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Journal articles on the topic 'Charge tranfer'

Author: Grafiati

Published: 9 March 2023

Last updated: 10 March 2023

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1

Fourmigue, M., K. Bechgaard, P. Auban, D. Jérôme, K. Boubekeur, and P. Batail. "Novel charge-tranfer salts based on the isoindolo[1,2,3-de]quinolizinium: An aza-analog of fluoranthene." Synthetic Metals 27, no. 3-4 (December 1988): 231–36. http://dx.doi.org/10.1016/0379-6779(88)90149-x.

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2

Vogler, A., and H. Kunkely. "Photochemistry of [MCo2(CO)8] (M = Zn, Cd, Hg) induced by metal to metal charge tranfer excitation." Journal of Organometallic Chemistry 355, no. 1-3 (November 1988): 1–6. http://dx.doi.org/10.1016/0022-328x(88)89005-3.

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3

Caricato, Marco, Silvia Díez González, Idoia Arandia Ariño, and Dario Pasini. "Homochiral BINOL-based macrocycles with π-electron-rich, electron-withdrawing or extended spacing units as receptors for C60." Beilstein Journal of Organic Chemistry 10 (June 6, 2014): 1308–16. http://dx.doi.org/10.3762/bjoc.10.132.

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The “one-pot” synthesis of several homochiral macrocycles has been achieved by using π-electron-rich, electron-deficient or extended aromatic dicarboxylic acids in combination with an axially-chiral dibenzylic alcohol, derived from enantiomerically-pure BINOL. Two series of cyclic adducts with average molecular D 2 and D 3 molecular symmetries, respectively, have been isolated in pure forms. Their yields and selectivities deviate substantially from statistical distributions. NMR and CD spectroscopic methods are efficient and functional in order to highlight the variability of shapes of the covalent macrocyclic frameworks. The larger D 3 cyclic adducts exhibit recognition properties towards C60 in toluene solutions (up to log K a = 3.2) with variable stoichiometries and variable intensities of the charge-tranfer band upon complexation.

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4

Samia, Anna C. S., John Cody, Christoph J. Fahrni, and Clemens Burda. "The Effect of Ligand Constraints on the Metal-to-Ligand Charge-Tranfer Relaxation Dynamics of Copper(I)−Phenanthroline Complexes: A Comparative Study by Femtosecond Time-Resolved Spectroscopy." Journal of Physical Chemistry B 108, no. 2 (January 2004): 563–69. http://dx.doi.org/10.1021/jp036857a.

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5

Lind, Thomas, and Hermann Bank. "Effect of Ligand Metal Charge Transfer and Intravalence Charge Transfer Bands on the Colour of Grossular Garnet." Neues Jahrbuch für Mineralogie - Monatshefte 1997, no. 1 (March 26, 1997): 1–14. http://dx.doi.org/10.1127/njmm/1997/1997/1.

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6

Platonov, Alexei N., Klaus Langer, Christian Chopin, Michael Andrut, and Michail N. Taran. "Fe2+ -Ti4+ charge-transfer in dumortierite." European Journal of Mineralogy 12, no. 3 (May 31, 2000): 521–28. http://dx.doi.org/10.1127/ejm/12/3/0521.

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7

Bardsley, J. N., P. Gangopadhyay, and B. M. Penetrante. "Symmetric charge transfer to multiply charged ions." Physical Review A 40, no. 5 (September 1, 1989): 2742–44. http://dx.doi.org/10.1103/physreva.40.2742.

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8

Platonov, Alexej N., Klaus Langer, Stanislas S. Matsuk, Mikhail N. Taran, and Xiaorui Hu. "Fe2+-Ti4+ charge-transfer in garnets from mantle eclogites." European Journal of Mineralogy 3, no. 1 (February 21, 1991): 19–26. http://dx.doi.org/10.1127/ejm/3/1/0019.

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9

Vikhnin, V. S., A. A. Kaplyanskii, A. B. Kutsenko, G. K. Liu, J. V. Beitz, and S. E. Kapphan. "“Charge transfer–lattice” clusters induced by charged impurities." Journal of Luminescence 94-95 (December 2001): 775–79. http://dx.doi.org/10.1016/s0022-2313(01)00364-7.

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10

Abbasov, I. I., and J. I. Huseynov. "Charge-Transfer Processes in (SnS)1 – x(PrS)x Alloys." Ukrainian Journal of Physics 62, no. 10 (November 2017): 883–88. http://dx.doi.org/10.15407/ujpe62.10.0883.

