• 제목/요약/키워드: $M{\"{o}}ssbauer$ spectroscopy

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Charge Structure of the Combined System (La0.6Sr0.4MnO3)0.7(La0.6Sr0.4FeO3)0.3 as Investigated by Mössbauer Spectroscopy

  • Uhm, Young Rang;Kim, Sam Jin;Kim, Chul Sung
    • Journal of Magnetics
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    • 제7권1호
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    • pp.18-20
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    • 2002
  • The charge structures of (LSMO) and of the combined system $(La_{ 0.6}Sr_{0.4}FeO_3$(LSMO) and of the combined system (La_{0.6}Sr_{0.4}MnO_3)_{0.7}(La_{0.6}Sr_{0.4}/FeO_3)_{0.3}$are investigated by using M$\ddot{o}$ssbauer spectroscopy. The antiferromagnetically ordered $(La_{0.6}Sr_{0.4}FeO_3$(LSFO) has possible charges of Fe^{3+} and Fe^{4+}$, which include a low-spin $Fe^{4+}$ state at and above 230 K. The temperature dependences of the M$\ddot{o}$ssbauer spectra for the $(La_{ 0.6}Sr_{0.4}FeO_3$ system and for the combined $(LSMO)_{ 0.7}(LSFO)_{0.3}$ system are fitted as three sets of Zeeman patterns corresponding to $Fe^{3+}$ and $Fe^{4+} below 230 K. At and above 230 K, the fitted M$\ddot{o}$ssbauer spectra for the combined system are the same in all temperature ranges. Above 230 K, $(La_{0.6}Sr_{0.4}FeO_3$ spectrum consists of two sets of six Lorentzians for $Fe^{3+}$ and one line for low spin $Fe^{4+}$. It is worth noting that large fields are induced in the combined system.

Crystallographic, Magnetic and Mössbauer Study of Phase Transition in LaVO3

  • Yoon, Sung-Hyun
    • Journal of Magnetics
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    • 제12권3호
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    • pp.108-112
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    • 2007
  • Nature of phase transition in $LaVO_3$ has been studied using X-ray diffraction, SQUID magnetometer, and $M\"{o}ssbauer$ spectroscopy with 1% of $^{57}Fe$ doped sample. The crystal structure was orthorhombic with space group Pnma. Antiferromagnetic phase transition temperature $T_N$ was 140K, below which a weak ferromagnetic trace has been found. $M\"{o}ssbauer$ spectra below $T_N$ were single set of hyperfine sextet, which enabled us to discard the possibility of two inequivalent magnetic sites or uncompensated antiferromagnetism. Hyperfine magnetic field abruptly disappeared as low as about 90K, much below $T_N$.

In 이온을 첨가한 $EuFeO_{3}$의 결정구조 및 자기적 성질 (The Crystallograpic and Magnetic Properties of EuFeO3 Doped with in ions)

  • 김정기;서정철;한은주
    • 한국자기학회지
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    • 제4권4호
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    • pp.335-339
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    • 1994
  • $Eu(Fe_{1-x}In_{x})O_{3}$ (x=0, 0.03과 0.05)의 결정구조와 자기적 성질을 상온에서의 X선 회절, $M\"{o}ssbauer$ 분광학 및 자기이력곡선 측정 방법에 의해서 연구하였다. X선 회절 분석 결과는 모든 시료가 orthorhombic 결정구조를 가지며, 단위포의 체적은 x=0을 제외하면 In 농도의 증가에 따라 증가함을 보인다. $M\"{o}ssbauer$ 스펙트럼은 두셋트 여섯 lines을 갖는다는 가정하에 분석하였다. 분석 결과는 각 셋트에서의 초미세 자기장은 x의 증가에 따라 감소하였다. 본 연구의 시료에서 공명 흡수선의 반폭이 x의 증 가에 따라 증가함은, 측정 data가 $Fe^{3+}$ 이온 주위 z개의 $In^{3+}$ 이온이 존재할 확률 분포, $_{n}P_{z}(x)$에 비례하는 초미세 구조에 의한 흡수선의 합으로 이루어졌음을 의미한다. 자기이력 곡선에서 $M_{s}$$H_{c}$는 각각 X의 증가에 따라 감소와 증가를 보인다.

