• Journal of Magnetics
• /
• 제17권4호
• /
• pp.255-260
• /
• 2012

In this study, we determine that the electron paramagnetic resonance line-width (EPRLW) is axially symmetric about the c-axis and analyze the spin Hamiltonian with an isotopic g-factor of 1.9920 at a frequency of 9.5 GHz. It should be noted that the electron paramagnetic resonance signals are Lorentzian. Our findings show that the EPRLW decreases exponentially with an increase in the temperature; i.e., its temperature dependence in the range 300-400 K obeys Arrhenius behavior, this kind of temperature dependence indicates an off-center a motional narrowing of the spectrum when $Mn^{2+}$ impurity ions substitute for $Nb^{5+}$ ions. The specific heats follow a linear dependence suggesting a simple Debye $T^3$ behavior.

• Bulletin of the Korean Chemical Society
• /
• 제21권2호
• /
• pp.251-258
• /
• 2000

• 한국자기학회지
• /
• 제13권5호
• /
• pp.204-210
• /
• 2003

강유전체 물질인 LiNbO$_3$ 및 LiTaO$_3$ 단결정 내에 불순물로 첨가되어 있는 상자성 전이원소인 Cr$^{3+}$ , $Mn^{2+}$, Fe$^{3+}$ 이온에 관한 전자 자기공명 연구를 하였다. 이들 두 단결정 내에 들어있는 불순물 이온에 대하여 중첩모델을 써서 계산한 영자기장 갈라지기 상수의 값을 실험에서 얻은 영자기장 갈라지기 값 및 기존에 보고된 많은 연구 논문과 비교 분석하여 상자성 불순물이 결정 내의 어느 자리를 치환하고 들어가는지를 연구하였다. LiNbO$_3$ 단결정 내의 Cr$^{3+}$ 이온이 불순물로 들어 갈 경우에는 두 가지 공명 중심이 가능하며, Li$^{+}$ 및 Nb$^{5+}$이온 자리를 각각 치환하고 들어간다. 또한 LiNbO$_3$ 결정 내의 $Mn^{2+}$ 및 Fe$^{3+}$ 이온의 경우에는 두 이온 모두 Nb$^{5+}$ 이온 자리를 치환하고 들어간다. LiTaO$_3$ 단결정 내에 불순물로 들어가 있는 Cr$^{3+}$ 및 Fe$^{3+}$ 이온은 모두 Li$^{+}$ 이온 자리를 치환하고있는 것으로 나타났다.

• Bulletin of the Korean Chemical Society
• /
• 제20권7호
• /
• pp.796-800
• /
• 1999

Three anthrylazacrown ethers in which the anthracene fluorophore π system is separated from the electron donor atoms by one methylene group were synthesized, and their photophysical study was accomplished. These fluorescent compounds showed a maximum fluorescence intensity at pH=5 in aqueous solutions and a decrease in fluorescence intensity upon binding of paramagnetic metal cations (Mn 2+ (d 5 ), Co 2+ (d 7 ), Cu 2+ (d 9 )). The decrease in fluorescence intensity may be attributed to the paramagnetic effect of metal cations to deactivate the excited state by the nonradiative quenching process. The benzylic nitrogen was found to play an important role in changing fluorescence intensity. From the observed linear Stern-Volmer plot and the fluorescence lifetime independence of the presence of metal ions, it was inferred that the chelation enhanced fluorescence quenching (CHEQ) mechanism in the system is a ground state static quenching process. Enhanced fluorescence was also observed when an excess Na + ion was added to the quenched aqueous solution, and it was attributed to cation displacement of a complexed fluorescence quencher.

• 한국자기학회:학술대회 개요집
• /
• 한국자기학회 2003년도 somma/kms meeting
• /
• pp.194-194
• /
• 2003

• 한국분말재료학회지
• /
• 제13권6호
• /
• pp.401-407
• /
• 2006

Effects of oxygen deficiency on the room temperature ferromagnetism in Fe-doped reduced $TiO_2$ have been investigated by comparing the air-annealed $Ti_{0.97}Fe_{0.03}O_2$ compound with secondly post-annealed one in vacuum ambience. The air-annealed sample showed a paramagnetic behavior at room temperature. However, when the sample was further annealed in vacuum, a strongly enhanced ferromagnetic behavior was observed at same temperature. $M{\"{o}}ssbauer$ spectra of air-annealed sample at 295K showed a single doublet of $Fe^{3+}$, suggesting that the Fe ions are paramagnetic. On the other hand, the absorption spectra after vacuum-annealing exhibited two doublets, in which one is the same component with air-annealed sample and the other is new doublet corresponding to $Fe^{2+}$ state. This result suggests that the occurrence of ferromagnetism in reduced sample may be interpreted as the contribution of unquenched orbital moment of $Fe^{2+}$ ions.

