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Vibrational and rotational excitation of CO in comets. Part 1: Non-equilibrium calculations. Part 2: Results of the calculation for standard bright comet, comet Iras-Araki-Alcock and comet Halley

The vibrational and rotational excitation of the CO molecule in cometary comae were investigated using a model which includes IR vibrational pumping by the solar flux, vibrational and rotational radiative decay, and collisional coupling among rotational states. Steady state was not assumed in solving the rate equations. The evolution of a shell of CO gas was monitored as it expanded from the nucleus into the outer coma. Collisional effects were treated using a kinetic temperature profile derived from theoretical work on the coma energy balance. The kinetic temperature was assumed to be extremely cold in the inner coma; this has significant consequences for the CO excitation. If optical depth effects are ignored, only low J transitions will be significantly excited in comets observed at high spatial resolution. Ground-based observations of CO co-vibrational and rotational transitions will be extremely difficult due to lack of sensitivity and/or terrestrial absorption. However, CO should be detectable from a large comet with favorable observing geometry if the CO is a parent molecule present at the 10% level (or greater) relative to H2O. Observations using cooled, spaceborne instruments should be capable of detecting CO emission from even moderately bright comets.

Chin, G.↗

Far-infrared emission lines of CO and OH in the Orion-KL molecular shock

Observations of far infrared rotational emission lines which arise in the shocked gas associated with Orion-Kl are presented, including detections of the CO J = 34 yields 33, J = 31 yields 30, J = 26 yields 25, and OH sup 2 PI sub (3/2) J sup P = 7/2(-) yields 5/2(+) emission lines, as well as improved measurements of the CO J = 22 yields 21 and OH sup 2 PI sub (3/2) J = 5/2 yields 3/2 lines. These lines are observed to have velocity widths of Del V approx. 20 to 30 km/sec, somewhat less than either the 2 micro H sub 2 lines or the high velocity plateau component of the millimeter wave CO lines seen in this object. An H sub 2 column density of approx. 3 x 10 to the 21st power, a total mass of approx. 1 solar mass and characteristic temperature and density T approx. 750 K and approx. 2 x 10 to the 6th power per cu cm can be derived from the CO intensities. The density is too low by at least an order of magnitude for the observed infrared H sub 2 and far infrared CO emission to be accounted for by a purely hydrodynamic shock, and support is lent to hydromagnetic shock models. From the present measurements, the relative abundance of CO is estimated to be CO H sub 2 = 1.2 x .0001, corresponding to 20% of the cosmic abundance of C existing in the form of CO. The average relative abundance of OH in the shocked gas is O/H sub 2 or = 5 x 10 to the -7th power. An upper limit to the intensity of the HD J = 1 yields 0 line is used to derive an upper limit of tau or = 3 for the D/H relative abundance in the Orion cloud core.

Watson, D. M.↗

Far-infrared emission lines of CO and OH in the Orion-KL molecular shock

Observations of far infrared rotational emission lines which arise in the shocked gas associted with Orion-Kl are presented, including detections of the CO J = 34 yields 33, J = 31 yields 30, J = 26 yields 25, and OH sup 2 PI sub (3/2) J sup P = 7/2(-) yields 5/2(+) emission lines, as well as improved measurements of the CO J = 22 yields 21 and OH sup 2 PI sub (3/2) J = 5/2 yields 3/2 lines. These lines are observed to have velocity widths of Del V approx. 20 to 30 km/sec, somewhat less than either the 2 micro H sub 2 lines or the high velocity plateau component of the millimeter wave CO lines seen in this object. An H sub 2 column density of aprox. 3 x 10 to the 21st power, a total mass of approx. 1 solar mass and characteristic temperature and density T approx. 750 K and approx. 2 x 10 to the 6th power per cu cm can be derived from the CO intensities. The density is too low by at least an order of magnitude for the observed infrared H sub 2 and far infrared CO emission to be accounted for by a purely hydrodynamic shock, and support is lent to hydromagnetic shock models. From the present measurements, the relative abundance of CO is estimated to be CO H sub 2 = 1.2 x .0001, corresponding to 20 percent of the cosmic abundance of C existing in the form of CO. The average relative abundance of OH in the shocked gas is O/H sub 2 or = 5 x 10 to the -7th power. An upper limit to the intensity of the HD J - 1 yields 0 line is used to derive an upper limit of tau or = 3 for the D/H relative abundance in the Orion cloud core.

