• 제목/요약/키워드: Fluorescence lifetime

검색결과 90건 처리시간 0.026초

대화면 BLU용 EEFL의 광학적 특성 (Optical Characteristics of EEFL (External Electrode Fluorescence Lamp) for Large Size BLU)

  • 최용성;이경섭;이상헌
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2006년도 영호남 합동 학술대회 및 춘계학술대회 논문집 센서 박막 기술교육
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    • pp.74-76
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    • 2006
  • An external electrode fluorescent lamp (EEFL) has an advantage of a long lifetime in the ear1y stages of the study on plasma discharge, interest in the lamp continues. Researches on the operation of external electrode fluorescent lamps have focused mainly on its use of a type of high frequency (MHz). By performing high brightness using a square wave operation method with the low frequency below 100kHz, which is applied to a narrowed tube type lamp that has several mm of lamp diameter, EEFL presented the possibility of using it as a light source for back-lights. However, because EEFL generates plasma using wall charges, which considers the impedance characteristics of glass based on the structural principle in discharge, it can be significant1y affected by frequency. Thus, this study verified the change in the characteristics of electromagnetic fields according to the change in frequency through a Maxwell's electromagnetic field simulation and examined the relationship between the change in the EEFL frequency and brightness by measuring the optical characteristics. In addition, the characteristics of the transformation of energy orbits were verified by investigating the characteristics of the wavelength according to the change in frequency through the OES.

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Synthesis and Characterization of Peripherally Ferrocene-modified Zinc Phthalocyanine for Dye-sensitized Solar Cell

  • An, Min-Shi;Kim, Soon-Wha;Hong, Jong-Dal
    • Bulletin of the Korean Chemical Society
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    • 제31권11호
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    • pp.3272-3278
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    • 2010
  • Synthesis and structural characterization of peripherally ferrocene-substituted zinc phthalocyanine (ZnPc-Fc) were carried out for efficient far-red/near-IR performance in dye-sensitized nanostructured $TiO_2$ solar cells. Incorporating ferrocene into phthalocyanine strongly improved the dye solubility in polar organic solvents, and reduced surface aggregation due to the steric effect of bulky ferrocene substituents. The involvement of electron transfer reaction pathways between ferrocene and phthalocyanine in ZnPc-Fc was evidenced by completely quenched fluorescence from S1 state (< 0.08% vs ZnPc). Strong absorption bands at 542 and 682 nm were observed in the transient absorption spectroscopy of ZnPc-Fc in DMSO, which was excited at a 670 nm laser pulse with a 15 ps full width at half maximum. Also, the excited state absorption signals at 450 - 600 and 750 - 850 nm appeared from the formation of charge separated state of phthalocyanine's anion. The lifetime of the charge separate state in ZnPc-Fc was determined to be $170{\pm}8$ ps, which was almost 17 times shorter than that of the ZnPc.

Solvent Effects on the Solvatochromism of 7-Aminocoumarin Derivatives in Neat and Binary Solvent Mixtures: Correlation of the Electronic Transition Energies with the Solvent Polarity Parameters

  • Choi, Jin-Yeong;Park, Eun-Ju;Chang, Seung-Hyun;Kang, Tai-Jong
    • Bulletin of the Korean Chemical Society
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    • 제30권7호
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    • pp.1452-1458
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    • 2009
  • The change in the electronic absorption and emission energy of 7-aminocoumarin derivatives in binary solvent mixtures has been studied. The electronic transition energy along with the Stokes' shift is correlated with the orientation polarizability of the solvent as well as the empirical solvent polarity parameters $E_T$ (30). It is observed that the emission peak shift traces the change of $E_T$ (30) value very closely in binary solvent mixtures. The emission transition more strongly depends on the solvent polarity than the absorption, which indicates the dipole moment gets larger on excitation. From the dependence of the Stokes’ shift of 7-aminocoumarins with the solvent polarity parameters and the ground state dipole moment obtained by the semi-empirical calculations, the excited state dipole moment was estimated. The fluorescence lifetime change of 7-aminocoumarins in binary solvent mixtures was measured and the results are explained in terms of molecular conformation and solvent polarity. The study indicates the empirical solvent polarity $E_T$ (30) is a good measure of microscopic solvent polarity and it probes in general the non-specific solvent interactions.