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11

Ito, H., Y. Chihara, Y. Suzuki, T. Hirayama, and T. Koizumi. "Multiple Charge Transfer by Slow Multi-Charged Xe Ions." Journal of Physics: Conference Series 58 (March 1, 2007): 311–14. http://dx.doi.org/10.1088/1742-6596/58/1/069.

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12

Kato, Takashi, and Tokio Yamabe. "Vibronic interactions and charge transfer in negatively charged chloroacenes." Chemical Physics 321, no. 1-2 (January 2006): 149–58. http://dx.doi.org/10.1016/j.chemphys.2005.07.041.

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13

Hvelplund, P., L. H. Andersen, C. Brink, D. H. Yu, D. C. Lorents, and R. Ruoff. "Charge transfer in collisions involving multiply charged C60 molecules." Zeitschrift f�r Physik D Atoms, Molecules and Clusters 30, no. 4 (December 1994): 323–26. http://dx.doi.org/10.1007/bf01426397.

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14

Pietsch, U. "Bond charges and electronic charge transfer in ternary semiconductors." physica status solidi (b) 134, no. 1 (March 1, 1986): 21–27. http://dx.doi.org/10.1002/pssb.2221340104.

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15

Hess, B., H. L. Lin, J. E. Niu, and W. H. E. Schwarz. "Electron Density Distributions and Atomic Charges." Zeitschrift für Naturforschung A 48, no. 1-2 (February 1, 1993): 180–92. http://dx.doi.org/10.1515/zna-1993-1-237.

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Abstract Accurate electron densities and X-ray form factors of Li, Be, F and their ions have been calculated. Electron correlation, crystal fields and ionic charge transfer change the form factors by up to a few percent, mainly in the range of sin θ/ λ < 1/3 Â -1 . Although electron correlation and crystal fields are small perturbations, their effects on the density and form factor are not additive. Densities or form factors of atomic and ionic systems are very similar; [Li0F0] and [Li+F-] procrystals differ by an effective charge transfer of not more than 0.4 e. Charge transfer and charge overlap in crystals cannot be distinguished uniquely. When the experimental data on Li2BeF4 (approximately reproduced by 3/4 atomic plus 1/4 ionic procrystal) are interpreted from the atomic partial charges are as low as 0.1 e (Li+ 0.12Be+ 0.2F- 0.14); when interpreted from the ionic viewpoint,the charges are much higher, namely 0.7 e. Intermediate viewpoints are also possible.

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16

Jain, Vishal, Hitesh Parmar, and Ketan Dodiya. "FTIR Spectra of Magnetic Charge Transfer Complexes of TEMPO Free Radical." International Journal of Trend in Scientific Research and Development 1, no. 2 (February 27, 2017): 8–13. http://dx.doi.org/10.31142/ijtsrd62.

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17

Lubinski, G., Z. Juhász, R. Morgenstern, and R. Hoekstra. "Low-Energy State-Selective Charge Transfer by Multiply Charged Ions." Physical Review Letters 86, no. 4 (January 22, 2001): 616–19. http://dx.doi.org/10.1103/physrevlett.86.616.

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18

Narits, A. A. "Charge transfer between fullerenes and highly charged noble gas ions." Journal of Physics B: Atomic, Molecular and Optical Physics 41, no. 13 (June 23, 2008): 135102. http://dx.doi.org/10.1088/0953-4075/41/13/135102.

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19

Furuhashi, Osamu, Tohru Kinugawa, Nobuyuki Nakamura, Suomi Masuda, Chikashi Yamada, and Shunsuke Ohtani. "Doubly Charged Molecular Ions Studied by Double Charge Transfer Spectroscopy." Journal of the Chinese Chemical Society 48, no. 3 (June 2001): 531–34. http://dx.doi.org/10.1002/jccs.200100080.

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20

Junghäuhnel, Gerhard, and Wolfgang Regenstein. "Charge-Transfer-Komplexe; Das Profil der Charge-Transfer-Bande gelöster Charge-Transfer-Komplexe." Zeitschrift für Chemie 13, no. 7 (September 1, 2010): 264–65. http://dx.doi.org/10.1002/zfch.19730130714.

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21

Maslinkov, Ivan. "Analysis and Modelling of Capacitive Transducers Based on the Charge Transfer Method." Indian Journal of Applied Research 4, no. 2 (October 1, 2011): 13–17. http://dx.doi.org/10.15373/2249555x/feb2014/185.

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22

Balaji, G. Naveen, S. Chenthur Pandian, and S. Giridharan S. Shobana J. Gayathri. "Dynamic and Non-Linear Charge Transfer through Opto-Deportation by Photovoltaic Cell." International Journal of Trend in Scientific Research and Development Volume-1, Issue-5 (August 31, 2017): 486–92. http://dx.doi.org/10.31142/ijtsrd2329.

