TN213 96063908一种发红光的电子陷获型红外上转换材料的制备=The synthesis of one kind of electrontrapping infrared up—conversion materialwhich emits red light[刊,中]/龚平,杜力,过晓晖,刘英,候洵(中科院西安光机所.陕西,西安...TN213 96063908一种发红光的电子陷获型红外上转换材料的制备=The synthesis of one kind of electrontrapping infrared up—conversion materialwhich emits red light[刊,中]/龚平,杜力,过晓晖,刘英,候洵(中科院西安光机所.陕西,西安(710068)),贾炜(佛航光信息联营有限公司.广东,佛山(528000))∥光子学报.—1995,24(4).—293—295研制的电子陷获(ET)型红外上转换材料是在改进传统工艺的基础上,使用硫化助熔法,在石英反应管中,基质合成和掺杂一次完成,具有工艺简单、生长周期短、重复性好的优点,由于反应在密闭系统中完成,安全可靠,对实验室环境保护好,用这种方法制备出的红外上转换材料,在室温下用紫外光或可见光激励后,用红外激发红光,并测量得了其激发光谱(红外)和发射光谱(红光)。展开更多
The rare earth ternary complex of Eu 3+ with thenoyltrifluoroacetone,and 4,7-2NH2 phenanthroline was synthesized and well characterized by UV,fluorescent,IR spectrometry and X-ray diffractometry(XRD)as well as element...The rare earth ternary complex of Eu 3+ with thenoyltrifluoroacetone,and 4,7-2NH2 phenanthroline was synthesized and well characterized by UV,fluorescent,IR spectrometry and X-ray diffractometry(XRD)as well as elemental analysis.The results show that the complex of Eu(III)emits strong red luminescence when excited by UV light,and Eu(TTA)3(2NH2-Phen)has the higher sensitized luminescent efficiency and longer lifetime than Eu(TTA)3(Phen).In device of ITO/PVK/Eu(TTA)3(2NH2-Phen)/Al,the spectra of Eu(TTA)3(2NH2-Phen)with different ratios for spin-cast film were monitored.The main emitting peak at 614 nm can be attributed to the transition of 5 D0→ 7 F2 of Eu 3+ and this process results in the enhancement of red emission from electroluminescence device.The effect and mechanism of the ligands on the luminescence properties of europium complex were discussed.The results show that the luminescence intensity of the title complexes greatly increases in comparison with that of their corresponding complexes,revealing that the second ligands form very good synergistic effect with the first ligands.The title complexes possess excellent thermal stability properties,and are hopefully developed into fine PL and EL red materials.展开更多
The product channels and mechanisms of the C2HC12＋O2 reaction are investigated by step-scan time-resolved Fourier transform infrared emission spectroscopy and the G3MP2// B3LYP/6-311G（d,p） level of electronic struc...The product channels and mechanisms of the C2HC12＋O2 reaction are investigated by step-scan time-resolved Fourier transform infrared emission spectroscopy and the G3MP2// B3LYP/6-311G（d,p） level of electronic structure calculations. Vibrationally excited products of HCI, CO, and CO2 are observed in the IR emission spectra and the product vibrational state distribution are determined which shows that HCI and CO are vibrationally excited with the nascent average vibrational energy estimated to be 59.8 and 51.8 kJ/mol respectively. In combination with the G3MP2//B3LYP/6-311G（d,p） calculations, the reaction mechanisms have been characterized and the energetically favorable reaction pathways have been suggested.展开更多
Normal vibrations of ethylbenzene in the first excited state have been studied using resonant two-photon ionization spectroscopy. The band origin of ethylbenzene of S1-S0 transition appeared at 37586 cm-1. A vibration...Normal vibrations of ethylbenzene in the first excited state have been studied using resonant two-photon ionization spectroscopy. The band origin of ethylbenzene of S1-S0 transition appeared at 37586 cm-1. A vibrational spectrum of 2000 cm-1 above the band origin in the first excited state has been obtained. Several chain torsions and normal vibrations are obtained in the spectrum. The energies of the first excited state are calculated by the time- dependent density function theory and configuration interaction singles （CIS） methods with various basis sets. The optimized structures and vibrational frequencies of the So and S1 states are calculated using Hartree-Fock and CIS methods with 6-311＋＋G（2d,2p） basis set. The calculated geometric structures in the So and $1 states are gauche conformations that the symmetric plane of ethyl group is perpendicular to the ring plane. All the observed spectral bands have been successfully assigned with the help of our calculations.展开更多
基金This work is by the National Natural Science Foundation of China(No.22203006,No.21927901,No.92261206,No.21627805,No.12174012,No.21673004,No.21821004,No.21674001,and No.21790363)Ministry of Science and Technology of China(a special talent program)and the Beijing City.