Watson, D. M.↗

CO aperture synthesis of NGC 4038/9 (ARP 244)

Researchers present high-resolution (approx. 6 seconds) CO observations of the merging galaxies NGC 4038/9 made with the Owens Valley Radio Observatory (OVRO) Millimeter Wave Interferometer. The CO observations of Arp 244 were obtained between April and June 1988 using the OVRO Millimeter Wave Interferometer. Two fields with phase centers near the NGC 4039 nucleus and near the NGC 4038 nucleus were observed. The size of the synthesized beam is approximately 6.5 x 7 seconds at PA=72 degrees. The rms in a single cleaned channel map is 0.06 Jy beam(exp -1), corresponding to a brightness temperature of 0.12 K over the synthesized beam. Contour maps of the integrated CO intensity for both interferometer fields are shown. Three CO concentrations are evident. Two are centered near the nuclei of NGC 4038 and NGC 4039, closely correlated with H alpha and radio continuum maxima. A third CO emission region lies about 25 seconds northeast of the NGC 4039 nucleus. A number of radio continuum, H alpha, and 10 micron emission knots appear in this region. The total integrated intensity at the northern nuclear source, 302 K km/s, leads to a molecular mass of 8.3 by 10 to the 8th power solar mass assuming a Galactic CO to H2 conversion factor of 3.0 x 10 to the 20th power H2 cm(-2) (K km/s)(-1). The integrated CO intensity of the southern nuclear source leads to a molecular mass of 2.4 x 10 to the 8th solar mass. The extranuclear CO concentration contains 1.2 x 10 to the 9th power solar mass of molecular gas, extending over 170 km/s, and is resolved in a number of channels. Its large size, mass, and morphology strongly suggest that it is an agglomeration of several clumps.

Stanford, S. A.↗

CO observations of southern mergers

There are good reasons to believe that the formation of some elliptical galaxies result from the merging of two disk galaxies, as Toomre and Toomre first suggested (1972, Ap. J. 178, 623). Such a process strongly enhances the star-formation activity of the system, thus consuming its molecular gas. This might account for the low cold-gas content of elliptical galaxies compared to that of spirals. Researchers present here CO(1-0) and CO(2-1) observations of a sequence of three objects, NGC 1614, NGC 3256, and NGC 7252, that present characteristic features of merger remnants: single body and extended tidal tails. NGC 3256 and 7252 even exhibit the r(exp 1/4) radial light distribution that is the signature of elliptical galaxies, which indicates that their stellar bodies are in late stages of relaxation. Both NGC 1614 and NGC 3256 undergo extended bursts of star formation revealed by their large far-infrared luminosities, and by the presence in the near-infrared spectrum of the 3.28 microns feature (Morwood: 1986, A. A. 166, 4) attributed to polycyclic aromatic hydrocarbons. On the other hand, NGC 7252 has a milder activity of star formation, as suggested by a lower infrared luminosity, and thus seems to have gone past the starburst phase. The CO data were collected with the Swedish-ESO 15 m Submillimeter Telescope (SEST) (beamsize = 43 seconds at 115 GHz, 23 seconds at 230 GHz). For NGC 7252, researchers have only observed the central position in CO-12(1-0). The spectrum is displayed together with an HI spectrum obtained with the Nancay radiotelescope. Researchers mapped NGC 1614 and NGC 3256 in CO-12(1-0) and CO-12(2-1), and also observed the nucleus of NGC 3256 in CO-13(1-0). The various CO spectra obtained towards the nuclei of both galaxies are presented. Characteristics of the galaxies are gathered, with luminosities and masses in solar units and temperatures in Kelvins.

Casoli, F.↗

Savanna burning and convective mixing in southern Africa - Implications for CO emissions and transport

Atmospheric data from both remote and direct measurements were used to compute the carbon monoxide (CO) emissions and mass transport from Africa south of the equator. The Measurement of Air Pollution from Satellites (MAPS) experiment flew on the Space Shuttle during October 5-13, 1984; the highest CO mixing ratios from the entire mission were measured over southern Africa. In addition to the MAPS data, surface CO mixing ratios were measured in the boundary layer at Cape Point, South Africa. A calibration factor for the remote MAPS CO measurements was determined by computing the ratio of the surface measurements from Cape Point during unpolluted periods to coincident MAPS measurements. The adjusted MAPS CO data were then used to compute the mass flux of CO from biomass burning in southern Africa during the MAPS mission. The transport calculations were compared to the estimated CO emissions from biomass burning to examine the efficiency in which the continental tropical clouds redistribute CO in the troposphere.

