Tellurium (Te)
metalloidSolid
标准原子量
127.6 u电子排布
[Kr] 5s2 4d10 5p4熔点
449.51 °C沸点
987.85 °C密度
6232 kg/m³氧化态
−2, −1, 0, +1, +2, +3, +4, +5, +6电负性（鲍林）
2.1第一电离能
9.009808 eV发现年份
1782原子半径
140 pm详细信息
Tellurium is a brittle metalloid in group 16, below selenium and above polonium. It is chemically related to sulfur and selenium but is more metallic, less abundant, and more easily reduced. In nature it occurs mainly as telluride minerals and as a minor constituent of copper ores. Its technological importance comes from semiconducting and thermoelectric compounds, cadmium telluride photovoltaics, and small alloying additions that modify machinability and corrosion behavior.
Crystalline tellurium has a silvery-white appearance, and when pure it exhibits a metallic luster. It is brittle and easily pulverized. Amorphous tellurium is found by precipitating tellurium from a solution of telluric or tellurous acid. Whether this form is truly amorphous, or made of minute crystals, is open to question. Tellurium is a p-type semiconductor, and shows greater conductivity in certain directions, depending on alignment of the atoms.
Its conductivity increases slightly with exposure to light. It can be doped with silver, copper, gold, tin, or other elements. In air, tellurium burns with a greenish-blue flames, forming the dioxide. Molten tellurium corrodes iron, copper, and stainless steel.
The name derives from the Latin Tellus, who was the Roman goddess of the Earth. Tellurium was discovered by Franz Joseph Müller von Reichenstein in 1782 and overlooked for 15 years until it was isolated by the German chemist Martin-Heinrich Klaproth in 1798. The Hungarian chemist Paul Kitaibel independently discovered tellurium in 1789, prior to Klaproth's work but after von Reichenstein.
Tellurium was discovered by Franz Joseph Müller von Reichenstein, a Romanian mining official, in 1782. Reichenstein was the chief inspector of all mines, smelters and saltworks in Transylvania. He also had an interest in chemistry and extracted a new metal from an ore of gold, known as aurum album, which he believed was antimony. He shortly realized that the metal he had produced wasn't antimony at all, but a previously unknown element. Reichenstein's work was forgotten until 1798 when Martin Heinrich Klaproth, a German chemist, mentioned the substance in a paper. Klaproth named the new element tellurium but gave full credit for its discovery to Reichenstein. Tellurium is found free in nature, but is most often found in the ores sylvanite (AgAuTe4), calaverite (AuTe2) and krennerite (AuTe2). Today, most tellurium is obtained as a byproduct of mining and refining copper.
From the Latin word tellus, earth. Discovered by Muller von Reichenstein in 1782; named by Klaproth, who isolated it in 1798.
Pure tellurium is a silvery-white to gray, lustrous, crystalline solid at ordinary conditions. It is brittle and can be powdered, but it is not malleable. The common trigonal form has helical chains of atoms, giving the element anisotropic electrical and thermal properties.
The largest modern use of tellurium is in cadmium telluride, CdTe, thin-film solar cells. Tellurium is also used in bismuth telluride, Bi₂Te₃, and related thermoelectric materials for cooling and power generation from temperature differences. Small additions to copper, steel, and lead improve machinability or modify mechanical properties. Tellurium compounds are used in some infrared optical materials, phase-change chalcogenide systems, and specialized vulcanization and glass applications, but these uses are smaller and material-specific.
Tellurium is a semiconductor and is frequently doped with copper, tin, gold or silver. Tellurium is also used to color glass and ceramics and is one of the primary ingredients in blasting caps.
Tellurium is primarily used as an alloying agent. Small amounts of tellurium are added to copper and stainless steel to make them easier to machine and mill. Tellurium is also added to lead to increase its strength and resistance to sulfuric acid (H2SO4).
Tellurium forms many compounds, but none that are commercially important. They include: tellourous acid (H2TeO2), tellurium tetrachloride (TeCl4), tellurium dichloride (TeCl2), tellurium trioxide (TeO3), tellurium monoxide (TeO) and sodium telluride (Na2Te).
