Silver (Ag)
transition-metalSolid
标准原子量
107.8682 u电子排布
[Kr] 5s1 4d10熔点
961.78 °C沸点
2161.85 °C密度
1.0501e+4 kg/m³氧化态
−2, −1, 0, +1, +2, +3电负性（鲍林）
1.93第一电离能
7.576234 eV发现年份
暂无原子半径
160 pm详细信息
Silver is a soft, dense transition metal in group 11, chemically related to copper and gold but more reactive than gold. It is the best elemental conductor of electricity and heat at ordinary temperatures and has exceptional optical reflectivity when freshly polished. In nature it occurs as native metal and in sulfide, sulfosalt, chloride, and telluride minerals, commonly associated with lead, zinc, copper, and gold ores.
Pure silver has a brilliant white metallic luster. It is a little harder than gold and is very ductile and malleable, being exceeded only by gold and perhaps palladium. Pure silver has the highest electrical and thermal conductivity of all metals, and possesses the lowest contact resistance. It is stable in pure air and water, but tarnishes when exposed to ozone, hydrogen sulfide, or air containing sulfur. The alloys of silver are important.
The name derives from the Anglo-Saxon seofor and siolfur, which is of unknown origin. The symbol Ag derives from the Latin argentum and Sanskrit argunas from "bright". Silver was known in prehistoric times.
Archaeological evidence suggests that people have been using silver for at least 5000 years. Silver can be obtained from pure deposits, from silver ores such as argentite (Ag2S) and horn silver (AgCl), and in conjunction with deposits of ores containing lead, gold or copper.
The Latin word for silver is argentum. Silver has been known since ancient times. It is mentioned in Genesis. Slag dumps in Asia Minor and on islands in the Aegean Sea indicate that man learned to separate silver from lead as early as 3000 B.C.
Pure silver is a bright white, highly lustrous metal with a clean metallic sheen. It is malleable and ductile, and it takes a very high polish. In air it does not oxidize rapidly, but exposed surfaces darken by tarnishing, mainly through reaction with sulfur compounds.
Silver is used in electrical contacts, conductive pastes, solders, brazing alloys, and high-reliability connectors because of its conductivity and workability. It remains important in jewelry, tableware, coinage, and decorative objects, usually as alloys to improve hardness. Silver mirrors and coatings serve optical applications. Silver halides were central to photographic film and paper, though that use has declined. Silver compounds and silver-containing surfaces are also used where controlled antimicrobial action is desired.
Silver and silver compounds have many uses. Pure silver is the best conductor of heat and electricity of all known metals, so it is sometimes used in making solder, electrical contacts and printed circuit boards. Silver is also the best reflector of visible light known, but silver mirrors must be given a protective coating to prevent them from tarnishing. Silver has also been used to create coins, although today other metals are typically used in its place. Sterling silver, an alloy containing 92.5% silver, is used to make silverware, jewelry and other decorative items. High capacity batteries can be made with silver and zinc and silver and cadmium. Silver nitrate (AgNO3) is light sensitive and is used to make photographic films and papers. Silver iodide (AgI) is used to seed clouds to produce rain.
Sterling silver is used for jewelry, silverware, etc. where appearance is paramount. This alloy contains 92.5% silver, the remainder being copper or some other metal. Silver is of the utmost importance in photography, about 30% of the U.S. industrial consumption going into this application. It is used for dental alloys. Silver is used in making solder and brazing alloys, electrical contacts, and high capacity silver-zinc and silver-cadmium batteries. Silver paints are used for making printed circuits. It is used in mirror production and may be deposited on glass or metals by chemical deposition, electrode position, or by evaporation. When freshly deposited, it is the best reflector of visible light known, but is rapidly tarnished and loses much of its reflectance. It is a poor reflector of ultraviolet. Silver fulminate, a powerful explosive, is sometimes formed during the silvering process. Silver iodide is used in seeding clouds to produce rain. Silver chloride has interesting optical properties as it can be made transparent; it also is a cement for glass. Silver nitrate, or lunar caustic, the most important silver compound, is used extensively in photography. Silver for centuries has been used traditionally for coinage by many countries of the world. In recent times, however, consumption of silver has greatly exceeded the output.
