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Carbon dioxide reduction mechanism on Ru-based electrocatalysts [Ru(bpy)(2)(CO)(2)](2+) : insights from first-principles theory

Damas, Giane Benvinda (author)
Uppsala universitet,Linköpings universitet,Kemi,Tekniska fakulteten,Uppsala Univ, Dept Phys & Astron, Mat Theory Div, Box 530, S-75121 Uppsala, Sweden.;Linköping Univ, Dept Phys Chem & Biol, S-58183 Linköping, Sweden.,Materialteori
Ivashchenko, Dmytro A. (author)
University Lyon, FRA,Univ Lyon 1, Univ Lyon, Ens Lyon, Lab Chim,UMR 5182,CNRS, Lyon, France.
Rivalta, Ivan (author)
University Lyon, FR;University Bologna, ITA,Univ Lyon 1, Univ Lyon, Ens Lyon, Lab Chim,UMR 5182,CNRS, Lyon, France.;Univ Bologna, Dipartimento Chim Ind Toso Montanari, Bologna, Italy.
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Araujo, Moyses, 1975- (author)
Uppsala universitet,Karlstads universitet,Institutionen för ingenjörsvetenskap och fysik (from 2013),Uppsala University,Uppsala Univ, Dept Phys & Astron, Mat Theory Div, Box 530, S-75121 Uppsala, Sweden.;Karlstad Univ, Dept Engn & Phys, S-65188 Karlstad, Sweden.,Materialteori
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 (creator_code:org_t)
2021
2021
English.
In: Sustainable Energy & Fuels. - : Royal Society of Chemistry. - 2398-4902. ; 5:23, s. 6066-6076
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Solar fuel production through the so-called artificial photosynthesis has attracted a great deal of attention to the development of a new world energy matrix that is renewable and environmentally friendly. This process is characterized by light absorption with enough photon energy to generate conduction electrons, which drive the carbon dioxide reduction to produce organic fuels. It is also common to couple Ru-complex electrocatalysts to form a more efficient and selective hybrid system for this application. In this work, we have undertaken a thorough investigation of the redox reaction mechanism of Ru-based electrocatalysts by means of density functional theory (DFT) methods under the experimental conditions that have been previously reported. More specifically, we have studied the electrochemistry and catalytic activity of the [Ru(bpy)(2)(CO)(2)](2+) coordination complex. Our theoretical assessment supports the following catalytic cycle: (i) [Ru(bpy)(2)(CO)(2)](2+) is transformed into [Ru(bpy)(2)(CO)](0) upon two-electron reduction and CO release; (ii) [Ru(bpy)(2)(CO)](0) is protonated to form the [Ru(bpy)(2)(CO)H](+) hydride complex; (iii) CO2 is activated by the hydride complex through an electrophilic addition to form the [Ru(bpy)(2)(CO)(OCHO)](+) intermediate; (iv) the resulting formic acid ligand is released in solution; and, finally, (v) the CO ligand is reattached to the complex to recover the initial [Ru(bpy)(2)(CO)(2)](2+) catalyst.

Subject headings

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)
NATURVETENSKAP  -- Fysik (hsv//swe)
NATURAL SCIENCES  -- Physical Sciences (hsv//eng)
NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)
NATURVETENSKAP  -- Kemi -- Annan kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Other Chemistry Topics (hsv//eng)
NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)

Keyword

Chemistry
Kemi

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