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Journal articles on the topic 'Tiem Resolved Spectroscopy'

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Published: 7 September 2023

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1

Yakovlev, V. "Time-resolved luminescence spectroscopy study of CsI:Eu crystal." Functional Materials 20, no. 4 (December 25, 2013): 451–56. http://dx.doi.org/10.15407/fm20.04.451.

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2

Liu Fan, 刘璠, 姚旭日 Yao Xuri, 刘雪峰 Liu Xuefeng, and 翟光杰 Zhai Guangjie. "基于压缩感知的单光子时间分辨成像光谱技术." Laser & Optoelectronics Progress 58, no. 10 (2021): 1011016. http://dx.doi.org/10.3788/lop202158.1011016.

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3

Gaft, Michael, Harold Seigel, Gerard Panczer, and Renata Reisfeld. "Laser-induced time-resolved luminescence spectroscopy of Pb2+ in minerals." European Journal of Mineralogy 14, no. 6 (November 25, 2002): 1041–48. http://dx.doi.org/10.1127/0935-1221/2002/0014-1041.

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4

DAI Zijie, 戴子杰, 康黎星 KANG Lixing, 龚诚 GONG Cheng, 刘政 LIU Zheng, and 刘伟伟 LIU Weiwei. "PtSe2薄膜的时间分辨太赫兹光谱特性研究（特邀）." ACTA PHOTONICA SINICA 50, no. 8 (2021): 0850206. http://dx.doi.org/10.3788/gzxb20215008.0850206.

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5

Qingli Zhou, Qingli Zhou, and Xicheng Zhang Xicheng Zhang. "Applications of time-resolved terahertz spectroscopy in ultrafast carrier dynamics (Invited Paper)." Chinese Optics Letters 9, no. 11 (2011): 110006–9. http://dx.doi.org/10.3788/col201109.110006.

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6

Fabelinskii, Immanuil L. "Time-resolved spectroscopy." Uspekhi Fizicheskih Nauk 152, no. 8 (1987): 722. http://dx.doi.org/10.3367/ufnr.0152.198708y.0722.

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7

Fabelinskiĭ, Immanuil L. "Time-resolved spectroscopy." Soviet Physics Uspekhi 30, no. 8 (August 31, 1987): 755–56. http://dx.doi.org/10.1070/pu1987v030n08abeh002959.

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8

Clark, R. J. H., R. E. Hester, and T. L. Gustafson. "Time Resolved Spectroscopy." Vibrational Spectroscopy 1, no. 1 (December 1990): 106–8. http://dx.doi.org/10.1016/0924-2031(90)80018-y.

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9

Beddard, G. S. "Time resolved spectroscopy." Spectrochimica Acta Part A: Molecular Spectroscopy 47, no. 2 (January 1991): 311. http://dx.doi.org/10.1016/0584-8539(91)80104-q.

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10

YAGI, Toshirou. "Time-Resolved Phonon Spectroscopy." Journal of the Spectroscopical Society of Japan 44, no. 5 (1995): 281–91. http://dx.doi.org/10.5111/bunkou.44.281.

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11

Görlach, Ekkehard, Hansruedi Gygax, Paolo Lubini, and Urs P. Wild. "Time resolved fluorescence spectroscopy." Proceedings / Indian Academy of Sciences 103, no. 3 (March 1991): 395–400. http://dx.doi.org/10.1007/bf02842096.

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12

Jones, W. J. "Time-Resolved Vibrational Spectroscopy." Optica Acta: International Journal of Optics 33, no. 9 (September 1986): 1096. http://dx.doi.org/10.1080/716099710.

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13

Atkinson, George H. "Time-Resolved Vibrational Spectroscopy." Journal of Physical Chemistry A 104, no. 18 (May 2000): 4129. http://dx.doi.org/10.1021/jp001015m.

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14

Bakker, Huib, Stephen R. Meech, and Edwin J. Heilweil. "Time-Resolved Vibrational Spectroscopy." Journal of Physical Chemistry A 122, no. 18 (May 10, 2018): 4389. http://dx.doi.org/10.1021/acs.jpca.7b12769.

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15

Millar, David P. "Time-resolved fluorescence spectroscopy." Current Opinion in Structural Biology 6, no. 5 (October 1996): 637–42. http://dx.doi.org/10.1016/s0959-440x(96)80030-3.

