 for T >500 K ? -10 -500 0 0 500 0 4 1 10 Fig. 5 Room temperature magnetic moment of Mn-PsB films as a function of growth temperature and chamber pressure. 4 1.6 3 1.2 1 0.8 2.5 2 1.5 1 0.6 0.4 (1kHz) (10kHz) (100kHz) (1MHz) 3.5 R.T = 0.3 -cm Eac ~ 0.012eV capacitance (pF) 0.17 0 field O e 1.4 0.50 0.19 for T < 500 K [24] 0.46 for T > 500 K [24] o 650 C 300m τ Ar -30 4 -1 10 log Res (ohm-cm) Activation energy (eV) Pure PsB o 650 C 200m τ Ar -20 Fig.4 X-ray diffraction pattern of Mn-PsB films grown by PLD at 450º C on MgO substrate Semiconductor nature Resistivity (k ⋅cm) 450 C 50m τ Ar 10 (c) 500 2.3 The bandgap of Mn-PsB film was determined by optical absorption method and it was found to be 2.3 eV which is in good agreement with the value reported in reference [21]. for PsB crystal. The value of 0.92 eV as reported by [24] appears to be too low. Being basically an insulator its bandgap cannot be comparable to narrow bandgap semiconductors. Figure 5 presents the magnetic loops for Mn-PsB films grown at different conditions of temperature and pressure. The best film with the highest value of magnetic moment is achieved for growth taking place at 450 ºC at 50 mT of Ar-pressure. This film has the magnetic moment of 25 emu/g with the coercivity of just 6.5 Oe. The loop saturates around 2 kOe. (e) 1000 (intrinsic) 6.3 for T <500 K (extrinsic) 0.92 [29] 0.5 3 3.5 4 4.5 5 5.5 -1 1000/T (K ) 6 6.5 0 -5 0 Voltage (V) 5 Fig.6 Temperature dependence of resistivity (left) and frequency dependence of capacitance (right). methods. The results are almost identical. Here in Figure 7 the MR measured with the 2-point probe method is shown. It decreases as the field increases and the curve is parabolic which is typical of all semiconductors. The solid curve is best fit of the experimental curve (fluctuating). Resistance (KOhm) The temperature (T) dependence of resistivity ( ) and capacitance C as a function of frequency ( ) is shown in Figure 6 for the Mn-PsB film. The nature of the vs. T-1 curve confirms the semiconductor nature of the film and its almost perfect linearity points to the high quality of the film. From this curve we get the room temperature value of the resistivity to be 0.3 ⋅cm and the activation energy of approximately 12 meV. These values also point to the device quality of the film. It is believed that the conduction in PsB appears to be polaron mediated [24]. It is argued that the conductivity in this material is due to the small polaron band conduction or small polaron hopping conduction. Since the polaron band conduction is possible only at low temperatures it is assumed that the conduction in PsB is due to polaron hopping. Very small value of the activation energy of 12 meV at room temperature could not be due to the intrinsic conduction. Such low values of the activation energy points to the presence of point defects and interstitials in the material [24]. The nature of the capacitance (C) vs. voltage (V) dependence, Fig.6, is typical of insulators. Also, the strong frequency dependence of C is typical of polar and non-polar dielectrics. The relative dielectric constant ( r) at room temperature is found to be approximately 7000. For pure PsB crystals it is reported that the r remains practically constant between 300 to 500 K and then it rises fast and reaches its maximum value around 900 K and then saturates [24]. This type of behavior puts pseudobrookite in the special class of dielectrics known as non-linear (possibly even polar) dielectrics and warrants more investigation. It is important to point out that conductivity, thermal power and dielectric constant show anomalous behavior around 500 K for PsB crystals [24]. The nature of this transition point is not well understood and warrants further studies. Since Mn-substituted PsB film with 40 atomic % Mn3+ shows excellent n-type conductivity and magnetization we decided to study its magnetic field dependence of resistivity and current-voltage (I-V) characteristics. Two experiments were designed: first, to determine the classical magneto-resistance; and second, to study the I-V relationship as function of magnetic field and temperature. The motivation for the second study comes from the non-linear I-V behavior found in IH samples and their prospects for fabricating “varistor” devices [4,5,7]. Radiation hardness of these devices have also been dealt with in references [5,7]. The magneto-resistance (MR) for the Mn-PsB film was measured using both the 2-point and 4-point probe 32.67 32.66 32.65 32.64 32.63 32.62 32.61 32.60 32.59 32.58 32.57 295 K 2 Point probe MR Poly. (2 Point probe MR) -12 -9 -6 -3 0 3 6 9 12 H (KGauss) Fig.7 Magneto-resistance of Mn-PsB film on MgO. Having established the MR effect we proceeded to examine the effect of temperature and magnetic field on the I-V characteristics of the Mn-substituted PsB film (0.6 Fe2TiO5.0.4Mn2O3). The initial I-V relations using the 4-point probe method at varying temperatures looked very linear. This technique was employed in order to eliminate any effect of contact resistance due to the Ag contacts and the interface. However, to exploit any possible non-linearity we took the best linear fit for the IV graph up to four significant digits, subtracted the