Eniya Listiani, Dewi and Kenichi, Oyaizu and Eishun, Tsuchida (2003) Four-electron reduction of dioxygen catalyzed by a decavanadium complex. Inorganica Chimica Acta (342). pp. 316-318.
[2003]_Four-electron_reduction_of_dioxygen_catalyzed_by_a_de.pdf
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Abstract
The electrochemical behavior of the modified electrodes: a Nikko Keisoku DPGS-1 dual potentiogalvanostat and a NFG-3 universal programmer were employed along with a Graphtec WX2400 X-Y recorder to obtain the voltammogram. The samples and electrolytes were set up in a conventional two-compartment cell in which a glassy carbon disk electrode served as the working electrode. The counter electrode was a platinum wire and the reference electrode was a saturated calomel electrode (SCE). , it was demonstrated that the vanadium multinuclear complex catalyzes the reduction of O2 at a high potential, which is promising to expand the wide application of the catalyst. Although the mechanism of this vanadium-based cluster complex 1 was not yet clarified, the oxophilic [V(III)] of oxovanadium(V) cluster complexes were predicted actively reacts with O2 to accomplish a four-electron reduction of O2 in acid condition as described in previous literature (2[V(III)] / O2/ 2[V(V)O]). (EMS2022)
Item Type: | Article |
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Additional Information: | DDC'23" 537.56 |
Uncontrolled Keywords: | Electrochemistry; Four-electron reduction; Dioxygen; Decavanadium |
Subjects: | Energy |
Depositing User: | - Hadiyati - |
Date Deposited: | 08 Oct 2022 01:54 |
Last Modified: | 22 Nov 2022 02:05 |
URI: | https://karya.brin.go.id/id/eprint/12221 |