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에이니그마타이트($Na_4(Fe^{2+},Ti,Fe^{3+}){_{12}}(Fe^{3+},Si){_{12}}O_{40}$)의 뫼스바우어 분광분석과 결정화학 ([ $M\ddot{o}ssbauer$ ] Spectroscopy and Crystal Chemistry of Aenigmatite, $Na_4(Fe^{2+},Ti,Fe^{3+}){_{12}}(Fe^{3+},Si){_{12}}O_{40}$)

  • 최진범
    • 한국광물학회지
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    • 제20권4호
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    • pp.367-376
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    • 2007
  • 에이니그마타이트($Na_4(Fe^{2+},Ti,Fe^{3+}){_{12}}(Fe^{3+},Si){_{12}}O_{40}$)는 Na가 풍부한 알칼리 화성암에 흔히 산출되는 광물이며, 분지 개방형 단쇄형 규산염광물로 분류된다. 3개의 산출이 다른 자연산 에이니그마타이트를 대상으로 뫼스바우어 분광분석을 실시하였으며 상세한 결정화학적 연구가 수행되었다. 뫼스바우어 분광분석 결과 9개의 흡수선이 분리되었는데, 3쌍의 흡수선은 팔면체 자리를 점유하는 $Fe^{2+}$의 피크이며, 저속도 구간의 독립적인 2개의 흡수선과 대응하는 한 개의 중첩된 흡수선은 각각 사면체와 팔면체 자리의 $Fe^{3+}$의 피크로 밝혀졌다. $Fe^{2+}$$Fe^{3+}$의 정확한 함량비에 의해 화학분석치가 재계산되었으며, Fe 양이온의 사면체 자리와 팔면체 자리에 대한 정확한 자리점유율로 상세한 결정화학적 정보를 제공하였다. 상당한 함량의 $Fe^{3+}/tet$는 사면체 자리점유에 있어 $Fe^{3+}$$Al^{3+}$보다 우위를 보여준다. 결정화학적로 규명된 에이니그마타이트(AEN1)의 상세한 화학조성은 $(Na_{3.97}Ca_{0.03})(Ca_{0.11}Mn_{0.59}Fe^{2+}{_{8.07}}Ti_{2.07}Mg_{0.70}Fe^{3+}{_{0.43}}Al_{0.04})(Fe^{3+}{_{0.56}}Al_{0.18}Si_{11.26})O_{40}$으로 밝혀졌다.

Superparamagnetic Properties of Ni0.7Zn0.3Fe2O4 Nanoparticles

  • Lee, Seung-Wha;Kim, Chul-Sung
    • Journal of Magnetics
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    • 제10권3호
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    • pp.84-88
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    • 2005
  • Nanoparticles $Ni_{0.7}Zn_{0.3}Fe_2O_4$ is fabricated by a sol-gel method. The magnetic and structural properties of powders were investigated with XRD, SEM, $M\ddot{o}ssbauer$ spectroscopy, and VSM. $Ni_{0.7}Zn_{0.3}Fe_2O_4$ powders annealed at $300^{\circ}C$ have a spinel structure and behaved superparamagnetically. The estimated size of $Ni_{0.7}Zn_{0.3}Fe_2O_4$ nanoparticle is about 11 nm. $Ni_{0.7}Zn_{0.3}Fe_2O_4$ annealed at 400 and $500^{\circ}C$ has a typical spinel structure and is ferrimagnetic in nature. The isomer shifts indicate that the iron ions were ferric at the tetrahedral (A) and the octahedral (B). Blocking temperature $(T_B)\;of\;Ni_{0.7}Zn_{0.3}Fe_2O_4$ nanoparticle is about 260 K. The magnetic anisotropy constant of $Ni_{0.7}Zn_{0.3}Fe_2O_4$ annealed $300^{\circ}C$ were calculated to be $1.7X10^6\;ergs/cm^3$. Also, temperature of the sample increased up to $43^{\circ}C$ within 7 minutes under AC magnetic field of 7 MHz.

