The structural and transport properties of Nd0.7-xLaxSr0.3MnO3 manganites with x=0, 0.1, and 0.2 prepared by solid state reaction route are studied. These compounds are found to be crystallized in orthorhombic structural form. A shift in the metal-semiconductor/insulator transition temperature (TMI) towards room temperature (289 K) with the substitution of Nd by La, as the value of x is varied in the sequence (0, 0.1, and 0.2), has been provided. The shift in the TMI, from 239 K (for x=0) to near the room temperature 289 K (for x=0.2), is attributed to the fact that the average radius 〈rA〉 of site-A increases with the percentage of La. The maximum temperature coefficients of resistance (TCR) of Nd0.7-xLaxSr0.3MnO3 (x=0.1 and 0.2) are found to be higher compared to its parent compound Nd0.7Sr0.3MnO3 which is almost independent of 〈rA〉. The electrical resistivity of the experimental results is explored by various theoretical models below and above TMI. An appropriate enlightenment for the observed behavior is discussed in detail.
1. Introduction
In the past few decades, AMnO3-type manganites have been extensively studied because of their richness in physical properties which is due to the simultaneous presence of spin, lattice, and orbital degrees of freedom [1–3]. Significant attention has been paid by many researchers in order to explore their potential for spacious technological applications such as read heads, magnetic information storage, low- and high-field magnetic sensors, IR detectors, and numerous other spintronic applications [4–11]. The substituted manganites provide high temperature coefficient of resistance (TCR) in bulk as well as in thin films at room temperature. This will motivate us to explore them for infrared radiation detectors (i.e., IR detector) for night vision applications [12]. Among all perovskite manganites, NdMnO3 is an antiferromagnetic insulator, characterized by a superexchange coupling between Mn3+ sites. This coupling is facilitated by a single egelectron predominated by strong correlation effects. On the other hand, partial substitution of Nd3+ ions with divalent cations (Sr, Ca, and Ba) results in mixed valance states of Mn, that is, Mn3+/Mn4+ which is responsible for the ferromagnetic Zener double exchange mechanism [13].
The most prevalent experimental way of affecting the physical properties of the manganites is either substituting cations at the A- or B-sites or varying the oxygen content in the regular perovskite structure [20–22]. The size mismatch at A-site generates internal chemical pressure within the lattice. Due to this structural disorder effect, the local oxygen displacement occurs, ensuing into bond angle fluctuations and bond length variations, further leading to carrier localization in perovskite lattice. This distortion can be controlled by the average size of the A-site cation which in turn modifies the Mn–O–Mn bond angle and Mn–O distances. The Mn–O–Mn bond angle is directly related to the hopping integral between Mn3+ and Mn4+ degenerate states. Goldschmidt’s tolerance factor τis defined asτ=〈rA〉+r0/2(rB+r0)where 〈rA〉 and rB are the radii of the average A-site and B-site ions and r0is the radius of oxygen ion. Forτ<1, Mn–O–Mn bond angle is decreasing due to rotation of MnO6 octahedra which in turn leads to lower symmetric structure. The transport properties of the substituted manganites are influenced by the local distortion of the lattice. This local distortion occurs by the size mismatch of different radii of A-site cation and also by cationic vacancies of rare earth (3+) and divalent alkaline earth (2+)elements. This disorder is quantified by means of the variance of the A-site cation radius distribution(σ2)defined as ∑yiri2-〈rA〉2 whereyiare the fractional occupancies of the species. Thus, the variations in ionic radii at A-sites lead to competing phases at a particular temperature, hence influencing electrical and magnetic transport properties of the perovskite manganites.
In the present research, the structural and transport properties of Nd-based manganites with composition Nd0.7-xLaxSr0.3MnO3 (where x = 0, 0.1, and 0.2) are studied in order to tune the TCR and TMI for application aspect. The present work is targeted to achieve favorable properties of manganites for IR detector applications.
