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Electrochemical CO2 Utilisation
CO2 Capture & Utilisation
CO2 Capture & Utilisation
CO2 Capture & Utilisation
CO2 Capture & Utilisation
Power production from combustion of fossil fuels releases CO2, which is mainly responsible for global warming and cause severe problems to both ecology and human beings. The rise in atmospheric CO2 levels must be slowed or reverted to avoid undesirable climate change. Materials capable of cost-effective CO2 conversion into chemicals and fuels would help in stabilizing the atmospheric levels of greenhouse gas. The potential products can be obtained with CO2 conversion are formic acid, methanol, CO and ethylene. At present there is no commercially viable process for the conversion of CO2 to useful chemicals and the current state-of-the-art materials are expensive, which limit commercial implementation. For example, although several materials are known for the electrochemical conversion of CO2, until now only precious metals such as Au and Ag could promote this process with Faradaic efficiency more than 80%. Because of the durability and poisoning effect many efficient catalysts are far beyond commercialization. We strategically focus on the synthesis of nanomaterials in various forms (metals, bimetals, alloys, intermetallic, core shell etc.) and study their efficiency in the photochemical, electrochemical and heterogeneous conversion of CO2 into fuel and chemicals. The reaction mechanism and kinteics are completely understood by a detailed electronic structure calculations. Our materials and methods are expected to have the potential to convert waste CO2 to produce gasoline, diesel fuel, jet fuel, and industrial chemicals.
Power production from combustion of fossil fuels releases CO2, which is mainly responsible for global warming and cause severe problems to both ecology and human beings. The rise in atmospheric CO2 levels must be slowed or reverted to avoid undesirable climate change. Materials capable of cost-effective CO2 conversion into chemicals and fuels would help in stabilizing the atmospheric levels of greenhouse gas. The potential products can be obtained with CO2 conversion are formic acid, methanol, CO and ethylene. At present there is no commercially viable process for the conversion of CO2 to useful chemicals and the current state-of-the-art materials are expensive, which limit commercial implementation. For example, although several materials are known for the electrochemical conversion of CO2, until now only precious metals such as Au and Ag could promote this process with Faradaic efficiency more than 80%. Because of the durability and poisoning effect many efficient catalysts are far beyond commercialization. We strategically focus on the synthesis of nanomaterials in various forms (metals, bimetals, alloys, intermetallic, core shell etc.) and study their efficiency in the photochemical, electrochemical and heterogeneous conversion of CO2 into fuel and chemicals. The reaction mechanism and kinteics are completely understood by a detailed electronic structure calculations. Our materials and methods are expected to have the potential to convert waste CO2 to produce gasoline, diesel fuel, jet fuel, and industrial chemicals.
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Publication List (2012)
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Metal flux crystal growth technique in the determination of ordered superstructure in EuInGe. Subbarao, U.; Sebastian, A.; Rayaprol, S.; Yadav, C. S.; Svane, A.; Vaitheeswaran, G. and Peter, S. C. Cryst. Growth Des., 2012, 13, 352.
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Metallic Yb2AuGe3: An ordered superstructure in the AlB2 type family with mixed valent Yb and a high temperature phase transition. Peter, S. C.; Sarkar, S.; and Kanatzidis, M.G. Inorg. Chem., 2012, 51, 10793.
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Single crystal growth of europium and ytterbium based intermetallic compounds using metal flux technique. Sarkar, S.; and Peter, S. C. J. Chem. Sci., 2012, 124, 385.
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Crystal structure of YbCu6In6 and mixed valence behavior of Yb in YbCu6-xIn6+x (x = 0, 1, 2) solid solution. Subbarao, U.; and Peter, S. C. Inorg. Chem., 2012, 51, 6326.
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EuLiGe2 and YbLiGe2 – A divalent and an intermediate-valent compound with CaLiSi2-type structures. Iyer, A.K.; and Peter, S. C. Eur. J. Inorg. Chem., 2012, 2012, 1790.
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The polygallides. Yb3Ga7Ge3 and YbGa4Ge2. Peter, S. C.; Malliakas, C.D.; Nakotte, H.; Kothapilli, K.; Rayaprol, S.; Schultz, A.J.; Kanatzidis, M.G. J. Solid State Chem., 2012, 187, 200.
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Yb4LiGe4 – A Yb mixed valent Zintl phase with strong electronic correlations. Peter, S. C.; Disseler, S. M.; Svensson, J. N.; Carretta, P.; and Graf, M. J. J. Alloys Compd., 2012, 516, 126.
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ThSi2 type ytterbium disilicide and its analogues YbTxSi2-x (T = Cr, Fe, Co). Peter, S.C.; and Kanatzidis, M. G. Z. Anorg. Allg. Chem., 2012, 638, 287.