Isotopes in Earth/Planetary Science
The measurement of relative amounts of 107Ag and 109Ag is used to study the processes responsible for the isotopic fractionation of silver isotopes in ore deposits, which depends on the specific minerals and environmental conditions. This is currently an area of active research and it is thought that the relative amounts of the isotopes of silver are altered during the formation of the ore [351] Y. Luo, E. Dabek-Zlotorzynska, V. Celo, D. C. Muir, L. Yang. Anal. Chem.82, 3922 (2010)., [352] A. V. Chugaev, I. V. Chernyshev. Geochim. Cosmochim. Acta Suppl.73, A225 (2009)..
Isotopes in Forensic Science and Anthropology
Silver isotope-amount ratiosn(107Ag)/n(109Ag) along with isotope-amount ratios of copper n(65Cu)/n(63Cu), and isotope-amount ratios of lead (n(206Pb)/n(204Pb), n(207Pb)/n(204Pb) and n(208Pb)/n(204Pb)) have been used to determine origins of European coins and information on the flow of goods in the world market over time (Fig. IUPAC.47.1). Metals from Peru and Mexico and those from European mining have distinct isotopic signatures that enable the origin of the metal to be determined by examining the isotopic compositions of silver, copper, and lead in the coins. Abundant silver sources, mined in Mexico and Peru in the 16 th century, were used to mint coins, but they were not a major influence in the European coin market until the 18 th century (Fig. IUPAC.47.1) [237] A. M. Desaulty, P. Telouk, E. Albalat, F. Albarede. Proc. Natl. Acad. Sci.108, 9002 (2011)..
Isotopes in Geochronology
The amount ratio n(107Pd)/n(107Ag) is used in geochronology to date major events in the Solar System [344] W. R. Kelly, G. J. Wasserburg. Geophys. Res. Lett.5 1079 (1978)., [345] G. J. Wasserburg, D. A. Papanastassiou. Some Short-Lived Nuclides in the Early Solar-System – A Connection with the Placental ISM, in Essays in Nuclear Astrophysics, C. A. Barnes, D. D. Clayton, and D. N. Schramm. Cambridge University Press, Cambridge, UK (1982)., [346] J. H. Chen, G. J. Wasserburg. Live 107Pd in the Early Solar System and Implications on Planetary Evolution, in Earth Processes: Reading the Isotopic Code, Geophysical Monograph 95, A. Basu and S. Hart. Amer. Geophys. U., Washington (1996)., [347] J. H. Chen, G. J. Wasserburg. Geochim. Cosmochim. Acta54, 1729 (1990)., [348] A. P. Dicken. Radiogenic Isotope Geology, Cambridge University Press, New York (1995)., [353] G. J. Wasserburg. “Short-lived nuclei in the early solar-system”, in Protostars and Planets, D. C. Black, M. S. Matthews (Eds.), Univ. Arizona Press, Tucson, Arizona, USA (1985).. Although 107Ag is naturally occurring, it is also the daughter product by beta decay of 107Pd. If both excess 107Ag and 107Pd are present in a sample of extraterrestrial origin, then the material would have formed sometime after 107Pd decayed (i.e. sometime after the 6.5-million-year half-life of 107Pd). The n(107Pd)/n(107Ag) amount ratio can be measured to help determine when the 107Pd decay process began and determine how much time has elapsed since the material was formed.
Isotopes in Industry
107Ag is being studied as a possible target for cyclotron production of 103Pd (with a half-life of 17 days) via the 107Ag (p, α n) 103Pd reaction. 103Pd releases X-rays and Auger electrons at the rate of about 80 X-rays and 186 Auger electrons per 100 decays of 103Pd, which makes this isotope an ideal candidate for internal radiotherapy for the treatment of cancers. The production of this isotope in a no-carrier form (not formed in another solution) is important for its medical uses. By using neutrons, photons, and charged particles to force reactions with isotopes of a higher mass number than 103, 103Pd will occur in a fraction of those reactions. The most common methods of 103Pd production use targets of rhodium or other isotopes of palladium. However, 107Ag has also been studied as a feasible option [349] M. Hussain, S. Sudar, M. N. Aslam, H. A. Shah, R. Ahmad, A. A. Malik, S. M. Qaim. Appl. Radiat. Isot.67, 1842 (2009)., [354] F. G. Perey. Phys. Rev. Lett.131, 745 (1963).. 109Ag is used to produce the gamma reference source 110mAg to help calibrate gamma detectors [349] M. Hussain, S. Sudar, M. N. Aslam, H. A. Shah, R. Ahmad, A. A. Malik, S. M. Qaim. Appl. Radiat. Isot.67, 1842 (2009)., [354] F. G. Perey. Phys. Rev. Lett.131, 745 (1963)..
