A Robust Molecular Catalyst Generated In?Situ for Photo- and Electrochemical Water Oxidation

Podrobná bibliografie
Parent link:ChemSusChem
Vol. 10, iss. 5.— 2017.— [P. 862-875]
Korporativní autor: Национальный исследовательский Томский политехнический университет (ТПУ) Институт природных ресурсов (ИПР) Кафедра технологии органических веществ и полимерных материалов (ТОВПМ)
Další autoři: Hassan H. A. Yo. Hussein Abdelazeem Younus, Ahmad N. Nazir, Chughtai A. H. Adeel, Vandichel M. Matthias, Busch M. Michael, Van H. K. Hecke Kristof, Yusubov M. S. Mekhman Suleiman-Ogly (Suleimanovich), Song Sh. Shaoxian, Verpoort F. V. K. Frensis Valter Kornelius
Shrnutí:Title screen
Water splitting is the key step towards artificial photosystems for solar energy conversion and storage in the form of chemical bonding. The oxidation of water is the bottle-neck of this process that hampers its practical utility; hence, efficient, robust, and easy to make catalytic systems based on cheap and earth-abundant materials are of exceptional importance. Herein, an in?situ generated cobalt catalyst, [CoII(TCA)2(H2O)2] (TCA=1-mesityl-1,2,3-1H-triazole-4-carboxylate), that efficiently conducts photochemical water oxidation under near-neutral conditions is presented. The catalyst showed high stability under photolytic conditions for more than 3?h of photoirradiation. During electrochemical water oxidation, the catalytic system assembled a catalyst film, which proved not to be cobalt oxide/hydroxide as normally expected, but instead, and for the first time, generated a molecular cobalt complex that incorporated the organic ligand bound to cobalt ions. The catalyst film exhibited a low overpotential for electrocatalytic water oxidation (360?mV) and high oxygen evolution peak current densities of 9 and 2.7?mA?cm?2 on glassy carbon and indium-doped tin oxide electrodes, respectively, at only 1.49 and 1.39?V (versus a normal hydrogen electrode), respectively, under neutral conditions. This finding, exemplified on the in?situ generated cobalt complex, might be applicable to other molecular systems and suggests that the formation of a catalytic film in electrochemical water oxidation experiments is not always an indication of catalyst decomposition and the formation of nanoparticles.
Jazyk:angličtina
Vydáno: 2017
Témata:
On-line přístup:http://dx.doi.org/10.1002/cssc.201601477
Médium: Elektronický zdroj Kapitola
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=656171

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200 1 |a A Robust Molecular Catalyst Generated In?Situ for Photo- and Electrochemical Water Oxidation  |f H. A. Yo. Hassan [et al.] 
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330 |a Water splitting is the key step towards artificial photosystems for solar energy conversion and storage in the form of chemical bonding. The oxidation of water is the bottle-neck of this process that hampers its practical utility; hence, efficient, robust, and easy to make catalytic systems based on cheap and earth-abundant materials are of exceptional importance. Herein, an in?situ generated cobalt catalyst, [CoII(TCA)2(H2O)2] (TCA=1-mesityl-1,2,3-1H-triazole-4-carboxylate), that efficiently conducts photochemical water oxidation under near-neutral conditions is presented. The catalyst showed high stability under photolytic conditions for more than 3?h of photoirradiation. During electrochemical water oxidation, the catalytic system assembled a catalyst film, which proved not to be cobalt oxide/hydroxide as normally expected, but instead, and for the first time, generated a molecular cobalt complex that incorporated the organic ligand bound to cobalt ions. The catalyst film exhibited a low overpotential for electrocatalytic water oxidation (360?mV) and high oxygen evolution peak current densities of 9 and 2.7?mA?cm?2 on glassy carbon and indium-doped tin oxide electrodes, respectively, at only 1.49 and 1.39?V (versus a normal hydrogen electrode), respectively, under neutral conditions. This finding, exemplified on the in?situ generated cobalt complex, might be applicable to other molecular systems and suggests that the formation of a catalytic film in electrochemical water oxidation experiments is not always an indication of catalyst decomposition and the formation of nanoparticles. 
461 |t ChemSusChem 
463 |t Vol. 10, iss. 5  |v [P. 862-875]  |d 2017 
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701 1 |a Hassan  |b H. A. Yo.  |c chemical engineer  |c assistant of Tomsk Polytechnic University  |f 1985-  |g Hussein Abdelazeem Younus  |3 (RuTPU)RU\TPU\pers\39720 
701 1 |a Ahmad  |b N.  |c chemical engineer  |c assistant of Tomsk Polytechnic University  |f 1981-  |g Nazir  |3 (RuTPU)RU\TPU\pers\39722 
701 1 |a Chughtai  |b A. H.  |g Adeel 
701 1 |a Vandichel  |b M.  |g Matthias 
701 1 |a Busch  |b M.  |g Michael 
701 1 |a Van  |b H. K.  |g Hecke Kristof 
701 1 |a Yusubov  |b M. S.  |c chemist  |c Professor of Tomsk Polytechnic University, Doctor of chemical sciences  |f 1961-  |g Mekhman Suleiman-Ogly (Suleimanovich)  |3 (RuTPU)RU\TPU\pers\31833 
701 1 |a Song  |b Sh.  |g Shaoxian 
701 1 |a Verpoort  |b F. V. K.  |c Chemical Engineer  |c Professor of Tomsk Polytechnic University, doctor of chemical Sciences  |f 1963-  |g Frensis Valter Kornelius  |3 (RuTPU)RU\TPU\pers\35059  |9 18334 
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