Connors, Vickie S.↗

High temperature co-axial winding transformers

The analysis and design of co-axial winding transformers is presented. The design equations are derived and the different design approaches are discussed. One of the most important features of co-axial winding transformers is the fact that the leakage inductance is well controlled and can be made low. This is not the case in conventional winding transformers. In addition, the power density of co-axial winding transformers is higher than conventional ones. Hence, using co-axial winding transformers in a certain converter topology improves the power density of the converter. The design methodology used in meeting the proposed specifications of the co-axial winding transformer specifications are presented and discussed. The final transformer design was constructed in the lab. Co-axial winding transformers proved to be a good choice for high power density and high frequency applications. They have a more predictable performance compared with conventional transformers. In addition, the leakage inductance of the transformer can be controlled easily to suit a specific application. For space applications, one major concern is the extraction of heat from power apparatus to prevent excessive heating and hence damaging of these units. Because of the vacuum environment, the only way to extract heat is by using a cold plate. One advantage of co-axial winding transformers is that the surface area available to extract heat from is very large compared to conventional transformers. This stems from the unique structure of the co-axial transformer where the whole core surface area is exposed and can be utilized for cooling effectively. This is a crucial issue here since most of the losses are core losses.

Divan, Deepakraj M.↗

The nature of the source of CO in Comet P/Halley

We show by numerical simulations that the CO distribution in the coma of Comet P/Halley as measured by neutral gas mass spectrometer aboard Giotto spacecraft (P. Eberhardt et al., 1987) can be explained by an extended jet source originating from vent 1 in the rotational model of M. J. S. Belton et al. (1991). This is an alternative interpretation for the origin of the CO distribution where Eberhardt et al. (1987) explained the observations in terms of a spherically symmetric extended source function. We still find nearly 1/3 of CO is due to CO sublimating directly at the nucleus, possibly from the vent itself. Approximately 50% of CO that originates in the extended jet source may be formed via photolysis of H2CO while the rest can be due to CO trapped in grain mantels and other C=O-bearing molecules. The overall production rates of CO in the two models differ by less than 29%. The prediction of the jet source model compares satisfactorily with the distribution of CO observed in the coma by the IUE satellite but unfortunately does not allow one to discriminate between the two models.

Samarasinha, Nalin H.↗

(12)CO (3-2) & (1-0) emission line observations of nearby starburst galaxy nuclei

New measurements of the (12)CO (1-0) and (12)CO (3-2) line emission are presented for the nuclei of seven nearby starburst galaxies selected from a complete sample of 21 nearby starburst galaxies for which the nuclear star formation rates are measured to be comparable to the archetype starburst galaxies M82 and NGC 253. The new observations capitalize on the coincidence between the beam size of the 45 m Nobeyama telescope at 115 GHz and that of the 15 m James Clerk Maxwell Telescope at 345 GHz to measure the value of the (12)CO (3-2)/(1-0) emission line ratio in a 15 sec (less than or equal to 2.5 kpc) diameter region centered on the nuclear starburst. In principle, the (12)CO (3-2)/(1-0) emission line ratio provides a measure of temperature and optical depth for the (12)CO gas. The error weighted mean value of the (12)CO (3-2)/(1-0) emission line ratio measured for the seven starburst galaxy nuclei is -0.64 +/- 0.06. The (12)CO (3-2)/(1-0) emission line ratio measured for the starburst galaxy nuclei is significantly higher than the average value measured for molecular gas in the disk of the Galaxy, implying warmer temperatures for the molecular gas in starburst galaxy nuclei. On the other hand, the (12)CO (3-2)/(1-0) emission line ratio measured for the starburst galaxy nuclei is not as high as would be expected if the molecular gas were hot, greater than 20 K, and optically thin, tau much less than 1. The total mass of molecular gas contained within the central 1.2-2.8 kpc diameter region of the starburst galaxy nuclei ranges from 10(exp 8) to 10(exp 9) solar mass. While substantial, the molecular gas mass represents only a small percentage, approximately 9%-16%, of the dynamical mass in the same region.