Silver chemistry is dominated by the +1 oxidation state, with Ag⁺ forming many salts and coordination complexes. Silver nitrate (AgNO₃) is a common soluble reagent and precursor for other silver compounds. Silver chloride (AgCl), silver bromide (AgBr), and silver iodide (AgI) are sparingly soluble, light-sensitive halides that underpinned traditional photography. Silver sulfide (Ag₂S) is the principal tarnish product and an important natural mineral. Higher oxidation states such as +2 and +3 exist in specialized compounds, usually with strong oxidizing ligands or solid-state structures.
See more information at the Silver compound page.
Massive metallic silver has low acute toxicity, but dusts, soluble salts, and fine particles require careful handling. Chronic intake of bioavailable silver compounds can cause argyria, a persistent gray-blue discoloration of skin and other tissues. Silver nitrate (AgNO₃) is corrosive and stains skin and organic materials. Some silver compounds are toxic to aquatic organisms. Molten silver presents ordinary burn and metal-fume hazards in foundry or refining work.
While silver itself is not considered to be toxic, most of its salts are poisonous. Exposure to silver (metal and soluble compounds, as Ag) in air should not exceed 0.01 mg/m3, (8-hour time-weighted average - 40 hour week). Silver compounds can be absorbed in the circulatory system and reduced silver deposited in the various tissues of the body. A condition, known as argyria, results with a grayish pigmentation of the skin and mucous membranes. Silver has germicidal effects and kills many lower organisms effectively without harm to higher animals.
Silver is a trace element in soils, sediments, natural waters, and living organisms, with no established essential biological role in humans. In the environment Ag⁺ is strongly complexed or immobilized by sulfide, chloride, organic matter, and mineral surfaces. Mining, smelting, photography wastes, electronics, and some antimicrobial products can add silver to waste streams. In anoxic sediments, formation of silver sulfide (Ag₂S) greatly reduces mobility and bioavailability.
Silver is produced both from primary silver mines and, very often, as a by-product of lead, zinc, copper, and gold mining. Supply therefore depends partly on the economics of other base and precious metals. Demand is split among industrial uses, jewelry and silverware, investment products, and smaller specialty applications. Recycling is important from photographic materials, jewelry, electronics, and industrial scrap, but recovery is uneven when silver is widely dispersed in small devices or coatings. Its price is volatile because it is both an industrial metal and a precious metal.
Silver occurs natively and in ores such as argentite (Ag2S) and horn silver (AgCl); lead, lead-zinc, copper, gold, and copper-nickel ores are principal sources. Mexico, Canada, Peru, and the U.S. are the principal silver producers in the western hemisphere.
Silver is far less abundant cosmically than lighter metals such as iron or magnesium. Its stable isotopes, ¹⁰⁷Ag and ¹⁰⁹Ag, are made mainly by neutron-capture processes in earlier generations of stars, including slow and rapid neutron-capture pathways. In planetary materials it behaves as a chalcophile and moderately siderophile element, concentrating in sulfide phases and metallic portions more than in silicate minerals.
- Silver has the highest electrical conductivity of any element.
- Sterling silver is usually 92.5% silver, with copper as the main hardening metal.
- Fresh silver mirrors reflect visible light very well but tarnish in sulfur-rich air.
- Silver halides darken because light can reduce Ag⁺ to metallic silver.
- Most mined silver is not obtained from mines worked only for silver.
- Native silver can form wires, plates, and dendritic crystals in some deposits.
