Cobalt sulfide

Last updated
Cobalt sulfide
FeS2structure.png
Sulfid kobaltnaty.PNG
Identifiers
PubChem CID
RTECS number
  • GG332500
UNII
Properties
CoxSy
Molar mass 90.9982 g/mol
Appearanceblack solid (alpha)
grayish-red crystals (beta)
Density 5.45 g/cm3
Melting point 1195 °C
0.00038 g/100 mL (18 °C)
Solubility slightly soluble in acid
+225.0·10−6 cm3/mol
Structure
octahedral (beta)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Yes check.svgY  verify  (what is  Yes check.svgYX mark.svgN ?)

Cobalt sulfide is the name for chemical compounds with a formula CoxSy. Well-characterized species include minerals with the formulas CoS, CoS2, Co3S4, and Co9S8. In general, the sulfides of cobalt are black, semiconducting, insoluble in water, and nonstoichiometric. [1]

Contents

Minerals and hydrometallurgy

Cobalt sulfides occur widely as minerals, comprising major sources of all cobalt compounds. Binary cobalt sulfide minerals include the cattierite (CoS2) and linnaeite (Co3S4). CoS2 (see image in table) is isostructural with iron pyrite, featuring disulfide groups, i.e. Co2+S22−. Linnaeite, also rare, adopts the spinel motif. [2] The Co9S8 compound is known as a very rare cobaltpentlandite (the Co analogue of pentlandite). [3] Mixed metal sulfide minerals include carrollite (CuCo2S4) and siegenite (Co3−xNixS4).

CoS is known as jaipurite. However, this species is questionable. [4] [5]

Cobalt sulfide minerals are converted to cobalt via roasting and extraction into aqueous acid. In some processes, cobalt salts are purified by precipitation when aqueous solutions of cobalt(II) ions are treated with hydrogen sulfide. Not only is this reaction useful in the purification of cobalt from its ores, but also in qualitative inorganic analysis. [1]

Applications and research

In combination with molybdenum, the sulfides of cobalt are used as catalysts for the industrial process called hydrodesulfurization, which is implemented on a large scale in refineries. Synthetic cobalt sulfides are widely investigated as electrocatalysts. [6]

Selected literature

Related Research Articles

<span class="mw-page-title-main">Cadmium sulfide</span> Chemical compound

Cadmium sulfide is the inorganic compound with the formula CdS. Cadmium sulfide is a yellow solid. It occurs in nature with two different crystal structures as the rare minerals greenockite and hawleyite, but is more prevalent as an impurity substituent in the similarly structured zinc ores sphalerite and wurtzite, which are the major economic sources of cadmium. As a compound that is easy to isolate and purify, it is the principal source of cadmium for all commercial applications. Its vivid yellow color led to its adoption as a pigment for the yellow paint "cadmium yellow" in the 18th century.

<span class="mw-page-title-main">Lead(II) sulfide</span> Chemical compound

Lead(II) sulfide is an inorganic compound with the formula PbS. Galena is the principal ore and the most important compound of lead. It is a semiconducting material with niche uses.

<span class="mw-page-title-main">Dye-sensitized solar cell</span> Type of thin-film solar cell

A dye-sensitized solar cell is a low-cost solar cell belonging to the group of thin film solar cells. It is based on a semiconductor formed between a photo-sensitized anode and an electrolyte, a photoelectrochemical system. The modern version of a dye solar cell, also known as the Grätzel cell, was originally co-invented in 1988 by Brian O'Regan and Michael Grätzel at UC Berkeley and this work was later developed by the aforementioned scientists at the École Polytechnique Fédérale de Lausanne (EPFL) until the publication of the first high efficiency DSSC in 1991. Michael Grätzel has been awarded the 2010 Millennium Technology Prize for this invention.

<span class="mw-page-title-main">Siegenite</span>

Siegenite (also called grimmite, or nickel cobalt sulfide) is a ternary transition metal dichalcogenide compound with the chemical formula (Ni,Co)3S4. It has been actively studied as a promising material system for electrodes in electrochemical energy applications due to its better conductivity, greater mechanical and thermal stability, and higher performance compared to metal oxides currently in use. Potential applications of this material system include supercapacitors, batteries, electrocatalysis, dye-sensitized solar cells, photocatalysis, glucose sensors, and microwave absorption.

Indium(III) sulfide (Indium sesquisulfide, Indium sulfide (2:3), Indium (3+) sulfide) is the inorganic compound with the formula In2S3.

