Cobalt Content Research Articles

Evaluation of Heavy Metals Pollution in the Sediments of Diyala River Lower Reaches, Eastern Iraq

Investigating the heavy metals in soil is important to the life of humans and living organisms. Diyala River Lower Reaches was chosen due to the changes in environmental characteristics that took place in recent years. Twelve sediment samples were collected from four different sites. The physical, and chemical properties and the concentrations of nine heavy metals were indicated. The results showed that the average concentrations of arsenic, copper, chromium, cobalt, iron, manganese, nickel, lead, and zinc are 8.5, 45.7, 538.5, 12.2, 5.07, 991.7, 183.5, 16.07, 136.5 ppm, respectively. They reflect contamination with arsenic, chromium, and nickel, while they are free of lead, and zinc contamination, according to the Environmental Protection Agency's (EPA) sediment quality guidelines. The measured contamination indices (the enrichment factor (EF), contamination factor (CF), degree of pollution (Cdeg), geographical accumulation index (Igeo), and pollution load index (PLI)), reflected high contamination factor for arsenic and chromium, and medium for manganese, nickel, lead, and zinc, while low for copper and cobalt. Based on all the results in all sampling sites indicate the presence of heavy element contamination in the sediments of the Diyala River Lower Reaches.

Serum Cobalt Concentration and DNA Methylation Signatures in Women with Obesity

Obesity, a multifactorial disorder, has been associated with alterations in metal metabolismand epigenetic modifications. This pilot case–control study aimed to investigate serum cobalt concentrations and associated DNA methylation patterns in women with obesity. Serum cobalt levels were measured using inductively coupled plasma mass spectrometry (ICP-MS), revealing significantly higher cobalt concentrations in participants with normal weight than in participants with obesity. Additionally, DNA methylation analysis identified differentially methylated positions (DMPs) associated with cobalt exposure, and DMPs between groups highlighted hypomethylation in the top DMPs in individuals with obesity. Functional enrichment analysis of these DMPs unveiled potential pathways implicated in apoptosis, cancer, and metabolic signaling, warranting further investigation into the mechanistic links. This study provides preliminary insights into the interplay between cobalt exposure, DNA methylation, and potential implications for obesity management.

Influence of bismuth and cobalt doping on structural, dielectric, and magnetic properties of M-type calcium hexagonal ferrites

M-type hexagonal ferrites have been getting considerable attention owing to their promising application in electronic fields. Though, the growth of nanosized M-type hexagonal ferrites is still a big challenge. Herein the fabrication of M-type hexaferrite with nominal composition Ca1-xBixFe12-xCoxO19 (x=0.00, 0.05, 0.10, 0.15, 0.20) with high quality is reported by the sol-gel auto combustion route. The objective of the study is to improve the structural, spectral, dielectric, and magnetic characteristics of M-type hexagonal ferrite which was achieved through the variation of concentration of Cobalt and Bismuth. X-ray diffraction (XRD) patterns confirmed the single-phase M-type hexagonal structure. The crystallite size of all samples was found to be in the range of 42–49 nm. Other parameters such as lattice parameters a & c, unit cell volume, crystallite size, X-ray density, Bulk density, and porosity were also calculated. The doping contents were found to decrease the bulk and X-ray densities while increasing the porosity. Fourier-transform infrared (FTIR) spectra showed the formation of metal-oxygen stretching vibrations that confirmed the formation of hexagonal ferrites. The scanning electron microscopy (SEM) images revealed a regular platelet hexagonal structure and homogeneously distributed grains were examined. The dielectric constant was high at low frequency and then decreased with increasing frequency, while the dielectric loss was decreased appreciably with doping. The saturation magnetization ranged from 15.51 to 38.27 emu/g, coercivity increased from 207.93 to 1359.69 Oe, and the squareness ratio was found to be in the range of 0.19–0.78. The dielectric and magnetic properties of Ca1-xBixFe12-xCoxO19 (x=0.00, 0.05, 0.10, 0.15, 0.20) with the variation of Co and Bi revealed that these materials are good candidates for modern devices.