2. Experimental Details
The polycrystalline samples of Nd0.7-xLaxSr0.3MnO3, where x = 0, 0.1, and 0.2 are synthesized by the solid state reaction route using ingredients Nd2O3, La2O3, SrCO3, and Mn2O3. The mixed powders are calcined at 1100°C in air for 24 hours. Thereafter, powder is pressed into pellets by applying a uniaxial pressure of 4-5 tons followed by sintering at 1300°C for 5 hours. The sintered pellets are annealed in an oxygen environment at 1000°C for 5 hours to retain the oxygen stoichiometry. The structure and phase purity of the samples are analyzed by powder X-ray diffraction (XRD) performed on a diffractometer (PANanalytical X’pert Pro) using CuKα radiation at 40 kV and 30 mA. The resistivity measurement without and with magnetic field (5T) are carried out using a four-probe method in the temperature range from 5 to 300 K on a quantum design Physical Property Measurement System (PPMS Model no. 6000).
3. Results and Discussion3.1. XRD Results
The XRD patterns of polycrystalline manganites Nd0.7-xLaxSr0.3MnO3 where x=0 (NLSMO 0), 0.1 (NLSMO 1), and 0.2 (NLSMO 2) prepared by solid state route are shown in Figure 1. The XRD patterns of all compounds exhibit single-phase orthorhombic unit cell with Pnma (no. 62, PCPDF ref no. 861534) space group. It can be observed from patterns that the peaks are slightly shifted toward lower angle side with the substitution of Nd by La. This small shift arises due to the mismatch of radius at A-site, that is, larger radius of La-ion (1.36 Å) in comparison to the radius of Nd-ion (1.27 Å) which causes increase in the volume of the lattice. Subsequently, an internal chemical pressure generated within the lattice due to the size mismatch at A-site, which results in slight shift in the peaks of XRD pattern. The increase in tolerance factor from 0.9408 (for NLSMO 0) to 0.9470 (for NLSMO 2) indicates that the Mn–O–Mn bond angle approaches towards angle 180° which reduces the distortion in MnO6. Less distortive structure promotes the hopping integral (t=cos(θ/2))and reduces the charge localization (especially below 40 K in our case) which is further supported by the resistivity data.
XRD patterns of perovskite manganites Nd0.7-xLaxSr0.3MnO3 where x = 0, 0.1, and 0.2.
3.2. Electrical Transport
The design and development of uncooled IR detector (Bolometer) require TMI around the room temperature with high TCR for improved sensitivity [12, 23]. The temperature-dependent resistivitiesρ(T)studied in the temperature range 5–300 K are shown in Figure 2. All samples are exhibiting metal-semiconductor/insulator transition (TMI). The shift in the TMI, from 239 K (for x=0) to near the room temperature 289 K (for x=0.2), is attributed to the fact that the average radius 〈rA〉 of site-A increases with the percentage of La. In perovskite manganites, the oxygen ions tend to move towards the center of MnO6 octahedra as 〈rA〉 decreases, which in turn leads to distortion. Hence, average A-site ionic radii induced distortion is influencing the reduction in Mn–O bond distances and Mn–O–Mn bond angle. This lattice distortion offers a localized state for the eg electron and causes possible electronic phase separation within the lattice. Therefore, hopping amplitude of the charge carrier from Mn3+ to Mn4+ is decreasing due to suppression of delocalized hopping sites [24]. As the average radius 〈rA〉 increases, the local lattice distortion reduces due to the shifting of Mn–O–Mn bond angle towards symmetrical side (180°). As a consequence, hopping amplitude increases which leads to shift in TMI towards higher temperature.
Temperature dependent resistivity behavior of Nd0.7-xLaxSr0.3MnO3 where x = 0, 0.1 and 0.2.
In order to understand the electrical transport mechanism of manganites, the temperature-dependent resistivity is categorized into two parts: low temperatureT<TMI and high temperature (T>TMI) behaviors. In case ofT<TMI, TCR is positive (i.e., dρ/dT>0), while it is negative (dρ/dT<0) forT>TMI.