Devereux, Nicholas↗

Observations of Middle Atmosphere CO from the UARS ISAMS during the Early Northern Winter 1991/92

Structure and kinematics of carbon monoxide in the upper stratosphere and lower mesosphere (10-0.03 hPa) are studied for the early northern winter 1991/92 using the Upper Atmosphere Research Satellite Improved Stratospheric and Mesospheric Sounder (ISAMS) measurements. The study is aided by data from a 6-week parameterized-chemistry run of the Goddard Space Flight Center 3D Chemistry and Transport Model (CTM), initialized on 8 December 1991. Generally, CO mixing ratios increase with height due to the increasing source contribution from CO, photolysis. In the tropical upper stratosphere. however, a local maximum in CO mixing ratio occurs. A simple photochemical model is used to show that this feature results largely from methane oxidation. In the extratropics the photochemical lifetime of CO is long, and therefore its evolution is dictated by large-scale motion of air. evidenced by strong correlation with Ertel potential vorticity. This makes CO one of the few useful observable tracers at the stratopause level and above. Thus CO maps are used to study the synoptic evolution of the polar vortex in early January 1992. Modified Lagrangian mean mixing diagnostics are applied to ISAMS and CTM data to examine the strength of the mixing barrier at the polar vortex edge. It is demonstrated that planetary wave activity weakens the barrier. promoting vortex erosion. The vortex erosion first appears in the lower mesosphere and subsequently descends through the upper stratosphere. and is attributed to effects of planetary wave dissipation. Agreement between ISAMS and CTM is good in the horizontal distribution of CO throughout the examined period, but vertical CO gradients in the CTM weaken with time relative to the ISAMS observations.

Allen, D. R.↗

Evaluation of Low Temperature CO Removal Catalysts

CO removal from spacecraft gas streams was evaluated for three commercial, low temperature oxidation catalysts: Carulite 300, Sofnocat 423, and Hamilton Sundstrand Pt1. The catalysts were challenged with CO concentrations (1-100 ppm) under dry and wet (50% humidity) conditions using 2-3 % O2. CO removal and CO2 concentration were measured at constant feed composition using a FTIR. Water vapor affected the CO conversion of each catalyst differently. An initial screening found that Caulite 300 could not operate in humid conditions. The presence of water vapor affected CO conversion of Sofnocat 423 for challenge concentrations below 40 ppm. The conversion of CO by Sofnocat 423 was 80% at CO concentrations greater than 40 ppm under both dry and moist conditions. The HS Pt1 catalyst exhibited CO conversion levels of 100% under both dry and moist conditions.

Low Temperature↗

On the Detectability of CO Molecules in the Interstellar Medium via X-Ray Spectroscopy

We present a study of the detectability of CO molecules in the Galactic interstellar medium using high-resolution X-ray spectra obtained with the XMM-Newton Reflection Grating Spectrometer. We analysed 10 bright low mass X-ray binaries (LMXBs) to study the CO contribution in their line of sights. A total of 25 observations were fitted with the ISMabs X-ray absorption model which includes photoabsorption cross-sections for Oi, Oii, Oiii and CO. We performed a Monte Carlo (MC) simulation analysis of the goodness of fit in order to estimate the significance of the CO detection. We determine that the statistical analysis prevents a significant detection of CO molecular X-ray absorption features, except for the lines of sight towards XTE J1718-330 and 4U 1636-53. In the case of XTE J1817-330, this is the first report of the presence of CO along its line of sight. Our results reinforce the conclusion that molecules have a minor contribution to the absorption features in the O K-edge spectral region. We estimate a CO column density lower limit to perform a significant detection with XMM-Newton of N(CO) greater than 6 x 10(exp 16) per sq cm for typical exposure times.