Tellurium improves the machinability of copper and stainless steel, and its addition to lead decreases the corrosive action of sulfuric acid on lead and improves its strength and hardness. Tellurium is used as a basic ingredient in blasting caps, and is added to cast iron for chill control. Tellurium is used in ceramics. Bismuth telluride has been used in thermoelectric devices.
Isotopes in Earth/Planetary Science
Tellurium isotopes are a mixture of r-process, s-process, and p-process nucleosynthesis products, making them useful for studying the contribution of stellar products to the molecular cloud from which the Sun and planets were formed (Fig. IUPAC.52.1) [378] M. Fehr. Tellurium Isotopes and their Applications in Cosmo- and Geochemistry, Swiss Federal Institute of Technology Zurich (2014), Feb. 26; http://e-collection.library.ethz.ch/eserv/eth:27380/eth-27380-01.pdf., [379] M. A. Fehr, M. Rehkämper, D. Porcelli, A. N. Halliday. Homogeneity of Tellurium Isotopes in Chondrites, Leachates of Allende and Canyon Diablo, Lunar and Planetary Science (2014), Feb. 26; http://www.lpi.usra.edu/meetings/lpsc2003/pdf/1655.pdf., [380] M. A. Fehr, M. Rehkämper, A. N. Halliday, U. Wiechert, B. Hattendorf, D. Günther, S. Ono, J. L. Eigenbrode, I. D. Rumble. Geochim. Cosmochim. Acta69, 5099 (2005)..
Isotopes in Geochronology
The double beta decay of 130Te (with a half-life of 7×1020 years) has been used for the determination of gas-retention ages of tellurium minerals [382] A. P. Meshik, C. M. Hohenberg, O. V. Pravdivtseva, T. J. Bernatowicz, Y. S. Kapustab. Nucl. Phys. A809, 275 (2008)..
Isotopes Used as a Source of Radioactive Isotope(s)
120Te is used for the production of 120gI, where “g” indicates ground state, via the 120Te (p, n) 120gI reaction, which is used as a positron emission tomography (PET) and beta-emitting isotope [383] A. Hohn, H. H. Coenen, S. M. Qaim. Appl. Radiat. Isot.49, 1493 (1998)., [384] H. Herzog, S. M. Qaim, L. Tellmann, S. Spellerberg, D. Kruecker, H. H. Coenen. Eur. J. Nucl. Med. Mol. Imaging33, 1249 (2006).. 120gI has a half-life of 1.36 h. 122Te is used in the production of the radioisotope 122I (with a half-life of 3.6 min) via the reaction 122Te (p, n) 122I, which is used in gamma imaging [385] A. Hohn, B. Scholten, H. H. Coenen, S. M. Qaim, Appl. Radiat. Isot.49, 93 (1998).. 123Te is used for the production of radioactive 123I (with a half-life of 13.2 h) via the 123Te (p, n) 123I reaction, which is used in thyroid imaging [386] T. Kakavand, M. Sadeghi, K. K. Moghaddam, S. S. Bonab, B. Fateh. Iran. J. Radiat. Res.5, 207 (2008). and for in vivo medical studies using single-photon emission computed tomography (SPECT) [386] T. Kakavand, M. Sadeghi, K. K. Moghaddam, S. S. Bonab, B. Fateh. Iran. J. Radiat. Res.5, 207 (2008).. 124Te is used for the production of both 123I and the PET isotope 124I via the 124Te (p, 2n) 123I and 124Te (p, n) 124I reactions, respectively [386] T. Kakavand, M. Sadeghi, K. K. Moghaddam, S. S. Bonab, B. Fateh. Iran. J. Radiat. Res.5, 207 (2008)., [387] M. L. Firouzbakht, D. J. Schlyer, R. D. Finn, G. Laguzzi, A. P. Wolf. Nucl. Instr. Methods Phys. Res. B79, 909 (1993)., [388] H. Herzog, L. Tellman, S. M. Qaim, S. Spellerberg, A. Schmid, H. H. Coenen. Appl. Radiat. Isot.56, 673 (2002)., [389] F. T. Lee, C. Hall, A. Rigopoulos, J. Zweit, K. Pathmaraj, G. J. O’Keefe, F. E. Smyth, S. Welt, L. J. Old, A. M. Scott. J. Nucl. Med.42, 764 (2001).. The half-life of 124I is 100 h.