linear component and examined the non-linear component of the data set. Figure 8 shows the average I-V behavior at 300 K(a) and 441 K(b).. The magnetic field applied were H= 1, 0, and –1 Tesla. We observe that the non-linear component is three orders of magnitude smaller than the original linear curve and here the magnetic field effect is quite pronounced which is practically indistinguishable in its linear counterparts. It is important to realize that the sample experiences no Joule heating (=i2R) because of the low currents applied and thereby we eliminate any thermal effects that could cause the non-linearity or field dependence. From Figure 8 we see clearly that the non-linearity in the I-V behavior is both magnetic field and temperature dependent. The dependence on temperature is quite understandable and is of no particular interest to technology. However, magnetic field dependence is of interest because non-linear devices based on Mn-PsB could be switched magnetically. 140 I (uA) 100 10 0 Acknowledgments: We thank the U.S. Office of Naval Research (Grant # N00014-03-1-0358) and the U.S. Department of Energy (Grant #DE-FG02-03ER46039 ) for their sponsorships. We also thank the staff of MINT Center and Dr. Mike Bersch of Central Analytical Facilities (CAF) at the University of Alabama for their technical support. -1 0 -2 0 -6 0 0 60 I (nA) applications. Spintronics, magneto-electronics, radhard electronics are its other possible applications. 20 -4 0 0 -2 0 0 0 200 V (m V ) 400 600 20 -2 0 -6 0 (a) -1 0 0 1 T e s la - 1 T e s la 300 K 0 T e s la -1 4 0 -6 0 0 -4 0 0 -2 0 0 0 200 400 600 V (m V ) 300 References I (uA) 60 200 30 0 -3 0 -6 0 -7 0 0 -5 0 0 -3 0 0 I (nA) -1 0 0 100 300 500 700 V (m V ) 100 0 -1 0 0 (b) -2 0 0 1 T e s la - 1 T e s la 0 T e s la 441 K -3 0 0 -8 0 0 -6 0 0 -4 0 0 -2 0 0 0 200 400 600 800 V (m V ) Fig. 8 Temperature and magnetic field dependence of non-linear I-V characteristics of Mn-PsB film: (a) 300 K and (b) 441 K. The inserts are the original linear curves. 4. Summary Only recently it has been realized that many members of the family of Fe-Ti-oxides possess fascinating properties that could be exploited for many novel applications. These are very robust materials, relatively less expensive to process and their raw materials are abundant. From the point of electronic technology some solid solutions of ilmenite-hematite (IH) and Mn-substituted pseudobrookite (Mn-PsB) are good candidates for emerging technologies of spintronics and radhard electronics. The paper deals primarily with Mn-PsB and shows its superiority, at least from application point of view, to the more established IH system. Like many IH it is also a wide bandgap semiconductor with bandgap of the order of 2.3 eV, magnetic moment approaching a value of 25 emu/g with the coercivity of just 6.5 Oe. Its dielectric constant is about 7000 which makes it also a very good material for gate-oxide and capacitor applications. Its well pronounced magneto-resistance and magnetic field dependence of the non-linearity of I-V characteristics add additional dimensions to its potential [1]. Y. Ishikawa, J. Phys. Soc. Japan, 13(1), p. 37, (1968). [2]. Y. Ishikawa, J. Phys. Soc. Japan, 12 (10), p. 1083, (1957). [3]. F. Zhou, S. Kotru and R. K. Pandey, Thin Solid Films, 408, p33, (2002). [4]. F. Zhou, S. Kotru, and R. K. Pandey, Mats. Lett. , 57, p. 2104, (2003). [5]. P. Padmini, M. Pulikkathara, R. Wilkins, and R. K Pandey, Appl. Phys. Lett., 82(4), p. 586, (2003). [6]. D. M. Allen, L. Navarrete, J. Dou, R. Schad, P. Padmini, P. Kale and R. K. Pandey, Appl. Phys. Lett., 85, p. 5902, (2004). [7]. P. Padmini, S. Ardalan, F. Tompkins, P. Kale, R. Wilkins and R. K. Pandey, J. Elec. Mats., 34(2), p. 1095, (2005). [8]. J. Dou, L. Navarrete, P. Padmini, P. Kale, R. K. Pandey and R. Schad, Session : GG (Spintronics), Paper # 6, MRS Spring Meeting, San Francisco, CA, (2006). [9].J.B. MacChesney and A. Muan, Am. Mineralogist, 46, p.572, (1961). [10]. L. A. Bursill, J.Solid State Chemistry, 10, p. 72, (1974). [11]. R.W.G. Wyckoff, Crystal Structures, 3, p.297, (1964). Wiley Publication. [12].S. Akimoto and T. Nagata, Nature, 179, p.37, (1957). [13]. L. Pauling, Z. Krist., 73, p.97, (1930). [14]. M. Shiojori, S. Sekimoto, T.. Maeda, Y. Ikeda, and K. Iwauchi, Phys. Stat. Sol., 84, p. 55, (1984). [15]. M. Drofenik, L. Golic, D. Hanzel, V. Krasevec, A. Pradan, M. Bakker and D. Kolar, 40, p. 47, (1981). [16]. E. Gurewitz and U. Atzmony, Phys. Rev. B, 26(11), p. 6093, (1982). [17].N.M.L. K che, P.C. Morais and K. S. Neto, Solid State Comm., 52(9), p. 781, (1984). [18]. R.K. Pandey, Ferroelectrics, Wiley Encyclopedia of RF and Microwave Engineering, Editor Kai Chang, Vol.2, p. 1516, (2005). [19]. L. Navarrete, J. Dou, A. M. Drew, R. Schad, P. Padmini, P. Kale and R.K. Pandey, J. Am. Cer. Soc., 89(5), p. 1601, (2006). [20]. G. Garton, S.H. Smith and B. M. Wanklyn, J. Crystal Growth, 13/14, p. 588, (1972). [21]. D.S. Ginley and R.J. Bauman, Mat. Res. Bull., 11, p. 1539, (1976). [22]. P. Colombo and M. Guglielmi, J. European Cer. Soc., 8, p.383, (1991). [23]. A. R. Phani and S. Santucci, Mats. Lett., 50, p. 240, (2001). [24]. R.S. Singh, T. H. Ansari and R.A. Singh, Solid State Comm., 94(12), p. 1003, (1995).