2012
DOI: 10.1002/cctc.201200209
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Towards Artificial Photosynthesis of CO2‐Neutral Fuel: Homogenous Catalysis of CO2‐Selective Reduction to Methanol Initiated by Visible‐Light‐Driven Multi‐Electron Collector

Abstract: And there was light! Electrochemical studies demonstrated the activation of CO2 by two‐electron‐reduced ruthenium complex [(bpy)2Ru(Q)]2+ (1). The CO2‐reduction cycle was initiated by complex 1 as a photoactive electron mediator. MeOH was afforded with good selectivity from the multicomponent system, which also consisted of cobalt catalyst [Co(NDS)2]2−, a primary alcohol as a co‐catalyst, and ascorbic acid in aqueous solution.

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Cited by 12 publications
(4 citation statements)
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“…Other reducing agents. Na et al 298 have demonstrated a visible light-driven multicomponent system, that is capable of selectively reducing CO 2 to MeOH. The RuQ complex (Fig.…”
Section: Production Of Dme From Co 2 Hydrogenation Over Heterogeneous...mentioning
confidence: 99%
“…Other reducing agents. Na et al 298 have demonstrated a visible light-driven multicomponent system, that is capable of selectively reducing CO 2 to MeOH. The RuQ complex (Fig.…”
Section: Production Of Dme From Co 2 Hydrogenation Over Heterogeneous...mentioning
confidence: 99%
“…[1][2][3] The (cooperative) activation of small molecules is of particular importance for solar fuel production, considering the fact that usually several redox equivalents are required in order to overcome thermodynamically unfavored stepwise monoelectronic pathways. [4][5][6][7] Various design motifs for multielectron storage in solar energy conversion schemes have been developed over the years, including dinuclear rhodium complexes, [8][9][10][11][12][13][14][15] or a multi-electron chargeable cobalt porphyrin catalyst. [16] Bimetallic activation of CO 2 was recently reported by Jurss et al in electrocatalytic studies on an anthracene-bridged dinuclear rhenium complex.…”
Section: Introductionmentioning
confidence: 99%
“…In keeping with Na et al ( 2012), the photocatalytic reduction use, harnessing sunlight for methanol synthesis, is an environmentally promising method explored by researchers [131]. Li et al (2012) synthesized TiO 2 nanotubes (TNTs) photocatalysts through a hydrothermal process and CdS (or BI 2 S 3 )/TiO 2 nanotubes photocatalysts through direct precipitation [132].…”
Section: E-methanol's Production and Infrastructurementioning
confidence: 84%
“…The BI 2 S 3 -modified TNTs photocatalyst demonstrated superior photocatalytic activity, CO 2 adsorption capacity, and visible light absorption compared to the CdS-modified counterpart. Particularly, after 5 h of visible light exposure, the Bi 2 S 3 -modified TNTs photocatalyst achieved a maximum methanol yield of 224.6 µmol/g, approximately 2.2 times that of TNTs [131,132].…”
Section: E-methanol's Production and Infrastructurementioning
confidence: 99%