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16

Erdmann, M., O. Rubner, Z. Shen, and V. Engel. "Time-resolved photoelectron spectroscopy:." Journal of Organometallic Chemistry 661, no. 1-2 (November 2002): 191–97. http://dx.doi.org/10.1016/s0022-328x(02)01822-3.

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17

Ajb. "Time-resolved Vibrational Spectroscopy." Journal of Molecular Structure 131, no. 1-2 (October 1985): 185. http://dx.doi.org/10.1016/0022-2860(85)85117-6.

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18

Andreoni, Alessandra. "Time-resolved fluorescence spectroscopy." Journal of Photochemistry and Photobiology B: Biology 9, no. 3-4 (June 1991): 379–80. http://dx.doi.org/10.1016/1011-1344(91)80178-k.

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19

Yuzawa, Tetsuro, Chihiro Kato, Michael W. George, and Hiro-O. Hamaguchi. "Nanosecond Time-Resolved Infrared Spectroscopy with a Dispersive Scanning Spectrometer." Applied Spectroscopy 48, no. 6 (June 1994): 684–90. http://dx.doi.org/10.1366/000370294774368947.

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A nanosecond time-resolved infrared spectroscopic system based on a dispersive scanning spectrometer has been constructed. This is an advanced version of a similar system reported in a previous paper; the time resolution has been improved from 1 μs to 50 ns and the sensitivity from 10−4 in intensity changes to 10−6. These have been achieved by the use of a high-temperature ceramic infrared light source, a photovoltaic MCT detector, and a low-noise, wide-band preamplifier developed specifically for the present purpose. Time-resolved infrared spectra of a few samples of photochemical and photobiological interests are presented to show the capability of the system. The origin of the thermal artifacts, which have been found to hamper the time-resolved infrared measurements seriously, is shown to be due to the transient reflectance change induced by a small temperature jump. The future prospect of time-resolved infrared spectroscopy is discussed with reference to other methods including infrared laser spectroscopy and Fourier transform infrared spectroscopy.
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20

TORIUMI, Hirokazu. "FT-IR time-resolved spectroscopy." Journal of the Spectroscopical Society of Japan 37, no. 4 (1988): 289–90. http://dx.doi.org/10.5111/bunkou.37.289.

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21

IWATA, Koichi, and Hiro-o. HAMAGUCHI. "Picosecond Time-resolved Raman Spectroscopy." Journal of the Spectroscopical Society of Japan 44, no. 2 (1995): 61–73. http://dx.doi.org/10.5111/bunkou.44.61.

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22

Pophristic, Milan, Frederick H. Long, Chuong Tran, and Ian T. Ferguson. "Time-Resolved Spectroscopy of InGaN." MRS Internet Journal of Nitride Semiconductor Research 5, S1 (2000): 803–9. http://dx.doi.org/10.1557/s109257830000510x.

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We have used time-resolved photoluminescence (PL), with 400 nm (3.1 eV) excitation, to examine InxGa1−xN/GaN light-emitting diodes (LEDs) before the final stages of processing at room temperature. We have found dramatic differences in the time-resolved kinetics between dim, bright and super bright LED devices. The lifetime of the emission for dim LEDs is quite short, 110 ± 20 ps at photoluminescence (PL) maximum, and the kinetics are not dependent upon wavelength. This lifetime is short compared to bright and super bright LEDs, which we have examined under similar conditions. The kinetics of bright and super bright LEDs are clearly wavelength dependent, highly non-exponential, and are on the nanosecond time scale (lifetimes are in order of 1 ns for bright and 10 ns for super bright LED at the PL max). The non-exponential PL kinetics can be described by a stretched exponential function, indicating significant disorder in the material. Typical values for β, the stretching coefficient, are 0.45 − 0.6 for bright LEDs, at the PL maxima at room temperature. We attribute this disorder to indium alloy fluctuations.From analysis of the stretched exponential kinetics we estimate the potential fluctuations to be approximately 75 meV in the super bright LED. Assuming a hopping mechanism, the average distance between indium quantum dots in the super bright LED is estimated to be 20 Å.
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23

Helbing, Jan, and Mathias Bonmarin. "Time-Resolved Chiral Vibrational Spectroscopy." CHIMIA International Journal for Chemistry 63, no. 3 (March 25, 2009): 128–33. http://dx.doi.org/10.2533/chimia.2009.128.