Crystallographic and Magnetic Properties of Co, Zn, Ni-Zn Substituted Nano-size Manganese Ferrites Synthesized by Sol-gel Method

  • Noh, Kwang Mo;Lee, Young Bae;Kwon, Woo Hyun;Kang, Jeoung Yun;Choi, Won-Ok;Chae, Kwang Pyo
    • Journal of Magnetics
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    • 제21권3호
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    • pp.308-314
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    • 2016
  • Cobalt-, zinc-, and nickel-zinc-substituted nano-size manganese ferrite powders, $MnFe_2O_4$, $Mn_{0.8}Co_{0.2}Fe_2O_4$, $Mn_{0.8}Zn_{0.2}Fe_2O_4$ and $Mn_{0.8}Ni_{0.1}Zn_{0.1}Fe_2O_4$, were fabricated using a sol-gel method, and their crystallographic and magnetic properties were subsequently studied. The $MnFe_2O_4$ ferrite powder annealed at temperatures above 523 K exhibited a spinel structure, and the particle size increased as the annealing temperature increased. All ferrites annealed at 773 K showed a single spinel structure, and the lattice constants and particle size decreased with the substitution of Co, Zn, and Ni-Zn. The $M{\ddot{o}}ssbauer$ spectrum of the $MnFe_2O_4$ ferrite powder annealed at 523 K only showed a doublet due to its superparamagnetic phase, and the $M{\ddot{o}}ssbauer$ spectra of the $MnFe_2O_4$, $Mn_{0.8}Co_{0.2}Fe_2O_4$, and $Mn_{0.8}Zn_{0.2}Fe_2O_4$ ferrite powders annealed at 773 K could be fitted as the superposition of two Zeeman sextets due to the tetrahedral and octahedral sites of the $Fe^{3+}$ ions. However, the $M{\ddot{o}}ssbauer$ spectrum of the $Mn_{0.8}Ni_{0.1}Zn_{0.1}Fe_2O_4$ ferrite powder annealed at 773 K consisted of two Zeeman sextets and one quadrupole doublet due to its ferrimagnetic and paramagnetic behavior. The area ratio of the $M{\ddot{o}}ssbauer$ spectra could be used to determine the cation distribution equation, and we also explained the variation in the $M{\ddot{o}}ssbauer$ parameters by using this cation distribution equation, the superexchange interaction and the particle size. Relative to pure $MnFe_2O_4$, the saturation magnetizations and coercivities were larger in $Mn_{0.8}Co_{0.2}Fe_2O_4$ and smaller in $Mn_{0.8}Zn_{0.2}Fe_2O_4$, and $Mn_{0.8}Ni_{0.1}Zn_{0.1}Fe_2O_4$. These variations could be explained using the site distribution equations, particle sizes and magnetic moments of the substituted ions.

Crystallographic and Magnetic Properties of MnxFe3-xO4 Powders

  • Kwon, Woo Hyun;Lee, Jae-Gwang;Choi, Won Ok;Chae, Kwang Pyo
    • Journal of Magnetics
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    • 제18권1호
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    • pp.26-29
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    • 2013
  • $Mn_xFe_{3-x}O_4$ powders have been fabricated by using sol-gel methods; their crystallographic and magnetic properties were investigated by using X-ray diffraction, scanning electron microscopy, M$\ddot{o}$ssbauer spectroscopy, and vibrating sample magnetometer. The $Mn_xFe_{3-x}O_4$ ferrite powders annealed at $500^{\circ}C$ had a single spinel structure regardless of the $Mn^{2+}$-doping amount and their lattice constants became larger as the $Mn^{2+}$ concentration was increased. Their Mossbauer spectra measured at room temperature were fitted with 2 Zeeman sextets due to the tetrahedral and octahedral sites of Fe ions, which made them ferrimagnetic. The magnetic behavior of $Mn_xFe_{3-x}O_4$ powders showed that the $Mn^{2+}$-doping amount made their saturation magnetization increase, but there were no severe effects on their coercivities. The saturation magnetization of the $Mn_xFe_{3-x}O_4$ powder varied from 38 emu/g to 70.0 emu/g and their minimum coercivity was 111.1 Oe.