ISM: structure↗

Analysis of CO Transport from Australia Fires and Its Impact to Ozone, Water Vapor and Clouds Using CrIS Single-Field-of-View Sounder Products and Other Remote Sensing and MERRA-2 Reanalysis Data

Australia’s unprecedented fire disasters at the end of 2019 to early 2020 emitted huge amounts of carbon monoxide (CO) and fire aerosol particles, and the long-range transport of the smoke plumes poses great impact to climate change, such as altering the Antarctic ozone (O3) hole. Spaceborne observations from satellites have been proven successful in monitoring CO from wildfires in the past decade and can be used to examine the associated CO transport. The primary remote sensing data used in this study is the Single Field of View (SFOV) Sounder Atmospheric Product (SiFSAP) derived from the Cross-track Infrared Sounder (CrIS) on SNPP, a new product that will be generated at NASA and released to the public in a few months. SiFSAP has a high spatial resolution of ~14 km and includes atmospheric profiles of temperature, water vapor, CO, O3, as well as cloud products, and as the SiFSAP algorithm performs both day- and night-time retrievals, it provides an additional observation for night-time in comparison to the day-time-only solar polar satellite instruments such as MOPPIT, OMPS, and TROPOMI. Most recent significant improvements in the quality of this product plus its good spatial resolution (better than most global weather and climate models) enable us to conduct process-oriented analysis of CO transport, and the variation of water vapor, O3 and clouds (optical depth, effective radius and cloud height) within and around the fire plumes. The wind fields from MERRA-2 reanalysis will be used to help characterize the transport. Other remote sensing data, such as CO from AIRS, MOPPIT and TROPOMI, O3 from OMPS and TROPOMI, as well as the UV aerosol index from OMI and OMPS, will be used and compared with SiFSAP sounder products. Cross-validation of CO and O3 from these different sensors with the corresponding MERRA-2 products will also be carried out. Along the plume transport path, some enhancement of O3 and correlation between fire aerosol, cloud optical depth and water vapor have been found but need further investigation. Using the transport of fire plumes over the Southern Pacific Ocean as a unique testbed, this study will demonstrate the trace species monitoring capability of current satellite observations, in particular, for CO and O3, and hopefully, it will provide some insight on the impacts on fire emissions on air quality and climate.

Xiaozhen (Shawn) Xiong↗

Optimizing Materials to Boost the Valorization of CO 2 : Tuning Cobalt–Cobalt Interactions on In 2 O 3 -Based Photothermal Catalysts

The valorization of CO 2 is an important challenge within the current panorama, since this molecule is probably the main contributor to climate change. In this study, the synthesis of materials based on a nanostructured batonnet-type indium oxide is carried out. In them, different amounts of Co are introduced, varying between 2 and 8% mol. It is verified that the most active sample in the transformation of carbon dioxide to carbon monoxide contains 6 mol %. of Co. This sample’s activity under dual excitation exceeds the thermal counterpart by more than 30%. After carrying out a complete physical and chemical characterization with the help of X-ray absorption spectroscopy and other techniques, it is shown that catalysts with amounts of cobalt equal to or below 4 mol % contain isolated single-atom species, while those with higher amounts of metal display a Co–Co interaction which triggers the evolution of the samples under reaction conditions. The optimum control of this Co–Co interaction and the nature of the final cobalt-containing species determine dual photothermal catalytic properties. In conclusion, this work establishes a structure–activity relationship to interpret the catalytic behavior of highly dispersed subnanometric cobalt species, and thus an avenue to optimize the photothermal valorization of carbon dioxide.

36 MATERIALS SCIENCE↗

Oxophilicity Drives Oxygen Transfer at a Palladium–Silver Interface for Increased CO Oxidation Activity

A single-layer AgO x phase grown on Ag(111) efficiently transfers oxygen to Pd domains at room temperature, rendering the Pd-decorated surface highly reactive toward CO oxidation. Here, oxygen transfer from AgO x to Pd and the surface reactivity toward CO were investigated as a function of the Pd coverage using X-ray photoelectron spectroscopy, surface infrared spectroscopy of adsorbed CO, temperature-programmed reaction spectroscopy, and density functional theory (DFT) calculations. Our results show that all of the oxygen from the AgO x layer (~0.375 monolayer) migrates to the surface of Pd during formation of a nearly complete Pd bilayer at 300 K and that the oxygen coverages generated on Pd increase as the Pd cluster size decreases, reaching values that exceed the oxygen concentration in the AgO x layer by as much as a factor of 2. Experimental measurements and DFT calculations show that preferential binding of oxygen on the edges of the Pd clusters enhances the oxygen coverage on Pd clusters of decreasing size and produces a heterogeneous spatial distribution of oxygen. CO adsorbs in high coverages at 100 K by binding on both the terraces and O-rich edges of the Pd clusters. During subsequent heating, oxidation of the adsorbed CO consumes nearly all of the oxygen that transferred from AgO x to the Pd domains; in contrast, the pure AgO x layer exhibits limited reactivity toward CO adsorbed at 100 K. These results demonstrate that differences in oxophilicity drive facile oxygen transfer from Ag to the edges of Pd nanoclusters and thereby give rise to an efficient pathway for CO oxidation on bimetallic PdAg surfaces. The cooperation between the Pd and Ag domains results in near-interfacial chemistry that may be broadly important in catalysis by bimetallic alloys.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Materials Data on CoHRu3(CO)13 by Materials Project

