CO2 Reduction Catalysts and Catalysis - Texas A&M … Reduction Catalysts and Catalysis CHEM 462...
Transcript of CO2 Reduction Catalysts and Catalysis - Texas A&M … Reduction Catalysts and Catalysis CHEM 462...
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CO2 Reduction Catalysts and Catalysis
CHEM 462 Kristina Goldstein
Soomin Park
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Why does CO2 matter?
https://www.skepticalscience.com/breathing-co2-carbon-dioxide.htm (accessed 11/1/14)
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Why does CO2 matter?
http://theenergycollective.com/nrdcswitchboard/299251/strong-climate-action-requires-moving-away-fossil-fuels (accessed 11/1/1
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Outline • Introduction • Catalysis
• Historical Background • Catalyst and Kinetic Energy • Catalytic Cycle
• CO2 Reduction
• Water Gas Shift Reaction • Introducing CO2 Reduction Catalysts
• Methods
• Synthesis of Catalysts and Chemical Environments • CV and Theory • IR-SEC
• Results
• Smieja • Franco • Riplinger • Fischer-Tropsch
• Conclusions
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• Jöns Jakob Berzelius (1835, Swedish chemist)
• Wilhelm Ostwald (1909 Nobel Prize in Chemistry)
• 20th Century
Catalytic Power (history)
http://en.wikipedia.org/wiki/Jöns_Jacob_Berzelius#mediaviewer/File:Jöns_Jacob_Berzelius_daguerreotype.jpg (accessed 11/1/1 http://en.wikipedia.org/wiki/Wilhelm_Ostwald#mediaviewer/File:Wilhelm_Ostwald.jpg (accessed 11/1/14)
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Catalyst
• Rate of Reaction
• Pathway
• Activation Energy(Ea)
• Equilibrium
http://en.wikipedia.org/wiki/Catalysis#mediaviewer/File:CatalysisScheme.png (accessed 11/1/14)
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Catalyst
• Rate of Reaction
• Pathway
• Activation Energy(Ea)
• Equilibrium (Keq)
http://en.wikipedia.org/wiki/Catalysis#mediaviewer/File:CatalysisScheme.png (accessed 11/1/14)
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Catalytic Cycle
http://en.wikipedia.org/wiki/Catalytic_cycle#mediaviewer/File:Catcycle.png (accessed 11/1/14)
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CO2 Reduction (1958)
Chemical Formula Name # of articles
HCO2H formic acid 5
HCHO formaldehyde 6
CH3OH methanol 7
CH4 methane 2
CO carbon monoxide many
J. Chem. Educ., 1958, 35 (9), 446-449
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CO2 Reduction
http://newenergyandfuel.com/wp-content/uploads/2010/12/Products-From-CO2-Reforming.gif (accessed 11/1/14)
CO2 + 2 H+ + 2 e- → CO + H2O
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Green Chemistry with Carbon Dioxide
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Water Gas Shift Reaction (WGSR)
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CO2 + H2 = H2O + CO
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Water Gas Shift Reaction (WGSR)
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CO2 + H2 = H2O + CO
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Water Gas Shift Reaction (WGSR)
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Chiang et al. Inorg. Chem., 2005, 44, 9007-9016; J. Chem. Educ., 1958, 35 (9), 446-449
CO2 Reduction 15
• Catalytic Hydrogenation
• Complex Metal Hydrides
• Electrochemical Reduction
• Photocatalysis
• Biological reduction
- Carbon Monoxide DeHydrogenase: CODH
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_dioxide#mediaviewer/File:TiO2nanotube.jpg (accessed 11/1/14); M. Asadi, Nat. Commun., 2014, 5; http://www.ratbehavior.org/im
Electrochemical Reduction
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TiO2 films MoS2 flakes
Fe-porphyrin
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Transition Metals Complexes
C. Riplinger at el, 2014, http://pubs.acs.org.lib-ezproxy.tamu.edu:2048/doi/pdf/10.1021/ja508192y
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Photocatalysis
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B. A. Parkinson, P. F. Weaver, Nature, 1984, 309, 148-149
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Biological Reduction
Carbon Monoxide DeHydrogenase (CODH)
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Synthesis of Catalysts
• Smieja Study
• Riplinger Study
(white)
M=Re (white crystal), Mn (orange crystal) (yellow)
Smieja et al. Inorg. Chem. 2013, 52, 2484-2491; Riplinger et al. J. Am. Chem. Soc. 2014 (Just Accepted Manuscript)
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Synthesis Continued
(yellow)
Franco et al. Chem. Commun., 2014, 00, 1-3; Chiang et al. Inorg. Chem., 2005, 44, 9007-9016
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• Franco Catalyst
• Why use a proton-assisted process?