Development and understanding of the lithiation/de-lithiation mechanism of a low cobalt and nickel-rich cathode material for lithium‐ion batteries

Nickel-rich LiNixMnyCo1−x−yO2 (NMC, with x ≥ 0.6) layered oxides are regarded as cathode candidates for high-energy density lithium-ion batteries (LIBs). However, this technology faces several challenges due to the scarcity of crucial raw materials such as cobalt precursors and the negative environmental impact of their extraction process. It is therefore, it becomes imperative to develop low cobalt content cathode compositions that offer alternative options with comparable electrochemical performance. Herein, we have used a systematic approach to modify the composition while keeping all other properties (particle size and morphology) constant to synthesise low-Co-cathode materials, namely LiNi0·8Mn0·1Co0·1O2 (NMC-10 %) and LiNi0·8Mn0·15Co0·05O2 (NMC-5%). A co-precipitation route using a continuous stirred thank reactor was used for synthesis. The physico-chemical properties, electrochemical performances, cycling stability, and rate capabilities of NMC-5% materials are comparable to those of NCM-10 % materials. NMC-10 % and NMC-5% half cells show initial specific discharge capacities of 191 mAh.g−1, and 185 mAh.g−1, respectively, in a voltage range of 2.8–4.3 V (vs. Li+/Li). The NMC-5% exhibits excellent thermal stability, characterized by a predominant exothermic peak at 432 °C and significantly lower total heat energy when compared to NMC-10 % counterpart, which displayed its main exothermic peak at 339 °C. The structural and electronic changes of both materials were evaluated through in operando synchrotron-based X-ray techniques. Regardless of the cobalt content, both materials show comparable structural and electronic evolution upon the de-intercalation/intercalation of Li+ ions. An irreversible phase transition at the first delithiation was observed as emphasized by diffraction of synchrotron radiations.

From Co-MOF to Co@carbon–comparison of needle-like catalysts in photo-driven hydrogen evolution

In response to the rising demand for catalytic hydrogen production, more attention is focused on noble-metal-free catalysts such as cobalt-based metal–organic frameworks (MOFs) and their derivatives. Due to the varying activity of cobalt forms in photocatalytic processes, the present study explores the performance of photo-driven hydrogen generation of cobalt nitrilotriacetate (Co-NTA) with metal ions and MOF-derived carbons containing Co/CoOx/CoNx. The needle-like morphology of the obtained Co-NTA template was preserved in carbon materials prepared through carbonization with and without furfuryl alcohol. Carbons featured nitrogen-containing graphitic structures and oxygen functional groups. They were also characterized by a more developed specific surface area and larger pore volume compared to their parent MOF. All materials evolved hydrogen under visible light in a photosensitized system. Owing to the high content of metallic cobalt on the surface of non-impregnated carbon, it produced three times more hydrogen (14.2 mmol g−1) than Co-NTA.

First-principles study of the structures and redox mechanisms of Ni-rich lithium nickel manganese cobalt oxides

To reduce the cobalt (Co) content in lithium-ion batteries, Ni-rich (high-Ni) lithium nickel manganese cobalt oxides (NMC) are pursued as one of the next-generation cathode materials. However, there is still debate on the crystal and electronic structures of the baseline, LiNiO2. Density Functional Theory (DFT) calculations were performed to provide a theoretical understanding of Ni-rich NMC. First, it was found that the commonly used R3¯m structure for LiNiO2 is metallic, contrary to the experimentally reported mix-conducting behavior. Among the four different space groups, R3¯m, C2/m, P21/c, and P2/c, P2/c with charge disproportionation of Ni2+ and Ni4+ is the most energetically stable and semiconducting structure of LiNiO2. Therefore, the atomic structures of representative Ni-rich NMC were built by partially replacing Ni with Co or Mn in the P2/c LiNiO2 to form LixNiyMnzCo1-y-zO2. In the fully lithiated (x = 1.0) high Ni content NMC (y > 0.5), the oxidation state of all Mn ions becomes 4+, while Co ions still maintain 3+, and part of the Ni ions become 2+ to compensate for the charge. Upon delithiation, the local environment shows more variation of the charge states on the transition metal (TM) ions. The average oxidation on each TM follows a sequence of losing electrons that starts from Ni2+ to Ni3+, then oxidizing Ni3+ and Co3+, while Mn4+ remains electrochemically inactive till x = 0. A general relationship for the oxidation state change in each TM as a function of x and y is derived and shows agreement with both modeling and experimental data.