Tellurium commonly shows oxidation states −2, +4, and +6, with +4 especially important in oxides and oxoanion chemistry. Hydrogen telluride, H₂Te, is an unstable and highly toxic hydride. Tellurium dioxide, TeO₂, is an amphoteric oxide used in tellurite glasses and as a chemical intermediate. Telluric acid, H₆TeO₆, contains tellurium in the +6 state. Metal tellurides include cadmium telluride, CdTe, and bismuth telluride, Bi₂Te₃, whose bonding and band structures are central to their electronic uses.
See more information at the Tellurium compound page.
Elemental tellurium has moderate acute toxicity, but dusts and fumes should be controlled because inhalation and ingestion can be harmful. Exposure to tellurium or some tellurium compounds can produce a persistent garlic-like odor in breath and sweat from volatile metabolites. Hydrogen telluride, H₂Te, is particularly hazardous. Cadmium telluride, CdTe, also requires controls because cadmium compounds are toxic, especially if dust is generated during manufacture or disposal.
Tellurium and its compounds are probably toxic and should be handled with care. Workmen exposed to as little as 0.01 mg/m3 of air, or less, develop "tellurium breath," which has a garlic-like odor.
Tellurium is a rare trace element in the crust and is strongly chalcophile, concentrating with sulfide and telluride mineral assemblages rather than forming abundant independent deposits. Weathering can release tellurium into soils and waters, where its speciation depends on redox conditions and pH. Tellurite and tellurate species can be mobile under some conditions, while reduction and adsorption tend to immobilize it. It has no known essential biological role for humans.
Tellurium is not usually mined as a primary product. Most commercial supply is recovered as a by-product from copper refining, especially from anode slimes produced during electrolytic purification. This dependence makes supply sensitive to copper ore composition, refinery practice, and the economics of by-product recovery rather than to tellurium demand alone. Demand is led by cadmium telluride photovoltaics and thermoelectric materials, with smaller metallurgical and chemical uses. Recycling is technically possible from manufacturing scrap and some end-of-life devices, but collection and separation can limit recovery.
Tellurium is occasionally found native, but is more often found as the telluride of gold (calaverite), and combined with other metals. It is recovered commercially from anode muds produced during the electrolytic refining of blister copper. The U.S., Canada, Peru, and Japan are the largest Free World producers of the element.
Tellurium is far less abundant in the universe than lighter chalcogens such as sulfur and selenium. Its stable isotopes are produced 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 element and is associated with sulfide-rich phases rather than silicate minerals.
