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Artículos de revistas sobre el tema "Electronic spectroscopy"

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Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 13 de julio de 2024

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1

Seddon, Kenneth R. "Inorganic Electronic Spectroscopy". Journal of Organometallic Chemistry 290, n.º 1 (julio de 1985): c11—c12. http://dx.doi.org/10.1016/0022-328x(85)80158-3.

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2

R, G. "Inorganic electronic spectroscopy". Journal of Molecular Structure 129, n.º 1-2 (junio de 1985): 180–81. http://dx.doi.org/10.1016/0022-2860(85)80208-8.

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3

Hybl, John D., Allison W. Albrecht, Sarah M. Gallagher Faeder y David M. Jonas. "Two-dimensional electronic spectroscopy". Chemical Physics Letters 297, n.º 3-4 (noviembre de 1998): 307–13. http://dx.doi.org/10.1016/s0009-2614(98)01140-3.

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4

Ramasesha, Sheela K. y Stephen A. Payne. "Electronic spectroscopy of KF:Cu+". Physica B: Condensed Matter 167, n.º 1 (octubre de 1990): 56–60. http://dx.doi.org/10.1016/0921-4526(90)90104-3.

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5

Pino, T., Y. Carpentier, G. Féraud, H. Friha, D. L. Kokkin, T. P. Troy, N. Chalyavi, Ph Bréchignac y T. W. Schmidt. "Electronic Spectroscopy of PAHs". EAS Publications Series 46 (2011): 355–71. http://dx.doi.org/10.1051/eas/1146037.

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6

Kaledin, Leonid A. y Michael C. Heaven. "Electronic Spectroscopy of UO". Journal of Molecular Spectroscopy 185, n.º 1 (septiembre de 1997): 1–7. http://dx.doi.org/10.1006/jmsp.1997.7383.

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7

Kharlamova, Marianna V. y Christian Kramberger. "Spectroscopy of Filled Single-Walled Carbon Nanotubes". Nanomaterials 12, n.º 1 (23 de diciembre de 2021): 42. http://dx.doi.org/10.3390/nano12010042.

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Many envisaged applications, such as nanoelectronics, photovoltaics, thermoelectric power generation, light-emission devices, energy storage and biomedicine, necessitate single-walled carbon nanotube (SWCNT) samples with specific uniform electronic properties. The precise investigation of the electronic properties of filled SWCNTs on a qualitative and quantitative level is conducted by optical absorption spectroscopy, Raman spectroscopy, photoemission spectroscopy and X-ray absorption spectroscopy. This review is dedicated to the description of the spectroscopic methods for the analysis of the electronic properties of filled SWCNTs. The basic principle and main features of SWCNTs as well as signatures of doping-induced modifications of the spectra of filled SWCNTs are discussed.
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8

Nedilko, S. "Luminescence spectroscopy and electronic structure of Eu3+-doped Bi-containing oxide compoundsLuminescence spectroscopy and electronic structure of Eu3+-doped Bi-containing oxide compounds". Functional Materials 20, n.º 1 (25 de marzo de 2013): 29–36. http://dx.doi.org/10.15407/fm20.01.029.

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9

Joung, Joonyoung F., Junwoo Baek, Youngseo Kim, Songyi Lee, Myung Hwa Kim, Juyoung Yoon y Sungnam Park. "Electronic relaxation dynamics of PCDA-PDA studied by transient absorption spectroscopy". Physical Chemistry Chemical Physics 18, n.º 33 (2016): 23096–104. http://dx.doi.org/10.1039/c6cp03858a.

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10

Krechkivska, Olha, Michael D. Morse, Apostolos Kalemos y Aristides Mavridis. "Electronic spectroscopy and electronic structure of diatomic TiFe". Journal of Chemical Physics 137, n.º 5 (7 de agosto de 2012): 054302. http://dx.doi.org/10.1063/1.4738958.

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11

Garcia, Maria A., Carolin Vietz, Fernando Ruipérez, Michael D. Morse y Ivan Infante. "Electronic spectroscopy and electronic structure of diatomic IrSi". Journal of Chemical Physics 138, n.º 15 (21 de abril de 2013): 154306. http://dx.doi.org/10.1063/1.4801328.