图片
性质
物理性质
- 原子半径（经验值）
- 160 pm 比较所有元素的原子半径（经验值） →
- 共价半径
- 145 pm 比较所有元素的共价半径 →
- 范德华半径
- 172 pm 比较所有元素的范德华半径 →
- 金属半径
- 134 pm 比较所有元素的金属半径 →
- 密度
- 1.0501 × 104 kg/m³ 比较所有元素的密度 →
- 摩尔体积
- 0.0103 L/mol
- 标准温度和压力下的物相
- 固态 比较所有元素的标准温度和压力下的物相 →
- 熔点
- 961.78 °C 比较所有元素的熔点 →
- 沸点
- 2161.85 °C 比较所有元素的沸点 →
- 热导率
- 429 W/(m·K) 比较所有元素的热导率 →
- 比热容
- 0.235 J/(g·K) 比较所有元素的比热容 →
- 摩尔热容
- 25.35 J/(mol·K) 比较所有元素的摩尔热容 →
- 晶体结构
- 面心立方 比较所有元素的晶体结构 →
化学性质
- 电负性（鲍林）
- 1.93 比较所有元素的电负性（鲍林） →
- 电负性（Allen）
- 1.87
- 电子亲和能
- 1.302 eV
- 第一电离能
- 7.576234 eV 比较所有元素的第一电离能 →
- 第二电离能
- 21.484474 eV 比较所有元素的第二电离能 →
- 第三电离能
- 34.80012 eV 比较所有元素的第三电离能 →
- 第四电离能
- 49.000169 eV 比较所有元素的第四电离能 →
- 第五电离能
- 65.000224 eV 比较所有元素的第五电离能 →
- 氧化态
- −2, −1, 0, +1, +2, +3 比较所有元素的氧化态 →
- 价电子
- 11 比较所有元素的价电子 →
- 电子排布
- [Kr] 5s1 4d10
热力学性质
- 临界点（温度）
- 6137 °C
- 熔化热
- 0.11690936 eV 比较所有元素的熔化热 →
- 汽化热
- 2.597295 eV 比较所有元素的汽化热 →
- 升华热
- 2.952791 eV
- 原子化热
- 2.952791 eV
- 原子化焓
- 2.952791 eV
核性质
- 质子
- 47 比较所有元素的质子 →
- 中子
- 60 比较所有元素的中子 →
- 已知同位素
- 42 比较所有元素的已知同位素 →
- 稳定同位素
- 2 比较所有元素的稳定同位素 →
- 最稳定同位素
- Ag-107
丰度
- 丰度（地壳）
- 0.075 mg/kg 比较所有元素的丰度（地壳） →
- 丰度（海洋）
- 4 × 10−5 mg/L 比较所有元素的丰度（海洋） →
晶体结构
- 晶格常数a
- 409 pm
电子结构
- 各电子层电子数
- 2, 8, 18, 18, 1 比较所有元素的各电子层电子数 →
标识符
- CAS登记号
- 7440-22-4 比较所有元素的CAS登记号 →
- 谱项符号
- 2S1/2
- InChI
- InChI=1S/Ag
- InChI Key
- BQCADISMDOOEFD-UHFFFAOYSA-N
电子排布 实测值
Ag: 4d¹⁰ 5s¹[Kr] 4d¹⁰ 5s¹1s² 2s² 2p⁶ 3s² 3p⁶ 3d¹⁰ 4s² 4p⁶ 4d¹⁰ 5s¹原子模型
不同同位素的中子数、质量和稳定性不同，但中性原子的电子排布不变。
原子模型示意图，未按比例绘制。
原子指纹
发射 / 吸收光谱
同位素分布
| 质量数 | 原子质量（u） | 天然丰度 | 半衰期 |
|---|---|---|---|
| 107 稳定 | 106.9050916 ± 0.0000026 | 51.8390% | 稳定 |
| 109 稳定 | 108.9047553 ± 0.0000014 | 48.1610% | 稳定 |
物相 / 状态
原因: 低于熔点（961.78 °C）936.8 °C
示意图，未按比例绘制
相变点
相变能
在熔点熔化1 mol物质所需的能量
在沸点汽化1 mol物质所需的能量
在升华点升华1 mol物质所需的能量
密度
标准条件下
标准条件下
高级
原子光谱
已显示10项，共47项。 按离子电荷升序排列。
收录能级 ?