- Tellurium was named from tellus, the Latin word for Earth.
- It is one of the few elements whose name refers to Earth rather than a celestial object or place of discovery.
- Natural tellurium contains several stable isotopes and very long-lived radioactive isotopes.
- The element can impart a garlic-like odor to breath at exposures far below severe poisoning levels.
- Tellurium improves the machinability of copper without requiring large alloy additions.
- Many useful tellurium materials are semiconductors rather than metallic conductors.
图片
性质
物理性质
- 原子半径（经验值）
- 140 pm 比较所有元素的原子半径（经验值） →
- 共价半径
- 138 pm 比较所有元素的共价半径 →
- 范德华半径
- 206 pm 比较所有元素的范德华半径 →
- 金属半径
- 137 pm 比较所有元素的金属半径 →
- 密度
- 6232 kg/m³ 比较所有元素的密度 →
- 摩尔体积
- 0.0205 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
- 449.51 °C 比较所有元素的熔点 →
- 沸点
- 987.85 °C 比较所有元素的沸点 →
- 热导率
- 14.3 W/(m·K) 比较所有元素的热导率 →
- 比热容
- 0.202 J/(g·K) 比较所有元素的比热容 →
- 摩尔热容
- 25.73 J/(mol·K) 比较所有元素的摩尔热容 →
- 晶体结构
- 六方密堆积 比较所有元素的晶体结构 →
化学性质
- 电负性（鲍林）
- 2.1 比较所有元素的电负性（鲍林） →
- 电负性（Allen）
- 2.158
- 电子亲和能
- 1.9708 eV
- 第一电离能
- 9.009808 eV 比较所有元素的第一电离能 →
- 第二电离能
- 18.600064 eV 比较所有元素的第二电离能 →
- 第三电离能
- 27.840096 eV 比较所有元素的第三电离能 →
- 第四电离能
- 37.415629 eV 比较所有元素的第四电离能 →
- 第五电离能
- 59.300204 eV 比较所有元素的第五电离能 →
- 氧化态
- −2, −1, 0, +1, +2, +3, +4, +5, +6 比较所有元素的氧化态 →
- 价电子
- 6 比较所有元素的价电子 →
- 电子排布
- [Kr] 5s2 4d10 5p4
热力学性质
- 临界点（温度）
- 2056 °C
- 熔化热
- 0.1812717 eV 比较所有元素的熔化热 →
- 汽化热
- 0.54412603 eV 比较所有元素的汽化热 →
- 升华热
- 2.041768 eV
- 原子化热
- 2.041768 eV
- 原子化焓
- 2.037622 eV
核性质
- 质子
- 52 比较所有元素的质子 →
- 中子
- 74 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
- 4 比较所有元素的稳定同位素 →
- 最稳定同位素
- Te-126
- 发现年份
- 1782
丰度
- 丰度（地壳）
- 0.001 mg/kg 比较所有元素的丰度（地壳） →
晶体结构
- 晶格常数a
- 445 pm
电子结构
- 各电子层电子数
- 2, 8, 18, 18, 6 比较所有元素的各电子层电子数 →
标识符
- CAS登记号
- 13494-80-9 比较所有元素的CAS登记号 →
- 谱项符号
- 3P2
- InChI
- InChI=1S/Te
- InChI Key
- PORWMNRCUJJQNO-UHFFFAOYSA-N
电子排布 实测值
Te: 4d¹⁰ 5s² 5p⁴[Kr] 4d¹⁰ 5s² 5p⁴1s² 2s² 2p⁶ 3s² 3p⁶ 3d¹⁰ 4s² 4p⁶ 4d¹⁰ 5s² 5p⁴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 |
|---|---|---|---|
| 122 稳定 | 121.9030435 ± 0.0000016 | 2.5500% | 稳定 |
| 124 稳定 | 123.9028171 ± 0.0000016 | 4.7400% | 稳定 |
| 125 稳定 | 124.9044299 ± 0.0000016 | 7.0700% | 稳定 |
| 126 稳定 | 125.9033109 ± 0.0000016 | 18.8400% | 稳定 |
物相 / 状态
原因: 低于熔点（449.51 °C）424.5 °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52项。 按离子电荷升序排列。
收录能级 ?
| 离子 | 电荷 | 能级 |
|---|---|---|
| Te I | 0 | 120 |
| Te II | +1 | 129 |
| Te III | +2 | 55 |
| Te IV | +3 | 16 |
| Te V | +4 | 45 |
| Te VI | +5 | 9 |
| Te VII | +6 | 60 |
| Te VIII | +7 | 2 |
| Te IX | +8 | 2 |
| Te X | +9 | 2 |
离子半径
| 电荷 | 配位 | 自旋 | 半径 |
|---|---|---|---|
| -2 | 6 | 暂无 | 221 pm |
| +4 | 3 | 暂无 | 52 pm |
| +4 | 4 | 暂无 | 66 pm |
| +4 | 6 | 暂无 | 97 pm |
| +6 | 4 | 暂无 | 43 pm |
| +6 | 6 | 暂无 | 56.00000000000001 pm |
化合物
同位素 (4)
Thirty isotopes of tellurium are known, with atomic masses ranging from 108 to 137. Natural tellurium consists of eight isotopes.