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24

Millers, D., L. Grigorjeva, V. Pankratov, S. Chernov, and A. Watterich. "Time-resolved spectroscopy of ZnWO4." Radiation Effects and Defects in Solids 155, no. 1-4 (November 2001): 317–21. http://dx.doi.org/10.1080/10420150108214131.

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25

Greetham, G. M., D. Sole, I. P. Clark, A. W. Parker, M. R. Pollard, and M. Towrie. "Time-resolved multiple probe spectroscopy." Review of Scientific Instruments 83, no. 10 (October 2012): 103107. http://dx.doi.org/10.1063/1.4758999.

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26

Betz, Timo, and Cécile Sykes. "Time resolved membrane fluctuation spectroscopy." Soft Matter 8, no. 19 (2012): 5317–26. http://dx.doi.org/10.1039/c2sm00001f.

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27

Bickerton, Steven, Carles Badenes, Thomas Hettinger, Timothy Beers, and Sonya Huang. "Time-Resolved Spectroscopy with SDSS." Proceedings of the International Astronomical Union 7, S285 (September 2011): 289–90. http://dx.doi.org/10.1017/s1743921312000816.

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AbstractWe present a brief technical outline of the newly-formed project, “Detection of Spectroscopic Differences over Time” (DS/DT). Our collaboration is using individual exposures from the SDSS spectroscopic archive to produce a uniformly-processed set of time-resolved spectra. Here we provide an overview of the properties and processing of the available data, and highlight the wide range of time base-lines present in the archive.
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28

Chernikov, Alexej, Thomas Feldtmann, Sangam Chatterjee, Martin Koch, Mackillo Kira, and Stephan W. Koch. "Time-resolved phonon-sideband spectroscopy." Solid State Communications 150, no. 37-38 (October 2010): 1733–36. http://dx.doi.org/10.1016/j.ssc.2010.07.034.

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29

Böhmer, Martin, Michael Wahl, Hans-Jürgen Rahn, Rainer Erdmann, and Jörg Enderlein. "Time-resolved fluorescence correlation spectroscopy." Chemical Physics Letters 353, no. 5-6 (February 2002): 439–45. http://dx.doi.org/10.1016/s0009-2614(02)00044-1.

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30

Stolow, Albert, Arthur E. Bragg, and Daniel M. Neumark. "Femtosecond Time-Resolved Photoelectron Spectroscopy." Chemical Reviews 104, no. 4 (April 2004): 1719–58. http://dx.doi.org/10.1021/cr020683w.

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31

Spoonhower, J. P., and M. S. Burberry. "Time-resolved spectroscopy of BaFBr:Eu2+." Journal of Luminescence 43, no. 4 (June 1989): 221–26. http://dx.doi.org/10.1016/0022-2313(89)90005-7.

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32

ISHIDA, Yukiaki. "Ultrafast Time-Resolved Photoemission Spectroscopy." Hyomen Kagaku 37, no. 1 (2016): 31–36. http://dx.doi.org/10.1380/jsssj.37.31.

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33

Lin, S. H., B. Fain, and C. Y. Yeh. "Ultrafast time-resolved fluorescence spectroscopy." Physical Review A 41, no. 5 (March 1, 1990): 2718–29. http://dx.doi.org/10.1103/physreva.41.2718.

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34

Plakhotnik, Taras, and Daniel Walser. "Time Resolved Single Molecule Spectroscopy." Physical Review Letters 80, no. 18 (May 4, 1998): 4064–67. http://dx.doi.org/10.1103/physrevlett.80.4064.

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35

Maklygina, Yu S., I. D. Romanishkin, A. S. Skobeltsin, T. A. Savelyeva, A. A. Potapov, G. V. Pavlova, I. V. Chekhonin, O. I. Gurina, and V. B. Loschenov. "Time-resolved fluorescence imaging technique for rat brain tumors analysis." Journal of Physics: Conference Series 2058, no. 1 (October 1, 2021): 012028. http://dx.doi.org/10.1088/1742-6596/2058/1/012028.

