Tb3+-doped CaNb2O6 (CaNb2O6:Tb3+) thin films were deposited on quartz substrates at a growth temperature of 300 °C using radio-frequency magnetron sputtering. The deposited thin films were annealed at several annealing temperatures for 20 min and characterized for their structural, morphological, and luminescent properties. The experimental results showed that the annealing temperature had a significant effect on the properties of the CaNb2O6:Tb3+ thin films. The crystalline structure of the as-grown CaNb2O6:Tb3+ thin films transformed from amorphous to crystalline after annealing at temperatures greater than or equal to 700 °C. The emission spectra of the thin films under excitation at 251 nm exhibited a dominant emission band at 546 nm arising from the 5D4 → 7F5 magnetic dipole transition of Tb3+ and three weak emission bands at 489, 586, and 620 nm, respectively. The intensity of the 5D4 → 7F5 (546 nm) magnetic dipole transition was greater than that of the 5D4 → 7F6 (489 nm) electrical dipole transition, indicating that the Tb3+ ions in the host crystal were located at sites with inversion symmetry. The average transmittance at wavelengths of 370~1,100 nm decreased from 86.8 % at 700 °C to 80.5 % at an annealing temperature of 1,000 °C, and a red shift was observed in the bandgap energy with increasing annealing temperature. These results suggest that the annealing temperature plays a crucial role in developing green light-emitting CaNb2O6:Tb3+ thin films for application in electroluminescent displays.

Polymeric materials have been widely used in energy-related applications including fabrication of batteries and fuel cells, pressure retarded osmosis, gas separation and reverse electrodialysis processes. Despite these various versatility, their poor mechanical properties still remain as obstacles for applying to industrial levels. As a way of improving the mechanical properties, Tröger's Base (TB) which is a rigid, V-shaped, and bridged bicyclic amine have been recently introduced. In this work, polyimides incorporating TB units (PI-TBs) were synthesized in-situ polycondensation reaction using dimethoxymethane (DMM). PI-TB membranes were prepared and physicochemical characteristics including mechancial properties were investigated.

CaAl2O4:RE3+(RE = Tb or Dy) phosphor powders were synthesized with different contents of activator ions Tb3+ and Dy3+ by using the solid-state reaction method. The effects of the content of activator ions on the crystal structure, morphology, and emission and excitation properties of the resulting phosphor particles were investigated. XRD patterns showed that all the synthesized phosphors had a monoclinic system with a main (220) diffraction peak, irrespective of the content and type of Tb3+ and Dy3+ ions. For the Tb3+-doped CaAl2O4 phosphor powders, the excitation spectra consisted of one broad band centered at 271 nm in the range of 220-320 nm and several weak peaks; the main emission band showed a strong green band at 552 nm that originated from the 5D4→ 7F5 transition of Tb3+ ions. For the Dy3+-doped CaAl2O4 phosphor, the emission spectra under ultraviolet excitation at 298 nm exhibited one strong yellow band centered at 581 nm and two weak bands at 488 and 672 nm. Concentration-dependent quenching was observed at 0.05 mol of Tb3+ and Dy3+ contents in the CaAl2O4 host lattice.

BaMoO4:Tb3+ phosphor powders were synthesized with different concentrations of Tb3+ ions using the solid-state reaction method. XRD patterns showed that all the phosphors, irrespective of the concentration of Tb3+ ions, had tetragonal systems with two main (112) and (004) diffraction peaks. The excitation spectra of the Tb3+-doped BaMoO4 phosphors consisted of an intense broad band centered at 290 nm in the range of 230-330 nm and two weak bands. The former broad band corresponded to the 4f8 →4f75d1 transition of Tb3+ ions; the latter two weak bands were ascribed to the 7F2→ 5D3 (471 nm) and 7F6→ 5D4 (492 nm) transitions of Tb3+. The main emission band, when excited at 290 nm, showed a strong green band at 550 nm arising from the 5D4→ 7F5 transition of Tb3+ ions. As the concentration of Tb3+ increased from 1 to 10 mol%, the intensities of all the emission lines gradually increased, approached maxima at 10 mol% of Tb3+ ions, and then showed a decreasing tendency with further increase in the Tb3+ ions due to the concentration quenching effect. The critical distance between neighboring Tb3+ ions for concentration quenching was calculated and found to be 12.3 Å, which indicates that dipoledipole interaction was the main mechanism for the concentration quenching of the 5D4→ 7F5 transition of Tb3+ in the BaMoO4:Tb3+ phosphors.

SrSnO3 phosphor powders were synthesized with two different contents of activator ions Eu3+ and Tb3+ using thesolid-state reaction method. The structural, morphological, and optical properties of the phosphors were investigated using X-ray diffractometry, field-emission scanning electron microscopy, and fluorescence spectrophotometry, respectively. All thephosphors showed a cubic structure, irrespective of the type and the content ratio of activator ions. For Eu3+-doped SrSnO3phosphors, the intensity of the 620nm red emission spectrum resulting from the 5D0→7F2 transition of Eu3+ was stronger thanthat of the 595nm orange emission signal due to the 5D0→7F1 transition in the range 0.01-0.05mol of Eu3+, but the ratio ofthe intensity was reversed in the range 0.10-0.20mol of Eu3+. The variation in the emission intensity indicates that the sitesymmetry of the Eu3+ ions around the host crystal was changed from non-inversion symmetry to inversion. For the Tb3+-dopedSrSnO3 phosphors under excitation at 281nm, one strong green emission band at 550nm and several weak bands wereobserved. These results suggest that the optimum red and green emission signals can be realized when the activator ion contentfor Eu3+- or Tb3+-doped SrSnO3 phosphors is 0.20mol and 0.15mol, respectively.