<span class="mw-page-title-main">Fast ion conductor</span>

In materials science, fast ion conductors are solid conductors with highly mobile ions. These materials are important in the area of solid state ionics, and are also known as solid electrolytes and superionic conductors. These materials are useful in batteries and various sensors. Fast ion conductors are used primarily in solid oxide fuel cells. As solid electrolytes they allow the movement of ions without the need for a liquid or soft membrane separating the electrodes. The phenomenon relies on the hopping of ions through an otherwise rigid crystal structure.

The polysulfide–bromine battery, is a type of rechargeable electric battery, which stores electric energy in liquids, such as water-based solutions of two salts: sodium bromide and sodium polysulfide. It is an example and type of redox (reduction–oxidation) flow battery.

<span class="mw-page-title-main">Carrollite</span>

Carrollite, CuCo2S4, is a sulfide of copper and cobalt, often with substantial substitution of nickel for the metal ions, and a member of the linnaeite group. It is named after the type locality in Carroll County, Maryland, US, at the Patapsco mine, Sykesville.

<span class="mw-page-title-main">PEDOT-TMA</span> Chemical compound

Poly(3,4-ethylenedioxythiophene)-tetramethacrylate or PEDOT-TMA is a p-type conducting polymer based on 3,4-ethylenedioxylthiophene or the EDOT monomer. It is a modification of the PEDOT structure. Advantages of this polymer relative to PEDOT are that it is dispersible in organic solvents, and it is non-corrosive. PEDOT-TMA was developed under a contract with the National Science Foundation, and it was first announced publicly on April 12, 2004. The trade name for PEDOT-TMA is Oligotron. PEDOT-TMA was featured in an article entitled "Next Stretch for Plastic Electronics" that appeared in Scientific American in 2004. The U.S. Patent office issued a patent protecting PEDOT-TMA on April 22, 2008.

<span class="mw-page-title-main">Lithium cobalt oxide</span> Chemical compound

Lithium cobalt oxide, sometimes called lithium cobaltate or lithium cobaltite, is a chemical compound with formula LiCoO
2
. The cobalt atoms are formally in the +3 oxidation state, hence the IUPAC name lithium cobalt(III) oxide.

A Direct Carbon Fuel Cell (DCFC) is a fuel cell that uses a carbon rich material as a fuel such as bio-mass or coal. The cell produces energy by combining carbon and oxygen, which releases carbon dioxide as a by-product. It is also called coal fuel cells (CFCs), carbon-air fuel cells (CAFCs), direct carbon/coal fuel cells (DCFCs), and DC-SOFC.

<span class="mw-page-title-main">Cobalt(II) hydroxide</span> Chemical compound

Cobalt(II) hydroxide or cobaltous hydroxide is the inorganic compound with the formula Co(OH)
2
, consisting of divalent cobalt cations Co2+
and hydroxide anions OH
. The pure compound, often called the "beta form" is a pink solid insoluble in water.

<span class="mw-page-title-main">Separator (electricity)</span>

A separator is a permeable membrane placed between a battery's anode and cathode. The main function of a separator is to keep the two electrodes apart to prevent electrical short circuits while also allowing the transport of ionic charge carriers that are needed to close the circuit during the passage of current in an electrochemical cell.

<span class="mw-page-title-main">Zinc–cerium battery</span>

Zinc–cerium batteries are a type of redox flow battery first developed by Plurion Inc. (UK) during the 2000s. In this rechargeable battery, both negative zinc and positive cerium electrolytes are circulated though an electrochemical flow reactor during the operation and stored in two separated reservoirs. Negative and positive electrolyte compartments in the electrochemical reactor are separated by a cation-exchange membrane, usually Nafion (DuPont). The Ce(III)/Ce(IV) and Zn(II)/Zn redox reactions take place at the positive and negative electrodes, respectively. Since zinc is electroplated during charge at the negative electrode this system is classified as a hybrid flow battery. Unlike in zinc–bromine and zinc–chlorine redox flow batteries, no condensation device is needed to dissolve halogen gases. The reagents used in the zinc-cerium system are considerably less expensive than those used in the vanadium flow battery.

<span class="mw-page-title-main">Cobalt oxide nanoparticle</span>

In materials and electric battery research, cobalt oxide nanoparticles usually refers to particles of cobalt(II,III) oxide Co
3
O
4
of nanometer size, with various shapes and crystal structures.