Serum trace elements during treatment in pancreatic cancer patients and their associations with cancer prognosis

Background & AimsIn this study, we assessed serum trace element concentrations in patients with pancreatic cancer and compared the results to those of healthy controls and patients with chronic pancreatitis. We evaluated the association between trace element concentrations during cancer treatment and the risk of cancer progression and mortality in pancreatic cancer patients. MethodsA retrospective cohort study was conducted at a tertiary center in Korea. Serum trace element concentrations of cobalt (Co), copper (Cu), selenium (Se), and zinc (Zn) were measured at diagnosis using an inductively coupled plasma-mass spectrometry in 124 pancreatic cancer patients, 50 chronic pancreatitis patients, and 120 healthy controls. Trace elements were measured after a median of 282.5 (95% confidence interval [CI], 224.0–326.5) days from treatment initiation to assess changes in trace element concentrations during treatment. ResultsSerum Co and Cu concentrations were significantly higher in patients with chronic pancreatitis and pancreatic cancer than in healthy controls, while serum Se and Zn concentrations were significantly lower. During treatment, serum concentrations of Cu, Se, and Zn were significantly decreased in patients with pancreatic cancer.During the follow-up (median 152.5; 95% CI, 142.8–160.0 months), 85.5% of patients experienced progression or relapse, and 84.7% of patients died. Patients with decreased Se and Zn concentrations during treatment had a higher mortality (hazard ratio [HR], 2.10; 95% CI, 1.31–3.38; P = 0.0020 for Se; HR, 1.72; 95% CI, 1.06–2.79; P = 0.0269 for Zn) compared to those with unchanged or increased trace element concentrations during treatment. Patients with a greater reduction in Zn concentrations during treatment had a higher mortality than those with a smaller reduction (HR, 1.59; 95% CI, 1.01–2.52; P = 0.0483). Patients whose Zn status changed to deficient after treatment had an increased mortality (HR, 1.76; 95% CI, 1.16–2.67, P = 0.0084). Patients with multiple (≥ 2) trace element deficiencies after treatment had poorer outcomes than those with no or single trace element deficiency. ConclusionsThis study revealed that decreases in Se and Zn concentrations during cancer treatment were associated with adverse outcomes in terms of cancer progression and mortality in patients with pancreatic cancer. Further prospective investigations are recommended.

Effect of Cobalt Ion Concentration and Thermal Annealing Temperature on Structural and Magnetic Properties of CoFe2O4 Nanoparticles

Effect of Cobalt Ion Concentration and Thermal Annealing Temperature on Structural and Magnetic Properties of CoFe2O4 Nanoparticles

Are Metal Ion Levels Elevated After Dual Mobility Acetabular Systems: Minimum Five-Year Analyses.

While dual mobility systems in total hip replacements have demonstrated reduced dislocation and revision occurrences, concerns persist about the potential elevation of metal ions in the bloodstream, leading to negative tissue reactions. Notably, there's a scarcity of research spanning over five years post-surgery that examines cobalt and chromium levels after such implants. This study aimed to delve into these metal ion concentrations after a five-year period, building on previous metal-ion findings. We focused on: (1) cobalt concentrations in blood and urine; (2) chromium concentrations in blood and urine; (3) cobalt variations based on follow-up duration and specific implant metrics (e.g., offset, cup dimension, stem, and neck inclination); and (4) chromium variations based on the same parameters. We tracked 57 individuals who received THA using modular dual mobility systems from January 1, 2011, to December 31, 2016, for an average span of six years (ranging from five to 10 years). At the final check-up, we measured cobalt and chromium levels in serum, plasma, blood, and urine. We also evaluated parameters like head composition and dimension, stem offset, cup dimension, and stem-neck inclination. Cobalt concentrations remained minimal, with average blood and urine values being 0.8+0.6mcg/L (standard <1.8mcg/L) and 1.2+1.0mcg/L (standard <2.8mcg/L), respectively. Two individuals exhibited a slight increase in blood cobalt concentration by 0.1 and 0.2mcg/L. Chromium averages in blood and urine were also minimal, with readings of 0.9+0.2mcg/L (standard <1.2mcg/L) and 1.3 + 0.5mcg/L (standard <2mcg/L), respectively. One individual had a marginally increased blood chromium concentration of 1.3mcg/L. Evaluations considering ceramic or cobalt-chrome heads, up to a decade of follow up, or varying implant metrics showed negligible variations in metal ion concentrations. The findings reveal that over a minimum of five years (average = six years; span, five to 10 years), cobalt and chromium concentrations in patients' systems remained within normal limits and were clinically insignificant, irrespective of the follow-up duration, head material, or implant specifications. This underscores the efficacy of dual mobility systems in ensuring minimal metal ion presence.