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12

Brugh, Dale J., Michael D. Morse, Apostolos Kalemos y Aristides Mavridis. "Electronic spectroscopy and electronic structure of diatomic CrC". Journal of Chemical Physics 133, n.º 3 (21 de julio de 2010): 034303. http://dx.doi.org/10.1063/1.3456178.

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13

Kharlamova, Marianna V. "Kinetics, Electronic Properties of Filled Carbon Nanotubes Investigated with Spectroscopy for Applications". Nanomaterials 13, n.º 1 (30 de diciembre de 2022): 176. http://dx.doi.org/10.3390/nano13010176.

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The paper is dedicated to the discussion of kinetics of growth, and electronic properties of filled carbon nanotubes investigated by spectroscopy for applications. The paper starts with discussion of growth of carbon nanotubes inside metallocene-filled carbon nanotubes. Nickelocene, cobaltocene are considered for growth of carbon nanotubes. Then, the investigations of filled carbon nanotubes by four spectroscopic techniques are discussed. Among them are Raman spectroscopy, near edge X-ray absorption fine-structure spectroscopy, photoemission spectroscopy, optical absorption spectroscopy. It is discussed that metal halogenides, metal chalcogenides, metals lead to changes in electronic structure of nanotubes with n- or p-doping. The filling of carbon nanotubes with different organic and inorganic substances results in many promising applications. This review adds significant contribution to understanding of the kinetics and electronic properties of filled SWCNTs with considering new results of recent investigations. Challenges in various fields are analyzed and summarized, which shows the author’s viewpoint of progress in the spectroscopy of filled SWCNTs. This is a valuable step toward applications of filled SWCNTs and transfer of existing ideas from lab to industrial scale.
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14

Фейер, В. М. "Electronic spectroscopy of Mg films". Scientific Herald of Uzhhorod University.Series Physics 10 (31 de diciembre de 2001): 26–30. http://dx.doi.org/10.24144/2415-8038.2001.10.26-30.

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15

Thakur, Pramod Kumar. "Electronic Spectroscopy And Its Interpretation". Himalayan Physics 5 (5 de julio de 2015): 112–15. http://dx.doi.org/10.3126/hj.v5i0.12888.

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Electronic Spectroscopy relies on the quantized nature of energy states. At given enough energy, an electron can be excited from its initial ground state or initial excited state (hot band) and briefly exist in a higher energy excited state. Electronic transitions involve exciting an electron from one principle quantum state to another. Without incentive, an electron will not transition to a higher level.. The Himalayan Physics Vol. 5, No. 5, Nov. 2014 Page: 112-115
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16

Zhang, Zhengyang, Adriana Huerta-Viga y Howe-Siang Tan. "Two-dimensional electronic-Raman spectroscopy". Optics Letters 43, n.º 4 (15 de febrero de 2018): 939. http://dx.doi.org/10.1364/ol.43.000939.

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17

Jochnowitz, E. B. y J. P. Maier. "Electronic spectroscopy of carbon chains". Molecular Physics 106, n.º 16-18 (20 de agosto de 2008): 2093–106. http://dx.doi.org/10.1080/00268970802208588.

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18

Courtney, Trevor L., Zachary W. Fox, Karla M. Slenkamp y Munira Khalil. "Two-dimensional vibrational-electronic spectroscopy". Journal of Chemical Physics 143, n.º 15 (21 de octubre de 2015): 154201. http://dx.doi.org/10.1063/1.4932983.

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19

Stienkemeier, Frank y Andrey F. Vilesov. "Electronic spectroscopy in He droplets". Journal of Chemical Physics 115, n.º 22 (2001): 10119. http://dx.doi.org/10.1063/1.1415433.

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20

Bacis, R., A. J. Bouvier y J. M. Flaud. "The ozone molecule: electronic spectroscopy". Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 54, n.º 1 (enero de 1998): 17–34. http://dx.doi.org/10.1016/s1386-1425(97)00259-x.