| 离子 | 电荷 | 能级 |
|---|---|---|
| Ag I | 0 | 107 |
| Ag II | +1 | 100 |
| Ag III | +2 | 64 |
| Ag IV | +3 | 2 |
| Ag V | +4 | 2 |
| Ag VI | +5 | 2 |
| Ag VII | +6 | 2 |
| Ag VIII | +7 | 2 |
| Ag IX | +8 | 2 |
| Ag X | +9 | 2 |
离子半径
已显示10项，共11项。
| 电荷 | 配位 | 自旋 | 半径 |
|---|---|---|---|
| +1 | 2 | 暂无 | 67 pm |
| +1 | 4 | 暂无 | 100 pm |
| +1 | 4 | 暂无 | 102 pm |
| +1 | 5 | 暂无 | 109.00000000000001 pm |
| +1 | 6 | 暂无 | 114.99999999999999 pm |
| +1 | 7 | 暂无 | 122 pm |
| +1 | 8 | 暂无 | 128 pm |
| +2 | 4 | 暂无 | 79 pm |
| +2 | 6 | 暂无 | 94 pm |
| +3 | 4 | 暂无 | 67 pm |
化合物
同位素 (2)
| 质量数 | 原子质量（u） | 天然丰度 | 半衰期 | 衰变方式 | |
|---|---|---|---|---|---|
| 107 稳定 | 106.9050916 ± 0.0000026 | 51.8390% ± 0.0080% | 稳定 | stable | |
| 109 稳定 | 108.9047553 ± 0.0000014 | 48.1610% ± 0.0080% | 稳定 | stable |
谱线
已显示50项，共125项。 默认仅显示具有实测强度的谱线。
| 波长（nm） | 强度 | 电离级 | 类型 | 跃迁 | 准确度 | 来源 | |
|---|---|---|---|---|---|---|---|
| 562.2482 nm | 21000 | Ag II | emission | 4d9.(2D<5/2>).5d 2[7/2] → 4d9.(2D<5/2>).4f 2[9/2]* | 实测值 | NIST | |
| 540.01037 nm | 20000 | Ag II | emission | 4d9.(2D<5/2>).5d 2[9/2] → 4d9.(2D<5/2>).4f 2[11/2]* | 实测值 | NIST | |
| 540.31323 nm | 15000 | Ag II | emission | 4d9.(2D<5/2>).5d 2[9/2] → 4d9.(2D<5/2>).4f 2[11/2]* | 实测值 | NIST | |
| 555.19264 nm | 12000 | Ag II | emission | 4d9.(2D<5/2>).5d 2[7/2] → 4d9.(2D<5/2>).4f 2[9/2]* | 实测值 | NIST | |
| 548.81562 nm | 8300 | Ag II | emission | 4d9.(2D<5/2>).5d 2[5/2] → 4d9.(2D<5/2>).4f 2[7/2]* | 实测值 | NIST | |
| 558.97829 nm | 4200 | Ag II | emission | 4d9.(2D<5/2>).5d 2[5/2] → 4d9.(2D<5/2>).4f 2[7/2]* | 实测值 | NIST | |
| 534.00267 nm | 2900 | Ag II | emission | 4d9.(2D<5/2>).5d 2[9/2] → 4d9.(2D<5/2>).4f 2[9/2]* | 实测值 | NIST | |
| 554.32121 nm | 2700 | Ag II | emission | 4d9.(2D<5/2>).5d 2[5/2] → 4d8.(3F).5s.5p.(3P*) 1F* | 实测值 | NIST | |
| 557.96782 nm | 2400 | Ag II | emission | 4d9.(2D<5/2>).5d 2[7/2] → 4d9.(2D<5/2>).4f 2[7/2]* | 实测值 | NIST | |
| 549.38302 nm | 2300 | Ag II | emission | 4d9.(2D<5/2>).5d 2[5/2] → 4d9.(2D<5/2>).4f 2[7/2]* | 实测值 | NIST | |
| 555.81412 nm | 2300 | Ag II | emission | 4d9.(2D<5/2>).5d 2[5/2] → 4d9.(2D<5/2>).4f 2[3/2]* | 实测值 | NIST | |
| 557.38257 nm | 2300 | Ag II | emission | 4d9.(2D<5/2>).5d 2[7/2] → 4d9.(2D<5/2>).4f 2[7/2]* | 实测值 | NIST | |
| 542.40509 nm | 2200 | Ag II | emission | 4d9.(2D<5/2>).5d 2[3/2] → 4d9.(2D<5/2>).4f 2[3/2]* | 实测值 | NIST | |
| 541.08117 nm | 1800 | Ag II | emission | 4d9.(2D<5/2>).5d 2[3/2] → 4d9.(2D<5/2>).4f 2[3/2]* | 实测值 | NIST | |
| 514.28157 nm | 1700 | Ag II | emission | 4d9.(2D<5/2>).5d 2[1/2] → 4d9.(2D<5/2>).4f 2[1/2]* | 实测值 | NIST | |
| 558.84183 nm | 1700 | Ag II | emission | 4d9.(2D<5/2>).5d 2[7/2] → 4d9.(2D<5/2>).4f 2[9/2]* | 实测值 | NIST | |