New experimental findings on the separation of cobalt and nickel from an ammonia-ammonium-based leach liquor using ammonium-saponified Cyanex 272

There is a need to improve cobalt and nickel recovery from industrial waste streams such as secondary leach solutions and rechargeable battery leach solutions due to the increasing economic value of these critical metals. Ammonia is an important lixiviant due to its limited environmental impact compared to acid based lixiviants, however, the subsequent selective extraction of cobalt and nickel from the leach liquor is a major challenge. This study presents new experimental findings on the treatment of a Base metal Refinery (BMR) secondary leach liquor that contains high concentrations of ammonia and ammonium sulphate, and low concentrations of cobalt (∼442 mg/L) and nickel (∼1624 mg/L) using partially saponified Cyanex 272. New knowledge that can be applied in the treatment of ammonia based leachates from various industrial wastes that contain residual cobalt and nickel is presented herein. The investigation was conducted through the determination of the optimum extraction temperature, percentage saponification, and organic to aqueous ratios. Partial saponification of Cyanex 272 increased ammonia-metal complex stability at the interphase and this limited cobalt extraction between 30 °C and 50 °C. However, a high cobalt extraction percentage, and a high separation factor of 94.07 %, and 1189.76 respectively were achieved at 60 °C, 20 % saponification, and 0.5 O/A loadings in a single contact. A second-stage batch extraction produced a nickel aqueous stream with no cobalt. Stripping of the loaded organic phase with dilute sulphuric acid produced a pure cobalt aqueous stream. Further, the extractant was successfully regenerated post stripping. Overall, partial ammonium-saponification increased the extent of cobalt extraction, and selectivity. The novel process conditions reported herein can be used to design sustainable cobalt-nickel separation processes.

Conversion of Lithium Chloride into Lithium Hydroxide Using a Two-Step Solvent Extraction Process in an Agitated Kühni Column

A significant consequence of the green transition is the growing demand of lithium-ion batteries (LIBs), as they are essential for electrical vehicles. In turn, the demand for the raw materials that are needed to produce LIBs is increasing. A common LIB cathode type for electrical cars is lithium nickel manganese cobalt oxide (NMC). Since cobalt is currently considered as a critical raw material, nickel-rich NMC cathodes are now designed with lower cobalt contents. The synthesis of these new NMC types requires LiOH instead of Li2CO3, which was used for Co-richer NMC materials in the past. Most production routes of LiOH start from Li2CO3 or Li2SO4. However, LiCl could also be a potential precursor for LiOH, as it could be obtained from various lithium sources. A two-step solvent extraction process (SX) was developed for direct conversion of LiCl into LiOH, using a phenol (butylhydroxytoluene or BHT) and a mixture of quaternary ammonium chlorides (Aliquat 336) in an aliphatic diluent (Shellsol D70) as the solvent. The SX process was validated in counter-current mode using a rotary agitated Kühni extraction column. The use of a column instead of mixer-settlers reduced the CO2 uptake by the final product (LiOH), which prevented the partial conversion of LiOH to Li2CO3. A total of 75 L of LiCl feed solution was processed in the Kühni column to obtain a solution of LiOH with a final purity of more than 99.95%, at a yield of 96%.Graphical

