Rising atmospheric levels of carbon dioxide and the depletion of fossil fuel reserves raise serious concerns about the ensuing effects on the global climate and future energy supply. Utilizing the abundant solar energy to convert CO2 into fuels such as methane or methanol could address both problems simultaneously as well as provide a convenient means of energy storage. In this Review, current approaches for the heterogeneous photocatalytic reduction of CO2 on TiO2 and other metal oxide, oxynitride, sulfide, and phosphide semiconductors are presented. Research in this field is focused primarily on the development of novel nanostructured photocatalytic materials and on the investigation of the mechanism of the process, from light absorption through charge separation and transport to CO2 reduction pathways. The measures used to quantify the efficiency of the process are also discussed in detail.

Photocatalytic reduction of CO2 on TiO2 and other semiconductors.

Since the time of the industrial revolution, the atmospheric CO(2) concentration has risen by nearly 35 % to its current level of 383 ppm. The increased carbon dioxide concentration in the atmosphere has been suggested to be a leading contributor to global climate change. To slow the increase, reductions in anthropogenic CO(2) emissions are necessary. Large emission point sources, such as fossil-fuel-based power generation facilities, are the first targets for these reductions. A benchmark, mature technology for the separation of dilute CO(2) from gas streams is via absorption with aqueous amines. However, the use of solid adsorbents is now being widely considered as an alternative, potentially less-energy-intensive separation technology. This Review describes the CO(2) adsorption behavior of several different classes of solid carbon dioxide adsorbents, including zeolites, activated carbons, calcium oxides, hydrotalcites, organic-inorganic hybrids, and metal-organic frameworks. These adsorbents are evaluated in terms of their equilibrium CO(2) capacities as well as other important parameters such as adsorption-desorption kinetics, operating windows, stability, and regenerability. The scope of currently available CO(2) adsorbents and their critical properties that will ultimately affect their incorporation into large-scale separation processes is presented.

Adsorbent Materials for Carbon Dioxide Capture from Large Anthropogenic Point Sources

http://ieeexplore.ieee.org/iel5/5610941/5624686/05624745.pdf

Power electronics

A review on the utilization of fly ash

Advances in CO2 capture technology—The U.S. Department of Energy's Carbon Sequestration Program ☆

A series of CdSe quantum dot (QD)-sensitized TiO2 heterostructures have been synthesized, characterized, and tested for the photocatalytic reduction of CO2 in the presence of H2O. Our results show that these heterostructured materials are capable of catalyzing the photoreduction of CO2 using visible light illumination (λ > 420 nm) only. The effect of removing surfactant caps from the CdSe QDs by annealing and using a hydrazine chemical treatment have also been investigated. The photocatalytic reduction process is followed using infrared spectroscopy to probe the gas-phase reactants and gas chromatography to detect the products. Gas chromatographic analysis shows that the primary reaction product is CH4, with CH3OH, H2, and CO observed as secondary products. Typical yields of the gas-phase products after visible light illumination (λ > 420 nm) were 48 ppm g−1 h−1 of CH4, 3.3 ppm g−1 h−1 of CH3OH (vapor), and trace amounts of CO and H2.

Visible Light Photoreduction of CO2 Using CdSe/Pt/TiO2 Heterostructured Catalysts

Active sites and structure–activity relationships for methanol synthesis from a stoichiometric mixture of CO2 and H2 were investigated for a series of coprecipitated Cu-based catalysts with temperature-programmed reduction (TPR), X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and N2O decomposition. Experiments in a reaction chamber attached to an XPS instrument show that metallic Cu exists on the surface of both reduced and spent catalysts and there is no evidence of monovalent Cu+ species. This finding provides reassurance regarding the active oxidation state of Cu in methanol synthesis catalysts because it is observed with 6 compositions possessing different metal oxide additives, Cu particle sizes, and varying degrees of ZnO crystallinity. Smaller Cu particles demonstrate larger turnover frequencies (TOF) for methanol formation, confirming the structure sensitivity of this reaction. No correlation between TOF and lattice strain in Cu crystallite...

Active Sites and Structure−Activity Relationships of Copper-Based Catalysts for Carbon Dioxide Hydrogenation to Methanol

http://absimage.aps.org/image/MAR10/MWS_MAR10-2009-001303.pdf

Visible light photoreduction of CO$_{2}$ using CdSe/Pt/TiO$_{2}$ heterostructured catalysts

http://www.netl.doe.gov/File%20Library/Research/Coal/ewr/co2/Improved-immobilized-carbon-dioxide-capture-sorbents.pdf

John P. Baltrus

Papers

Visible Light Photoreduction of CO2 Using CdSe/Pt/TiO2 Heterostructured Catalysts

Active Sites and Structure−Activity Relationships of Copper-Based Catalysts for Carbon Dioxide Hydrogenation to Methanol

Visible light photoreduction of CO$_{2}$ using CdSe/Pt/TiO$_{2}$ heterostructured catalysts

Improved immobilized carbon dioxide capture sorbents

Performance of immobilized tertiary amine solid sorbents for the capture of carbon dioxide