scholarly journals A bioinspired molybdenum–copper molecular catalyst for CO2 electroreduction

2020 ◽  
Vol 11 (21) ◽  
pp. 5503-5510 ◽  
Author(s):  
Ahmed Mouchfiq ◽  
Tanya K. Todorova ◽  
Subal Dey ◽  
Marc Fontecave ◽  
Victor Mougel

A bimetallic Mo–Cu complex inspired by the active site of the carbon monoxide dehydrogenase enzyme mediates the electroreduction of carbon dioxide to formic acid.

1998 ◽  
Vol 272 (1-2) ◽  
pp. 38-42 ◽  
Author(s):  
Immacolata Tommasi ◽  
Michele Aresta ◽  
Potenzo Giannoccaro ◽  
Eugenio Quaranta ◽  
Carlo Fragale

2020 ◽  
Author(s):  
Brian Skinn ◽  
Sujat Sen ◽  
McLain Leonard ◽  
DAN WANG ◽  
Fikile R. Brushett ◽  
...  

Space programs around the globe have begun to consider the logistical demands of missions beyond the orbital neighborhood of Earth. Unlike local installations such as the International Space Station, long-range missions will not have the option to resupply critical materials from Earth. Thus, the development of capabilities for what is often termed “In-Situ Resource Utilization” (ISRU) have been a continuing focus of research through NASA and other agencies. One particular long-range mission of interest is to place human astronauts on Mars; the major component of the thin Martian atmosphere is carbon dioxide, making CO2 a natural input to ISRU technologies for production of carbon-containing materials. Production of mission consumables from in-situ Mars resources will be critical to enabling human exploration of Mars, in part by minimizing the number and size of descent/ascent vehicles. Potential ISRU products from CO2 include that seem likely to provide significant mission benefits with minimal infrastructure required are propellants (e.g., hydrocarbons), fuel cell reactants (e.g., formic acid, methanol, carbon monoxide), and life support consumables (e.g., oxygen). The first portion of this talk will comprise a high-level overview of the chemical transformations that can be imparted to CO2 via electrocatalysis on gas-diffusion electrodes (GDEs), in the form of a summary of literature reports on the catalytic performance of a wide variety of single-metallic and metal-alloy systems. The remainder will encompass an exposition of the electrocatalytic performance of tin and copper single-metal GDE electrocatalysts prepared by pulsed electrodeposition. These metals are well known for their ability to reduce carbon dioxide to formic acid and hydrocarbons/carbon monoxide, respectively, and are under active development in numerous academic research groups and industrial entities to this end. These experimental results clearly demonstrate the power and flexibility of the pulse/pulse-reverse electrodeposition approach to catalyst fabrication, as evidenced by the appreciable effects of the pulsed-waveform electrodeposition parameters on CO2 electroreduction product distribution and total current density.


1930 ◽  
Vol 3 (3) ◽  
pp. 241-251 ◽  
Author(s):  
J. C. McLennan F.R.S. ◽  
J. V. S. Glass B.A.

This paper deals with the action of cathode rays on gases and gas mixtures. Methane, methane-oxygen mixtures, carbon monoxide and carbon monoxide-oxygen mixtures were examined. Methane gave small percentages of hydrogen and ethane. Methane and oxygen mixtures gave as gaseous products, carbon monoxide, carbon dioxide and hydrogen, the only other products being water and formic acid. The relative proportions of the products do not vary widely under a wide variation of conditions.The reaction was found to be of the first order with respect to pressure. The reaction rate increases linearly with the voltage up to a certain value, after which it becomes nearly independent of the voltage.The action of cathode rays on carbon monoxide produces carbon dioxide and a solid brown suboxide which is extremely soluble in water, and its composition corresponds to a formula (C3O)n. If the carbon monoxide is moist, no visible amount of solid or liquid is found and there is less carbon dioxide.Carbon monoxide-oxygen mixtures under the action of cathode rays form carbon dioxide. Presence of water vapor has a retarding effect on the reaction. For mixtures of the same composition the reaction rate is proportional to the total pressure. For dry mixtures the product increases with the carbon monoxide present; when moist it is much less, and independent of the carbon monoxide.


2002 ◽  
Vol 184 (21) ◽  
pp. 5894-5897 ◽  
Author(s):  
Jongyun Heo ◽  
Marcus T. Wolfe ◽  
Christopher R. Staples ◽  
Paul W. Ludden

ABSTRACT Substitution of one amino acid for another at the active site of an enzyme usually diminishes or eliminates the activity of the enzyme. In some cases, however, the specificity of the enzyme is changed. In this study, we report that the changing of a metal ligand at the active site of the NiFeS-containing carbon monoxide dehydrogenase (CODH) converts the enzyme to a hydrogenase or a hydroxylamine reductase. CODH with alanine substituted for Cys531 exhibits substantial uptake hydrogenase activity, and this activity is enhanced by treatment with CO. CODH with valine substituted for His265 exhibits hydroxylamine reductase activity. Both Cys531 and His265 are ligands to the active-site cluster of CODH. Further, CODH with Fe substituted for Ni at the active site acquires hydroxylamine reductase activity.


Biochemistry ◽  
2003 ◽  
Vol 42 (1) ◽  
pp. 222-230 ◽  
Author(s):  
Manuel Gnida ◽  
Reinhold Ferner ◽  
Lothar Gremer ◽  
Ortwin Meyer ◽  
Wolfram Meyer-Klaucke

1998 ◽  
Vol 120 (30) ◽  
pp. 7502-7510 ◽  
Author(s):  
William K. Russell ◽  
Christina M. V. Stålhandske ◽  
Jinqiang Xia ◽  
Robert A. Scott ◽  
Paul A. Lindahl

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