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21

Loukianov, Anton, Andrew Niedringhaus, Brandon Berg, Jie Pan, S. Seckin Senlik y Jennifer P. Ogilvie. "Two-Dimensional Electronic Stark Spectroscopy". Journal of Physical Chemistry Letters 8, n.º 3 (24 de enero de 2017): 679–83. http://dx.doi.org/10.1021/acs.jpclett.6b02695.

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22

Dorohoi, Dana. "Electronic spectroscopy of N-ylids". Journal of Molecular Structure 704, n.º 1-3 (octubre de 2004): 31–43. http://dx.doi.org/10.1016/j.molstruc.2004.01.047.

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23

Brümmer, O. y W. Heichler. "Auger Spectroscopy and Electronic Structure". Zeitschrift für Kristallographie 195, n.º 1-2 (enero de 1991): 156. http://dx.doi.org/10.1524/zkri.1991.195.1-2.156.

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24

Sherman, Bradford Charles y William B. Euler. "Electronic spectroscopy of poly(propylmethylazine)". Chemistry of Materials 6, n.º 7 (julio de 1994): 899–906. http://dx.doi.org/10.1021/cm00043a007.

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25

Eden, S., B. Barc, N. J. Mason, S. V. Hoffmann, Y. Nunes y P. Limão-Vieira. "Electronic state spectroscopy of C2Cl4". Chemical Physics 365, n.º 3 (noviembre de 2009): 150–57. http://dx.doi.org/10.1016/j.chemphys.2009.10.010.

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26

Swanson, J. G. y V. Montgomery. "Opto-electronic modulation spectroscopy (OEMS)". Journal of Electronic Materials 19, n.º 1 (enero de 1990): 13–18. http://dx.doi.org/10.1007/bf02655546.

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27

Yeh, C. S., D. L. Robbins, J. S. Pilgrim y M. A. Duncan. "Photoionizaton electronic spectroscopy of AgK". Chemical Physics Letters 206, n.º 5-6 (mayo de 1993): 509–14. http://dx.doi.org/10.1016/0009-2614(93)80176-p.

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28

Pilgrim, J. S., D. L. Robbins y M. A. Duncan. "Photoionization electronic spectroscopy of AlOH". Chemical Physics Letters 202, n.º 3-4 (enero de 1993): 203–8. http://dx.doi.org/10.1016/0009-2614(93)85266-q.

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29

López Arbeloa, F., T. López Arbeloa y I. López Arbeloa. "Electronic spectroscopy of pyrromethene 546". Journal of Photochemistry and Photobiology A: Chemistry 121, n.º 3 (marzo de 1999): 177–82. http://dx.doi.org/10.1016/s1010-6030(98)00453-5.

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30

Maier, John P. "Electronic spectroscopy of carbon chains". Chemical Society Reviews 26, n.º 1 (1997): 21. http://dx.doi.org/10.1039/cs9972600021.

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31

Maier, John P. "Electronic Spectroscopy of Carbon Chains". Journal of Physical Chemistry A 102, n.º 20 (mayo de 1998): 3462–69. http://dx.doi.org/10.1021/jp9807219.

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32

Jochnowitz, Evan B. y John P. Maier. "Electronic Spectroscopy of Carbon Chains". Annual Review of Physical Chemistry 59, n.º 1 (mayo de 2008): 519–44. http://dx.doi.org/10.1146/annurev.physchem.59.032607.093558.

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33

MASON, S. F. "The Electronic Spectroscopy of Dyes". Journal of the Society of Dyers and Colourists 84, n.º 12 (22 de octubre de 2008): 604–12. http://dx.doi.org/10.1111/j.1478-4408.1968.tb02796.x.

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34

Krechkivska, Olha y Michael D. Morse. "Electronic Spectroscopy of Diatomic VC". Journal of Physical Chemistry A 117, n.º 50 (12 de julio de 2013): 13284–91. http://dx.doi.org/10.1021/jp404710s.

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35

Robbins, D. L., C. S. Yeh, J. S. Pilgrim, G. L. Lang y M. A. Duncan. "Photoionization electronic spectroscopy of AlAg". Journal of Chemical Physics 100, n.º 7 (abril de 1994): 4775–83. http://dx.doi.org/10.1063/1.466268.

