Silver sulfide
{{chembox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 455355846
| Name =
| ImageFile = Ag2S-bas.png
| ImageSize = 160px
| ImageName = Ball-and-stick model of silver sulfide
| ImageFile1 = Sulfid stříbrný.PNG
| ImageSize1 =
| ImageName1 = Sample of silver sulfide
| IUPACName = Silver(I) sulfide
| OtherNames = Silver sulfide
Argentous sulfide
| SystematicName =
| Section1 = {{Chembox Identifiers
| Abbreviations =
| CASNo = 21548-73-2
| CASNo_Ref = {{cascite|correct|CAS}}
| EC_number = 244-438-2
| PubChem = 166738
| RTECS =
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 145878
| UNII = 9ZB10YHC1C
| UNII_Ref = {{fdacite|changed|FDA}}
| SMILES = S(Ag)Ag
| StdInChI = 1S/2Ag.S/q2*+1;-2
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = XUARKZBEFFVFRG-UHFFFAOYSA-N
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
}}
| Section2 = {{Chembox Properties
| Ag=2 | S=1
| Appearance = Grayish-blackish crystal
| Odor = Odorless
| Density = 7.234 g/cm3 (25 °C)
7.12 g/cm3 (117 °C)
| MeltingPtC = 836
| MeltingPt_ref = {{CRC90}}
| Solubility = 6.21·10−15 g/L (25 °C)
| SolubleOther = Soluble in aq. HCN, aq. citric acid with KNO3
Insoluble in acids, alkalies, aqueous ammoniums{{cite book|page = [https://archive.org/details/in.ernet.dli.2015.171090/page/n861 835]|title = A Dictionary of Chemical Solubilities: Inorganic|url = https://archive.org/details/in.ernet.dli.2015.171090|edition = 2nd|first1 = Arthur Messinger|last1 = Comey|first2 = Dorothy A.|last2 = Hahn|place = New York|publisher = The MacMillan Company|date = February 1921}}
| SolubilityProduct = 6.31·10−50
}}
| Section3 = {{Chembox Structure
| CrystalStruct = Monoclinic, mP12 (α-form)
Cubic, cI8 (β-form)
Cubic, cF12 (γ-form){{cite book|url = https://books.google.com/books?id=uo8wVw9Gq7wC&pg=PA13|title = High Pressure Phase Transformations: A Handbook|volume = 1|first = E. Yu|last = Tonkov|publisher = Gordon and Breach Science Publishers|year = 1992|isbn = 978-2-88124-761-3|page = 13}}
| SpaceGroup = Im{{overline|3}}m, No. 229 (α-form)
P21/n, No. 14 (β-form)
Fm{{overline|3}}m, No. 225 (γ-form)
| PointGroup = 2/m (α-form)
4/m {{overline|3}} 2/m (β-form, γ-form)
| LattConst_a = 4.23 Å
| LattConst_b = 6.91 Å
| LattConst_c = 7.87 Å (α-form)
| LattConst_beta = 99.583
| Coordination =
}}
| Section4 = {{Chembox Thermochemistry
| DeltaHf = −32.59 kJ/mol{{cite book|last = Pradyot|first = Patnaik|year = 2003|title = Handbook of Inorganic Chemicals|publisher = The McGraw-Hill Companies, Inc.|isbn = 978-0-07-049439-8|page = 845}}
| HeatCapacity = 76.57 J/mol·K
}}
| Section5 =
| Section6 =
| Section7 = {{Chembox Hazards
| MainHazards = May cause irritation
| GHSPictograms = {{GHS07}}{{Sigma-Aldrich| id=241474 |name=Silver sulfide|accessdate=2014-07-13}}
| GHSSignalWord = Warning
| HPhrases = {{H-phrases|315|319|335}}
| PPhrases = {{P-phrases|261|305+351+338}}
| NFPA-H = 0
| NFPA-F = 0
| NFPA-R = 0
| LD50 =
}}
}}
Silver sulfide is an inorganic compound with the formula {{chem|Ag|2|S}}. A dense black solid, it is the only sulfide of silver. It is useful as a photosensitizer in photography. It constitutes the tarnish that forms over time on silverware and other silver objects. Silver sulfide is insoluble in most solvents, but is degraded by strong acids. Silver sulfide is a network solid made up of silver (electronegativity of 1.98) and sulfur (electronegativity of 2.58) where the bonds have low ionic character (approximately 10%).