• Sustained catalysis in homogeneous solution even in the absence of Brønsted acids
• Reduce the large overpotentials required for multi-electron catalysis, specifically during protonation
• Long durability in solution and high selective conversion of CO2 into CO at relatively low potentials
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Chemical Environments
• Addition of protons through a variety of acids (H2O, TFE, MeOH)
• Changes to atmospheric environment
• Exposure to CO2
• Inert conditions (N2, Ar)
• Addition of different metals to ligands (Mn, Re, Pd, Rh, Ni, Fe, Co)
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Cyclic Voltammetry
• What is Cyclic Voltammetry?
• Provides insights into both the kinetic and thermodynamic details of many chemical systems via redox reactions
• Includes a working electrode, reference electrode, counter electrode, and supporting electrolyte
• Types: homogenous and heterogeneous
• Dependent on scan rate, concentration and pH
Marken et al. Electroanalytical Methods, 2010, 2, 57-105
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Theory Behind CV
• Rate of the homogeneous electron transfer step can be determined based on the measurement of peak potential and peak current data as a function of scan rate
• Reversibility determined by ratio between anodic and cathodic, peak current densities
• Internal standard consists of ferrocene, because it is completely reversible!
• Counter electrode applies current to system to keep voltage constant as the chemical system absorbs electrons
• Ohm’s Law: V=IR
• Position of electrodes matter due to effects of IR(ohmic) drop
Marken et al. Electroanalytical Methods, 2010, 2, 57-105
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Infrared-Spectroelectrochemistry (IR-SEC)
• A compliment to cyclic voltammetry
• Resolves the ambiguity of voltammetric data due to equilibrium of fast/slow steps on a voltammetric timescale in both the forward and backward direction
• Combines the thermodynamic data obtained from IR and the kinetic data obtained from CV
Marken et al. Electroanalytical Methods, 2010, 2, 57-105; Smieja et al. Inorg. Chem. 2013, 52, 2484-2491
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Smieja Results • Increased response as more equivalents of acid
were added to the CV cell
• The stronger the acid, the stronger the catalytic response
• Activated catalytic species: [Mn(bpy-tBu)(CO)3]-
• Mn(bpy-tBu)(CO)3 Br in MeCN under an Ar atmosphere
• Less overpotential than its Re counterpart
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Franco Catalyst
• Contains two acidic OH groups close to the metal centre, which showed a sustained catalytic response in homogeneous solution in the absence of acids
• Under a CO2 atmosphere in anhydrous MeCN
• Partial stabilization of intermediate due to interaction between OH-Br and O-N(bpy)
• 2-/3- reduction wave due to formation of a metal hydride
• Protons required for the catalytic process are supposed to be supplied by the Hofmann degradation of the supporting electrolyte, or hydrogen abstraction from the solvent
• Formation of HCOOH and CO confirm the presence of competing pathways and the hypothesis of hydride formation
Franco et al. Chem. Commun., 2014, 00, 1-3
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Catalytic Activation
Riplinger et al. J. Am. Chem. Soc. 2014
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CO/H2 Generation
Riplinger et al. J. Am. Chem. Soc. 2014
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Fischer-Tropsch Process • Originated from need of liquid fuels by Germany
during World War II
• Syngas from Water Shift Gas Reaction to Hydrocarbons
• Involves CO activation, C-C coupling, hydrogenation and desorption of the hydrocarbon product
• “hydrogen mediated catalytic reductive polymerization of carbon monoxide”
• Atomic details are still unclear for these steps
• Exothermic reaction, increasing heat release with longer hydrocarbon chains
• Different metal centers contribute to different hydrocarbon formations
• Interest motivated by economic viability, environmental and energy security concerns
Olusola et al. RSC Adv., 2012, 2, 7347–7366
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Conclusions
• Increasing interest in the industrial and academic communities
• A way to use a harmful greenhouse gas for synthesis of industrial compounds (CH4, CO, CH2O, Syngas)
• Multiple studies
• Purification and concentration of CO2 from the atmosphere to use the harmful levels of this greenhouse gas for energy storage
• Continue the approach to local proton sources on chelate ligands and mimicking naturally occurring catalytic systems
• Application of a solar cell to power catalysis, and separation of byproducts
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Questions ?
(accessed 2NOV2014) http://inhabitat.com/northwestern-university-develops-more-efficient-organic-solar-cell-using-algorithm-based-on-natural-evolution/
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