1974
DOI: 10.1039/c39740000158
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Electrocatalysis by metal phthalocyanines in the reduction of carbon dioxide

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Cited by 278 publications
(185 citation statements)
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“…This article must therefore be hereby marked "advertisement" in accordance with 18 U. S. C. §1734 solely to indicate this fact. On the other hand, metal complexes in general, and cobalt complexes in particular, are able to bind CO2 (24)(25)(26)(27)(28)(29)(30)(31)(32) and to act as electrocatalysts for its reduction (33)(34)(35)(36), for instance to CO by the overall reaction 4 (36).…”
mentioning
confidence: 99%
“…This article must therefore be hereby marked "advertisement" in accordance with 18 U. S. C. §1734 solely to indicate this fact. On the other hand, metal complexes in general, and cobalt complexes in particular, are able to bind CO2 (24)(25)(26)(27)(28)(29)(30)(31)(32) and to act as electrocatalysts for its reduction (33)(34)(35)(36), for instance to CO by the overall reaction 4 (36).…”
mentioning
confidence: 99%
“…126 In aqueous solutions of tetraalkylammonium salts, current-potential curves at a cobalt phthalocyanine (Co-Pc)-coated graphite electrode showed a reduction current peak whose height was proportional to the CO2 concentration and to the square root of the potential sweep rate at a given CO2 concentration. On electrolysis, oxalic acid and glycolic acid were detected, but formic acid was not.…”
Section: Metal Complexes Of N-macrocyclesmentioning
confidence: 99%
“…Such anchoring sites are part of molecular structures of quite different complexity: by controlling the structural parameters of the ligands, it is possible to control the utilization of the metal complexes in the reduction of CO 2 . Mono-, di-and poly-dentate phosphines with moieties of various basicity and acidity strongly influence the properties of the catalyst [19]. N-macrocyclic ligands have been intensively investigated [20][21][22] as well as dipyridine [23].…”
Section: The Direct Electro-reduction Of Carbon Dioxide In Watermentioning
confidence: 99%