3.2.1. Low Temperature (T<TMI) Behavior
Based on the temperature-dependent polynomial equations, the variation of resistivity at low temperatures (T<TMI)and comparative strengths of the different scattering mechanisms are explained [14–19]. These equations are used to explain the low temperature resistivity of manganites which is given in Table 1. From these equations, the conduction phenomenon of different scattering mechanisms is well explained.
Various models found in the literature to explain the conduction mechanism in low-temperature regime (below TMI) of manganites.
Author
Equation
Material
Ref
Schiffer et al. and Vlakhov et al.
ρ=ρ0+ρ2.55T2.5
La0.7Ca0.3MnO3 polycrystalline pellets and film
[14, 15]
Urushibara et al.
ρ=ρ0+ρ2T2
LSMO
[16]
Kubo and Ohata
ρ=ρ0+ρ4.5T4.5
Doped LaMnO3
[17]
Snyder et al.
ρ=ρ0+ρ2T2+ρ4.5T4.5
La0.67A0.33MnO3, A = Ca/Sr thin film/bulk
[18]
Jaime et al.
ρ=ρ0+ρ2T2+ρ5T5
La0.67A0.33MnO3, A = Pb/Ca
[19]
In the equations, ρ0is the temperature-independent residual resistivity which arises due to the grain/domain boundary effects, scattering by impurities, defects, and domain walls [18, 25]. Since polycrystalline materials have many grain boundaries, their substantial contribution to the resistivity is proved in microwave measurement [26]. Hence, ρ0plays a main role in the conduction phenomena. The term ρ2T2 describes the resistivity due to electron-electron scattering phenomenon [27, 28], while the term ρ2.5T2.5 gives resistivity due to the phenomenon of single magnon scattering process in ferromagnetic phase [18, 26, 29]. The last terms ρ4.5T4.5 ascribe due to the process of electron-magnon scattering process in the ferromagnetic region [28] and ρ5T5 contributes to the resistivity due to the phenomenon of electron-phonon interaction [19].
The experimental data of our samples are fitted with general polynomial ρ=ρ0+ρ2T2+ρ4.5T4.5 equation and their related fitting graphs and parameters are shown in Figure 3 and Table 2, respectively. From these data, the corresponding fitted parameters are decreasing with increase of A-site average radius 〈rA〉. It can be observed from the graphs of Figure 3; the residual resistivity of the original data is slightly higher than the fitting parameter values. This slight variation in residual resistivity arises may be due to the presence of grain boundary effects in the polycrystalline materials as well as localization effects particularly at low temperature. From Figure 4, it can be concluded that the residual resistivity is decreasing with increase of the average radius 〈rA〉 of A-site. These results are consistent with the reported literature [30]. As shown in Table 2, the values of ρ2and ρ4.5 are obtained from fitting polynomial (Figure 3) and are also decreasing with increase of A-site average radius 〈rA〉.
Theoretical fitted parameters below TMI, and maximum %TCR (see Figure 4) with respect to average radius 〈rA〉 of NLSMO series.
Composition
Sample code
Average radius 〈rA〉 Å
ρ0 (Ω cm)
ρ2(Ω cm K−2)
ρ4.5(Ω cm K−4.5)
Maximum TCR% (K−1)
Nd0.7Sr0.3MnO3
NLSMO 0
1.321
0.05036
3.32E-6
4.31E-12
1.40
Nd0.6La0.1Sr0.3MnO3
NLSMO 1
1.330
0.02208
1.40E-6
-5.15E-13
2.66
Nd0.5La0.2Sr0.3MnO3
NLSMO 2
1.339
0.00341
2.10E-7
-6.41E-14
2.65
Fitted curves of the resistivity data using polynomial equation ρ=ρ0+ρ2T2+ρ4.5T4.5 below the metal-insulator transition (T<TMI) temperature.
Residual resistivityρ0versus A-site average radius 〈rA〉. Inset shows maximum TCR% versus A-site average radius 〈rA〉.