| 质量数 | 原子质量（u） | 天然丰度 | 半衰期 | 衰变方式 | |
|---|---|---|---|---|---|
| 122 稳定 | 121.9030435 ± 0.0000016 | 2.5500% ± 0.1200% | 稳定 | stable | |
| 124 稳定 | 123.9028171 ± 0.0000016 | 4.7400% ± 0.1400% | 稳定 | stable | |
| 125 稳定 | 124.9044299 ± 0.0000016 | 7.0700% ± 0.1500% | 稳定 | stable | |
| 126 稳定 | 125.9033109 ± 0.0000016 | 18.8400% ± 0.2500% | 稳定 | stable |
谱线
已显示50项，共74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 | |
|---|---|---|---|---|---|---|---|
| 486.623 nm | 2300 | Te II | emission | 5s2.5p2.(3P).6p 4D* → 5s2.5p2.(3P).6d 4F | 实测值 | NIST | |
| 557.636 nm | 2100 | Te II | emission | 5s2.5p2.(1D).6s 2D → 5s2.5p2.(1D).6p 2F* | 实测值 | NIST | |
| 570.812 nm | 1900 | Te II | emission | 5s2.5p2.(3P).6s 4P → 5s2.5p2.(3P).6p 4D* | 实测值 | NIST | |
| 483.13 nm | 1600 | Te II | emission | 5s2.5p2.(3P).6p 4D* → 5s2.5p2.(3P).6d 4P | 实测值 | NIST | |
| 564.926 nm | 1500 | Te II | emission | 5s2.5p2.(3P).6s 4P → 5s2.5p2.(3P).6p 4D* | 实测值 | NIST | |
| 575.586 nm | 1500 | Te II | emission | 5s2.5p2.(3P).6s 4P → 5s2.5p2.(3P).6p 4D* | 实测值 | NIST | |
| 544.984 nm | 1400 | Te II | emission | 5s2.5p2.(3P).6s 4P → 5s2.5p2.(3P).6p 4P* | 实测值 | NIST | |
| 468.691 nm | 1310 | Te II | emission | 5s2.5p2.(3P).6p 4P* → 5s2.5p2.(3P).6d 4D | 实测值 | NIST | |
| 476.605 nm | 1300 | Te II | emission | 5s2.5p2.(3P).6p 2D* → 5s2.5p2.(3P).6d 2F | 实测值 | NIST | |
| 490.442 nm | 1300 | Te II | emission | 5s2.5p2.(3P).6p 2D* → 5s2.5p2.(3P).6d 2F | 实测值 | NIST | |
| 566.622 nm | 1200 | Te II | emission | 5s2.5p2.(3P).6s 2P → 5s2.5p2.(3P).6p 2D* | 实测值 | NIST | |
| 597.468 nm | 1200 | Te II | emission | 5s2.5p2.(3P).6s 4P → 5s2.5p2.(3P).6p 4P* | 实测值 | NIST | |
| 548.795 nm | 1100 | Te II | emission | 5s2.5p2.(3P).5d 2P → 5s2.5p2.(3P).6p 4D* | 实测值 | NIST | |
| 484.29 nm | 1000 | Te II | emission | 5s2.5p2.(3P).5d 2D → 5s2.5p2.(3P).4f 4D* | 实测值 | NIST | |
| 486.513 nm | 1000 | Te II | emission | 5s2.5p2.(3P).6p 4D* → 5s2.5p2.(3P).6d 4D | 实测值 | NIST | |
| 482.712 nm | 900 | Te II | emission | 5s2.5p2.(3P).6p 4P* → 5s2.5p2.(3P).6d 4D | 实测值 | NIST | |
| 447.865 nm | 830 | Te II | emission | 5s2.5p2.(3P).6p 4P* → 5s2.5p2.(3P).6d 4D | 实测值 | NIST | |
| 500.081 nm | 810 | Te II | emission | 5s2.5p2.(3P).6s 4P → 5s2.5p2.(3P).6p 2D* | 实测值 | NIST | |
| 477.155 nm | 800 | Te II | emission | 5s2.5p2.(3P).6p 4D* → 5s2.5p2.(3P).6d 4F | 实测值 | NIST | |
| 593.615 nm | 730 | Te II | emission | 5s2.5p2.(3P).6s 4P → 5s2.5p2.(3P).6p 4S* | 实测值 | NIST | |
| 464.111 nm | 680 | Te II | emission | 5s2.5p2.(3P).6p 4D* → 5s2.5p2.(3P).6d 4D | 实测值 | NIST | |
| 470.654 nm | 670 | Te II | emission | 5s2.5p2.(1D).6s 2D → 5s2.5p2.(1D).6p 2P* | 实测值 | NIST | |
| 436.402 nm | 650 | Te II | emission | 5s2.5p2.(3P).5d 4P → 5s2.5p2.(3P).4f 4D* | 实测值 | NIST | |
| 636.713 nm | 570 | Te II | emission | 5s.(2S).5p4.(1D) 2D → 5s2.5p2.(3P).6p 4D* | 实测值 | NIST | |
| 469.638 nm | 560 | Te II | emission | 5s2.5p2.(3P).5d 4P → 5s2.5p2.(3P).4f 2D* | 实测值 | NIST | |