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Abstract The paper presents a new approach to assessing the state of tissues that differ in phenotype and in the degree of immunocompetent cells activity using photosensitizers (PS) and time-resolved fluorescence analysis methods. The main attention is paid to the detection of differences between tumor cells and tumor-associated macrophages (TAM) using spectroscopic and microscopic methods by the fluorescent kinetics signal and the difference in the accumulation of PS (the accumulation is several times greater in macrophages). The results of the PS photoluminescence study were obtained using two different techniques: time-resolved spectroscopy and time-resolved fluorescence microscopy (FLIM). Time-resolved spectroscopic analysis of the PS fluorescence lifetime was performed on adult female rats with induced C6 glioma in vivo. 5-ALA-induced Pp IX, which is widely used in clinical practice for carrying out effective conduction photodiagnostics and PDT, was used as the PS.
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36

Silviu, Gurlui, Cazacu Marius Mihai, Timofte Adrian, Rusu Oana, Bulai Georgiana, and Dan Dimitriu. "Space- and time-resolved raman and breakdown spectroscopy: advanced lidar techniques." EPJ Web of Conferences 176 (2018): 01028. http://dx.doi.org/10.1051/epjconf/201817601028.

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DARLIOES - the advanced LIDAR is based on space- and time-resolved RAMAN and breakdown spectroscopy, to investigate chemical and toxic compounds, their kinetics and physical properties at high temporal (2 ns) and spatial (1 cm) resolution. The high spatial and temporal resolution are needed to resolve a large variety of chemical troposphere compounds, emissions from aircraft, the self-organization space charges induced light phenomena, temperature and humidity profiles, ice nucleation, etc.
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37

Stephenson, Kirk A. J., Julia Zhu, Adrian Dockery, Laura Whelan, Tomás Burke, Jacqueline Turner, James J. O’Byrne, G. Jane Farrar, and David J. Keegan. "Clinical and Genetic Re-Evaluation of Inherited Retinal Degeneration Pedigrees following Initial Negative Findings on Panel-Based Next Generation Sequencing." International Journal of Molecular Sciences 23, no. 2 (January 17, 2022): 995. http://dx.doi.org/10.3390/ijms23020995.

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Although rare, inherited retinal degenerations (IRDs) are the most common reason for blind registration in the working age population. They are highly genetically heterogeneous (>300 known genetic loci), and confirmation of a molecular diagnosis is a prerequisite for many therapeutic clinical trials and approved treatments. First-tier genetic testing of IRDs with panel-based next-generation sequencing (pNGS) has a diagnostic yield of ≈70–80%, leaving the remaining more challenging cases to be resolved by second-tier testing methods. This study describes the phenotypic reassessment of patients with a negative result from first-tier pNGS and the rationale, outcomes, and cost of second-tier genetic testing approaches. Removing non-IRD cases from consideration and utilizing case-appropriate second-tier genetic testing techniques, we genetically resolved 56% of previously unresolved pedigrees, bringing the overall resolve rate to 92% (388/423). At present, pNGS remains the most cost-effective first-tier approach for the molecular assessment of diverse IRD populations Second-tier genetic testing should be guided by clinical (i.e., reassessment, multimodal imaging, electrophysiology), and genetic (i.e., single alleles in autosomal recessive disease) indications to achieve a genetic diagnosis in the most cost-effective manner.
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38

Saito, Mitsunori, Takahiro Koketsu, and Yusuke Itai. "Time-space conversion for time-resolved spectroscopy." OSA Continuum 2, no. 5 (April 29, 2019): 1726. http://dx.doi.org/10.1364/osac.2.001726.

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39

Moffat, Anthony F. J. "Time-resolved optical-UV spectroscopy of colliding wind effects." Symposium - International Astronomical Union 193 (1999): 278–88. http://dx.doi.org/10.1017/s0074180900205548.

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It is in the ultraviolet-optical domain where the strongest known emission lines arise in hot star winds. In the case of hot-star binaries, culminating in the relatively common, strong-wind WR+O systems, similar line-emission is seen in the cooling flows downstream from the highly compressed, X-ray emitting heads of the bow shock regions produced when the two winds collide. Time-resolved UV-optical spectroscopy of these flows around a complete orbit can provide important constraints not only on the colliding wind process itself, but also on the winds and the orbit. Spectroscopic wind-wind collision effects have now been seen in every relatively close WR+O system (P ≲ 100 d) that has been adequately observed so far.
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40

Satoh, Azusa, Mamoru Kitaura, Kei Kamada, Akimasa Ohnishi, Minoru Sasaki, and Kazuhiko Hara. "Time-resolved photoluminescence spectroscopy of Ce:Gd3Al2Ga3O12crystals." Japanese Journal of Applied Physics 53, no. 5S1 (January 1, 2014): 05FK01. http://dx.doi.org/10.7567/jjap.53.05fk01.

