Metabolic modulation of carbon monoxide toxicity.

, the potential for metabolic intervention is likely.

Nitrite Oxidation with Copper-Cobalt Nanoparticles on Carbon Nanotubes Doped Conducting Polymer PEDOT Composite.

As a result of their nanostructure and the synergic effect between

, the Cu-Co/PEDOT/CNTs composites exhibited significantly enhanced catalytic activity towards the electrochemical oxidation of nitrite.

Studies on copper and cobalt in dairy calves.

 alone had no effect on any of the measurements taken, but it had an additive effect on weight gains to 

 supplementation during the grazing period.

Tryptophan 2,3-dioxygenase: a review of the roles of the heme and copper cofactors in catalysis.

, can inhibit catalysis by binding to either or to both the 

Purification and properties of the enzyme ATP-sulfurylase and its relation to vitamin A.

Oxidation of Ethanol in Cu-Faujasites Studied by IR Spectroscopy

In this study, IR studies of the coadsorption of ethanol and CO on Cu+ cations evidenced the transfer of electrons from ethanol to Cu+, … the band attributed to CO bonded to the same Cu+ cation due to the more effective π back donation of d electrons of

Rational design and effective control of gold-based bimetallic electrocatalyst for boosting CO2 reduction reaction: a first-principles study.

, and Rh substrates below Au monolayer could enhance the activity and selectivity for 

 production than pure Au, in which the limiting potential reduced from -0.74 to -0.63, -0.69, and -0.71 V respectively.

An as-cast high-entropy alloy with remarkable mechanical properties strengthened by nanometer precipitates.

, or Ni is higher than those of mixing between any two of Cr, Co, Ni and Mn, which leads to the separation of Cu from the CoCrCuMnNi HEA.

Desorption products during linear heating of copper zeolites with pre-adsorbed methanol.

 formation and desorption in larger amounts at lower temperatures compared to the bare zeolites.

Potential-Dependent Competitive Electroreduction of CO2 into CO and Formate on Cu(111) from an Improved H Coverage-Dependent Electrochemical Model with Explicit Solvent Effect

Simultaneously, the present study shows that the blocked

 can explain why the initial CO formation pathway is unfavorable at the high overpotentials.

Extraction of Li and Co from industrially produced Li-ion battery waste - Using the reductive power of waste itself.

 and Al-rich larger size fractions, the extraction efficiencies of 

 and Li increased up to over 99%, to leave a leach residue that is rich in graphite.

Copper adparticle enabled selective electrosynthesis of n-propanol

 shows activity toward multi-carbon products from 

 reduction, with reaction selectivity favoring two-carbon products; however, efficient conversion of CO to higher carbon products such as n-propanol, a liquid fuel, has yet to be achieved.

CuO/Co(OH)2 Nanosheets: A Novel Kind of Electrocatalyst for Highly Efficient Electrochemical Oxidation of Methanol.

The electronic structure interaction between

, which results in the Co ion binding-energy elevation, is considered to be the origin of high MOR performance.

Dopant-induced electron localization drives CO2 reduction to C2 hydrocarbons

Simulations show that the ability to tune the average oxidation state of

 adsorption and dimerization, and makes it possible to implement a preference for the electrosynthesis of C2 products.

Electronic structure of Al, Ga, In and Cu doped ZnO/Cu(111) bilayer films.

 doping results in a stronger interaction with 

 and a large red-shift of the CO stretching frequency.

In situ measurements of micronutrient dynamics in open seawater show that complex dissociation rates may limit diatom growth

On the basis of their labile metal complex pools, we discovered that Fe and

 co-limiting to diatom growth, contrary to the generally accepted view that phosphorus (phosphate) is the growth limiting element in the Mediterranean Sea.

Single atom detachment from Cu clusters, and diffusion and trapping on CeO2(111): implications in Ostwald ripening and atomic redispersion.

 reduces its detachment energy, which helps in the formation of single atom species on CeO2(111).

Sinter-Resistant and Highly Active Sub-5 nm Bimetallic Au-Cu Nanoparticle Catalysts Encapsulated in Silica for High-Temperature Carbon Monoxide Oxidation.

 conversion at low to intermediate temperatures (50-300 °C), silica encapsulation of the Au-Cu nanocomposites facilitated remarkable stability of the catalyst.

Structural behaviour of copper chloride catalysts during the chlorination of CO to phosgene.

Moreover, the data show that unique to the chlorine pre-treated sample,

 exposure at elevated temperature results in a short-lived oxidation of the 

Low temperature growth of fully covered single-layer graphene using a CoCu catalyst.

The growth outcome is found to vary significantly as the

 concentration is varied, with ∼1 at% Cu added to 

 yielding complete coverage single-layer graphene growth for the conditions used.

X-ray photoemission spectroscopy shows that

 form an alloy at high temperatures, which has a drastically lower carbon solubility, as determined by using the calculated Co-Cu-C ternary phase diagram.

Synergistic degradation of phenols using peroxymonosulfate activated by CuO-Co3O4@MnO2 nanocatalyst.

A remarkable synergetic effect was found between bi-metallic oxides of

: 0.5%Cu-2%Co-MnO2 can efficiently degrade 100% of 30ppm phenol, while 0.5%Cu@MnO2 or 2%Co@MnO2 alone is apparently sluggish for the degradation of organic contaminants.

The Effect of Copper Addition on the Activity and Stability of Iron-Based CO2 Hydrogenation Catalysts

 significantly increases the CO2 conversion, and decreases methane and carbon 

 selectivity, without significantly altering the crystallinity and structure of the catalyst itself.