| 416.977 nm | 540 | Te II | emission | 5s2.5p2.(3P).5d 2D → 5s2.5p2.(3P).4f 2F* | 实测值 | NIST | |
| 463.062 nm | 540 | Te II | emission | 5s2.5p2.(3P).6p 4S* → 5s2.5p2.(3P).7s 2P | 实测值 | NIST | |
| 478.488 nm | 510 | Te II | emission | 5s2.5p2.(1D).6s 2D → 5s2.5p2.(1D).6p 2P* | 实测值 | NIST | |
| 455.778 nm | 480 | Te II | emission | 5s2.5p2.(3P).6p 4S* → 5s2.5p2.(3P).6d 4D | 实测值 | NIST | |
| 683.7663 nm | 430 | Te I | emission | 5p3.(4S*).6p 5P → 5p3.(4S*).8d 5D* | 实测值 | NIST | |
| 404.716 nm | 400 | Te II | emission | 5s2.5p2.(3P).5d 4P → 5s2.5p2.(3P).4f 2D* | 实测值 | NIST | |
| 428.583 nm | 370 | Te II | emission | 5s2.5p2.(3P).6p 2S* → 5s2.5p2.(3P).6d 4D | 实测值 | NIST | |
| 394.798 nm | 340 | Te II | emission | 5s2.5p2.(3P).5d 4P → 5s2.5p2.(3P).4f 4F* | 实测值 | NIST | |
| 422.572 nm | 340 | Te II | emission | 5s2.5p2.(3P).5d 4P → 5s2.5p2.(3P).4f 4D* | 实测值 | NIST | |
| 396.921 nm | 320 | Te II | emission | 5s.(2S).5p4.(1D) 2D → 5s2.5p2.(1D).6p 2D* | 实测值 | NIST | |
| 410.105 nm | 320 | Te II | emission | 5s2.5p2.(1D).5d 2S → 5s2.5p2.(3P).4f 2D* | 实测值 | NIST | |
| 412.732 nm | 320 | Te II | emission | 5s2.5p2.(1D).5d 2S → 5s2.5p2.(3P).4f 4D* | 实测值 | NIST | |
| 496.187 nm | 320 | Te II | emission | 5s2.5p2.(3P).6p 4P* → 5s2.5p2.(3P).6d 4D | 实测值 | NIST | |
| 400.653 nm | 310 | Te II | emission | 5s.(2S).5p4.(3P) 4P → 5s2.5p2.(3P).6p 4D* | 实测值 | NIST | |
| 438.51 nm | 310 | Te II | emission | 5s2.5p2.(3P).5d 4P → 5s2.5p2.(3P).4f 2D* | 实测值 | NIST | |
| 417.929 nm | 300 | Te II | emission | 5s2.5p2.(3P).5d 4P → 5s2.5p2.(1S).6p 2P* | 实测值 | NIST | |
| 427.343 nm | 300 | Te II | emission | 5s2.5p2.(3P).6p 2S* → 5s2.5p2.(3P).7s 2P | 实测值 | NIST | |
| 679.109 nm | 300 | Te I | emission | 5p3.(4S*).6p 5P → 5p3.(4S*).8d 3D* | 实测值 | NIST | |
| 669.0154 nm | 290 | Te I | emission | 5p3.(4S*).6p 5P → 5p3.(4S*).8d 5D* | 实测值 | NIST | |
| 453.708 nm | 260 | Te II | emission | 5s2.5p2.(3P).5d 4P → 5s2.5p2.(3P).4f 4F* | 实测值 | NIST | |
| 397.592 nm | 250 | Te II | emission | 5s.(2S).5p4.(1D) 2D → 5s2.5p2.(1D).6p 2F* | 实测值 | NIST | |
| 416.356 nm | 250 | Te II | emission | 5s2.5p2.(3P).5d 4P → 5s2.5p2.(3P).4f 4D* | 实测值 | NIST | |
| 398.176 nm | 240 | Te II | emission | 5s2.5p2.(3P).6s 2P → 5s2.5p2.(1D).6p 2P* | 实测值 | NIST | |
| 425.114 nm | 240 | Te II | emission | 5s2.5p2.(3P).5d 2D → 5s2.5p2.(3P).4f 2F* | 实测值 | NIST | |
| 404.888 nm | 230 | Te II | emission | 5s.(2S).5p4.(3P) 4P → 5s2.5p2.(3P).6p 4S* | 实测值 | NIST |
扩展性质
共价半径（扩展）
- 共价半径（Pyykkö）
- 136 pm
- 共价半径（Pyykkö，双键）
- 128 pm
- 共价半径（Pyykkö，三键）
- 121 pm
- 共价半径（Bragg）
- 133 pm
范德华半径
- Bondi
- 206 pm
- Batsanov
- 210 pm
- Alvarez
- 199 pm
- UFF
- 447 pm
- MM3
- 244 pm
- Dreiding
- 423 pm
原子半径与金属半径
- 原子半径（Rahm）
- 242 pm
- 金属半径（C12）
- 160 pm
编号标度
- Mendeleev
- 102
- Pettifor
- 92
- Glawe
- 94
电负性标度
- Ghosh
- 0
- Gunnarsson–Lundqvist
- 6
- Robles–Bartolotti
- 4
极化率与色散
- 偶极极化率
- 38 a.u.