<span class="mw-page-title-main">Solid dispersion redox flow battery</span>

A solid dispersion redox flow battery is a type of redox flow battery using dispersed solid active materials as the energy storage media. The solid suspensions are stored in energy storage tanks and pumped through electrochemical cells while charging or discharging. In comparison with a conventional redox flow battery where active species are dissolved in aqueous or organic electrolyte, the active materials in a solid dispersion redox flow battery maintain the solid form and are suspended in the electrolyte. Further development expanded the applicable active materials. The solid active materials, especially with active materials from lithium-ion battery, can help the suspensions achieve much higher energy densities than conventional redox flow batteries. This concept is similar to semi-solid flow batteries in which slurries of active materials accompanied by conductive carbon additives to facilitate electrons conducting are stored in energy storage tanks and pumped through the electrochemical reaction cells. Based upon this technique, an analytical method was developed to measure the electrochemical performance of lithium-ion battery active materials, named dispersed particle resistance (DPR).

Dispersed particle resistance (DPR) is a measured parameter to characterize battery active materials. It is seen as an indicator of lithium-ion battery active material rate capability. It is the slope of voltage-current linear fit for active material samples in suspensions. It can be obtained by applying different voltages on a suspension and measuring the currents, after which the data points are plotted. The slope of the plot is referred to as dispersed particle resistance. It can also be done in the opposite way where different currents are applied and voltages are measured. The key advantage of this dispersed particle resistance technique is fast and accurate comparing with the conventional characterization method for which batteries need to be fabricated and tested for a long time.

Scanning vibrating electrode technique (SVET), also known as vibrating probe within the field of biology, is a scanning probe microscopy (SPM) technique which visualizes electrochemical processes at a sample. It was originally introduced in 1974 by Jaffe and Nuccitelli to investigate the electrical current densities near living cells. Starting in the 1980s Hugh Isaacs began to apply SVET to a number of different corrosion studies. SVET measures local current density distributions in the solution above the sample of interest, to map electrochemical processes in situ as they occur. It utilizes a probe, vibrating perpendicular to the sample of interest, to enhance the measured signal. It is related to scanning ion-selective electrode technique (SIET), which can be used with SVET in corrosion studies, and scanning reference electrode technique (SRET), which is a precursor to SVET.

Electro-oxidation(EO or EOx), also known as anodic oxidation or electrochemical oxidation (EC), is a technique used for wastewater treatment, mainly for industrial effluents, and is a type of advanced oxidation process (AOP). The most general layout comprises two electrodes, operating as anode and cathode, connected to a power source. When an energy input and sufficient supporting electrolyte are provided to the system, strong oxidizing species are formed, which interact with the contaminants and degrade them. The refractory compounds are thus converted into reaction intermediates and, ultimately, into water and CO2 by complete mineralization.

<span class="mw-page-title-main">Lithium nickel manganese cobalt oxides</span> Lithium ion battery cathode material

Lithium nickel manganese cobalt oxides (abbreviated NMC, Li-NMC, LNMC, or NCM) are mixed metal oxides of lithium, nickel, manganese and cobalt with the general formula LiNixMnyCo1-x-yO2. These materials are commonly used in lithium-ion batteries for mobile devices and electric vehicles, acting as the positively charged cathode.

References

  1. 1 2 John D. Donaldson, Detmar Beyersmann "Cobalt and Cobalt Compounds" in Ullmann's Encyclopedia of Industrial Chemistry 2005, Wiley-VCH, Weinheim. doi : 10.1002/14356007.a07_281.pub2
  2. Greenwood, Norman N.; Earnshaw, Alan (1984). Chemistry of the Elements. Oxford: Pergamon Press. ISBN   978-0-08-022057-4.
  3. "Home". mindat.org.
  4. "Jaipurite".
  5. "List of Minerals". 21 March 2011.
  6. Mathew, Simon; Yella, Aswani; Gao, Peng; Humphry-Baker, Robin; Curchod, Basile F. E.; Ashari-Astani, Negar; Tavernelli, Ivano; Rothlisberger, Ursula; Nazeeruddin, Md. Khaja (2014). "Dye-sensitized solar cells with 13% efficiency achieved through the molecular engineering of porphyrin sensitizers". Nature Chemistry. 6 (3): 242–247. Bibcode:2014NatCh...6..242M. doi:10.1038/nchem.1861. PMID   24557140.