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36

Nakajima, Atsushi, Kuniyoshi Hoshino, Katsura Watanabe, Yuji Konishi, Tsuyoshi Kurikawa, Suehiro Iwata y Koji Kaya. "Photoionization electronic spectroscopy of AlNa". Chemical Physics Letters 222, n.º 4 (mayo de 1994): 353–57. http://dx.doi.org/10.1016/0009-2614(94)87074-8.

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37

Turowski, Michał, Urszula Szczepaniak, Thomas Custer, Marcin Gronowski y Robert Kołos. "Electronic Spectroscopy of Methylcyanodiacetylene (CH3C5N)". ChemPhysChem 17, n.º 24 (5 de diciembre de 2016): 4068–78. http://dx.doi.org/10.1002/cphc.201600949.

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38

Fougère, Scott G., Walter J. Balfour, Jianying Cao y Charles X. W. Qian. "Electronic Spectroscopy of Rhodium Mononitride". Journal of Molecular Spectroscopy 199, n.º 1 (enero de 2000): 18–25. http://dx.doi.org/10.1006/jmsp.1999.7972.

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39

Rohringer, Nina. "X-ray Raman scattering: a building block for nonlinear spectroscopy". Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 377, n.º 2145 (abril de 2019): 20170471. http://dx.doi.org/10.1098/rsta.2017.0471.

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Ultraintense X-ray free-electron laser pulses of attosecond duration can enable new nonlinear X-ray spectroscopic techniques to observe coherent electronic motion. The simplest nonlinear X-ray spectroscopic concept is based on stimulated electronic X-ray Raman scattering. We present a snapshot of recent experimental achievements, paving the way towards the goal of realizing nonlinear X-ray spectroscopy. In particular, we review the first proof-of-principle experiments, demonstrating stimulated X-ray emission and scattering in atomic gases in the soft X-ray regime and first results of stimulated hard X-ray emission spectroscopy on transition metal complexes. We critically asses the challenges that have to be overcome for future successful implementation of nonlinear coherent X-ray Raman spectroscopy. This article is part of the theme issue ‘Measurement of ultrafast electronic and structural dynamics with X-rays’.
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40

Xiao Changtao, 肖常涛, 宋寅 Song Yin y 赵维谦 Zhao Weiqian. "超快二维电子光谱（特邀）". Laser & Optoelectronics Progress 61, n.º 1 (2024): 0130002. http://dx.doi.org/10.3788/lop232753.

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41

Garcia, Maria A. y Michael D. Morse. "Electronic Spectroscopy and Electronic Structure of Copper Acetylide, CuCCH". Journal of Physical Chemistry A 117, n.º 39 (12 de marzo de 2013): 9860–70. http://dx.doi.org/10.1021/jp312841q.

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42

Solomon, Edward I., Lipika Basumallick, Peng Chen y Pierre Kennepohl. "Variable energy photoelectron spectroscopy: electronic structure and electronic relaxation". Coordination Chemistry Reviews 249, n.º 1-2 (enero de 2005): 229–53. http://dx.doi.org/10.1016/j.ccr.2004.02.016.

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43

Dong, Chung-Li. "(Invited) Probing the Atomic and Electronic Structure of Working Energy Materials with x-Ray Spectroscopy". ECS Meeting Abstracts MA2022-01, n.º 36 (7 de julio de 2022): 1578. http://dx.doi.org/10.1149/ma2022-01361578mtgabs.

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Improving energy conversion/generation/storage efficiency of energy materials has always been a great challenge. Monitoring the atomic/electronic structures close to interface in many important energy materials, such as nanostructured catalysts, artificially photosynthesizing materials, smart materials, and energy storage devices, is of great importance. Designing such a material with improved performance without understanding its atomic/electronic structures, and their changes under operating conditions, is difficult. Understanding and controlling the interfacial electronic structures of energy materials require in-situ characterizations, of which synchrotron x-ray spectroscopy is the one with many unique features. The last decade has witnessed a golden age of in situ synchrotron x-ray spectroscopy for energy materials. X-ray absorption spectroscopy can be used to determine unoccupied electronic structures while X-ray emission spectroscopy can be utilized to examine occupied electronic structure. The additional use of resonant inelastic X-ray scattering further reveals inter-band d-d excitation or intra-band charge transfer excitation that can reflect the fundamental chemical and physical properties. An emerging technique, scanning transmission x-ray microscopy is a spectro-microscopic approach, providing regional x-ray absorption spectroscopy, is also gearing up for energy science. This presentation will report recent studies and perspectives of the application of in situ/operando synchrotron x-ray spectroscopy to energy materials. Tamkang University (TKU) end-stations constructed at the Taiwan Photon Source (TPS) 45A & 27A beamlines for the x-ray spectroscopic investigation of energy materials will also be introduced.
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44

