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Artykuły w czasopismach na temat „Metal-metal charge transfer”

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Data publikacji: 6 września 2023

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1

Lind, Thomas, i 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, nr 1 (26.03.1997): 1–14. http://dx.doi.org/10.1127/njmm/1997/1997/1.

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2

Labadz, A. F., i J. Lowell. "Charge transfer across metal-SiO2interfaces". Journal of Physics D: Applied Physics 24, nr 8 (14.08.1991): 1416–21. http://dx.doi.org/10.1088/0022-3727/24/8/028.

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3

Lachinov, A. N., T. G. Zagurenko, V. M. Kornilov, A. I. Fokin, I. V. Aleksandrov i R. Z. Valiev. "Charge transfer in a metal-polymer-nanocrystalline metal system". Physics of the Solid State 42, nr 10 (październik 2000): 1935–41. http://dx.doi.org/10.1134/1.1318890.

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4

Akande, A. R., i J. Lowell. "Charge transfer in metal/polymer contacts". Journal of Physics D: Applied Physics 20, nr 5 (14.05.1987): 565–78. http://dx.doi.org/10.1088/0022-3727/20/5/002.

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5

Liu, Tao, Yan-Juan Zhang, Shinji Kanegawa i Osamu Sato. "Photoinduced Metal-to-Metal Charge Transfer toward Single-Chain Magnet". Journal of the American Chemical Society 132, nr 24 (23.06.2010): 8250–51. http://dx.doi.org/10.1021/ja1027953.

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6

Zhao, Jianjun, Matthias Wasem, Christopher R. Bradbury i David J. Fermín. "Charge Transfer across Self-Assembled Nanoscale Metal−Insulator−Metal Heterostructures". Journal of Physical Chemistry C 112, nr 18 (15.04.2008): 7284–89. http://dx.doi.org/10.1021/jp7101644.

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7

Glass, Elliot N., John Fielden, Zhuangqun Huang, Xu Xiang, Djamaladdin G. Musaev, Tianquan Lian i Craig L. Hill. "Transition Metal Substitution Effects on Metal-to-Polyoxometalate Charge Transfer". Inorganic Chemistry 55, nr 9 (15.04.2016): 4308–19. http://dx.doi.org/10.1021/acs.inorgchem.6b00060.

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8

Chisholm, Malcolm H. "Charge distribution in metal to ligand charge transfer states of quadruply bonded metal complexes". Coordination Chemistry Reviews 282-283 (styczeń 2015): 60–65. http://dx.doi.org/10.1016/j.ccr.2014.03.034.

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9

Jiang, Wenjing, Chengqi Jiao, Yinshan Meng, Liang Zhao, Qiang Liu i Tao Liu. "Switching single chain magnet behaviorviaphotoinduced bidirectional metal-to-metal charge transfer". Chemical Science 9, nr 3 (2018): 617–22. http://dx.doi.org/10.1039/c7sc03401f.

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10

Rogers, David M., i J. Olof Johansson. "Metal-to-metal charge-transfer transitions in Prussian blue hexacyanochromate analogues". Materials Science and Engineering: B 227 (styczeń 2018): 28–38. http://dx.doi.org/10.1016/j.mseb.2017.10.003.

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11

Kunkely, Horst, Valeri Pawlowski i Arnd Vogler. "Optical metal-to-metal charge transfer of (μ-cyano) decaamminediosmium((III)". Inorganica Chimica Acta 238, nr 1-2 (październik 1995): 1–3. http://dx.doi.org/10.1016/0020-1693(95)04740-z.

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12

Govor, L. V., G. Reiter i J. Parisi. "When hole extraction determines charge transfer across metal-organic-metal structure". EPL (Europhysics Letters) 113, nr 5 (1.03.2016): 57002. http://dx.doi.org/10.1209/0295-5075/113/57002.

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13

Meng, Yin-Shan, Osamu Sato i Tao Liu. "Manipulating Metal-to-Metal Charge Transfer for Materials with Switchable Functionality". Angewandte Chemie International Edition 57, nr 38 (20.08.2018): 12216–26. http://dx.doi.org/10.1002/anie.201804557.

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14

Watson, R. E., M. Weinert i G. W. Fernando. "Charge transfer in transition-metal alloying: Charge-tailing effects". Physical Review B 43, nr 2 (15.01.1991): 1446–54. http://dx.doi.org/10.1103/physrevb.43.1446.

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15

Hubig, Stephan M., Sergey V. Lindeman i Jay K. Kochi. "Charge-transfer bonding in metal–arene coordination". Coordination Chemistry Reviews 200-202 (maj 2000): 831–73. http://dx.doi.org/10.1016/s0010-8545(00)00322-2.