Magnetorefractive effect in metallic Co/Pt nanostructures

Objectives. To carry out a theoretical investigation of the features of magnetorefractive effect for metal-to-metal nanostructures. This study uses the example of multilayer Co/Pt nanostructures (ferromagnetic metal–paramagnetic metal) with a different ratio of ferromagnetic and paramagnetic phases in the visible and near-infrared (IR) spectral regions.Methods. The dependence was expressed explicitly using the basic formulas for permittivity, refraction and extinction coefficients, and optical conductivity. This then confirms the common nature of these two effects. The magnetorefractive effect for s-polarization of light was calculated using Fresnel formulas for a three-layer structure. This took into account the thickness of the samples and the influence of the substrate. Effective medium methods were used to calculate the dielectric permittivity of materials. Since the average range of cobalt concentrations was being studied, the Bruggeman approximation was used to establish the effective permittivity of nanostructures. The reflection coefficient at normal incidence was calculated for all nanostructures.Results. Since the permittivity of inhomogeneous samples was replaced by a common effective parameter depending on the permittivity of each component, we were able to apply the Drude–Lorentz theory for conductors in a high-frequency alternating field and then estimate the parameters of the electronic structure of the samples being studied. Plasma and relaxation frequencies were calculated for each sample. This made it possible for the number of free electrons to be estimated and scattering in nanostructures to be investigated.Conclusions. It was shown that Langmuir shielding can be observed in the given energy range in the IR region of the spectrum. The calculated values correlate well with the experimental data.

Cobalt concentration effect on the Structural, Magnetic and Optical properties of Zn1-xCoxSe Nanoparticles

Cobalt doped Zinc selenide (Zn1-xCoxSe where x = 0.00,0.03, 0.05, 0.07, 0.09, 0.1, 0.15) nanoparticles are synthesized using co-precipitation method. For studying structural properties of prepared samples, nanoparticles are characterized by XRD (X-ray diffraction),SEM (Scanning Electron Microscope) with EDX (Energy Dispersive X-ray Diffractometer), HRTEM (High resolution transmission electron microscope),Elemental composition confirmed by EDX (Energy Dispersive X-ray Diffractometer), Inductively coupled plasma (ICP) spectroscopy test and XPS (X-ray photoelectron microscope). XRD study confirms that prepared samples are crystalline in nature and size is appeared in nanometer range with cubic structure. Optical investigation is done by UV–visible spectra and PL spectra at room temperature which indicates change in energy band gap as doping of cobalt increases in host material due to quantum confinement which shows the altered optical properties due to doping of transition metal in host material. FTIR (Fourier transform infra-red) spectroscopy reports presence of different functional groups in nanoparticles and thermal stability is confirmed by TG/DTA(Thermogravimetric) analysis. Magnetic analysis by using ESR (electron spin resonance) and VSM (Vibrating Sample Magnetometer) confirms presence of ferromagnetic coupling in cobalt doped zinc selenide nanoparticles which make these nanoparticles suitable for using in different devices e.g. in magnetic storage devices, magnetic imaging, magneto-optics and sensors etc. Combined semiconducting and magnetic nature of these Co doped ZnSe nanoparticles make them useful in spintronics, magnetic storage devices etc applications.

Effects of Co on the microstructure evolution and mechanical properties of Ti-4Al-6Cr-5Mo-8 Nb alloy by ultrasonic vacuum melting

An investigation was conducted into the impact of low cobalt content on the microstructure and mechanical properties of titanium alloys. Ti-4Al-6Cr-5Mo-8 Nb-xCo (x = 0, 2, 3, 4, and 5) alloys were prepared by ultrasonic-assisted melting and casting. The changes in microstructure, mechanical properties, and the strengthening and toughening mechanisms were researched. Results show that, when the cobalt content increases from 0 to 5 wt%, the as-cast structure is all β phase. The lattice parameter of the β phase decreases from 0.3663 to 0.3114 nm, a 15% decrease. The size of primary β grains decreases from 676.8 to 310.7 μm, a 54% decrease. When the cobalt content exceeds 3 wt%, the segregation energy of cobalt increases and grain boundary segregation occurs. Grain refinement is due to constitutional supercooling caused by the β-stable element cobalt, as well as the solute drag caused by the differences in intragranular and grain boundary compositions. In addition, the size mismatch between cobalt and titanium atoms leads to lattice distortion. As the cobalt content increases from 0 to 3 wt%, the tensile strength increases from 918.1 to 1147.8 MPa, a 25% increase, while the fracture toughness increases from 51.7 to 59.7 MPa·m1/2, a 15% increase. At 5 wt% cobalt, the tensile strength and fracture toughness diminished to 247.5 MPa and 14.8 MPa·m1/2, respectively. The decrease in lattice parameters mainly lead to an increase in strength. The secondary crack leads to an increase in toughness. The decline in strength and toughness results from cobalt segregating at grain boundaries, leading to embrittlement.

