quick-relievers 发表于 2025-3-21 18:30:39

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学术讨论会 发表于 2025-3-21 20:15:26

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脖子 发表于 2025-3-22 02:25:45

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公社 发表于 2025-3-22 06:05:22

https://doi.org/10.1007/978-1-4020-5281-1the solvation of electrodes quantitatively. Exceptions are the attempts that have been made to evaluate the contribution of the . potential to the total potential drop at the metal-solution interface, but even here there is still controversy as to magnitude and even sign (cf. Chapter 5 on potentials of zero charge).

同音 发表于 2025-3-22 12:22:34

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Nefarious 发表于 2025-3-22 14:04:03

Ye Yaoxian,Niu Zezhen,Huang Jiguanglayer; . is the Faraday; .. is the charge of the ionic species ., including the sign; and .. is the surface excess of that component in the interphase, in moles per unit area of the interface. The charge on the solution side of the double layer .. is equal and opposite in sign to the charge on the metal (.. = −..)

Nefarious 发表于 2025-3-22 18:52:29

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glamor 发表于 2025-3-22 23:41:16

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易改变 发表于 2025-3-23 02:33:14

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欢乐中国 发表于 2025-3-23 07:57:39

tion in the double layer. Such "maps of the double layer" can be given with reasonable certainty up to concentrations of about 1 N for mercury in contact with solutions of inorganic ions. However, this is-or was until very recently-the extent of the know­ ledge. The problems confronting a fundamental approach978-1-4684-1733-3978-1-4684-1731-9
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查看完整版本: Titlebook: Electrosorption; Eliezer Gileadi Book 1967 Plenum Press 1967 Atom.Diffusion.Langmuir.Sorption.adsorption.catalysis.catalyst.electrochemist