Ingestion Exposure to Nitrosamines in Chlorinated Drinking Water

  • Kim, He-Kap;Han, Ki-Chan
    • Environmental Analysis Health and Toxicology
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    • 제26권
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    • pp.2.1-2.7
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    • 2011
  • Objectives: N-Nitrosodimethylamine (NDMA) is classified as a probable human carcinogen by the United States Environmental Protection Agency (US EPA) and is formed during the chlorination of municipal drinking water. In this study, selected nitrosamines were measured in chlorinated drinking water collected from Chuncheon, Kangwon-do, Republic of Korea, and a risk assessment for NDMA was conducted. Methods: Twelve water samples were collected from 2 treatment plants and 10 household taps. Samples were analyzed for 6 nitrosamines via solid-phase extraction cleanup followed by conversion to dansyl derivatives and high-performance liquid chromatography-fluorescence detection (HPLC-FLD). Considering the dietary patterns of Korean people and the concentration change of NDMA by boiling, a carcinogenic risk assessment from ingestion exposure was conducted following the US EPA guidelines. Results: NDMA concentrations ranged between 26.1 and 112.0 ng/L. NDMA in water was found to be thermally stable, and thus its concentration at the end of boiling was greater than before thermal treatment owing to the decrease in water volume. The estimated excess lifetime carcinogenic risk exceeded the regulatory baseline risk of $10^{-5}$. Conclusions: This result suggests that more extensive studies need to be conducted on nitrosamine concentration distributions over the country and the source of relatively high nitrosamine concentrations.

Spectroscopic Characterization of Aqueous and Colloidal Am(III)-CO3 Complexes for Monitoring Species Evolution

  • Hee-Kyung Kim
    • 방사성폐기물학회지
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    • 제20권4호
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    • pp.371-382
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    • 2022
  • Carbonates are inorganic ligands that are abundant in natural groundwater. They strongly influence radionuclide mobility by forming strong complexes, thereby increasing solubility and reducing soil absorption rates. We characterized the spectroscopic properties of Am(III)-carbonate species using UV-Vis absorption and time-resolved laser-induced fluorescence spectroscopy. The deconvoluted absorption spectra of aqueous Am(CO3)2- and Am(CO3)33- species were identified at red-shifted positions with lower molar absorption coefficients compared to the absorption spectrum of aqua Am3+. The luminescence spectrum of Am(CO3)33- was red-shifted from 688 nm for Am3+ to 695 nm with enhanced intensity and an extended lifetime. Colloidal Am(III)-carbonate compounds exhibited absorption at approximately 506 nm but had non-luminescent properties. Slow formation of colloidal particles was monitored based on the absorption spectral changes over the sample aging time. The experimental results showed that the solubility of Am(III) in carbonate solutions was higher than the predicted values from the thermodynamic constants in OECD-NEA reviews. These results emphasize the importance of kinetic parameters as well as thermodynamic constants to predict radionuclide migration. The identified spectroscopic properties of Am(III)-carbonate species enable monitoring time-dependent species evolution in addition to determining the thermodynamics of Am(III) in carbonate systems.

Ho3+ 첨가 비정질 유전체 : 1.6μm 헝광의 방출 및 여기 스펙트럼 (Ho3+-Doped Amorphous Dielectrics:Emission and Excitation Spectra of the 1.6 μm Fluorescence)

