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Lead(II) iodide

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Lead(II) iodide
Lead(II) iodide
Lead(II) iodide
Names
Other names Plumbous iodide
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.030.220 Edit this at Wikidata
EC Number
  • 233-256-9
PubChem CID
UNII
UN number 2291 3077
CompTox Dashboard (EPA)
InChI
  • InChI=1S/2HI.Pb/h2*1H;/q;;+2/p-2Key: RQQRAHKHDFPBMC-UHFFFAOYSA-L
  • InChI=1/2HI.Pb/h2*1H;/q;;+2/p-2Key: RQQRAHKHDFPBMC-NUQVWONBAP
SMILES
  • II
Properties
Chemical formula PbI
2
Molar mass 461.01 g/mol
Appearance bright yellow powder
Odor odorless
Density 6.16 g/cm
Melting point 410 °C (770 °F; 683 K)
Boiling point 872 °C (1,602 °F; 1,145 K) decomp.
Solubility in water
  • 0.44 g/L (0 °C)
  • 0.76 g/L (20 °C)
  • 4.1 g/L (100 °C)
Solubility product (Ksp) 4.41×10 (20 °C)
Solubility
Band gap 2.34 eV (direct)
Magnetic susceptibility (χ) −126.5·10 cm/mol
Structure
Crystal structure Hexagonal hP6
Space group P63mc, No. 186
Lattice constant a = 0.4556 nm, b = 0.4556 nm, c = 1.3973 nmα = 90°, β = 90°, γ = 120°°
Formula units (Z) 2
Coordination geometry octahedral
Thermochemistry
Heat capacity (C) 77.4 J/(mol·K)
Std molar
entropy
(S298)
174.9 J/(mol·K)
Std enthalpy of
formation
fH298)
-175.5 kJ/mol
Gibbs free energyfG) -173.6 kJ/mol
Hazards
GHS labelling:
Pictograms GHS07: Exclamation markGHS08: Health hazardGHS09: Environmental hazard
Signal word Danger
Hazard statements H302, H332, H360, H373, H410
Precautionary statements P201, P202, P260, P261, P264, P270, P271, P273, P281, P301+P312, P304+P312, P304+P340, P308+P313, P312, P314, P330, P391, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
3 0 0
Flash point Non-flammable
Related compounds
Other anions
Other cations Tin(II) iodide
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒verify (what is  ?) Infobox references
Chemical compound

Lead(II) iodide (or lead iodide) is a chemical compound with the formula PbI
2. At room temperature, it is a bright yellow odorless crystalline solid, that becomes orange and red when heated. It was formerly called plumbous iodide.

The compound currently has a few specialized applications, such as the manufacture of solar cells, X-rays and gamma-ray detectors. Its preparation is an entertaining and popular demonstration in chemistry education, to teach topics such as precipitation reactions and stoichiometry. It is decomposed by light at temperatures above 125 °C (257 °F), and this effect has been used in a patented photographic process.

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.

Preparation

PbI
2 is commonly synthesized via a precipitation reaction between potassium iodide KI and lead(II) nitrate Pb(NO
3)2 in water solution:

Pb(NO3)2 + 2 KI → PbI2 + 2 KNO3

While the potassium nitrate KNO
3 is soluble, the lead iodide PbI
2 is nearly insoluble at room temperature, and thus precipitates out.

Other soluble compounds containing lead(II) and iodide can be used instead, for example lead(II) acetate and sodium iodide.

The compound can also be synthesized by reacting iodine vapor with molten lead between 500 and 700 °C.

A thin film of PbI
2 can also be prepared by depositing a film of lead sulfide PbS and exposing it to iodine vapor, by the reaction

PbS + I2 → PbI2 + S

The sulfur is then washed with dimethyl sulfoxide.

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". Larger crystals can be obtained by autoclaving the PbI
2 with water under pressure at 200 °C.

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.

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.

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 PbI
2 crystals in zero gravity, in an experiment flown on the Space Shuttle Discovery.