The observed maximum %TCR {=100[(1/ρ)*(dρ/dT)]}versus average radius of A-site, 〈rA〉 is given in the inset of Figure 4. The maximum %TCR values of the compounds are increasing with average radius 〈rA〉 of A-site but %TCR values are slightly equal in x = 0.1 and 0.2 as compared to the parent compound. It is worth to mention here that %TCR have values 2.66 (for x=0.1) and 2.65 (for x=0.2) which are independent with〈rA〉. To design a room temperature uncooled resistive bolometer (IR detector), the potential materials are α-Si, polycrystalline SiGe, semiconducting YBCO, VO2, and VOx having maximum TCR values of 2% to 6% [31, 32], 7% [33], 2.9% [34], 1.7% [35, 36], and 3.3% K−1) [37], respectively. The present results of our %TCR values are comparative with the existing materials. Hence, the present study enriches the possibility of further improvement in operating around room temperature for bolometer applications without sacrificing an optimum %TCR value.
3.2.2. High Temperature (T>TMI) Behavior
In paramagnetic or semiconducting/insulating phase, the electrical resistivity generally exhibits strong temperature dependence. Several conduction mechanisms are used to explain the electrical transport properties at high temperature above TMI. The most prevalent models are used to describe the conduction mechanisms by Mott’s variable range hopping model (TMI<T<θD/2) [38] and another one small polaron hopping model (T>θD/2) where θD is the Debye temperature [39]. Two models are linearly best fitted with experimental results. The experimental data of NLSMO 2 are fitted within a narrow temperature regime due to higher TMI; however, the obtained theoretical parameters are reasonably accountable as summarized in Table 3.
Fitting parameters by using different models for NLSMO series above TMI.
Composition
(T0)1/4 (K1/4)
N(EF) (eV−1 cm−3)
Ep (meV)
NLSMO 0
66.2743
1.052*1020
112.9
NLSMO 1
39.8132
8.083*1020
83.50
NLSMO 2
17.5069
2.16*1022
52.08
According to Mott’s variable range hopping model (VRH), the characteristic hopping length increases with lowering temperature and density of states are obtained from the well-established Mott law. Hopping conduction results from the states whose energies are focused in a narrow band near the vicinity of Fermi level is given by the equation ρ=ρ0exp(T0/T)1/4 whereT0=16α3/kβN(EF), kβ Boltzmann’s constant, and N(EF) is the density of states at the Fermi level. Here we have taken α value 2.22 nm−1 which is estimated and reported for manganites in [40]. (T0)1/4values are measured by slope of ln(ρ) versus 1/(T)1/4 which is useful for measurement of density of the states at the Fermi level, and the values obtained from Figure 5 are given in Table 3. The density of states N(EF) are increasing with increase of A-site average radius that affect the conducting nature of the samples.
Fitted curves of ln(ρ) versus (1/T)1/4 for ρ=ρ0exp(T0/T)1/4 equation above TMI.
Small polaron hopping models are used to explain the conductivity mechanism by either adiabatic polaron hopping ρ=ρ0Texp(EP/kβT) or nonadiabatic polaron hoppingρ=ρ0T3/2exp(EP/kβT). Here ρ0 is the residual resistivity and EP is the polaron activation energy. Jung [41] have pointed out that the higher value of N(EF) is due to the effect of adiabatic small polaron hopping process. The higher order density of states N(EF)(1022)is indicating the applicability of the adiabatic hopping mechanism. Based on this, the adiabatic small polaron hopping model is used in the present investigation rather than nonadiabatic small polaron hopping model. Polaron activation energy (EP)of the samples has been obtained from the slopes of ln(ρ/T) versus 1/Tcurves of Figure 6. These values are given in Table 3. Henceforth, it can be concluded that the decrease in polaron activation energies with the increase in average radius 〈rA〉occur due to the shift in Mn–O–Mn bond angle towards 180° which is shown in Figure 7. The hopping of charge carrier from one site to another site in the lattice will be enhanced with the decrease of polaron activation energy.