| 536.27883 nm | 1600 | Ag II | emission | 4d9.(2D<5/2>).5d 2[3/2] → 4d9.(2D<5/2>).4f 2[7/2]* | 实测值 | NIST | |
| 539.24682 nm | 1500 | Ag II | emission | 4d9.(2D<5/2>).5d 2[3/2] → 4d9.(2D<5/2>).4f 2[5/2]* | 实测值 | NIST | |
| 547.86589 nm | 1500 | Ag II | emission | 4d9.(2D<5/2>).5d 2[3/2] → 4d9.(2D<5/2>).4f 2[1/2]* | 实测值 | NIST | |
| 533.25049 nm | 1300 | Ag II | emission | 4d9.(2D<5/2>).5d 2[9/2] → 4d9.(2D<5/2>).4f 2[7/2]* | 实测值 | NIST | |
| 531.24574 nm | 1200 | Ag II | emission | 4d9.(2D<5/2>).5d 2[9/2] → 4d9.(2D<5/2>).4f 2[9/2]* | 实测值 | NIST | |
| 520.9078 nm | 1000 | Ag I | emission | 4d10.5p 2P* → 4d10.5d 2D | 实测值 | NIST | |
| 546.54853 nm | 1000 | Ag I | emission | 4d10.5p 2P* → 4d10.5d 2D | 实测值 | NIST | |
| 441.196 nm | 830 | Ag II | emission | 4d9.(2D<5/2>).6p 2[7/2]* → 4d9.(2D<5/2>).8s 2[5/2] | 实测值 | NIST | |
| 541.19338 nm | 740 | Ag II | emission | 4d9.(2D<5/2>).5d 2[3/2] → 4d9.(2D<5/2>).4f 2[3/2]* | 实测值 | NIST | |
| 513.72469 nm | 720 | Ag II | emission | 4d9.(2D<5/2>).5d 2[1/2] → 4d8.(3F).5s.5p.(3P*) 1D* | 实测值 | NIST | |
| 421.09542 nm | 700 | Ag I | emission | 4d10.5p 2P* → 4d10.6d 2D | 实测值 | NIST | |
| 431.959 nm | 630 | Ag II | emission | 4d9.(2D<5/2>).6p 2[7/2]* → 4d9.(2D<5/2>).8s 2[5/2] | 实测值 | NIST | |
| 443.063 nm | 580 | Ag II | emission | 4d9.(2D<3/2>).6p 2[5/2]* → 4d9.(2D<3/2>).8s 2[3/2] | 实测值 | NIST | |
| 408.59155 nm | 470 | Ag II | emission | 4d9.(2D<3/2>).5p 2[5/2]* → 4d8.5s2 1G | 实测值 | NIST | |
| 449.492 nm | 410 | Ag II | emission | 4d9.(2D<5/2>).6p 2[5/2]* → 4d9.(2D<5/2>).8s 2[5/2] | 实测值 | NIST | |
| 453.041 nm | 410 | Ag II | emission | 4d9.(2D<5/2>).6p 2[5/2]* → 4d9.(2D<5/2>).8s 2[5/2] | 实测值 | NIST | |
| 405.5475 nm | 400 | Ag I | emission | 4d10.5p 2P* → 4d10.6d 2D | 实测值 | NIST | |
| 431.354 nm | 290 | Ag II | emission | 4d9.(2D<3/2>).6p 2[5/2]* → 4d9.(2D<3/2>).8s 2[3/2] | 实测值 | NIST | |
| 436.409 nm | 290 | Ag II | emission | 4d9.(2D<3/2>).6p 2[1/2]* → 4d9.(2D<3/2>).8s 2[3/2] | 实测值 | NIST | |
| 444.917 nm | 290 | Ag II | emission | 4d9.(2D<3/2>).6p 2[3/2]* → 4d9.(2D<3/2>).8s 2[3/2] | 实测值 | NIST | |
| 478.83966 nm | 260 | Ag II | emission | 4d9.(2D<3/2>).5p 2[3/2]* → 4d8.5s2 1D | 实测值 | NIST | |
| 418.547499 nm | 250 | Ag II | emission | 4d9.(2D<3/2>).5p 2[5/2]* → 4d8.5s2 1D | 实测值 | NIST | |
| 723.9381 nm | 250 | Ag II | emission | 4d9.(2D<5/2>).6s 2[5/2] → 4d8.(3F).5s.5p.(3P*) 5G* | 实测值 | NIST | |
| 398.51904 nm | 220 | Ag II | emission | 4d9.(2D<5/2>).5p 2[3/2]* → 4d8.5s2 3P | 实测值 | NIST | |
| 433.316 nm | 210 | Ag II | emission | 4d9.(2D<5/2>).6p 2[7/2]* → 4d9.(2D<5/2>).8s 2[5/2] | 实测值 | NIST | |
| 447.909 nm | 210 | Ag II | emission | 4d9.(2D<5/2>).6p 2[3/2]* → 4d9.(2D<5/2>).8s 2[5/2] | 实测值 | NIST | |