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16

Watson, R. E., i M. Weinert. "Charge transfer in gold–alkali-metal systems". Physical Review B 49, nr 11 (15.03.1994): 7148–54. http://dx.doi.org/10.1103/physrevb.49.7148.

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17

Kulakowski, K., i A. Z. Maksymowicz. "Charge Transfer in Chromium-Transition Metal Alloys". physica status solidi (b) 130, nr 2 (1.08.1985): 629–35. http://dx.doi.org/10.1002/pssb.2221300226.

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18

Peisert, Heiko, Johannes Uihlein, Fotini Petraki i Thomas Chassé. "Charge transfer between transition metal phthalocyanines and metal substrates: The role of the transition metal". Journal of Electron Spectroscopy and Related Phenomena 204 (październik 2015): 49–60. http://dx.doi.org/10.1016/j.elspec.2015.01.005.

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19

Li, Chenfei, Xin Ying Kong, Zheng Hao Tan, Crystal Ting Yang i Han Sen Soo. "Emergence of ligand-to-metal charge transfer in homogeneous photocatalysis and photosensitization". Chemical Physics Reviews 3, nr 2 (czerwiec 2022): 021303. http://dx.doi.org/10.1063/5.0086718.

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Light energy can be harnessed by photosensitizers or photocatalysts so that some chemical reactions can be carried out under milder conditions compared to the traditional heat-driven processes. To facilitate the photo-driven reactions, a large variety of chromophores that are operated via charge transfer excitations have been reported because of their typically longer excited-state lifetimes, which are the key to the downstream photochemical processes. Although both metal-to-ligand charge transfers and ligand-to-metal charge transfers are well-established light absorption pathways; the former has been widely adopted in photocatalysis, whereas the latter has recently taken on greater importance in photosensitization applications. In this article, we review the latest developments on ligand-to-metal charge transfer photosensitization by molecular complexes across the periodic table by focusing homogeneous photocatalysis and the use of photophysical measurements and computational calculations to understand the electronic structures, photochemical processes, structure–activity relationships, and reaction mechanisms. We also present our perspectives on the possible future developments in the field.
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20

Lindsay, R., E. Michelangeli, B. G. Daniels, M. Polcik, A. Verdini, L. Floreano, A. Morgante, J. Muscat, N. M. Harrison i G. Thornton. "Surface to bulk charge transfer at an alkali metal/metal oxide interface". Surface Science 547, nr 1-2 (grudzień 2003): L859—L864. http://dx.doi.org/10.1016/j.susc.2003.10.014.

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21

Kunkely, Horst, i Arnd Vogler. "Photoredox reaction of chloromercurioferrocene induced by metal-to-metal charge transfer excitation". Journal of Photochemistry and Photobiology A: Chemistry 143, nr 2-3 (październik 2001): 209–11. http://dx.doi.org/10.1016/s1010-6030(01)00494-4.

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22

Oldenburg, Karin, i Arnd Vogler. "Optical metal-to-metal charge transfer in [FeIII(C5H4PPh2)2Re1(CO)3Cl]+". Journal of Organometallic Chemistry 544, nr 1 (październik 1997): 101–3. http://dx.doi.org/10.1016/s0022-328x(97)00329-x.

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23

Meyer, T. J. "Photochemistry of metal coordination complexes: metal to ligand charge transfer excited states". Pure and Applied Chemistry 58, nr 9 (1.01.1986): 1193–206. http://dx.doi.org/10.1351/pac198658091193.

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24

Azuma, Masaki, Yuki Sakai, Takumi Nishikubo, Masaichiro Mizumaki, Tetsu Watanuki, Takashi Mizokawa, Kengo Oka, Hajime Hojo i Makoto Naka. "Systematic charge distribution changes in Bi- and Pb-3d transition metal perovskites". Dalton Transactions 47, nr 5 (2018): 1371–77. http://dx.doi.org/10.1039/c7dt03244g.

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Charge distribution changes in Bi- and Pb-3d transition metal perovskite type oxides were examined. The change in the depth of the d level of the transition metal causes the intermetallic charge transfer.
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25

Nagae, Moichiro. "Charge transfer and coherent charge propagation in metal-insulator junctions". Physical Review B 36, nr 17 (15.12.1987): 9025–44. http://dx.doi.org/10.1103/physrevb.36.9025.

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26

Montejo-Alvaro, Fernando, Jesus A. Martínez-Espinosa, Hugo Rojas-Chávez, Diana C. Navarro-Ibarra, Heriberto Cruz-Martínez i Dora I. Medina. "CO2 Adsorption over 3d Transition-Metal Nanoclusters Supported on Pyridinic N3-Doped Graphene: A DFT Investigation". Materials 15, nr 17 (4.09.2022): 6136. http://dx.doi.org/10.3390/ma15176136.