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23

Afanasyev, D. A. "Charge transfer and properties of localized plasmon resonance in Ag-TiO2 nanostructures." Bulletin of the Karaganda University. "Physics" Series 95, no. 3 (September 30, 2019): 8–16. http://dx.doi.org/10.31489/2019ph3/8-16.

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24

Li, Xiaolong, Yin Xiao, Shirong Wang, Yuhao Yang, Yongning Ma, and Xianggao Li. "Polymorph-induced photosensitivity change in titanylphthalocyanine revealed by the charge transfer integral." Nanophotonics 8, no. 5 (February 28, 2019): 787–97. http://dx.doi.org/10.1515/nanoph-2018-0223.

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AbstractThe crystal form of semiconductor materials is keenly correlated with the photosensitivity of optoelectronic devices. Thus, understanding the crystal form-dependent photosensitivity mechanism is critical. In this work, the microemulsion phase transfer method was adopted to prepare α- and β-titanylphthalocyanine (TiOPc NPs) with an average diameter of 35 nm. The photosensitivity (E1/2) of α-TiOPc NPs was 2.73 times better than that of β-TiOPc NPs, which was characterized by photoconductors under the same measurement conditions. DFT was performed to explain the relationship between crystal form and photosensitivity by systematically calculating the charge transfer integrals for all possible dimers in the two different crystal forms. The hole and electron reorganization energies of TiOPc were respectively calculated to be 53.5 and 271.5 meV, revealing TiOPc to be a typical p-type semiconductor. The calculated total hole transfer mobility (μ+) ratio (2.83) of α- to β-TiOPc was almost identical to the experimental E1/2 ratio (2.73) and the calculated photogeneration quantum efficiency (ηe-h) ratio (2.23). In addition, the optimum hole transfer routes in the crystal of α- and β-TiOPc were all along with the [1 0 0] crystal orientation, which was determined by the calculated μ+. A high charge transfer mobility leads to a high photosensitive TiOPc crystal. Consequently, these results indicate that the selected theoretical calculation method is reasonable for indirectly explaining the relationship between crystal form and photosensitivity. The TiOPc molecular solid-state arrangements, namely, the crystal forms of TiOPc, have a strong influence on the charge transport behavior, which in turn, affects its photosensitivity.

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25

Moore, Barry, Haitao Sun, Niranjan Govind, Karol Kowalski, and Jochen Autschbach. "Charge-Transfer Versus Charge-Transfer-Like Excitations Revisited." Journal of Chemical Theory and Computation 11, no. 7 (June 17, 2015): 3305–20. http://dx.doi.org/10.1021/acs.jctc.5b00335.

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26

Marsagishvili, Tamaz, Jimsher Aneli, and Gennady Zaikov. "On the Processes of the Charge Transfer in the Electrical Conducting Polymer Materials." Chemistry & Chemical Technology 7, no. 2 (June 10, 2013): 175–80. http://dx.doi.org/10.23939/chcht07.02.175.

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27

Gichan, O. I. "Dynamic instabilities on a charged boundary: influence of mass transfer." Reports of the National Academy of Sciences of Ukraine, no. 10 (November 16, 2016): 47–53. http://dx.doi.org/10.15407/dopovidi2016.10.047.

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28

Song, Hongwei, Baojiu Chen, Hongshang Peng, and Jisen Zhang. "Light-induced change of charge transfer band in nanocrystalline Y2O3:Eu3+." Applied Physics Letters 81, no. 10 (September 2, 2002): 1776–78. http://dx.doi.org/10.1063/1.1501441.

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29

Shiraki, Y., and K. Ohta. "Formation of negatively-charged excitions and charge transfer in quantum dots." Microelectronic Engineering 47, no. 1-4 (June 1999): 107–9. http://dx.doi.org/10.1016/s0167-9317(99)00163-x.

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30

Shilstein, S. Sh. "Interrelation of charge transfer and crystal volume change in complex oxides." Physica C: Superconductivity 370, no. 1 (April 2002): 59–62. http://dx.doi.org/10.1016/s0921-4534(01)00963-7.

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31

Bao-Wei, Ding, and Hu Bi-Tao. "Ionization and Charge Transfer of Atomic Hydrogen by Highly Charged Ions." Chinese Physics Letters 27, no. 4 (April 2010): 043401. http://dx.doi.org/10.1088/0256-307x/27/4/043401.