| 451.558 nm | 210 | Ag II | emission | 4d9.(2D<5/2>).6p 2[5/2]* → 4d9.(2D<5/2>).8s 2[5/2] | 实测值 | NIST | |
| 381.09396 nm | 200 | Ag I | emission | 4d10.5p 2P* → 4d10.7d 2D | 实测值 | NIST | |
| 699.906 nm | 200 | Ag II | emission | 4d8.(3F).5s.5p.(3P*) 5D* → 4d9.(2D<3/2>).7s 2[3/2] | 实测值 | NIST | |
| 392.01238 nm | 180 | Ag II | emission | 4d9.(2D<5/2>).5p 2[3/2]* → 4d8.5s2 3P | 实测值 | NIST | |
| 462.00355 nm | 170 | Ag II | emission | 4d9.(2D<3/2>).5p 2[5/2]* → 4d8.5s2 1D | 实测值 | NIST | |
| 394.9435 nm | 160 | Ag II | emission | 4d9.(2D<5/2>).5p 2[3/2]* → 4d8.5s2 3P | 实测值 | NIST | |
| 502.73432 nm | 160 | Ag II | emission | 4d9.(2D<3/2>).5p 2[3/2]* → 4d8.5s2 1D | 实测值 | NIST | |
| 390.930327 nm | 140 | Ag II | emission | 4d9.(2D<5/2>).5p 2[5/2]* → 4d8.5s2 1D | 实测值 | NIST |
扩展性质
共价半径（扩展）
- 共价半径（Pyykkö）
- 128 pm
- 共价半径（Pyykkö，双键）
- 139 pm
- 共价半径（Pyykkö，三键）
- 137 pm
- 共价半径（Bragg）
- 177 pm
范德华半径
- Batsanov
- 210 pm
- Alvarez
- 253 pm
- UFF
- 314.8 pm
- MM3
- 243 pm
原子半径与金属半径
- 原子半径（Rahm）
- 225 pm
- 金属半径（C12）
- 144 pm
编号标度
- Mendeleev
- 72
- Pettifor
- 71
- Glawe
- 67
电负性标度
- Ghosh
- 0
- Miedema
- 4
- Gunnarsson–Lundqvist
- 4
- Robles–Bartolotti
- 3
极化率与色散
- 偶极极化率
- 55 a.u.
- 偶极极化率（不确定度）
- 8 a.u.
- C₆ (Gould–Bučko)
- 341 Ha·Bohr6
Miedema参数
- Miedema摩尔体积
- 10.25 cm3/mol
- Miedema电子密度
- 3
供应风险与经济性
- 生产集中度
- 19
- 相对供应风险
- 6
- 储量分布
- 23
- 政治稳定性（最大生产国）
- 23
- 政治稳定性（最大储量国）
- 20
相变与同素异形体
| 熔点 | 1234.93 K |
| 沸点 | 2435.15 K |
| 临界点（温度） | 6410.15 K |
氧化态分类
高级参考数据
屏蔽常数 (10)
| n | 轨道 | σ |
|---|---|---|
| 1 | s | 0.9577 |
| 2 | p | 4.0806 |
| 2 | s | 12.3658 |
| 3 | d | 14.4602 |
| 3 | p | 17.1914 |
| 3 | s | 16.9688 |
| 4 | d | 32.2372 |
| 4 | p | 28.4376 |
| 4 | s | 27.1352 |
| 5 | s | 40.2445 |
晶体半径详情 (11)
| 电荷 | CN | 自旋 | rcrystal (pm) | 来源 |
|---|---|---|---|---|
| 1 | II | 81 | ||
| 1 | IV | 114 | calculated, | |
| 1 | IVSQ | 116 | ||
| 1 | V | 123 | calculated, | |
| 1 | VI | 129 | calculated, | |
| 1 | VII | 136 | ||
| 1 | VIII | 142 | ||
| 2 | IVSQ | 93 | ||
| 2 | VI | 108 | ||
| 3 | IVSQ | 81 |
同位素衰变方式 (68)
| 同位素 | 模式 | 强度 |
|---|---|---|
| 92 | B+ | — |
| 92 | p | — |
| 93 | p | — |
| 93 | B+ | — |
| 93 | B+p | — |
| 94 | B+ | 100% |
| 94 | B+p | 0.2% |
| 95 | B+ | 100% |
| 95 | B+p | 2.3% |
| 96 | B+ | 100% |
X射线散射因子 (508)
| 能量 (eV) | f₁ | f₂ |
|---|---|---|
| 10 | — | 1.18566 |
| 10.1617 | — | 1.22941 |
| 10.3261 | — | 1.27478 |
| 10.4931 | — | 1.32182 |
| 10.6628 | — | 1.38215 |
| 10.8353 | — | 1.45541 |
| 11.0106 | — | 1.53256 |
| 11.1886 | — | 1.61379 |
| 11.3696 | — | 1.69933 |
| 11.5535 | — | 1.78755 |
补充数据
Estimated Crustal Abundance
The estimated element abundance in the earth's crust.