• BMB Reports
• /
• 제28권4호
• /
• pp.311-315
• /
• 1995

Exogenous $Cu^{2+}$ or $Zn^{2+}$ at micromolar concentration had a strong inhibitory effect on detergent-solubilized cytochrome c oxidase. A similar effect was observed when $Cu^{2+}$ was added to vesicular cytochrome c oxidase, although the extent of inhibition was significantly larger for the uncoupled state than for the coupled state. Interestingly, the inhibition by $Zn^{2+}$ was almost negligible for both the coupled and uncoupled states. These results suggest that the binding sites for $Cu^{2+}$ ions are exposed to the extravesicular side. whereas those for $Zn^{2+}$ are exposed to the matrix side. The EPR spectra of bound $Cu^{2+}$ ions at 77 K indicate that each of the first two $Cu^{2+}$ ions is ligated by three or four histidine residues, as evidenced by distinct $^{14}N$ superhyperfine splitting. These $Cu^{2+}$ ions can not be removed readily by EDTA and inhibit the enzyme activity by as much as 80%.

• 한국자기학회지
• /
• 제5권1호
• /
• pp.54-57
• /
• 1995

넓은 범위의 $^{1}H$ 핵자기공명 자기장에서 Heisenberg 반강자성체인 $MnCl_{2}.4H_{2}O$에 대하여 상온 수소 핵자기완화를 연구하였다. $MnCl_{2}.4H_{2}O$는 상온에서 밀접한 상자성 $Mn^{++}$ 이온계이지만 희박한 상자성계에서 예상되는 특성을 보인 반면에 희박한 상자성 근사와 매우 다른 결과도 보였다. 또한 수소 원자핵들은 0.7 T의 외부자기장 부근에서 스핀-격자 완화시간의 이상거동을 보였다.

• Journal of Magnetics
• /
• 제19권2호
• /
• pp.116-120
• /
• 2014

The spin-lattice relaxation time, $T_1$, for $^{69}Ga$, $^{71}Ga$, and $^{75}As$ nuclei in GaAs:$Mn^{2+}$ single crystals was measured as a function of temperature. The values of $T_1$ for $^{69}Ga$, $^{71}Ga$, and $^{75}As$ nuclei were found to decrease with increasing temperature. The $T_1$ values in GaAs:$Mn^{2+}$ crystal are similar to those in pure GaAs crystal. The calculated activation energies for the $^{69}Ga$, $^{71}Ga$, and $^{75}As$ nuclei are 4.34, 4.07, and 3.99 kJ/mol. It turns out that the paramagnetic impurity effect of $Mn^{2+}$ ion doped in GaAs single crystal was not strong on the spin-lattice relaxation time.

• Journal of Magnetics
• /
• 제16권2호
• /
• pp.134-139
• /
• 2011

Magnetic properties of highly zinc-substituted manganese ferrites are discussed on the basis of cation distribution. High throughput neutron powder diffractometry indicates that the prepared samples possess a nearly normal spinel structure, where the substitution of nonmagnetic zinc ions mainly causes the dilution of magnetic ions in the A-sublattice and consequently affects bond-randomness in the B-sublattice. On the other hand, the estimated occupancy of manganese ions in the B site indicates that random anisotropy effects due to local Jahn-Teller distortions gradually weaken with the substitution. Bulk magnetometry indicates that the substitution smears the transition from a paramagnetic phase to a soft-magnetic phase. Furthermore, at lower temperatures, such a soft-magnetic phase is destabilized and a magnetic glassy state appears. These features of the magnetic properties of dilute spinel ferrites are discussed from the viewpoint of the above-mentioned various types of disorders.