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CO2 adsorption on bare 3d transition-metal nanoclusters and 3d transition-metal nanoclusters supported on pyridinic N3-doped graphene (PNG) was investigated by employing the density functional theory. First, the interaction of Co13 and Cu13 with PNG was analyzed by spin densities, interaction energies, charge transfers, and HUMO-LUMO gaps. According to the interaction energies, the Co13 nanocluster was adsorbed more efficiently than Cu13 on the PNG. The charge transfer indicated that the Co13 nanocluster donated more charges to the PNG nanoflake than the Cu13 nanocluster. The HUMO-LUMO gap calculations showed that the PNG improved the chemical reactivity of both Co13 and Cu13 nanoclusters. When the CO2 was adsorbed on the bare 3d transition-metal nanoclusters and 3d transition-metal nanoclusters supported on the PNG, it experienced a bond elongation and angle bending in both systems. In addition, the charge transfer from the nanoclusters to the CO2 molecule was observed. This study proved that Co13/PNG and Cu13/PNG composites are adequate candidates for CO2 adsorption and activation.
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27

Chisholm, Malcolm H. "ChemInform Abstract: Charge Distribution in Metal to Ligand Charge Transfer States of Quadruply Bonded Metal Complexes". ChemInform 46, nr 47 (listopad 2015): no. http://dx.doi.org/10.1002/chin.201547222.

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28

Shin, Yeung-gyo K., Bruce S. Brunschwig, Carol Creutz i Norman Sutin. "Electroabsorption Spectroscopy of Charge-Transfer States of Transition-Metal Complexes. 2. Metal-to-Ligand and Ligand-to-Metal Charge-Transfer Excited States of Pentaammineruthenium Complexes1". Journal of Physical Chemistry 100, nr 20 (styczeń 1996): 8157–69. http://dx.doi.org/10.1021/jp953395v.

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29

Siles, P. F., T. Hahn, G. Salvan, M. Knupfer, F. Zhu, D. R. T. Zahn i O. G. Schmidt. "Tunable charge transfer properties in metal-phthalocyanine heterojunctions". Nanoscale 8, nr 16 (2016): 8607–17. http://dx.doi.org/10.1039/c5nr08671j.

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The transport properties of phthalocyanine heterojunctions are precisely tuned via engineering of the organic heterostructure. Conductive AFM techniques allow identifying transport mechanisms and performing nanoscale spatial mapping of carrier mobility.
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30

Davydov, S. Yu. "Charge transfer in epitaxial graphene-metal substrate system". Technical Physics Letters 37, nr 5 (maj 2011): 476–77. http://dx.doi.org/10.1134/s1063785011050191.

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31

Hunt, M. R. C., S. Modesti, P. Rudolf i R. E. Palmer. "Charge transfer and structure inC60adsorption on metal surfaces". Physical Review B 51, nr 15 (15.04.1995): 10039–47. http://dx.doi.org/10.1103/physrevb.51.10039.

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32

Herber, Rolfe H., Israel Nowik i Tomoyuki Mochida. "Metal atom dynamics in a charge transfer complex". Journal of Organometallic Chemistry 696, nr 8 (kwiecień 2011): 1698–700. http://dx.doi.org/10.1016/j.jorganchem.2011.01.037.

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33

Wang, Jianyu, Deyu Lu, Chaoran Li, Yaguang Zhu, Jorge Anibal Boscoboinik i Guangwen Zhou. "Measuring Charge Transfer between Adsorbate and Metal Surfaces". Journal of Physical Chemistry Letters 11, nr 16 (29.07.2020): 6827–34. http://dx.doi.org/10.1021/acs.jpclett.0c02002.

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34

Chen, Pingyun, i Thomas J. Meyer. "Medium Effects on Charge Transfer in Metal Complexes". Chemical Reviews 98, nr 4 (czerwiec 1998): 1439–78. http://dx.doi.org/10.1021/cr941180w.

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35

Wiertel, M., R. Taranko i E. Taranko. "Charge Transfer Dynamics in Atom-Metal Surface Collisions". Acta Physica Polonica A 96, nr 6 (grudzień 1999): 769–83. http://dx.doi.org/10.12693/aphyspola.96.769.

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36

Muhammed, Mufasila Mumthaz, Aalyah Saqer Alotaibi, Fathima Alkhashman i Junais Habeeb Mokkath. "Charge-transfer excitons of metal intercalated pentacene dimers". Chemical Physics Letters 729 (sierpień 2019): 1–5. http://dx.doi.org/10.1016/j.cplett.2019.05.017.