- 偶极极化率（不确定度）
- 4 a.u.
- C₆
- 445 Ha·Bohr6
- C₆ (Gould–Bučko)
- 471 Ha·Bohr6
相变与同素异形体
| 熔点 | 722.66 K |
| 沸点 | 1261.15 K |
| 临界点（温度） | 2329.15 K |
氧化态分类
高级参考数据
屏蔽常数 (11)
| n | 轨道 | σ |
|---|---|---|
| 1 | s | 1.0432 |
| 2 | p | 4.14 |
| 2 | s | 13.6688 |
| 3 | d | 14.1607 |
| 3 | p | 17.9911 |
| 3 | s | 18.0019 |
| 4 | d | 32.04 |
| 4 | p | 28.878 |
| 4 | s | 27.5916 |
| 5 | p | 41.1915 |
晶体半径详情 (6)
| 电荷 | CN | 自旋 | rcrystal (pm) | 来源 |
|---|---|---|---|---|
| -2 | VI | 207 | Pauling's (1960) crystal radius, | |
| 4 | III | 66 | ||
| 4 | IV | 80 | ||
| 4 | VI | 111 | ||
| 6 | IV | 57 | calculated, | |
| 6 | VI | 70 |
同位素衰变方式 (67)
| 同位素 | 模式 | 强度 |
|---|---|---|
| 104 | A | 100% |
| 105 | A | 100% |
| 106 | A | 100% |
| 107 | A | 70% |
| 107 | B+ | — |
| 107 | B+p | — |
| 108 | B+ | 51% |
| 108 | A | 49% |
| 108 | B+p | 2.4% |
| 108 | B+A | 0.1% |
X射线散射因子 (508)
| 能量 (eV) | f₁ | f₂ |
|---|---|---|
| 10 | — | 9.70237 |
| 10.1617 | — | 9.72653 |
| 10.3261 | — | 9.75076 |
| 10.4931 | — | 9.77506 |
| 10.6628 | — | 9.7994 |
| 10.8353 | — | 9.77638 |
| 11.0106 | — | 9.72308 |
| 11.1886 | — | 9.67008 |
| 11.3696 | — | 9.61736 |
| 11.5535 | — | 9.54395 |
补充数据
Estimated Crustal Abundance
The estimated element abundance in the earth's crust.
1×10-3 milligrams per kilogram
参考文献 (1)
- [5] Tellurium https://education.jlab.org/itselemental/ele052.html
Estimated Oceanic Abundance
The estimated element abundance in the earth's oceans.
Not Applicable
参考文献 (1)
- [5] Tellurium https://education.jlab.org/itselemental/ele052.html
Sources
Sources of this element.
Tellurium is occasionally found native, but is more often found as the telluride of gold (calaverite), and combined with other metals. It is recovered commercially from anode muds produced during the electrolytic refining of blister copper. The U.S., Canada, Peru, and Japan are the largest Free World producers of the element.
参考文献 (1)
- [6] Tellurium https://periodic.lanl.gov/52.shtml
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 Tellurium.
The element property data was retrieved from publications.