基金Supported by Natural Science Foundation of Jilin Province(20220101024JC,20200201247JC,20170520110JH)National Natural Science Foundation of China(11504029,11474035)。
文摘TN213 96063908一种发红光的电子陷获型红外上转换材料的制备=The synthesis of one kind of electrontrapping infrared up—conversion materialwhich emits red light[刊,中]/龚平,杜力,过晓晖,刘英,候洵(中科院西安光机所.陕西,西安(710068)),贾炜(佛航光信息联营有限公司.广东,佛山(528000))∥光子学报.—1995,24(4).—293—295研制的电子陷获(ET)型红外上转换材料是在改进传统工艺的基础上,使用硫化助熔法,在石英反应管中,基质合成和掺杂一次完成,具有工艺简单、生长周期短、重复性好的优点,由于反应在密闭系统中完成,安全可靠,对实验室环境保护好,用这种方法制备出的红外上转换材料,在室温下用紫外光或可见光激励后,用红外激发红光,并测量得了其激发光谱(红外)和发射光谱(红光)。
基金Project(B201015)supported by the Natural Science Foundation of Heilongjiang Province,ChinaProject(11551482)supported by the Scientific and Technical Research Project of Education Department of Heilongjiang Province,China+3 种基金Projects(L2010-124,L2010-144)supported by the Research Fund for Jiamusi University,ChinaProject(E08050204)supported by the Research Fund for the Provincial Key Laboratory of Biomaterials Jiamusi University,ChinaProject(2009-360)supported by Health Commission of Heilongjiang Province,ChinaProject supported by Key Laboratory of Luminescence and Optical Information,Beijing Jiaotong University,China
文摘The rare earth ternary complex of Eu 3+ with thenoyltrifluoroacetone,and 4,7-2NH2 phenanthroline was synthesized and well characterized by UV,fluorescent,IR spectrometry and X-ray diffractometry(XRD)as well as elemental analysis.The results show that the complex of Eu(III)emits strong red luminescence when excited by UV light,and Eu(TTA)3(2NH2-Phen)has the higher sensitized luminescent efficiency and longer lifetime than Eu(TTA)3(Phen).In device of ITO/PVK/Eu(TTA)3(2NH2-Phen)/Al,the spectra of Eu(TTA)3(2NH2-Phen)with different ratios for spin-cast film were monitored.The main emitting peak at 614 nm can be attributed to the transition of 5 D0→ 7 F2 of Eu 3+ and this process results in the enhancement of red emission from electroluminescence device.The effect and mechanism of the ligands on the luminescence properties of europium complex were discussed.The results show that the luminescence intensity of the title complexes greatly increases in comparison with that of their corresponding complexes,revealing that the second ligands form very good synergistic effect with the first ligands.The title complexes possess excellent thermal stability properties,and are hopefully developed into fine PL and EL red materials.
基金V. ACKNOWLEDGMENTS This work was supported by the National Natural Science Foundation of China （No.20733005, No.20673126, and No.20973179）, the National Basic Research Program of China （No.2007CB815200 and No.2007AA02Z116）, and the Chinese Academy of Sciences.
文摘The product channels and mechanisms of the C2HC12＋O2 reaction are investigated by step-scan time-resolved Fourier transform infrared emission spectroscopy and the G3MP2// B3LYP/6-311G（d,p） level of electronic structure calculations. Vibrationally excited products of HCI, CO, and CO2 are observed in the IR emission spectra and the product vibrational state distribution are determined which shows that HCI and CO are vibrationally excited with the nascent average vibrational energy estimated to be 59.8 and 51.8 kJ/mol respectively. In combination with the G3MP2//B3LYP/6-311G（d,p） calculations, the reaction mechanisms have been characterized and the energetically favorable reaction pathways have been suggested.
文摘Normal vibrations of ethylbenzene in the first excited state have been studied using resonant two-photon ionization spectroscopy. The band origin of ethylbenzene of S1-S0 transition appeared at 37586 cm-1. A vibrational spectrum of 2000 cm-1 above the band origin in the first excited state has been obtained. Several chain torsions and normal vibrations are obtained in the spectrum. The energies of the first excited state are calculated by the time- dependent density function theory and configuration interaction singles （CIS） methods with various basis sets. The optimized structures and vibrational frequencies of the So and S1 states are calculated using Hartree-Fock and CIS methods with 6-311＋＋G（2d,2p） basis set. The calculated geometric structures in the So and $1 states are gauche conformations that the symmetric plane of ethyl group is perpendicular to the ring plane. All the observed spectral bands have been successfully assigned with the help of our calculations.