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41

Ostensen, R. "Time resolved spectroscopy of Balloon 090100001." Communications in Asteroseismology 150 (2007): 265–66. http://dx.doi.org/10.1553/cia150s265.

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42

Ashfold, Michael, Majed Chergui, Ingo Fischer, Lingfeng Ge, Gilbert Grell, Misha Ivanov, Adam Kirrander, et al. "Time-resolved ultrafast spectroscopy: general discussion." Faraday Discussions 228 (2021): 329–48. http://dx.doi.org/10.1039/d1fd90024b.

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43

Weidner, H., and R. E. Peale. "Event-Locked Time-Resolved Fourier Spectroscopy." Applied Spectroscopy 51, no. 8 (August 1997): 1106–12. http://dx.doi.org/10.1366/0003702971941917.

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A low-cost method of adding time-resolving capability to commercial Fourier transform spectrometers with a continuously scanning Michelson interferometer has been developed. This method is specifically designed to eliminate noise and artifacts caused by mirror-speed variations in the interferometer. The method exists of two parts: (1) a novel timing scheme for synchronizing the transient events under study and the digitizing of the interferogram and (2) a mathematical algorithm for extracting the spectral information from the recorded data. The novel timing scheme is a modification of the well-known interleaved, or stroboscopic, method. It achieves the same timing accuracy, signal-to-noise ratio, and freedom from artifacts as step-scan time-resolving Fourier spectrometers by locking the sampling of the interferogram to a stable time base rather than to the occurrences of the HeNe fringes. The necessary pathlength-difference information at which samples are taken is obtained from a record of the mirror speed. The resulting interferograms with uneven pathlength-difference spacings are transformed into wavenumber space by least-squares fits of periodic functions. Spectra from the far-infrared to the upper visible at resolutions up to 0.2 cm−1 are used to demonstrate the utility of this method.
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44

Buchner, Franziska, Andrea Lübcke, Nadja Heine, and Thomas Schultz. "Time-resolved photoelectron spectroscopy of liquids." Review of Scientific Instruments 81, no. 11 (November 2010): 113107. http://dx.doi.org/10.1063/1.3499240.

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45

Drescher, M., M. Hentschel, R. Kienberger, M. Uiberacker, V. Yakovlev, A. Scrinzi, Th Westerwalbesloh, U. Kleineberg, U. Heinzmann, and F. Krausz. "Time-resolved atomic inner-shell spectroscopy." Nature 419, no. 6909 (October 2002): 803–7. http://dx.doi.org/10.1038/nature01143.

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46

Diaz, Marcos P. "Time‐resolved Spectroscopy of V Sagittae." Publications of the Astronomical Society of the Pacific 111, no. 755 (January 1999): 76–83. http://dx.doi.org/10.1086/316289.

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47

Remacle, F., U. Even, and R. D. Levine. "Time and Frequency Resolved ZEKE Spectroscopy." Journal of Physical Chemistry 100, no. 51 (January 1996): 19735–39. http://dx.doi.org/10.1021/jp963005k.

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48

Khasanov, Oleg, Tatiana Smirnova, Olga Fedotova, Grigory Rusetsky, Vladimir Gayvoronsky, and Sergey Pokutnyi. "Time resolved femtosecond spectroscopy of nanocomposites." EPJ Web of Conferences 190 (2018): 03004. http://dx.doi.org/10.1051/epjconf/201819003004.

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Characterization methods of nanocomposites consisted of semiconductor metal-oxide quantum dots (QD) incorporated into a dielectric matrix have been elaborated on the base of time resolved four-wave mixing and photon echo. Large permanent dipole moment, inherent to QDs under study, local field effect, the QD spatial dispersion and distribution function of the transition dipole moments in QDs are taken into account. New responses at multiple frequencies in directions differed from spatial synchronism conditions of well-known signals have been predicted.
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49

Noyan, Mehmet A., and James M. Kikkawa. "Time-resolved orbital angular momentum spectroscopy." Applied Physics Letters 107, no. 3 (July 20, 2015): 032406. http://dx.doi.org/10.1063/1.4927321.

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50

Guelachvili, Guy. "Time-resolved spectroscopy of stable molecules." Vibrational Spectroscopy 29, no. 1-2 (July 2002): 21–26. http://dx.doi.org/10.1016/s0924-2031(01)00173-4.

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