7.5×10-2 milligrams per kilogram
参考文献 (1)
Estimated Oceanic Abundance
The estimated element abundance in the earth's oceans.
4×10-5 milligrams per liter
参考文献 (1)
Sources
Sources of this element.
Silver occurs natively and in ores such as argentite (Ag2S) and horn silver (AgCl); lead, lead-zinc, copper, gold, and copper-nickel ores are principal sources. Mexico, Canada, Peru, and the U.S. are the principal silver producers in the western hemisphere.
参考文献 (1)
- [6] Silver https://periodic.lanl.gov/47.shtml
Production
Production of this element (from raw materials or other compounds containing the element).
Silver is also recovered during electrolytic refining of copper. Commercial fine silver contains at least 99.9% silver. Purities of 99.999+% are available commercially.
参考文献 (1)
- [6] Silver https://periodic.lanl.gov/47.shtml
Isotopes in Forensic Science and Anthropology
Information on the use of this element's isotopes in forensic science and anthropology.
Silver isotope-amount ratiosn(107Ag)/n(109Ag) along with isotope-amount ratios of copper n(65Cu)/n(63Cu), and isotope-amount ratios of lead (n(206Pb)/n(204Pb), n(207Pb)/n(204Pb) and n(208Pb)/n(204Pb)) have been used to determine origins of European coins and information on the flow of goods in the world market over time (Fig. IUPAC.47.1). Metals from Peru and Mexico and those from European mining have distinct isotopic signatures that enable the origin of the metal to be determined by examining the isotopic compositions of silver, copper, and lead in the coins. Abundant silver sources, mined in Mexico and Peru in the 16 th century, were used to mint coins, but they were not a major influence in the European coin market until the 18 th century (Fig. IUPAC.47.1) [237] A. M. Desaulty, P. Telouk, E. Albalat, F. Albarede. Proc. Natl. Acad. Sci.108, 9002 (2011)..
参考文献 (2)
- [237] A. M. Desaulty, P. Telouk, E. Albalat, F. Albarede. Proc. Natl. Acad. Sci.108, 9002 (2011).
- [4] IUPAC Periodic Table of the Elements and Isotopes (IPTEI) https://doi.org/10.1515/pac-2015-0703
参考文献
(9)
Data deposited in or computed by PubChem
The half-life and atomic mass data was provided by the Atomic Mass Data Center at the International Atomic Energy Agency.
Element data are cited from the Atomic weights of the elements (an IUPAC Technical Report). The IUPAC periodic table of elements can be found at https://iupac.org/what-we-do/periodic-table-of-elements/. Additional information can be found within IUPAC publication doi:10.1515/pac-2015-0703 Copyright © 2020 International Union of Pure and Applied Chemistry.
The information are cited from Pure Appl. Chem. 2018; 90(12): 1833-2092, https://doi.org/10.1515/pac-2015-0703.
Thomas Jefferson National Accelerator Facility (Jefferson Lab) is one of 17 national laboratories funded by the U.S. Department of Energy. The lab's primary mission is to conduct basic research of the atom's nucleus using the lab's unique particle accelerator, known as the Continuous Electron Beam Accelerator Facility (CEBAF). For more information visit https://www.jlab.org/
The periodic table at the LANL (Los Alamos National Laboratory) contains basic element information together with the history, source, properties, use, handling and more. The provenance data may be found from the link under the source name.
The periodic table contains NIST's critically-evaluated data on atomic properties of the elements. The provenance data that include data for atomic spectroscopy, X-ray and gamma ray, radiation dosimetry, nuclear physics, and condensed matter physics may be found from the link under the source name. Ref: https://www.nist.gov/pml/atomic-spectra-database
This section provides all form of data related to element Silver.
The element property data was retrieved from publications.