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32

Schreiber, M. "Charge Transfer Instability with Structural Change: Three-Sites Three-Electrons System." Journal of the Physical Society of Japan 56, no. 3 (March 15, 1987): 1029–42. http://dx.doi.org/10.1143/jpsj.56.1029.

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33

Munn, R. W., W. G. Mabbott, and M. Pope. "Metastable binding of excess charges to charge-transfer excitons in tetracene." Chemical Physics 139, no. 2-3 (December 1989): 339–45. http://dx.doi.org/10.1016/0301-0104(89)80146-6.

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34

Borse, Dinesh Dadasaheb, and Dr D. M. Gujarathi Dr. D. M. Gujarathi. "Direct Cash Transfer- A Real Game Changer." Paripex - Indian Journal Of Research 2, no. 1 (January 15, 2012): 12–13. http://dx.doi.org/10.15373/22501991/jan2013/5.

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35

Nakajima, Yusuke, and Tetsuo Koizumi. "Transfer ionization processes in charge-transfer reactions between slowly moving, highly charged ions and atoms." Physica Scripta T156 (September 1, 2013): 014035. http://dx.doi.org/10.1088/0031-8949/2013/t156/014035.

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36

Vikhnin, V. S. "Charge Transfer Vibronic Excitons: Charge-Transfer Lattice-Instability Effects." Physics of the Solid State 47, no. 8 (2005): 1548. http://dx.doi.org/10.1134/1.2014512.

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37

Junghäuhnel, Gerhard, and Wolfgang Regenstein. "Charge-Transfer-Komplexe; Die Charge-Transfer-Bande fester Komplexe." Zeitschrift für Chemie 13, no. 8 (September 1, 2010): 306–8. http://dx.doi.org/10.1002/zfch.19730130825.

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38

Schröder, Christian, Alex Lyons, and Steven W. Rick. "Polarizable MD simulations of ionic liquids: How does additional charge transfer change the dynamics?" Physical Chemistry Chemical Physics 22, no. 2 (2020): 467–77. http://dx.doi.org/10.1039/c9cp05478b.

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A new model for treating charge transfer in ionic liquids is developed and applied to 1-ethyl-3-methylimidazolium tetrafluoroborate. The model allows for us to examine the roles of charge transfer, polarizability, and charge scaling effects on the dynamics of ionic liquids.

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39

Kusakabe, T., T. Horiuchi, N. Nagai, H. Hanaki, I. Konomi, and M. Sakisaka. "Charge transfer of multiply charged slow argon, krypton and xenon ions on atomic and molecular targets. Single-charge transfer cross sections." Journal of Physics B: Atomic and Molecular Physics 19, no. 14 (July 28, 1986): 2165–74. http://dx.doi.org/10.1088/0022-3700/19/14/011.

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40

Junghähnel, Gerhard, Roland Gall, Herbert Götz, and Gerold Proksch. "Charge-Transfer-Komplexe: Zum experimentellen Nachweis von Charge-Transfer-Mehrfachbanden im Reflexionsspektrum adsorbierter Charge-Transfer-Komplexe." Zeitschrift für Chemie 11, no. 7 (September 1, 2010): 271–72. http://dx.doi.org/10.1002/zfch.19710110721.

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41

RAJARAM, Otthakal V., and William H. SAWYER. "Effects of charged lipids on the interaction of cholesteryl ester transfer protein with lipid microemulsions." Biochemical Journal 322, no. 1 (February 15, 1997): 159–65. http://dx.doi.org/10.1042/bj3220159.

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This study reports the effects of charged lipids on the transfer of cholesteryl-1-pyrene decanoate (Py-CE) between apolipoprotein-free microemulsion particles mediated by cholesteryl ester transfer protein (CETP). The surface charge characteristics of microemulsion particles composed of cholesteryl oleate and egg yolk phosphatidylcholine were altered by incorporating phosphatidylserine, oleate or stearylamine into the phosphatidylcholine that forms the surface monolayer of the particle. The transfer of Py-CE was measured continuously by following the decrease in excimer fluorescence that accompanies the transfer of the probe from donor to acceptor particles [Rajaram, Chan and Sawyer (1994) Biochem. J. 304, 423Ő430]. The inclusion of 20 mol% phosphatidylserine relative to the phospholipid in the surface monolayer of the emulsion caused a 64% decrease in the first-order rate constant describing the transfer. An increase in ionic strength caused a partial reversal of this effect, indicating that electrostatic factors are only partially responsible for the interaction with lipid. Complete inhibition of transfer was observed when 10 mol% sodium oleate was incorporated into the surface monolayer. The incorporation of stearylamine into the emulsion caused a 32% increase in the transfer rate. The binding of CETP to the different emulsion surfaces was also examined using a surface plasmon resonance biosensor. The presence of negatively charged lipid (phosphatidylserine or oleic acid) decreased the rate of association of CETP with the emulsion without a significant change in the dissociation rate constant. The presence of the positively charged lipid stearylamine increased the rate of association of CETP with the lipid surface. It is concluded that a negative surface charge on the monolayer decreases the rate of transfer by decreasing the affinity of CETP for these particles.