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37

Winter, J., H. Kuzmany, A. Soldatov, P. A. Persson, P. Jacobsson i B. Sundqvist. "Charge transfer in alkali-metal-doped polymeric fullerenes". Physical Review B 54, nr 24 (15.12.1996): 17486–92. http://dx.doi.org/10.1103/physrevb.54.17486.

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38

van Ipenburg, M. E., G. J. Dirksen i G. Blasse. "Charge-transfer excitation of transition-metal-ion luminescence". Materials Chemistry and Physics 39, nr 3 (styczeń 1995): 236–38. http://dx.doi.org/10.1016/0254-0584(94)01432-g.

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39

Ciarrocchi, Carlo, Guido Colucci, Massimo Boiocchi, Donatella Sacchi, Maduka L. Weththimuni, Alessio Orbelli Biroli i Maurizio Licchelli. "Interligand Charge-Transfer Processes in Zinc Complexes". Chemistry 4, nr 3 (21.07.2022): 717–34. http://dx.doi.org/10.3390/chemistry4030051.

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Electron donor–acceptor (EDA) complexes are characterized by charge-transfer (CT) processes between electron-rich and electron-poor counterparts, typically resulting in a new absorption band at a higher wavelength. In this paper, we report a series of novel 2,6-di(imino)pyridine ligands with different electron-rich aromatic substituents and their 1:2 (metal/ligand) complexes with zinc(II) in which the formation of a CT species is promoted by the metal ion coordination. The absorption properties of these complexes were studied, showing the presence of a CT absorption band only in the case of aromatic substituents with donor groups. The nature of EDA interaction was confirmed by crystallographic studies, which disclose the electron-poor and electron-rich moieties involved in the CT process. These moieties mutually belong to both the ligands and are forced into a favorable spatial arrangement by the coordinative preferences of the metal ion.
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40

Varadwaj, Pradeep R., Arpita Varadwaj i Bih-Yaw Jin. "Ligand(s)-to-metal charge transfer as a factor controlling the equilibrium constants of late first-row transition metal complexes: revealing the Irving–Williams thermodynamical series". Physical Chemistry Chemical Physics 17, nr 2 (2015): 805–11. http://dx.doi.org/10.1039/c4cp03953j.

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41

McGhee, Joseph, i Vihar P. Georgiev. "Simulation Study of Surface Transfer Doping of Hydrogenated Diamond by MoO3 and V2O5 Metal Oxides". Micromachines 11, nr 4 (20.04.2020): 433. http://dx.doi.org/10.3390/mi11040433.

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In this work, we investigate the surface transfer doping process that is induced between hydrogen-terminated (100) diamond and the metal oxides, MoO3 and V2O5, through simulation using a semi-empirical Density Functional Theory (DFT) method. DFT was used to calculate the band structure and charge transfer process between these oxide materials and hydrogen terminated diamond. Analysis of the band structures, density of states, Mulliken charges, adsorption energies and position of the Valence Band Minima (VBM) and Conduction Band Minima (CBM) energy levels shows that both oxides act as electron acceptors and inject holes into the diamond structure. Hence, those metal oxides can be described as p-type doping materials for the diamond. Additionally, our work suggests that by depositing appropriate metal oxides in an oxygen rich atmosphere or using metal oxides with high stochiometric ration between oxygen and metal atoms could lead to an increase of the charge transfer between the diamond and oxide, leading to enhanced surface transfer doping.
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42

Al Maadhede, Taif Saad, Hadi J. M. Al-Agealy i Methaq Abdul Razzaq Mohsin. "Investigating the Probability of the Charging Transition Rate in Cu Contact to P6 System Devices". Key Engineering Materials 949 (26.07.2023): 5–12. http://dx.doi.org/10.4028/p-8edaer.

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In this paper, we investigate the probability of the charge transfer interaction process from Cu metal to P6 molecule systems using charge transfer rate calculations. The charge transfer rate from donor Cu metal to an acceptor P6 molecule dye is presented with reorientation energy, electronic drive force, and barrier height emphasis on the effects of transfer processes in the Cu/P6 system. Charge transfer flow probability from Cu metal contacts to P6 dye molecule has recently been considered within the perturbation theory method, where the charge transfer rates have been found to be affected by strength coupling and reorientation energy. The charge transfer could be occurred even at large reorientation energy, less driving force energy, and low potential barrier. It requires to reorientation the donor to acceptor energy levels to start the charge transfer. It has been found that the rate of charge transfer processes enhance the flow rate yield of the transfer cross interface dependent on the potential barrier.
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43

Barandiarán, Zoila, Andries Meijerink i Luis Seijo. "Configuration coordinate energy level diagrams of intervalence and metal-to-metal charge transfer states of dopant pairs in solids". Physical Chemistry Chemical Physics 17, nr 30 (2015): 19874–84. http://dx.doi.org/10.1039/c5cp02625c.

