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      Photoredox systems with biocatalysts for CO 2utilization

      1 , 2 , 3 , 4 , 5
      Sustainable Energy & Fuels
      Royal Society of Chemistry (RSC)

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          Abstract

          Visible-light driven CO 2reduction and utilization systems involving the photoreduction of NAD(P) +or bipyridinium salt (viologen)-based electron mediators and biocatalysts are introduced.

          Abstract

          Visible-light driven redox systems have been attracting significant research attention due to their ability to produce hydrogen and reduce and utilize CO 2for the production of solar fuels and chemicals. Generally, visible-light driven redox systems consist of an electron donor, a photocatalytic dye, an electron mediator and a catalyst. One of the important components in visible-light driven redox systems is an effective catalyst for hydrogen production and reduction and utilization of CO 2. The catalysts used in visible-light driven redox systems are classified into metal nanoparticles, molecular catalysts and biocatalysts. Among them, biocatalysts are promising due to their excellent reaction and substrate selectivity, especially for the reduction and utilization of CO 2, which is remarkably higher than that of other catalysts. Among the biocatalysts for CO 2reduction and utilization, NAD(P) +-dependent dehydrogenases, which are commercially available, are widely used in visible-light driven redox systems. Formate dehydrogenase (FDH) from Candida boidiniiis a typical NAD(P) +-dependent dehydrogenase for the visible-light driven redox reduction of CO 2to formate. Furthermore, the addition of commercially available aldehyde (aldDH), formaldehyde (FldDH) and alcohol (ADH) dehydrogenase to this system results in the reduction of CO 2to methanol viaformate and formaldehyde as intermediates in visible-light driven redox systems. Furthermore, NAD(P) +-dependent dehydrogenases for decarboxylation are also commercially available and widely used for the visible-light driven formation of carbon–carbon bonds from CO 2and organic molecules. Malic enzyme (ME) from chicken liver is a typical NAD(P) +-dependent dehydrogenase with decarboxylating ability for the visible-light driven production of malate, which is based on the formation of carbon–carbon bonds from CO 2and pyruvate. In this review, visible-light driven CO 2reduction and utilization systems involving the photoreduction of NAD(P) +and biocatalysts are introduced. Furthermore, visible-light driven CO 2reduction and utilization systems involving the photoreduction of bipyridinium salt (viologen)-based electron mediators and biocatalysts also are introduced. In particular, the simplification of visible-light driven CO 2reduction and utilization systems by utilizing viologen-based electron mediators and the improvement in their efficiency without changing the structure of the biocatalyst are also discussed.

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          Most cited references186

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          New insights into the electrochemical reduction of carbon dioxide on metallic copper surfaces

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            Direct Capture of CO2 from Ambient Air.

            The increase in the global atmospheric CO2 concentration resulting from over a century of combustion of fossil fuels has been associated with significant global climate change. With the global population increase driving continued increases in fossil fuel use, humanity's primary reliance on fossil energy for the next several decades is assured. Traditional modes of carbon capture such as precombustion and postcombustion CO2 capture from large point sources can help slow the rate of increase of the atmospheric CO2 concentration, but only the direct removal of CO2 from the air, or "direct air capture" (DAC), can actually reduce the global atmospheric CO2 concentration. The past decade has seen a steep rise in the use of chemical sorbents that are cycled through sorption and desorption cycles for CO2 removal from ultradilute gases such as air. This Review provides a historical overview of the field of DAC, along with an exhaustive description of the use of chemical sorbents targeted at this application. Solvents and solid sorbents that interact strongly with CO2 are described, including basic solvents, supported amine and ammonium materials, and metal-organic frameworks (MOFs), as the primary classes of chemical sorbents. Hypothetical processes for the deployment of such sorbents are discussed, as well as the limited array of technoeconomic analyses published on DAC. Overall, it is concluded that there are many new materials that could play a role in emerging DAC technologies. However, these materials need to be further investigated and developed with a practical sorbent-air contacting process in mind if society is to make rapid progress in deploying DAC as a means of mitigating climate change.
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              Particle size effects in the catalytic electroreduction of CO₂ on Cu nanoparticles.

              A study of particle size effects during the catalytic CO2 electroreduction on size-controlled Cu nanoparticles (NPs) is presented. Cu NP catalysts in the 2-15 nm mean size range were prepared, and their catalytic activity and selectivity during CO2 electroreduction were analyzed and compared to a bulk Cu electrode. A dramatic increase in the catalytic activity and selectivity for H2 and CO was observed with decreasing Cu particle size, in particular, for NPs below 5 nm. Hydrocarbon (methane and ethylene) selectivity was increasingly suppressed for nanoscale Cu surfaces. The size dependence of the surface atomic coordination of model spherical Cu particles was used to rationalize the experimental results. Changes in the population of low-coordinated surface sites and their stronger chemisorption were linked to surging H2 and CO selectivities, higher catalytic activity, and smaller hydrocarbon selectivity. The presented activity-selectivity-size relations provide novel insights in the CO2 electroreduction reaction on nanoscale surfaces. Our smallest nanoparticles (~2 nm) enter the ab initio computationally accessible size regime, and therefore, the results obtained lend themselves well to density functional theory (DFT) evaluation and reaction mechanism verification.
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                Author and article information

                Contributors
                Journal
                SEFUA7
                Sustainable Energy & Fuels
                Sustainable Energy Fuels
                Royal Society of Chemistry (RSC)
                2398-4902
                2018
                2018
                : 2
                : 9
                : 1928-1950
                Affiliations
                [1 ]Advanced Research Institute for Natural Science and Technology
                [2 ]Osaka City University
                [3 ]Osaka 558-8585
                [4 ]Japan
                [5 ]Research Center for Artificial Photosynthesis
                Article
                10.1039/C8SE00209F
                93560b23-f78f-4e97-9b03-8c8f03784f26
                © 2018

                Free to read

                http://rsc.li/journals-terms-of-use#chorus

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