A Direct Grain-Boundary-Activity Correlation for CO Electroreduction on Cu Nanoparticles

 catalyzes the electrochemical reduction of 

 to valuable C2+ products including ethanol, acetate, propanol, and ethylene.

Activation of Cu(111) surface by decomposition into nanoclusters driven by CO adsorption

Eren et al. present an extreme example for

 (CO) adsorption on the (111) surface of 

Effect of Transition Metal Substitution on the Structure and Properties of a Clathrate-Like Compound Eu7Cu44As23

 and Fe can only substitute less than 20% of 

Tracking a Common Surface-Bound Intermediate during CO2-to-Fuels Catalysis

Therefore, the kinetics and thermodynamics of

 play a central role in determining fuel-formation selectivity and efficiency, highlighting the need for direct observation of CO surface binding equilibria under catalytic conditions.

A density functional theory study of CO oxidation on CuO1-x(111)

 has a great influence on the adsorption of 

On the remarkable thermal stability of nanocrystalline cobalt via alloying

A remarkable thermal stability is achieved by alloying

 resulting in stabilized nanostructures even after annealing for long times at high temperatures.

Atomic Interdiffusion and Diffusive Stabilization of Cobalt by Copper During Atomic Layer Deposition from Bis(N-tert-butyl-N'-ethylpropionamidinato) Cobalt(II).

 producing a transition layer on the Cu nearly as thick as the Co-rich overlayer.

Design and synthesis of copper-cobalt catalysts for the selective conversion of synthesis gas to ethanol and higher alcohols.

As revealed by energy-dispersive X-ray nanospectroscopy and temperature-resolved X-ray diffraction, superior mixing of

 species promotes formation of CuCo alloy nanocrystals after activation, leading to two orders of magnitude higher yield to high alcohols than a benchmark CuCoCr catalyst.

Interaction of various gas molecules with paddle-wheel-type open metal sites of porous coordination polymers: theoretical investigation.

 significantly contributes to the shift in the end-on coordination gas molecules such as 

NO oxidation catalysis on copper doped hexagonal phase LaCoO3: a combined experimental and theoretical study.

The role of Cu in degrading adsorption of CO on the PtnCu clusters.

The adsorption energies indicate that the introduction of a

 decreases the adsorption ability of the 

Bipolar charge storage characteristics in copper and cobalt co-doped zinc oxide (ZnO) thin film.

) can stabilize the bipolar charge, whereas Cu doping only stabilizes the positive charge in ZnO thin films.

The effect of Cu substitution on microstructure and thermoelectric properties of LaCoO3 ceramics.

 increased the electrical conductivity greatly and the absolute Seebeck coefficient, whose sign was also reversed from negative to positive.

Alleviation of Copper-Induced Oxidative Damage in Chlamydomonas reinhardtii by Carbon Monoxide

 increased the activity of catalase with 

Electrodeposition efficiency of Co and Cu in the fabrication of multilayer nanowires by polymeric track-etched templates.

 separately, a decrease of current efficiency is observed when the charge density is increased and the pore diameter is reduced; on the …, changing the degree of polarization for each deposition step of the different metals results in a sensible reduction of this effect.

High-pressure CO adsorption on Cu-based catalysts: Zn-induced formation of strongly bound CO monitored by ATR-IR spectroscopy.

 can reduce ZnO to Zn in the presence of 

, resulting in the formation of a CuZn(x) surface alloy.

A density functional study on cationic Au(n)Cu(m)+ clusters and their monocarbonyls.

, which can be understood by the frontier molecular orbital theory.

Adsorption of CO on Cu (110) and (100) surfaces using COSMO-based DFT

Solvent effects can improve the stability of

 (110) and (100) surfaces and the extent of CO activation.

Ensemble vs. electronic effects on the reactivity of two-dimensional Pd alloys: a comparison of CO and CH3OH adsorption on Zn/Pd(111) and Cu/Pd(111).

 addition to the Pd(111) surface was found to alter the preferred adsorption sites for 

 from threefold to bridge Pd sites and decrease the activity for the dehydrogenation of CH(3)OH.

Photoinduced carbon monoxide migration in a synthetic heme-copper complex.

In CH(3)CN, a significant fraction of the photodissociated

 (nu(CO)(Cu) = 2091 cm(-)(1)) giving [((6)L)Fe(II)..Cu(I)(CO)](+) (4), with an observed rate constant, k(1) = 1.5 x 10(5) s(-)(1).

Role of copper chloride in the formation of polychlorinated dibenzo-p-dioxins and dibenzofurans during incineration.

 concentration in the flue gas and reduced the formation of PCDDs and PCDFs during incineration.

Separation of no-carrier-added 64Cu from a proton irradiated 64Ni enriched nickel target.

 fraction is higher than 99% and recoveries of 64Cu and 64Ni are higher than 95%.

Microwave spectra, geometries, and hyperfine constants of OCCuX (X = F, Cl, Br).

, Cl, and Br nuclear quadrupole coupling constants indicate that substantial charge rearrangement takes place on coordination with 

, consistent with the formation of strong Cu-C bonds.

Step-induced unusual magnetic properties of ultrathin Co/Cu films: Ab initio study.

The effect is mainly due to hybridization of Co and Cu $d$ electrons when

2 pi resonance features in the electronic spectra of chemisorbed CO.

Oxidation of two high-palladium PFM alloys.

 on the oxide formation is such that it suppresses the oxide formation of 

 relative to Ga, as well as the formation of SnO 2 .

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Research Papers that Mention the Interaction