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Titlebook: Electrochemical Activation of Catalysis; Promotion, Electroch Costas G. Vayenas,Symeon Bebelis,Demetrios Tsiplak Book 2001 Springer Science

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發(fā)表于 2025-3-21 16:36:51 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Electrochemical Activation of Catalysis
副標(biāo)題Promotion, Electroch
編輯Costas G. Vayenas,Symeon Bebelis,Demetrios Tsiplak
視頻videohttp://file.papertrans.cn/306/305845/305845.mp4
圖書封面Titlebook: Electrochemical Activation of Catalysis; Promotion, Electroch Costas G. Vayenas,Symeon Bebelis,Demetrios Tsiplak Book 2001 Springer Science
描述I knew nothing of the work of C. G. Vayenas on NEMCA until the early nineties. Then I learned from a paper of his idea (gas interface reactions could be catalyzed electrochemically), which seemed quite marvelous; but I did not understand how it worked. Consequently, I decided to correspond with Professor Vayenas in Patras, Greece, to reach a better understanding of this concept. I think that my early papers (1946, 1947, and 1957), on the relationship between the work function of metal surfaces and electron transfer reactions thereat to particles in solution, held me in good stead to be receptive to what Vayenas told me. As the electrode potential changes, so of course, does the work function at the interface, and gas metal reactions there involve adsorbed particles which have bonding to the surface. Whether electron transfer is complete in such a case, or whether the effect is on the desorption of radicals, the work function determines the strength of their bonding, and if one varies the work function by varying the electrode potential, one can vary the reaction rate at the interface. I got the idea. After that, it has been smooth sailing. Dr. Vayenas wrote a seminal article in Mod
出版日期Book 2001
關(guān)鍵詞Ion; catalysis; electrolyte; kinetics
版次1
doihttps://doi.org/10.1007/b115566
isbn_softcover978-1-4757-8234-9
isbn_ebook978-0-306-47551-1
copyrightSpringer Science+Business Media New York 2001
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 22:22:49 | 只看該作者
板凳
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地板
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on the desorption of radicals, the work function determines the strength of their bonding, and if one varies the work function by varying the electrode potential, one can vary the reaction rate at the interface. I got the idea. After that, it has been smooth sailing. Dr. Vayenas wrote a seminal article in Mod978-1-4757-8234-9978-0-306-47551-1
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發(fā)表于 2025-3-22 09:50:30 | 只看該作者
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Electrochemical Promotion and Metal-support Interactions,
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Costas G. Vayenas,Symeon Bebelis,Demetrios Tsiplak
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https://doi.org/10.1007/b115566Ion; catalysis; electrolyte; kinetics
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