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42

Tetsuo, KUWABARA, SATAKE Ryota, GUO Haocheng, KATSUMATA Masayo, TAKAHASHI Masaki, SUZUKI Yasutada, OHTSUKI Takashi, SATO Tetsuya, and KUROKAWA Hideki. "Ion Detection by Intramolecular Charge-transfer Absorption of Benzocrown-bipyridinium Conjugate Appending Octadecyl Chain." Journal of Ion Exchange 27, no. 2 (2016): 27–32. http://dx.doi.org/10.5182/jaie.27.27.

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43

Xu Xiang, 徐翔, 张莹 Zhang Ying, 刘增辉 Liu Zenghui, 白杏 Bai Xing, 王骏 Wang Jun, 闫庆 Yan Qing, and 华灯鑫 Hua Dengxin. "层间电荷转移增强二硫化铼/石墨烯异质结薄膜的反饱和吸收特性." Acta Optica Sinica 41, no. 20 (2021): 2016002. http://dx.doi.org/10.3788/aos202141.2016002.

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44

Chubykalo, Andrew, and Viktor Kuligin. "The Tesla Currents in Electrodynamics." Applied Physics Research 10, no. 5 (September 27, 2018): 79. http://dx.doi.org/10.5539/apr.v10n5p79.

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The paper theoretically shows that the Maxwell equations in the Lorentz gauge deal with not only inertial charged particles, but also charged particles that do not have inertia (virtual charges). Virtual charges appear on the surface of metals. Their movement is the currents of Tesla. Experiments confirming their existence are presented, and some features that reveal them. The influence of virtual currents on the process of transfer of conduction electrons in p-n junctions of semiconductor devices is especially interesting. The results obtained can change our understanding of phenomena in the microcosm.

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45

Revathi Shree, K. "Inductive Power Transfer to Charge Electric Bicycles." Asian Journal of Electrical Sciences 8, S1 (June 5, 2019): 25–28. http://dx.doi.org/10.51983/ajes-2019.8.s1.2313.

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Inductive power transfer is nothing but wireless power transfer. That is transferring power from transmitter to receiver side without any physical contact. Nowadays this technique has wide applications. Mainly it is used to charge the batteries of the electric vehicles (EV). Due to the increasing pollution rate and scarcity of fuel in future days, the demand for the electric vehicles is increasing. Charging EV’s using IPT is simpler and risk free when compared to traditional wired charging systems. Using IPT technique the battery can be charged in constant current (CC) and constant voltage (CV) modes without using any feedback. A switch (consists of 2 AC switches and capacitor) is used to change the mode from CC to CV. The current output from the CC and the voltage output from the CV mode are load independent. This can be obtained by proper selection of inductances and capacitors. Here the feedback control techniques are not required to regulate the output according to charging profile. This IPT technique to charge battery is economical because using a single inverter many batteries can be charged at a time. The possibility of this method of charging is tested with an experimental prototype for efficiency and using MATLAB/SIMULINK software the simulation results are obtained for stability of current and voltage output of CC and CV mode.

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46

Martiradonna, Luigi. "Tunable charge transfer." Nature Materials 15, no. 1 (December 18, 2015): 3. http://dx.doi.org/10.1038/nmat4530.

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47

Mulliken, Robert S. "Charge-Transfer Spectra." Molecular Crystals and Liquid Crystals 126, no. 1 (January 1985): 1–7. http://dx.doi.org/10.1080/15421408508084149.

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48

Dennerl, Konrad. "Charge Transfer Reactions." Space Science Reviews 157, no. 1-4 (December 2010): 57–91. http://dx.doi.org/10.1007/s11214-010-9720-5.

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49

Philipp, Hal. "Charge transfer sensing." Sensor Review 19, no. 2 (June 1999): 96–105. http://dx.doi.org/10.1108/02602289910266250.

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50

Xu, Kang. "Diffusionless charge transfer." Nature Energy 4, no. 2 (January 28, 2019): 93–94. http://dx.doi.org/10.1038/s41560-019-0328-z.

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