[17]
Hc ~ K1Ms (1) From equation (1) it is clear that K1 is main factor for Hc variation. It means that the changes in the relative position between Fe ions caused by lattice contractions can result in an increase in magnetocrystalline anisotropy which must be responsible for the increase in coercivity in YIG-doped ferrites. Table 2. Magnetic properties of NdxY(1-x)Fe5O12 (x = 0.0, 0.2, 0.5, 0.8). No. Sample Comp. x, Magnetic Properties Hc (kOe) Ms (emu.g-1) 1. YFe5O12 0.0 0.012 35.70 2. Nd0.2Y0.8Fe5O12 0.2 0.014 33.90 3. Nd0.5Y0.5Fe5O12 0.5 0.018 36.70 4. Nd0.8Y0.2Fe5O12 0.8 0.031 35.30 The particle morphologies from non-doped and Nd-doped samples for different concentration are shown in Figure 4. The Figures indicate that all samples are composed of particles with irregular shapes and relatively narrow particle size distribution. The grain size estimations show that there is no significant change due to Nd doping. The Figure indicates that all samples are composed of particles with irregular shapes and relatively narrow particle size distribution. The sample with x = 0.0 (YNd-0) and x = 0.8 (YNd-0.8) consisted of particles with size in the range from ~ 0.8 µm to ~ 4 µm, as seen in Figure 4(a) and (b). These indicate that the substitution of Nd3+ into the YIG with different variation concentration does not modify the morphology shape of the particles. Figure 4. The SEM image of Y(1-x)NdxFe5O12 for for (a). x = 0.0, (b). x = 0.8. The elements in the sample were identified using an energy dispersive spectrophotometer (EDS) incorporated in the SEM equipment. The results of enumeration with EDS are listed in Table 3. It can be seen that the elements detected inside the sample only contained Y, Fe, Nd and O elements. It appears that the Y atomic decreased with the addition of Nd atoms. Meanwhile, for O and Fe atomic presentation is almost constant. The comparison between the elements Y and Nd (in% atoms) for each sample has a different content, but the difference is not too significan. Table 3. EDS observation of the samples. No. Samples Atomic (%) O Fe Y Nd 1. Y 29.32 40.52 30.16 - 2. YNd-02 33.16 37.32 28.07 1.45 3. YNd-05 33.15 38.14 24.61 4.10 4. YNd-08 32.07 39.23 22.68 6.02 Figure 5 shows the variation of the reflection loss (RL) versus frequency observed in Y(1-x)NdxFe5O12 (X = 0.0, 0.2, 0.5, 0.8) in the frequency range of 7 – 12GHz. It is seen that the matching frequencies is observed in the samples owing to the spin resonance at frequency at about 9GHz. The list the absorption data for the prepared samples are listed in Table 4. It can be seen that RL value of un-doped sample with x = 0.0 in YNd-0 was found to be 7.50(-dB). By the substitution of Nd3+ for x = 0.2 in YNd-02 sample, the value of RL change to 6.50(-dB). With the addition of Nd3+ substitution, the RL increase to 8.15 (-dB) for x = 0.5 in YNd-05 sample and continue increase to 8.66 (-dB) for x = 0.8 in YNd-08 sample. The optimum value of microwave absorption was found on the phase composition of Y2.2Nd0.8Fe5O12 (YNd-08) sample for x = 0.8 which was heat treated at 1300oC. It is known that doping with Nd3+ ions can effectively increase the attenuation characteristic as compared to Y3Fe5O12 un-doped sample for x = 0.0. Figure 5. Absorption characteristics of Y(1-x)NdxFe5O12 for x = 0.0, 0.2, 0.5 and 0.8. Table 4. Microwave absorption of Nd substituted yttrium iron garnet (YIG). Sample Codes Comp. of x RLoss (-dB) Thickness, d (mm) Frequency (GHz) YNd-0 0.0 7.20 2 9.80 YNd-02 0.2 6.70 2 9.70 YNd-05 0.5 8.15 2 9.40 YNd-08 0.8 8.66 2 9.50 Summary Neodymium-doped yttrium iron garnet, Y3−xNdxFe5O12 for x = 0.0, 0.2, 0.5 and 0.8 has been prepared by mechanochemical method using high energy milling (HEM), followed by sintering at 1300oC for 5 h, respectively. XRD refinement confirmed that no formation of secondary phases of Nd doped YIG with Nd3+ contents. The lattice constant (a) and cell volume (Vcell) were found to increase with increasing Nd3+ concentrations. All the measured samples show ferrimagnetic behavior attributed to the intrinsic structure. The saturation magnetization (Ms) obtained for all the samples is in the range of 34–37emu.g-1, while the coercivity (Hc) was increase with Nd doping from 12Oe to 31Oe. The microwave absorption optimum was found on the phase composition of Y2.2Nd0.8Fe5O12 with x = 0.8 in YNd-08 sample for reflection loss (RL) of 8.66 (-dB).. Acknowledgement The financial support of this research to the DIPA 2019/2020 of Indonesia National Nuclear Energy Agency project is gratefully acknowledged. Referrences.
Google Scholar
[1]
E. Baños-López, F. Sánchez-De Jesús, C. Cortés-Escobedo, A. Barba-Pingarrón, and A. Bolarín-Miró, Enhancement in Curie Temperature of Yttrium Iron Garnet by Doping with Neodymium,, Materials (Basel)., vol. 11, no. 9, p.1652, (2018).