  • 최용규
    • 한국세라믹학회지
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    • 제41권8호
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    • pp.618-622
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    • 2004
  • 플로라이드, 설파이드 및 셀레나이드 유리에 각각 첨가된 홀뮴 이온의 $^{5}$ I$_{5}$ \$\longrightarrow$$^{5}$ I$_{7}$ 전자천이에 기인하는 1.6$\mu$m 형광의 여기 스펙트럼을 $^{5}$ I$_{5}$ 준위가 위치하는 ∼900nm 대역에서 측정하였다. $^{5}$ $F_{1}$ 준위로의 상향전이가 발생하는 특정 파장대역에서 1.6$\mu$m발광의 여기효율이 감소하는 현상이 플로라이드 및 설파이드 유리에서 관찰되었으나 셀레나이드 유리에서는 $^{5}$ I$_{8}$ \$\longrightarrow$$^{5}$ I$_{5}$ 흡수 스펙트럼과 여기 스펙트럼의 모양이 유사하였으며, 이러한 현상은 각 비정질 유전체 재료의 광학적 비선형성과 단파장쪽 투과단의 차이에 기인한다. 한편, Tb$^{3+}$ , Dy$^{3+}$ , Eu$^{3+}$ 또는 N$d^{3+}$ 이온을 공동 첨가함으로써 $^{5}$ I$_{7}$ 준위의 형광수명을 효과적으로 감소시킬 수 있으나 Eu$^{3+}$ 이온을 제외한 나머지 공동 첨가제는 기저상태 흡수를 통하여 1.6 $\mu$m 대역에서의 흡수 손실을 크게 한다. 따라서 형광수명 감소 효과가 Tb$^{3+}$ 이온보다 크지는 않지만 추가적인 흡수 손실이 없는 Eu$^{3+}$ 이온이 공동 첨가제로 더 적합하다.

N-메틸루티돈의 루미네센스에 관한 연구 (Luminescence Studies of N-Methyllutidone, an Unusually High Triplet Energy Sensitizer)

  • 심상철;현명호;채규호
    • 대한화학회지
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    • 제22권1호
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    • pp.45-51
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    • 1978
  • $77^{\circ}C$K 에탄올 매트릭스에서 N-메틸루티돈의 발광에 대한 연구를 하였다. 형광은 관찰되지 않았으나 양자 수득률이 0.1과 수명 0.2초의 강한 인광이 관찰되었다. 인광의 0-0 띠로부터 이 화물합의 삼중상태 에너지가 85.1kcal/mole임을 알았으며 2-헥센, 트란스-1,4-디클로로부텐-2와 같은 높은 삼중상태 에너지를 가진 올레핀들이 N-메틸루티돈에 의해 효과적으로 시스${\leftrightarrow}$트란스광이성질화 반응을 일으키는 것으로 보아 이 높은 삼중상태 에너지가 정당함을 알 수 있다. 0-0띠의 polarization이 음의 값을 갖는 것으로 부터 발광상태가 $({\pi},{\pi})^3$ 상태임을 알 수 있다. LiCl과 같은 알카리염의 양이온과 N-메틸루티돈이 배위결합을 함으로써 $({\pi},{\pi})^3$$(n,{\pi})^3$상태 사이의 에너지 차이가 크게 되기 때문에 알카리 금속염은 인광의 세기를 증가시킨다.

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A Fiber Optic Sensor for Determination of 2,4-Dichlorophenol Based on Oxygen Oxidation Catalyzed by Iron(III) Tetrasulfophthalocyanine

  • Tong, Yilin;Li, Dapeng;Huang, Jun;Zhang, Cong;Li, Kun;Ding, Liyun
    • Bulletin of the Korean Chemical Society
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    • 제34권11호
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    • pp.3307-3311
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    • 2013
  • A new fiber optical sensor was developed for the determination of 2,4-dichlorophenol (DCP). The sensor was based on DCP oxidation by oxygen with the catalysis of iron(III) tetrasulfophthalocyanine (Fe(III)PcTs). The optical oxygen sensing film with $Ru(bpy)_3Cl_2$ as the fluorescence indicator was used to determine the consumption of oxygen in solution. A lock-in amplifier was used for detecting the lifetime of the oxygen sensing film by measuring the phase delay change of the sensor head. The different variables affecting the sensor performance were evaluated and optimized. Under the optimal conditions (i.e. pH 6.0, $25^{\circ}C$, Fe(III)PcTs concentration of 0.62 mg/mL), the linear detection range and response time of the sensor are $1.0{\times}10^{-6}-9.0{\times}10^{-6}$ mol/L and 250 s, respectively. The sensor displays high selectivity, good repeatability and stability, and can be used as an effective tool in analyzing DCP concentration in practical samples.