Temperature Dependent Cation Distribution in Tb2Bi1Ga1Fe4O12

  • Park, Il-Jin;Park, Chu-Sik;Kang, Kyoung-Soo;Kim, Chul-Sung
    • Journal of Magnetics
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    • 제13권3호
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    • pp.110-113
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    • 2008
  • In this study, heavy rare earth garnet $Tb_2Bi_1Ga_1Fe_4O_{12}$ powders were fabricated by a sol-gel and vacuum annealing process. The crystal structure was found to be single-phase garnet with a space group of Ia3d. The lattice constant $a_0$ was determined to be 12.465 ${\AA}$. From the analysis of the vibrating sample magnetometer (VSM) hysteresis loop at room temperature, the saturation magnetization and coercivity of the sample are 7.64 emu/g and 229 Oe, respectively. The N$\acute{e}$el temperature($T_N$) was determined to be 525 K. The M$\ddot{o}$ssbauer spectrum of $Tb_2Bi_1Ga_1Fe_4O_{12}$ at room temperature consists of 2 sets of 6 Lorentzians, which is the pattern of single-phase garnet. From the results of the M$\ddot{o}$ssbauer spectrum at room temperature, the absorption area ratios of Fe ions on 24d and 16a sites are 74.7% and 25.3%(approximately 3:1), respectively. These results show that all of the non-magnetic Ga atoms occupy the 16a site by a vacuum annealing process. Absorption area ratios of Fe ions are dependent not only on a sintering condition but also on the temperature of the sample. It can then be interpreted that the Ga ion distribution is dependent on the temperature of the sample. The M$\ddot{o}$ssbauer measurement was carried out in order to investigate the atomic migration in $Tb_2Bi_1Ga_1Fe_4O_{12}$.

상온 및 액체질소 온도에서 고속 중성자 조사된 원자로 압력 용기의 취화 현상에 관한 연구 (A Study on Embrittlement of Fast Neutron-irradiated Nuclear Reactor Pressure Vessel Steels at Room- and Liquid Nitrogen-temperature)

  • 김형배;김형상;김순구;신동훈;유연봉;고정대
    • 한국자기학회지
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    • 제15권2호
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    • pp.142-147
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    • 2005
  • 고속 중성자 조사한 원자로 압력 용기의 취하현상을 상온에서 X-선 회절 실험과 액체 질손 온도에서 M$\ "{o}$ssbauer 분광법으로 조사하였다. 시료의 중성자 조사량은 $10^{12},\;10^{13},\;10^{14},\;10^{15},\;10^{16},\;10^{17},\;10^{18}\;n/{\cal}cm^2$이다. X-선 회절 패턴에서 중성자 조사하지 않은 시료는 bcc 형태를 나타내었으나, 중성자 조사량이 $10^{17}\;n/{\cal}cm^2$ 이상인 시료에서는 bcc 구조가 사라지는 심각한 손상을 보였다. 모든 시료의 $M\ddot{o}ssbauer$ 스펙트럼은 두개 혹은 그 이상의 sextet의 중첩을 보였다. 모든 $M\ddot{o}ssbauer$ 스펙트럼은 본문에서는 3조의 sextet로 fitting 하였다. 이성질체 이동치와 사중극자 분열치는 거의 영에 가까운 값을 나타내었다. 액체 질소 온도에서 중성자 조사량이 $10^{17}\~10^{18}\;n/{\cal}cm^2$인 시료에서 S1 sextet의 초미세 자기장과 흡수 면적이 급격히 상승하는 현상을 관측하였으며, 상온에서 또한 이 현상을 관측하였다. 이는 중성자 조사에 의한 시료 내부의 $^{55}Mn$ 혹은 $^{56}Fe$$^{57}Fe$의 천이에 의한 $^{57}Fe$$M\ddot{o}ssbauer$ 핵종의 증가에 기인하는 것으로 추측된다.