Bibliografías temáticas / Marcus-Hush formalism

Literatura académica sobre el tema "Marcus-Hush formalism"

Autor: Grafiati
Publicado: 6 de septiembre de 2023

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Artículos de revistas sobre el tema "Marcus-Hush formalism"

1

Protsenko, V. S. y F. I. Danilov. "Application of dimensional analysis and similarity theory for simulation of electrode kinetics described by the Marcus–Hush–Chidsey formalism". Journal of Electroanalytical Chemistry 669 (marzo de 2012): 50–54. http://dx.doi.org/10.1016/j.jelechem.2012.01.028.

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Woźna, Agnieszka y Andrzej Kapturkiewicz. "The luminescence properties of the heteroleptic [Re(CO)3(N∩N)Cl] and [Re(CO)3(N∩N)(CH3CN)]+ complexes in view of the combined Marcus–Jortner and Mulliken–Hush formalism". Physical Chemistry Chemical Physics 17, n.º 45 (2015): 30468–80. http://dx.doi.org/10.1039/c5cp05167c.

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Unified description of the radiative kr and non-radiative knr rate constants characterizing the 3*MLCT → S0 processes allows deeper insights into the luminescence properties of the heteroleptic [Re(CO)3(α-diimine)(CH3CN)]+ and [Re(CO)3(α-diimine)Cl] chelates.
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3

Kamecka, Anna y Andrzej Kapturkiewicz. "The luminescence properties of heteroleptic [OsCl(CO)(N∩N)(P∩P)]+complexes – radiative and non-radiative deactivation of the excited3*MLCT state". Physical Chemistry Chemical Physics 17, n.º 36 (2015): 23332–45. http://dx.doi.org/10.1039/c5cp03299g.

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4

Suwatchara, Danu, Martin C. Henstridge, Neil V. Rees, Eduardo Laborda y Richard G. Compton. "Comparative evaluation of the symmetric and asymmetric Marcus–Hush formalisms of electrode kinetics – The one-electron oxidation of tetraphenylethylene in dichloromethane on platinum microdisk electrodes". Journal of Electroanalytical Chemistry 677-680 (julio de 2012): 120–26. http://dx.doi.org/10.1016/j.jelechem.2012.05.015.

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5

Suwatchara, Danu, Neil V. Rees, Martin C. Henstridge, Eduardo Laborda y Richard G. Compton. "Experimental comparison of the Butler–Volmer and Marcus–Hush–Chidsey formalisms of electrode kinetics: The reduction of cyclooctatetraene at mercury hemispherical electrodes via cyclic and square wave voltammetries". Journal of Electroanalytical Chemistry 665 (enero de 2012): 38–44. http://dx.doi.org/10.1016/j.jelechem.2011.11.009.

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6

Zhu, Guang Yuan, Yi Qin, Miao Meng, Suman Mallick, Hang Gao, Xiaoli Chen, Tao Cheng et al. "Crossover between the adiabatic and nonadiabatic electron transfer limits in the Landau-Zener model". Nature Communications 12, n.º 1 (19 de enero de 2021). http://dx.doi.org/10.1038/s41467-020-20557-7.

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AbstractThe semiclassical models of nonadiabatic transition were proposed first by Landau and Zener in 1932, and have been widely used in the study of electron transfer (ET); however, experimental demonstration of the Landau-Zener formula remains challenging to observe. Herein, employing the Hush-Marcus theory, thermal ET in mixed-valence complexes {[Mo2]-(ph)n-[Mo2]}+ (n = 1–3) has been investigated, spanning the nonadiabatic throughout the adiabatic limit, by analysis of the intervalence transition absorbances. Evidently, the Landau-Zener formula is valid in the adiabatic regime in a broader range of conditions than the theoretical limitation known as the narrow avoided-crossing. The intermediate system is identified with an overall transition probability (κel) of ∼0.5, which is contributed by the single and the first multiple passage. This study shows that in the intermediate regime, the ET kinetic results derived from the adiabatic and nonadiabatic formalisms are nearly identical, in accordance with the Landau-Zener model. The obtained insights help to understand and control the ET processes in biological and chemical systems.
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