Kim, Yujeong, Jin Kim, Linh K. Nguyen, Yong-Min Lee, Wonwoo Nam y Sun Hee Kim. "EPR spectroscopy elucidates the electronic structure of [FeV(O)(TAML)] complexes". Inorganic Chemistry Frontiers 8, n.º 15 (2021): 3775–83. http://dx.doi.org/10.1039/d1qi00522g.

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The complete hyperfine tensor of 17O of the FeV-oxo moeity was probed by ENDOR spectroscopy. The EPR spectroscopic results reported here provide a conclusive experimental basis for elucidating the electronic structure of the FeV-oxo complex.
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45

Kositzki, Ramona, Stefan Mebs, Nils Schuth, Nils Leidel, Lennart Schwartz, Michael Karnahl, Florian Wittkamp et al. "Electronic and molecular structure relations in diiron compounds mimicking the [FeFe]-hydrogenase active site studied by X-ray spectroscopy and quantum chemistry". Dalton Transactions 46, n.º 37 (2017): 12544–57. http://dx.doi.org/10.1039/c7dt02720f.

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46

Koleva, Bojidarka, Rositsa Nikolova, Atanas Tchapkanov, Tsonko Kolev, Heike Mayer-Figge, Michael Spiteller y William Sheldrick. "Crystal structure and spectroscopic properties of 4-acetaminopyridine and its protonated form". Polish Journal of Chemical Technology 11, n.º 3 (1 de enero de 2009): 35–40. http://dx.doi.org/10.2478/v10026-009-0033-y.

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Crystal structure and spectroscopic properties of 4-acetaminopyridine and its protonated form 4-Acetaminopyridine dihydrate and its protonated form, stabilized as the hydrochloride salt have been synthesized and spectroscopic elucidated in solution and in the solid-state by means of the inear-polarized solid state IR-spectroscopy (IR-LD), UV-spectroscopy, TGA, DSC, and the positive and negative ESI MS. Quantum chemical calculations were used to obtain the electronic structure, vibrational data and the electronic spectra. The spectroscopic and theoretical data are compared with the structure of the first compound obtained by single crystal X-ray diffraction. The effect of Npy protonation on the optical and magnetic properties of a 4-acetaminopyridine is discussed.
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47

Kim, Youngsang y Hyunwook Song. "Noise spectroscopy of molecular electronic junctions". Applied Physics Reviews 8, n.º 1 (marzo de 2021): 011303. http://dx.doi.org/10.1063/5.0027602.

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48

Persinger, Thomas D., Jiande Han y Michael C. Heaven. "Electronic Spectroscopy and Photoionization of LiMg". Journal of Physical Chemistry A 125, n.º 17 (21 de abril de 2021): 3653–63. http://dx.doi.org/10.1021/acs.jpca.1c01656.

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49

SHABLAEV, S. I. y R. V. PISAREV. "TWO-PHOTON ABSORPTION SPECTROSCOPY OF ELECTRONIC". Journal of the Magnetics Society of Japan 11, S_1_ISMO (1987): S1_19–22. http://dx.doi.org/10.3379/jmsjmag.11.s1_19.

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50

Zalecki, R., A. Kołodziejczyk, N. T. H. Kim-Ngan, A. Adamska, A. Kowalczyk, T. Toliński y M. Mihalik. "Electronic States of UNi2from Photoemission Spectroscopy". Acta Physica Polonica A 113, n.º 1 (enero de 2008): 407–12. http://dx.doi.org/10.12693/aphyspola.113.407.

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