$Er^{3+}$첨가 중금속 산화물 유리의 다중포논 완화와 주파수 상향 전이 현상 (Multiphonon relaxation and frequency upconversion of $Er^{3+}$ ions in heavy metal oxide glasses)

  • 최용규;김경헌;허종
    • 한국광학회지
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    • 제9권4호
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    • pp.221-226
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    • 1998
  • $Er_2O_3$를 첨가한 $PbO-Bi_2O_3-Ga_2O_3$ 삼성분계 중금속 산화물 유리로부터 발생하는 $1.5\mu\textrm{m}$와 2.7$\mu\textrm{m}$ 등의 형광에 대하여 복사 천이율, 형광 수명, 흡수 및 유도 방출 단면적 등을 조사하였다. 중금속 산화물 유리의 낮은 포논 에너지($~500cm^{-1}$)로 인하여 기존 산화물 유리로부터 관찰할 수 없었던 형광들의 양자 효율이 크게 높아졌으며 방출 단면적도 증가하였다. 한편, 798 nm 여기광의 상향 전이를 통한 녹색과 적색의 형광이 방출됨을 확인하였고, 각 에너지 준위의 형광 수명을 이용하여 다중포논 완화(multiphonon relaxation)를 정량적으로 규명하였다. $Er^{3+}:^4S_{3/2}{\rightarrow}^4I_{15/2}$ 천이에 의한 녹색 형광은 기지 유리(host glass)의 밴드 갭(band gap)흡수에 의한 비복사 천이의 영향을 받으므로 이 형광의 양자 효율을 높이기 위해서는 유리를 불활성 기체 분위기에서 용융하거나 자외선쪽 투과단이 짧은 유리 망목 형성제(glass-vetwork former)가 첨가된 기지 조성을 선택하는 것이 바람직하다.

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방사분석과 분광학을 이용한 Am(III) 가수분해와 옥살레이트 착물 화학종 연구 (Radioanalytical and Spectroscopic Characterizations of Hydroxo- and Oxalato-Am(III) Complexes)

  • 김희경;조혜륜;정의창;차완식
    • 방사성폐기물학회지
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    • 제16권4호
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    • pp.397-410
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    • 2018
  • 아메리슘(Am)은 사용후핵연료의 장기 방사성 독성에 크게 영향을 주기 때문에 고준위 방사성 폐기물 처분의 장기 안전성 평가에 필수적으로 고려되어야 할 원소이다. 분광학적 방법을 이용한 일부 악티나이드 원소의 화학반응 연구가 활발히 진행되고 있는 반면, 아메리슘에 대한 연구는 아직까지 미비한 상황이다. 이 연구에서는 고순도의 시료를 필요로 하는 화학반응 연구를 위하여 $^{241}Am$ 시료를 정제한 후, 액체섬광계수기와 감마선 및 알파선 스펙트럼을 이용하여 정량과 정성분석을 하였다. 액체 광도파 모세관 셀을 이용한 고감도의 UV-Vis 흡수 분광학과 시간분해 레이저 형광 분광학을 이용하여 Am(III) 가수분해물과 옥살레이트(oxalate, Ox) 착물반응을 조사하였다. 산성조건에서 $Am^{3+}$은 503 nm에서 최대 흡수봉우리를 보이며, 몰흡광계수는 $424{\pm}8cm^{-1}{\cdot}M^{-1}$임을 확인하였다. 중성 이상의 pH 조건에서 형성되는 $Am(OH)_3(s)$ 콜로이드 입자에서는 506-507 nm 파장에서 최대 흡수봉우리가 관측되었다. ${Am(Ox)_3}^{3-}$ 착물은 $Am^{3+}$에 비교하여 흡수 및 발광스펙트럼이 각각 4와 5 nm정도 장파장으로 이동하였고 몰흡광계수와 발광세기도 크게 증가하였다. ${Am(Ox)_3}^{3-}$의 발광수명은 23에서 56ns으로 증가하였고 이는 Am(III)의 내부권에 결합하고 있던 약 여섯 개의 물분자가 옥살레이트의 카르복실기로 치환되었음을 의미한다. 이 결과로부터 ${Am(Ox)_3}^{3-}$은 각 옥살레이트 리간드가 두 자리 결합(bidentate)을 하고 있다는 것을 제안하였다.