Electrochemical cobalt oxidation in chloride media

The green transition, despite recent advances in cobalt-free battery technologies, is still highly dependent on the availability of critical cobalt-based materials. Consequently, there has been increasing interest towards the development of new methods that maximize critical metals recovery from industrial hydrometallurgical solutions. In the current study, direct anodic oxidation of cobalt species from cobalt chloride solutions was studied as one alternative future strategy for cobalt recovery. Electrochemical methods were used (cyclic voltammetry, potentiostatic anodic deposition) and the effect of pH, temperature, and the concentration of cobalt and chloride ions on cobalt precipitation were investigated. The increase of pH and temperature was shown to stabilize the electrochemical oxidation of cobalt, while a decrease in cobalt concentration had a negative effect on precipitation. Scanning Electron Microscope, Atomic Force Microscopy and X-ray Photoelectron Spectroscopy were exploited to evaluate the morphology, structure, and composition of obtained anodic product. Calculated for potentiostatic anodic deposition (at highest studied potential of 1300 mV vs. Ag/AgCl) nucleation mechanism shows that the rate of nucleation for oxygen-cobalt species is faster than the subsequent growth rate of nuclei (instantaneous mechanism). XPS results confirmed that mixed Co3O4/Co(OH)2/CoOOH precipitate could be obtained by optimized anodic potentiostatic deposition in the range from 900 to 1150 mV and pH from 3 to 6 at 60 °C.

Eco-Friendly Remediation: Tea Leaves and Fibres as Adsorbents for High Cobalt Concentrations; Thermodynamics, Isotherms and Kinetic Studies

Increasing industrialization has produced huge amounts of liquid effluents, which are a key source of ecological unrest in diverse ecosystems. The high toxicity level of cobalt in surface water has drawn a lot ofattention; hence,a low-cost adsorbent made from leaves and fibres of Camellia sinensis has been developed to remove cobalt from wastewater. The kinetics of the pseudo-first and second-order sorption interaction, as well as the physicochemical parameters of the precursor adsorbent, was investigated. There was a linear relationship between Cobalt uptake and biosorbent dosage under ideal conditions; the optimum dosage was 4 g. Between 10 to 40 minutes of contact time, clearance of cobalt was greater than 90 per cent. The Gibb’s free energy (∆Go) at various temperatures ranges from -9980 to -1020, indicating a spontaneous system, viable for both parts of the precursor adsorbent. The entropy change (∆So) was found to be +31.05 and +35.12 for tea leaves and fibre respectively, implying a highly disordered biosorption interface. The enthalpy (∆Ho) was found to be-8.58 and -10.03 for tea leaves and fibres hence, an exothermic system was suggested by the enthalpy with a second order kinetics. Therefore, Camellia sinensis is a suitable adsorbent for the effective removal of high cobalt concentrations in wastewater.

A cobalt ion concentration detection model with temperature interference resistance via a novel contrastive neural network

Accurately detecting the concentration of cobalt ions in zinc solution is of great significance for improving the energy efficiency and stability of zinc hydrometallurgy. However, traditional cobalt ion detection methods have low efficiency and are susceptible to temperature interference. For this purpose, we collected spectral data of cobalt zinc solutions with different concentrations under multiple temperature conditions using a self-developed automatic detection system. Based on this dataset, we proposed a novel comparative neural network with self-attention layer, and optimized its parameters through comparative experiments. The test results indicate that the network can effectively eliminate temperature interference in spectral data. In addition, the problems of distortion and redundant dimension in the output features of comparative neural networks were discovered, and feature correction and screening were completed using isometric mapping and competitive adaptive reweighting sampling algorithms. Finally, the partial least squares regression was used to regress the obtained features, and the final regression accuracy reached 0.064 mg/L. The test results show that the accuracy of this model is 4.52 times that of the neural network model that directly maps spectral data to concentration.