Formation
Silver sulfide naturally occurs as the tarnish on silverware. When combined with silver, hydrogen sulfide gas creates a layer of black silver sulfide patina on the silver, protecting the inner silver from further conversion to silver sulfide.{{cite book|last1=Zumdahl|first1=Steven S.|url=https://books.google.com/books?id=hsuV9JTGaP8C&pg=PA505|title=Chemical Principles|last2=DeCoste|first2=Donald J.|year=2013|isbn=978-1-111-58065-0|edition=7th|page=505|publisher=Cengage Learning }} Silver whiskers can form when silver sulfide forms on the surface of silver electrical contacts operating in an atmosphere rich in hydrogen sulfide and high humidity.{{Cite web|date=2002|title=Degradation of Power Contacts in Industrial Atmosphere: Silver Corrosion and Whiskers|url=https://nepp.nasa.gov/whisker/reference/tech_papers/chudnovsky2002-paper-silver-corrosion-whiskers.pdf}} Such atmospheres can exist in sewage treatment and paper mills.{{Cite journal|last1=Dutta|first1=Paritam K.|last2=Rabaey|first2=Korneel|last3=Yuan|first3=Zhiguo|last4=Rozendal|first4=René A.|last5=Keller|first5=Jürg|date=2010|title=Electrochemical sulfide removal and recovery from paper mill anaerobic treatment effluent|journal=Water Research|volume=44|issue=8|pages=2563–2571|doi=10.1016/j.watres.2010.01.008|issn=0043-1354|pmid=20163816|bibcode=2010WatRe..44.2563D }}{{Cite web|title=Control of Hydrogen Sulfide Generation {{!}} Water & Wastes Digest|url=https://www.wwdmag.com/corrosion/control-hydrogen-sulfide-generation|access-date=2018-07-05|website=www.wwdmag.com|date=5 March 2012 |language=en}}
Structure and properties
Three forms are known: monoclinic acanthite (α-form), stable below 179 °C, body centered cubic so-called argentite (β-form), stable above 180 °C, and a high temperature face-centred cubic (γ-form) stable above 586 °C.{{cite book|doi = 10.1007/10681727_86|pages = 1–4|year = 1998|isbn = 978-3-540-31360-1|volume = 41C|publisher = Springer Berlin Heidelberg|chapter-url = https://link.springer.com/static-content/lookinside/996/chp%253A10.1007%252F10681727_86/000.png|title = Non-Tetrahedrally Bonded Elements and Binary Compounds I|series = Landolt-Börnstein - Group III Condensed Matter|chapter = Silver sulfide (Ag2S) crystal structure}} The higher temperature forms are electrical conductors. It is found in nature as relatively low temperature mineral acanthite. Acanthite is an important ore of silver. The acanthite, monoclinic, form features two kinds of silver centers, one with two and the other with three near neighbour sulfur atoms.Frueh, A. J. (1958). The crystallography of silver sulfide, Ag2S. Zeitschrift für Kristallographie-Crystalline Materials, 110(1-6), 136-144. Argentite refers to a cubic form, which, due to instability in "normal" temperatures, is found in form of the pseudomorphosis of acanthite after argentite.
Exceptional ductility of α-Ag<sub>2</sub>S
Relative to most inorganic materials, α-Ag2S displays exceptional ductility at room temperature.{{Cite journal |last=Chen |first=Lidong |year=2018 |title=Room-temperature ductile inorganic semiconductor |url=https://www.nature.com/articles/s41563-018-0047-z |journal=Nature Materials |volume=17 |pages=421-426}}{{Cite journal |last=Chen |first=Lidong |title=Flexible thermoelectrics based on ductile semiconductors |url=https://www.science.org/doi/full/10.1126/science.abq0682 |journal=Science |volume=377 |issue=6608 |pages=854-858}} This material can undergo extensive deformation, akin to metals, without fracturing. Such behavior is evident in various mechanical tests; for instance, α-Ag2S can be easily machined into cylindrical or bar shapes and can withstand substantial deformation under compression, three-point bending, and tensile stresses. The material sustains over 50% engineering strain in compression tests and up to 20% or more in bending tests.
The intrinsic ductility of alpha-phase silver sulfide (α-Ag2S) is underpinned by its unique structural and chemical bonding characteristics. At the atomic level, its monoclinic crystal structure, which remains stable up to 451 K, enables the movement of atoms and dislocations along well-defined crystallographic planes known as slip planes. Additionally, the dynamic bonding within the crystal structure supports both the sliding of atomic layers and the maintenance of material integrity during deformation. The interatomic forces within the slip planes are sufficiently strong to prevent the material from cleaving while still allowing for considerable flexibility. Further insights into α-Ag2S's ductility come from density functional theory calculations, which reveal that the primary slip planes align with the [100] direction and slipping occurs along the [001] direction. This arrangement permits atoms to glide over each other under stress through minute adjustments in the interlayer distances, which are energetically favorable as indicated by low slipping energy barriers (ΔEB) and high cleavage energies (ΔEC). These properties ensure significant deformation capability without fracture. Silver and sulfur atoms in α-Ag2S form transient, yet robust interactions that enable the material to retain its integrity while deforming. This behavior is akin to that of metals, where dislocations move with relative ease, providing α-Ag2S with a unique combination of flexibility and strength, making it exceptionally resistant to cracking under mechanical stress.
History
In 1833 Michael Faraday noticed that the resistance of silver sulfide decreased dramatically as temperature increased. This constituted the first report of a semiconducting material.{{cite web|title=1833 - First Semiconductor Effect is Recorded|url=http://www.computerhistory.org/semiconductor/timeline/1833-first.html|access-date=24 June 2014|website=Computer History Museum}}
Silver sulfide is a component of classical qualitative inorganic analysis.{{Greenwood&Earnshaw2nd}}
References
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External links
- [http://www.vam.ac.uk/content/journals/conservation-journal/issue-18/tarnishing-of-silver-a-short-review/ Tarnishing of Silver: A Short Review] V&A Conservation Journal
- [https://nepp.nasa.gov/whisker/other_whisker/silver/index.htm Images of silver whiskers] NASA
{{Commons category|Silver sulfide}}
{{Silver compounds}}
{{Sulfides}}
{{Authority control}}