DOI: 10.3390/ma11091652
Google Scholar
[2]
J. Liu, P. Yu, Q. Jin, C. Zhang, M. Zhang, and V. G. Harris, Microwave-accelerated rapid synthesis of high- quality yttrium iron garnet nano powders with improved magnetic properties,, Mater. Res. Lett., vol. 6, no. 1, p.36–40, (2018).
DOI: 10.1080/21663831.2017.1386240
Google Scholar
[3]
V. Sharma, J. Saha, S. Patnaik, and B. K. Kuanr, Synthesis and characterization of yttrium iron garnet ( YIG ) nanoparticles - Microwave material,, AIP Adv., vol. 7, no. May, p.1–8, (2017).
DOI: 10.1063/1.4973199
Google Scholar
[4]
E. J. J. Mallmann, A. S. B. Sombra, J. C. Goes, and P. B. A. Fechine, Yttrium Iron Garnet: Properties and Applications Review,, Solid State Phenom., vol. 202, p.65–96, (2013).
DOI: 10.4028/www.scientific.net/ssp.202.65
Google Scholar
[5]
R. Bhalekar, A. and N. Singh, L., Review Article- Al Substituted Yttrium Iron Garnet Nanoparticles,, Int. J. o Sci. Eng. Res., vol. 9, no. 6, p.284–288, (2018).
Google Scholar
[6]
M. A. Musa, R. S. Azis, N. H. Osman, J. Hassan, and M. M. Dihom, Structural and magnetic properties of yttrium aluminum iron garnet (YAlG) nanoferrite prepared via auto-combustion sol–gel synthesis,, J. Aust. Ceram. Soc., vol. 54, no. 1, p.55–63, (2018).
DOI: 10.1007/s41779-017-0126-7
Google Scholar
[7]
T. Arun, M. Vairavel, S. Gokul Raj, and R. Justin Joseyphus, Crystallization kinetics of Nd-substituted yttrium iron garnet prepared through sol-gel auto-combustion method,, Ceram. Int., vol. 38, no. 3, p.2369–2373, (2012).
DOI: 10.1016/j.ceramint.2011.10.090
Google Scholar
[8]
Y. Y. Kim, Thermal Conductivity of a Nanoscale Yttrium Iron Garnet Thin-Film Prepared by the Sol-Gel Process,, Nanomaterials, vol. 7, no. 247, p.2–10, (2017).
DOI: 10.3390/nano7090247
Google Scholar
[9]
P. Paulo et al., Synthesis , structure and magnetic properties of Y 3 Fe 5-x Al x O 12 garnets prepared by the soft chemical method,, Prcessing Appl. Ceram., vol. 8, no. 4, p.211–218, (2014).
Google Scholar
[10]
M. Majerová et al., Magnetic Properties of Yttrium Iron Garnet Polycrystalline Material Prepared by Spray-Drying Synthesis Department of Magnetometry , Institute of Measurement Science , Slovak Academy of Sciences , Dúbravská cesta 9 , 841 04 Bratislava , Slovakia Vitrum Lau,, Meas. 2015, Proceeding 10th Int. Conf. Smolenice, Slovakia, p.285–288, (2015).
DOI: 10.21909/sp.2017.03.739
Google Scholar
[11]
V. Sharma and B. K. Kuanr, Magnetic and crystallographic properties of rare-earth substituted yttrium-iron garnet,, J. Alloys Compd., vol. 748, p.591–600, (2018).
DOI: 10.1016/j.jallcom.2018.03.086
Google Scholar
[12]
Q. I. Mohaidat, M. Lataifeh, K. Hamasha, S. H. Mahmood, I. Bsoul, and M. Awawdeh, The Structural and the Magnetic Properties of Aluminum Substituted Yttrium Iron Garnet,, Mater. Res., vol. 21, no. 3, p.1–7, (2018).
DOI: 10.1590/1980-5373-mr-2017-0808
Google Scholar
[13]
M. C. Onbasli et al., Optical and magneto-optical behavior of Cerium Yttrium Iron Garnet thin films at wavelengths of 200 – 1770 nm,, Nat. Publ. Gr., no. March, p.1–10, (2016).
DOI: 10.1038/srep23640
Google Scholar
[14]
K. J. Khan, F. Saleemi, T. Abbas, and I. Sadiq, Substitutional effect of rare earth element Ho3+ on structural and magnetic properties of yttrium iron garnets,, J. Ovonic Res., vol. 11, no. 6, p.263–270, (2015).
Google Scholar
[15]
W. R. Agami, Effect of neodymium substitution on the electric and dielectric properties of Mn-Ni-Zn ferrite,, Phys. B Phys. Condens. Matter, vol. DOI: 10.10, (2018).
DOI: 10.1016/j.physb.2018.01.021
Google Scholar
[16]
N. Yahya et al., Morphology and Magnetic Characterisation of Aluminium Substituted Yttrium-Iron Garnet Nanoparticles Prepared Using Sol Gel Technique,, J. Nano Sci. Nanotechnology., vol. 11, no. 2, p.2652–2656, (2011).
DOI: 10.1166/jnn.2011.2723
Google Scholar
[17]
F. Chen et al., Crystal structure tailored microwave magnetodielectric effect in Yb x Y 3-x Fe 5 O 12 ceramics,, J. Alloys Compd., vol. 726, p.1030–1039, (2017).
Google Scholar