Fitted curves of the ln(ρ/T)versus 1/T for adiabatic equation ρ=ρ0Texp(Ep/KβT) above TMI.
Variation of polaron hopping energy and (T0)1/4 versus A-site average radius 〈rA〉.
From Table 3, density of statesN(EF)values are increasing with average radius〈rA〉. ThisN(EF)specifies the carrier effective mass in other sense narrowing of the band width, consequently results in a large change in the resistivity and sharpening of the resistivity peak in the vicinity of TMI [42]. The higher values of density of states at the Fermi level lead to a higher value of conductivity [41].
3.3. Magnetoresistance
Figure 8 shows the electrical resistivity behavior of the Nd0.7-xLaxSr0.3MnO3 where x =0, 0.1, and 0.2 samples in a constant magnetic field of 5T. In the presence of an external magnetic field, the resistivity decreases significantly. This suggests that the external magnetic field (5T) facilitates the hopping of egelectron between neighbouring Mn ions, which agrees with the double exchange mechanism [13].
Variation of resistivity with temperature of NLSMO series with (5T) and without magnetic field. Inset shows the variation of %MR with temperature.
The magnetoresistance MR is defined as %MR =100*[ρ(0,T)-ρ(H,T)]/ρ(0,T)whereρ(0,T)and ρ(H,T)are the resistivities at temperature without magnetic field and in the applied magnetic field H, respectively. The highest percentage MR (at TMI) values of the Nd0.7-xLaxSr0.3MnO3 are 46%, 52%, and 50% for x = 0, 0.1, and 0.2 as shown in inset of Figure 8. The %MR values are increasing slightly higher than the parent compound with varying of 〈rA〉; this will be useful for potential applications [8, 43]. The misalignment of adjacent magnetic domains/grains or phase separation scenario are responsible for low-temperature MR. Hopping of charge carriers become easier across the domain wall boundaries and the resistivity decreases, which in turn leads to significant MR at low temperature. Colossal magnetoresistance at TMI is due to the alignment of adjacent Mn ions in the presence of field which directly influence the double exchange mechanism.
4. Conclusion
In this paper, the influence of La substitution at Nd site on the electrical and magnetotransport properties in Nd0.7-xLaxSr0.3MnO3 (x = 0, 0.1 and 0.2) has been extensively studied. TMI is shifting towards room temperature with La content. Conduction mechanism behavior is explained by the polynomial equation in low-temperature region and the high-temperature behavior is described using different prevalent existing models. From the present study, it can be concluded that the residual resistivityρ0and the polaron activation energies are decreasing with increase of average radius of site-A. An interesting observation is that NLSMO 2 provides TMI around the room temperature and maximum percentage of TCR values are independent with average radius 〈rA〉 in x=0.1 and x=0.2. However, the TCR value is not satisfactorily high for the development of sensitive microbolometer; this study will be useful in future to optimize the working temperature without affecting the TCR. Moreover, the present research can further be extended for the optimization of the composition to achieve high TCR with TMI around the room temperature for the development of MEMS-based uncooled microbolometer for night vision cameras.