СУЧАСНІ ТЕНДЕНЦІЇ РИНКУ ЛІТІЙ-ІОННИХ БАТАРЕЙ ДЛЯ ЕЛЕКТРОННИХ ПРИСТРОЇВ

A detailed review is presented in this work on the future perspectives of lithium-ion batteries with emphasis on potential of their application in portable electronic devices. As specific energy and power are key criteria in portable electronics applications, the Li-ion batteries have a clear advantage over other chemistries. The portable electronics sector requires miniaturization of batteries, while maintaining high capacity and power as well as complying with strict safety standards. Although LCO batteries still are dominant chemistry for portable electronics, it will gradually lose market share to NMC and NCA cells. These also have advantage of lower content of cobalt, which will become necessary within the overall strongly growing Li-ion battery market.

NEXAFS and XPS Studies of Co Doped Bismuth Magnesium Tantalate Pyrochlores

Co doped bismuth magnesium tantalate with a pyrochlore structure (sp. gr. Fd-3m) was synthesized for the first time using the standard ceramic method. Single phase Bi2Mg1−xCoxTa2O9 samples were found to be formed when x &lt; 0.7 in the X-ray phase analysis. However, with a higher cobalt content in the samples, the impurity phase β-BiTaO4 (sp. gr. P-1) is detected, and its amount is proportional to the degree of cobalt doping. The formation of solid solutions is evidenced by a uniform increase in the unit cell parameter of the Co,Mg co doped bismuth tantalate phase with an increase in the content of cobalt ions in the samples from 10.5412(8) (x = 0.3) to 10.5499(8) Å (x = 0.7). The samples exhibit a porous microstructure consisting of chaotically oriented and partially fused elongated grains measuring 1–2 μm. The dependence of the ceramic grain size on the n(Mg)/n(Co) ratio was not determined. X-ray spectroscopy (ear dge X-ray bsorption ine tructure (NEXAFS) and X-ray photoelectron spectroscopy (XPS)) was used to study the charge state of ions in Bi2Mg1−xCoxTa2O9. The NEXAFS and XPS data showed that doping with cobalt and magnesium did not change the bismuth and tantalum oxidation states in pyrochlore; in particular, the ions maintained their oxidation states of Bi(+3), Mg(+2) and Ta(+5). The energy position of the peaks of the Ta4f-, Ta5p-, Ta4d spectra had a characteristic shift towards lower energies compared to the binding energy in pentavalent tantalum oxide Ta2O5. A shift towards lower energies is characteristic of a decrease in the effective positive charge; in particular, for the Ta4f and Ta4d spectra we presented, this energy shift was ΔE = 0.65 eV, and in the region of the Ta4d edge—0.55 eV. This in turn allowed for us to assume that tantalum atoms have the same effective charge +(5-δ). The oxidation state of cobalt ions was predominantly 2+ and partially 3+, according to NEXAFS spectroscopy data.

Revealing the effect of cobalt content and ligand exchange in the bimetallic Ni–Co MOF for stable supercapacitors with high energy density

Metal-organic frameworks (MOF) exhibit considerable potential as electrode materials for supercapacitors. Nevertheless, the electrochemical performance of the MOF is impeded by its low electrical conductivity and chemical stability. In this study, we investigate the impact of cobalt composition and ligand exchange on the performance of bimetallic NiCo-MOF to unlock its optimal performance. Our results reveal that integrating cobalt affects the abundance of Ni3+ and Co2+, which serve as electrochemical active species. Additionally, ligand exchange with a phosphate group leads to further modifications in both abundance and surface area. The result indicates that a Ni/Co ratio of 10:1 in NiCo-MOF exhibits superior performance (437 C g−1 at 0.5 A g−1), surpassing the performance of other ratios. Furthermore, the process of ligand exchange in NiCo-MOF with a Ni/Co ratio of 10:1 yields an even higher capacity of 522 C g−1 at 0.5 A g−1, with an energy density of 22 Wh kg−1 at 363 W kg−1 when assembled in an asymmetric supercapacitor cell. The supercapacitor cell demonstrates a remarkable capacity retention of 99 % at 5 A g−1 over 5000 cycles. This study provides insight into the pivotal role of cobalt composition and ligand exchange in improving the electrochemical performance of NiCo-MOF.