This paper presents new type magnetostrictive optical systems. The suggested wireless optical systems are developed by using two types of magnetostrictive thin film actuators. The first is a seesaw type wireless-controlled compact optical switch, and another is a comb type TbDyFeNi thin film actuator by silicon micromachining techniques with DC magnetron sputtering. In the seesaw type, TbDyFe films are selectively deposited on the micromachined switch matrix. For the optical switching operation, switch is arranged in a 1×2 array (mirror size of 5mm × 800μm × 50μm) and has different length from the supporting point. Mirrors are also actuated by externally applied magnetic fields up to 0.5T. In the comb type, the effect of Ni content on the magneto-mechanical properties of the Tb0.24Dy0.76Fe2 system is investigated with the effect of deposited film thickness of TbDyFeNi on silicon substrate for wireless microactuator. As results, magneto-mechanical characteristics are investigated. using magnetization and deflected angle variation

Green phosphors K2BaW2O8:Tb3+(1.0mol%) were synthesized by solid state reaction method. Differential thermalanalysis was applied to trace the reaction processes. Three endothermic values of 95, 706, and 1055oC correspond to the lossof absorbed water, the release of carbon dioxide, and the beginning of the melting point, respectively. The phase purity of thepowders was examined using powder X-ray diffraction(XRD). Two strong excitation bands in the wavelength region of 200-310nm were found to be due to the WO42− exciton transition and the 4f-5d transition of Tb3+ in K2BaW2O8. The excitationspectrum presents several lines in the range of 310-380nm; these are assigned to the 4f-4f transitions of the Tb3+ ion. The strongemission line at around 550nm, due to the 5D4→7F5 transition, is observed together with weak lines of the 5D4→7FJ(J=3,4, and 6) transitions. A broad emission band peaking at 530nm is observed at 10K, while it disappears at room temperature.The decay times of Tb3+ 5D4→7F5 emission are estimated to be 4.8 and 1.4ms, respectively, at 10 and 295 K; those of theWO42− exciton emissions are 22 and 0.92µs at 10 and 200K, respectively.

비정질 Tb45.7 Fe54.3-x /Cox 및 Tb50.2 /Fe 49.8-x/Cox (0≤x≤9.6) 합금박막의 자기적 특성 및 자기변형특성에 대하여 체계적으로 조사하였다. 박막제조는 Fe 타게트에 Tb, Co 소편으로 구성된 복합타겟 방식의 rf 마그네트론 스퍼터링법에 의해 제조하였다. XRD 조사에의 한 박막의 미세구조는 잘 발달된 비정질 구조를 나타내었다. Tb45.7 Fe54.3-x Cox (x=2~4)에서 우수한 고유자기변형특성 및 저자기장자기변형특성을 얻었다. 즉, 100 Oe의 저자장에서 130ppm의 자기변형을 나타내었으며 고유자기변형 (인가 자기장, 5 kOe)은 330ppm에서 400ppm으로 증가하였다.

Tb3+ 이온이 첨가 된 NaCa(PO3)3 형광체의 여기 및 방출 스펙트럼 및 레이저 분광 측정을 통하여 형광특성을 조사 하였다. 고상법으로 NaCa(PO3)3:Tb3+ 형광체를 합성하였다. X선 회절측정(XRD)을 사용하여 형광체의 결정 구조 및 결정성을 분석하여 Tb3+ 이온이 30 mol%까지 첨가되어도 형광체의 결정구조가 NaCa(PO3)3의 결정상을 유지하였다. NaCa(PO3)3:Tb3+(0.01 - 30mol %)형광체의 여기 및 방출 스펙트럼과 형광의 감쇠곡선을 상온에서 측정 하였다. NaCa(PO3)3:Tb3+의 여기 스펙트럼에서 205 ~ 245 nm 영역에서 넓은 Tb3+의 4f – 5d 전이에 의한 f - d 밴드가 나타났다. NaCa(PO3)3:Tb3+의 방출 스펙트럼에서 5D4 → 7FJ 전이에 의한 강한 피크와 5D3 → 7FJ 전이에 약한 피크가 관찰 되었다. 방출 스펙트럼의 형광 강도와 형광의 수명시간 분석을 통하여 Tb3+ 이온 사이의 에너지 전이 및 교차 이완이 확인되었다.

본 연구에서는 연성을 형광체 층이 가질 수 있다면 외부의 기계적 외력에 대하여 장기간 안정성을 확보 할 수 있을 것으로 기대하였다. 이에 본 연구에서는 스크린 프린팅 공법을 통하여 유연한 Gd2O2S:Tb 증감 지를 제작하였고 장기적인 외력에 의한 피로누적과 반복적인 외력에 의한 피로누적에 따른 영향을 고찰하 고자 RMS 분석과 히스토그램을 분석을 통하여 영상 균일도를 평가하였다. 연구 결과, 지속적인 외력에 대 하여는 지배적인 픽셀 영역이 일정하게 유지되면서 RSD가 10% 이내를 만족하였으나, 반복적인 외력의 경우 지배적인 픽셀 영역이 3 영역으로 분할되며 영상 균일도에 악영향을 미치며 RSD가 10% 이상으로 증가 하는 것으로 나타났다. 이러한 결과를 바탕으로 기존 방사선증감지에 대비하여 기계적 안정성을 확보함으 로써 곡면 검출기의 적용 가능성을 제시하였으나 아직까지 플렉시블 검출기에 적용하기 위해서는 추가적 인 연구가 필요할 것으로 사료된다. 이러한 결과 유연성을 가진 방사선 증감지는 다양한 곡면에 적용이 가 능하므로 향후 핵의학, 치료용, 산업 분야 등과 같은 다양한 분야에 적용할 수 있을 것으로 기대된다.