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Configuration coordinate diagrams, which are normally used in a qualitative manner for the energy levels of active centers in phosphors, are quantitatively obtained here for intervalence charge transfer (IVCT) states of mixed valence pairs and metal-to-metal charge transfer (MMCT) states of heteronuclear pairs, in solid hosts.
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44

Rojanasuwan, Sunit, Pakorn Prajuabwan, Annop Chanhom, Anuchit Jaruvanawat, Adirek Rangkasikorn i Jiti Nukeaw. "The Effect of the Central Metal Atom on the Structural Phase Transition of Indium Doped Metal Phthalocyanine". Advanced Materials Research 717 (lipiec 2013): 146–52. http://dx.doi.org/10.4028/www.scientific.net/amr.717.146.

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We investigate the effect of central metal atom on the phthalocyanine (Pc) molecular crystals as intercalated with indium. As dopant, indium has physical interaction with some atom in the ring of Pc molecule and there is charge transfer between indium atom and Pc ring atom. Since In-doped Pc is a hole doping which increase positive charge carriers and the HOMO of ZnPc, CuPc, NiPc and MgPc are localized on the phthalocyanine ring, then, the central metal atom e.g. Zn, Cu, Ni and Mg are not directly involved with the charge transfer between indium dopant and their Pc molecule. The structural phase transition from α phase to β phase of ZnPc upon doping with indium is another evidence for the existing of charge transfer between dopant atom and matrix Pc molecule. A comparative experiment of optical absorption spectrum of each metal Pc reveals that the central metal atom will affect the forming of crystal structure whether will be α phase or β phase as intercalated with indium.
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45

Vetrova, Daria A., i Sergey A. Kuznetsov. "Study of alkaline earth metals cations influence on the electrochemical behaviour of the Ti (IV) / Ti (III) redox couple in the CsCl — CsF melt". Transactions of the Kоla Science Centre of RAS. Series: Engineering Sciences 13, nr 1/2022 (27.12.2022): 51–57. http://dx.doi.org/10.37614/2949-1215.2022.13.1.008.

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The influence of the alkaline earth metal cations (Mg2+, Ca2+, Sr2+ и Ва2+) on the charge transfer kinetics of the Ti (IV) / Ti (III) redox couple in melts of alkali metal halides was studied by cyclic voltammetry method. Standard rate constants of charge transfer have been determined by the Nicholson method. The activation energies of the charge transfer process in the CsCl — CsF (10 wt. %) — K2TiF6 melt with the addition of alkaline earth metal cations were calculated.
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46

Freccero, Riccardo, Pavlo Solokha i Serena De Negri. "Unpredicted but It Exists: Trigonal Sc2Ru with a Significant Metal–Metal Charge Transfer". Inorganic Chemistry 60, nr 14 (9.07.2021): 10084–88. http://dx.doi.org/10.1021/acs.inorgchem.1c01168.

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47

Ma, Yuguang, Houyu Zhang, Jiacong Shen i Chiming Che. "Electroluminescence from triplet metal—ligand charge-transfer excited state of transition metal complexes". Synthetic Metals 94, nr 3 (maj 1998): 245–48. http://dx.doi.org/10.1016/s0379-6779(97)04166-0.

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48

Dakhnovskii, Yuri, Vassiliy Lubchenko i Rob D. Coalson. "Multiphoton absorption by metal–metal long distance charge‐transfer complexes in polar solvents". Journal of Chemical Physics 105, nr 21 (grudzień 1996): 9441–53. http://dx.doi.org/10.1063/1.472778.

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49

Zych, Aleksander, Annemarie Reinhardt i Barbara Albert. "Metal-to-metal charge transfer emission, its mechanism and quenching in Y2Sn2O7:Ce3+". Journal of Alloys and Compounds 723 (listopad 2017): 30–35. http://dx.doi.org/10.1016/j.jallcom.2017.06.225.

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50

Bernhardt, Paul V., Fernando Bozoglian, Brendan P. Macpherson i Manuel Martinez. "Tuning the metal-to-metal charge transfer energy of cyano-bridged dinuclear complexes". Dalton Trans., nr 16 (2004): 2582–87. http://dx.doi.org/10.1039/b407185a.

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Do bibliografii