CoeyJ. M. D.ViretM.Von MolnárS.Mixed-valence manganites1999482167293ManhD. H.PhongP. T.ThanhT. D.HongL. V.PhucN. X.La0.7Ca0.3MnO3 perovskite synthesized by reactive milling method: the effect of particle size on the magnetic and electrical properties20104911-28122-s2.0-7484914029110.1016/j.jallcom.2009.10.164SiwachP. K.SinghH. K.SrivastavaO. N.Low field magnetotransport in manganites2008202727320110.1088/0953-8984/20/27/273201SeikhM. M.SudheendraL.RaoC. N. R.Magnetic properties of La0.5-xLnxSr0.5MnO3 (Ln = Pr, Nd, Gd and Y)2004177103633363910.1016/j.jssc.2004.06.004Von HelmoltR.WeckerJ.HolzapfelB.SchultzL.SamwerK.Giant negative magnetoresistance in perovskitelike La2/3Ba1/3MnOx ferromagnetic films199371142331233310.1103/PhysRevLett.71.2331JinS.TiefelT. H.McCormackM.FastnachtR. A.RameshR.ChenL. H.Thousandfold change in resistivity in magnetoresistive La-Ca-Mn-O films199426451574134152-s2.0-23444434665Haghiri-GosnetA.-M.RenardJ.-P.CMR manganites: physics, thin films and devices2003368R127R15010.1088/0022-3727/36/8/201HeremansJ.Solid state magnetic field sensors and applications1993268114911682-s2.0-002764714410.1088/0022-3727/26/8/001JinS.McCormackM.TiefelT. H.RameshR.Colossal magnetoresistance in La-Ca-Mn-O ferromagnetic thin films (invited)19947610692969332-s2.0-2154446765710.1063/1.358119MiraJ.RivasJ.HuesoL. E.RivadullaF.López QuintelaM. A.RamosC. A.Strong reduction of lattice effects in mixed-valence manganites related to crystal symmetry2002652502441810.1103/PhysRevB.65.024418HuesoL.MathurN.Dreams of a hollow future200442769723013042-s2.0-164245839910.1038/427301aKimJ.-H.GrishinA. M.Free-standing epitaxial La1-x(Sr,Ca)xMnO3 membrane on Si for uncooled infrared microbolometer2005873303350210.1063/1.1996845ZenerC.Interaction between the d-shells in the transition metals. II. Ferromagnetic compounds of manganese with Perovskite structure195182340340510.1103/PhysRev.82.403SchifferP.RamirezA. P.BaoW.CheongS. W.Low temperature magnetoresistance and the magnetic phase diagram of La1-xCaxMnO319957518333633392-s2.0-034292330510.1103/PhysRevLett.75.3336VlakhovE. S.ChakalovR. A.ChakalovaR. I.NenkovK. A.DörrK.HandsteinA.MüllerK. H.Influence of the substrate on growth and magnetoresistance of La0.7Ca0.3MnOz thin films deposited by magnetron sputtering1998834215221572-s2.0-0001225439UrushibaraA.MoritomoY.ArimaT.AsamitsuA.KidoG.TokuraY.Insulator-metal transition and giant magnetoresistance in La1-xSrxMnO31995512014103141092-s2.0-424410102910.1103/PhysRevB.51.14103KuboK.OhataN.A quantum theory of double exchange. I19723312131SnyderG. J.HiskesR.DiCarolisS.BeasleyM. R.GeballeT. H.Intrinsic electrical transport and magnetic properties of La0.67Ca0.33MnO3 and La0.67Sr0.33MnO3 MOCVD thin films and bulk material199653211443414444JaimeM.LinP.SalamonM. B.HanP. D.Low-temperature electrical transport and double exchange in La0.67(Pb,Ca)0.33MnO319985810R5901R59042-s2.0-0001184368SudheendraL.RaoC. N. R.Electronic phase separation in the rare-earth manganates (La1-xLnx)0.7Ca0.3MnO3 (Ln = Nd, Gd and Y)200315193029304010.1088/0953-8984/15/19/306AsthanaS.BahadurD.NigamA. K.MalikS. K.Magneto-transport studies on (Pr1/3Sm2/3)2/3A1/3MnO3 (A = Ca, Sr and Ba) compounds20041629529753072-s2.0-334301582410.1088/0953-8984/16/29/020AsthanaS.BahadurD.NigamA. K.MalikS. K.Lattice effect on the magnetic and magneto-transport