RuRu2HCo(CO)4(CO)9 crystallizes in the monoclinic P2_1/c space group. The structure is zero-dimensional and consists of thirty-six formaldehyde molecules, four ruthenium molecules, four Co(CO)4 clusters, and four Ru2H clusters. In each Co(CO)4 cluster, Co2+ is bonded in a distorted trigonal pyramidal geometry to four C+0.92+ atoms. There are a spread of Co–C bond distances ranging from 1.75–1.89 Å. There are four inequivalent C+0.92+ sites. In the first C+0.92+ site, C+0.92+ is bonded in a distorted bent 150 degrees geometry to one Co2+ and one O2- atom. The C–O bond length is 1.18 Å. In the second C+0.92+ site, C+0.92+ is bonded in a linear geometry to one Co2+ and one O2- atom. The C–O bond length is 1.16 Å. In the third C+0.92+ site, C+0.92+ is bonded in a distorted single-bond geometry to one Co2+ and one O2- atom. The C–O bond length is 1.18 Å. In the fourth C+0.92+ site, C+0.92+ is bonded in a distorted single-bond geometry to one Co2+ and one O2- atom. The C–O bond length is 1.18 Å. There are four inequivalent O2- sites. In the first O2- site, O2- is bonded in a single-bond geometry to one C+0.92+ atom. In the second O2- site, O2- is bonded in a single-bond geometry to one C+0.92+ atom. In the third O2- site, O2- is bonded in a single-bond geometry to one C+0.92+ atom. In the fourth O2- site, O2- is bonded in a single-bond geometry to one C+0.92+ atom. In each Ru2H cluster, Ru+3.67+ is bonded in a 1-coordinate geometry to one H1+ atom. The Ru–H bond length is 1.80 Å. H1+ is bonded in a bent 120 degrees geometry to two equivalent Ru+3.67+ atoms.

36 MATERIALS SCIENCE↗

Materials Data on Co(NO5)2 by Materials Project

Co(NO5)2 crystallizes in the triclinic P-1 space group. The structure is zero-dimensional and consists of one Co(NO5)2 cluster. Co is bonded in an octahedral geometry to six O atoms. There is four shorter (1.75 Å) and two longer (2.22 Å) Co–O bond length. N is bonded in a trigonal planar geometry to three O atoms. There are a spread of N–O bond distances ranging from 1.24–1.28 Å. There are five inequivalent O sites. In the first O site, O is bonded in a single-bond geometry to one Co atom. In the second O site, O is bonded in a single-bond geometry to one Co atom. In the third O site, O is bonded in a bent 120 degrees geometry to one Co and one N atom. In the fourth O site, O is bonded in a single-bond geometry to one N atom. In the fifth O site, O is bonded in a single-bond geometry to one N atom.

36 MATERIALS SCIENCE↗

Materials Data on Co(ClO3)2 by Materials Project

Co(O3Cl)2 crystallizes in the monoclinic C2/m space group. The structure is one-dimensional and consists of two Co(O3Cl)2 ribbons oriented in the (0, 1, 0) direction. Co is bonded in an octahedral geometry to four equivalent O and two equivalent Cl atoms. All Co–O bond lengths are 1.94 Å. Both Co–Cl bond lengths are 2.24 Å. There are two inequivalent O sites. In the first O site, O is bonded in a water-like geometry to two equivalent O atoms. Both O–O bond lengths are 1.36 Å. In the second O site, O is bonded in a distorted water-like geometry to one Co and one O atom. Cl is bonded in a single-bond geometry to one Co atom.

36 MATERIALS SCIENCE↗