PbI
2 can also be crystallized from powder by sublimation at 390 °C, in near vacuum or in a current of argon with some hydrogen.

Large high-purity crystals can be obtained by zone melting or by the Bridgman–Stockbarger technique. These processes can remove various impurities from commercial PbI
2.

Applications

Lead iodide is a precursor material in the fabrication of highly efficient Perovskite solar cell. Typically, a solution of PbI
2 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 CH
3NH
3I and annealed, turning it into the double salt methylammonium lead iodide CH
3NH
3PbI
3, with a perovskite structure. The reaction changes the film's color from yellow to light brown.

PbI
2 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.

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." However, due to the toxicity and instability of the compound it is no longer used as such. It may still be used in art for bronzing and in gold-like mosaic tiles.

Stability

Common material characterization techniques such as electron microscopy can damage samples of lead(II) iodide. Thin films of lead(II) iodide are unstable in ambient air. Ambient air oxygen oxidizes iodide into elemental iodine:

2 PbI2 + O2 → 2 PbO + 2 I2

Toxicity

Lead iodide is very toxic to human health. Ingestion will cause many acute and chronic consequences characteristic of lead poisoning. Lead iodide has been found to be a carcinogen in animals suggesting the same may hold true in humans. Lead iodide is an inhalation hazard, and appropriate respirators should be used when handling powders of lead iodide.

Structure

The structure of PbI
2, 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. 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. The solid can also take an R6 rhombohedral structure.

  • Lead(II) iodide precipitates when solutions of potassium iodide and lead(II) nitrate are combined Lead(II) iodide precipitates when solutions of potassium iodide and lead(II) nitrate are combined
  • Experiment "golden rain" where iodide of lead(II) was recrystallized from hot solution by cooling, forming crystals of golden-yellow Experiment "golden rain" where iodide of lead(II) was recrystallized from hot solution by cooling, forming crystals of golden-yellow

See also

References

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Cited sources

External links

Lead compounds
Pb(II)
Pb(II,IV)
Pb(IV)
Salts and covalent derivatives of the iodide ion
HI
+H
He
LiI BeI2 BI3
+BO3
CI4
+C
NI3
NH4I
+N
I2O4
I2O5
I2O6
I4O9
IF
IF3
IF5
IF7
Ne
NaI MgI2 AlI
AlI3
SiI4 PI3
P2I4
+P
PI5
S2I2 ICl
ICl3
Ar
KI CaI2 ScI3 TiI2
TiI3
TiI4
VI2
VI3
CrI2
CrI3
CrI4
MnI2 FeI2
FeI3
CoI2 NiI2
-Ni
CuI ZnI2 GaI
GaI3
GeI2
GeI4
+Ge
AsI3
As2I4
+As
Se IBr
IBr3
Kr
RbI
RbI3
SrI2 YI3 ZrI2
ZrI3
ZrI4
NbI4
NbI5
MoI2
MoI3
TcI3 RuI3 RhI3 PdI2 AgI CdI2 InI
InI3
SnI2
SnI4
SbI3
+Sb
TeI4
+Te
I
I
3
Xe
CsI
CsI3
BaI2   LuI3 HfI3
HfI4
TaI4
TaI5
WI2
WI3
WI4
ReI3
ReI
4
OsI
OsI2
OsI3
IrI3
IrI
4
PtI2
PtI4
AuI
AuI3
Hg2I2
HgI2
TlI
TlI3
PbI2 BiI3 PoI2
PoI4
AtI Rn
Fr RaI2   Lr Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
LaI2
LaI3
CeI2
CeI3
PrI2
PrI3
NdI2
NdI3
PmI3 SmI2
SmI3
EuI2
EuI3
GdI2
GdI3
TbI3 DyI2
DyI
3
HoI3 ErI3 TmI2
TmI3
YbI2
YbI3
AcI3 ThI2
ThI3
ThI4
PaI4
PaI5
UI3
UI4
NpI3 PuI3 AmI2
AmI3
CmI3 BkI
3
CfI
2

CfI
3
EsI2
EsI3
Fm Md No
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