properties of (La1/3Sm2/3)0.67Ba0.33-x SrxMnO3 (x=0.0, 0.1, 0.2 and 0.33) compounds20084501-213614110.1016/j.jallcom.2006.10.067YongG. J.KolaganiR. M.AdhikariS.DruryO. B.GardnerC.BiontaR. M.FriedrichS.Heteroepitaxy of Nd0.67Sr0.33MnO3 on silicon for bolometric x-ray detector application20108111611390610.1063/1.3499244BhattacharyaS.MukherjeeR. K.ChaudhuriB. K.YangH. D.Effect of Li doping on the magnetotransport properties of La0.7Ca0.3-yLiyMnO3 system: decrease of metal-insulator transition temperature200382234101410310.1063/1.1580650De TeresaJ. M.IbarraM. R.BlascoJ.GarcíaJ.MarquinaC.AlgarabelP. A.ArnoldZ.KamenevK.RitterC.Von HelmoltR.Spontaneous behavior and magnetic field and pressure effects on La2/3Ca1/3MnO3 perovskite199654211871193DominguezM.BhagatS. M.LoflandS. E.RamachandranJ. S.XiongG. C.JuH. L.VenkatesanT.GreeneR. L.Giant magnetoresistance at microwave frequencies1995324, article 34910.1209/0295-5075/32/4/011BanerjeeA.PalS.ChaudhuriB. K.Nature of small-polaron hopping conduction and the effect of Cr doping on the transport properties of rare-earth manganite La0.5Pb0.5Mn1-xCrxO3200111531550155810.1063/1.1378018UrushibaraA.MoritomoY.ArimaT.AsamitsuA.KidoG.TokuraY.Insulator-metal transition and giant magnetoresistance in La1-xSrxMnO31995512014103141092-s2.0-424410102910.1103/PhysRevB.51.14103PiL.ZhengL.ZhangY.Transport mechanism in polycrystalline La0.825Sr0.175Mn1-xCuxO32000611389178921AsthanaS.JoonghoeD.BahadurD.Effects of A-site ionic size variation on the magnetic and transport properties of (PrxSm1-x)2/3Sr1/3MnO3 (0≤×≤1)2007244124542454510.1002/pssb.200777399ZerovV. Y.MalyarovV. G.Heat-sensitive materials for uncooled microbolometer arrays200168129399482-s2.0-0141535296MalyarovV. G.Uncooled thermal IR arrays200269107507602-s2.0-0036820257SedkyS.FioriniP.BaertK.HermansL.MertensR.Characterization and optimization of infrared poly SiGe bolometers19994646756822-s2.0-003265125710.1109/16.753700AlmasriM.Çelik-ButlerZ.ButlerD. P.YaradanakulA.YildizA.Uncooled multimirror broad-band infrared microbolometers20021155285352-s2.0-003677234910.1109/JMEMS.2002.803413GruzdevaA. P.ZerovV. Y.KonovalovaO. P.KulikovY. V.MalyarovV. G.KhrebtovI. A.ShaganovI. I.Bolometric and noise properties of elements for uncooled IR arrays based on vanadium dioxide films19976412111011132-s2.0-0031362331ChenC.YiX.ZhangJ.ZhaoX.Linear uncooled microbolometer array based on VOx thin films2001422879010.1016/S1350-4495(01)00058-5ZerovV. Y.MalyarovV. G.KhrebtovI. A.KulikovY. V.ShaganovI. I.SmirnovA. D.Uncooled membrane-type linear microbolometer array based on a VOx film20016864284312-s2.0-0141484567DionneG. F.Magnetic exchange and charge transfer in mixed-valence manganites and cuprates1996798517251742-s2.0-0001286780MottN. F.Conduction in glasses containing transition metal ions196811117ViretM.RannoL.CoeyJ. M. D.Magnetic localization in mixed-valence manganites1997551380678070JungW.-H.Evaluation of Mott's parameters for hopping conduction in La0.67Ca0.33MnO3 above Tc1998171513171319EweL. S.HamadnehI.SalamaH.HamidN. A.HalimS. A.Abd-ShukorR.Magnetotransport properties of La0.67Ca0.33MnO3 with different grain sizes20099524574632-s2.0-6234913751310.1007/s00339-008-4908-1ZhangW.BoydI. W.ElliottM.Herrenden-HarkerandW.Transport properties and giant magnetoresistance behavior in La-Nd-Sr-Mn-O films199669811541156