Lead(II) iodide
Lead(II) iodide (or lead iodide) is a chemical compound with the formula Template:Chem/link. At room temperature, it is a bright yellow odorless crystalline solid, that becomes orange and red when heated.[1] It was formerly called plumbous iodide.
The compound currently has a few specialized applications, such as the manufacture of solar cells,[2] X-rays and gamma-ray detectors.[3] Its preparation is used in chemistry education to teach topics such as precipitation reactions and stoichiometry.[4] It is decomposed by light at temperatures above Script error: No such module "convert"., and this effect has been used in a patented photographic process.[5][6]
Lead iodide was formerly employed as a yellow pigment in some paints, with the name iodide yellow. However, that use has been largely discontinued due to its toxicity and poor stability.[7]
Preparation
Template:Chem/link is commonly synthesized via a precipitation reaction between iodide Template:Chem/link and lead(II) Template:Chem/link2 in water solution:
The lead iodide Template:Chem/link is nearly insoluble at room temperature, and thus precipitates out.[8]
Other soluble compounds containing lead(II) and iodide can be used instead, for example lead(II) acetate[2] and sodium iodide.
The compound can also be synthesized by reacting iodine vapor with molten lead between 500 and 700 °C.[9]
A thin film of Template:Chem/link can also be prepared by depositing a film of lead sulfide Template:Chem/link and exposing it to iodine vapor, by the reaction
The sulfur is then washed with dimethyl sulfoxide.[10]
Crystallization
Lead iodide prepared from cold solutions usually consists of many small hexagonal platelets, giving the yellow precipitate a silky appearance. Larger crystals can be obtained by exploiting the fact that solubility of lead iodide in water (like those of lead chloride and lead bromide) increases dramatically with temperature. The compound is colorless when dissolved in hot water, but crystallizes on cooling as thin but visibly larger bright yellow flakes, that settle slowly through the liquid — a visual effect often described as "golden rain".[11] Larger crystals can be obtained by autoclaving the Template:Chem/link with water under pressure at 200 °C.[12]
Even larger crystals can be obtained by slowing down the common reaction. A simple setup is to submerge two beakers containing the concentrated reactants in a larger container of water, taking care to avoid currents. As the two substances diffuse through the water and meet, they slowly react and deposit the iodide in the space between the beakers.[13]
Another similar method is to react the two substances in a gel medium, that slows down the diffusion and supports the growing crystal away from the container's walls. Patel and Rao have used this method to grow crystals up to 30 mm in diameter and 2 mm thick.[14]
The reaction can be slowed also by separating the two reagents with a permeable membrane. This approach, with a cellulose membrane, was used in September 1988 to study the growth of Template:Chem/link crystals in zero gravity, in an experiment flown on the Space Shuttle Discovery.[15]
Template:Chem/link can also be crystallized from powder by sublimation at 390 °C, in near vacuum[16] or in a current of argon with some hydrogen.[17]
Large high-purity crystals can be obtained by zone melting or by the Bridgman–Stockbarger technique.[9][16] These processes can remove various impurities from commercial Template:Chem/link.[18]
Applications
Lead iodide is a precursor material in the fabrication of highly efficient Perovskite solar cell. Typically, a solution of Template:Chem/link in an organic solvent, such as dimethylformamide or dimethylsulfoxide, is applied over a titanium dioxide layer by spin coating. The layer is then treated with a solution of methylammonium iodide Template:Chem/link and annealed, turning it into the double salt methylammonium lead iodide Template:Chem/link, with a perovskite structure. The reaction changes the film's color from yellow to light brown.[2]
Template:Chem/link is also used as a high-energy photon detector for gamma-rays and X-rays, due to its wide band gap which ensures low noise operation.[5][3][16]
Lead iodide was formerly used as a paint pigment under the name "iodine yellow". It was described by Prosper Mérimée (1830) as "not yet much known in commerce, is as bright as orpiment or chromate of lead. It is thought to be more permanent; but time only can prove its pretension to so essential a quality. It is prepared by precipitating a solution of acetate or nitrate of lead, with potassium iodide: the nitrate produces a more brilliant yellow color."[7] However, due to the toxicity and instability of the compound it is no longer used as such.[7] It may still be used in art for bronzing and in gold-like mosaic tiles.[5]
Stability
Common material characterization techniques such as electron microscopy can damage samples of lead(II) iodide.[19] Thin films of lead(II) iodide are unstable in ambient air.[20] Ambient air oxygen oxidizes iodide into elemental iodine:
Toxicity
Lead iodide is very toxic to human health. Ingestion will cause many acute and chronic consequences characteristic of lead poisoning.[21] Lead iodide has been found to be a carcinogen in animals suggesting the same may hold true in humans.[22] Lead iodide is an inhalation hazard, and appropriate respirators should be used when handling powders of lead iodide.
Structure
The structure of Template:Chem/link, as determined by X-ray powder diffraction, is primarily hexagonal close-packed system with alternating between layers of lead atoms and iodide atoms, with largely ionic bonding. Weak van der Waals interactions have been observed between lead–iodide layers.[3] The most common stacking forms are 2H and 4H. The 4H polymorph is most common in samples grown from the melt, by precipitation, or by sublimation, whereas the 2H polymorph is usually formed by sol-gel synthesis.[23] The solid can also take an R6 rhombohedral structure.[24]
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See also
References
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Cited sources
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External links
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