Selenium is a chemical element with symbol Se and atomic number 34. It is a nonmetal with properties that are intermediate between those of its periodic table column-adjacent chalcogen elements sulfur and tellurium. It rarely occurs in its elemental state in nature, or as pure ore compounds.
Selenium is a metalloid of group 16 that presents the oxidation states -2, +4 and +6, the +4 and +6 being the most stable. Its electronegativity of 2.55 (Pauling scale) configures it as an element with properties intermediate between metals and non-metals, slightly more non-metal than sulfur. Its predominant bond is covalent, with a tendency to form two angular directed bonds. Exceptions: grey crystalline selenium exhibits semiconductor properties, with the ability to increase its conductivity in the presence of light (photoconductive effect).
Se + 2 NaOH -> Na2SeO3 + H2O
Selenium reacts with hot strong base to form sodium selenite, showing selenium's amphoteric behaviour in basic medium.
Se + 2 HNO3 -> H2SeO3 + 2 NO2
Selenium reacts with concentrated nitric acid, being oxidised to selenite, a stable selenium oxide.
Se + 2 H2O -> H2Se + O2 (posteriormente H2SeO3, con oxigeno)
Selenium reacts with oxygen at high temperatures forming selenium oxides, which subsequently react with water to give selenous acid.
| Compound | Formula | Use or importance |
|---|---|---|
| Zinc selenide | ZnSe | Semiconductor semiconductor material; used in diodes, transistors and light emitters |
| Cadmium selenide | CdSe | Semiconductor semiconductor; used in Photocell, screens and reddish pigments |
| Selenous acid | H2SeO3 | Compound in the +4 oxidation state; precursor of selenium salts and compounds |
| Selenic acid | H2SeO4 | Compound in the +6 oxidation state; strong oxidant and precursor of selenate salts |
Natural selenium is composed of six stable isotopes: selenium-74 (⁷⁴Se, 0.89%), selenium-76 (⁷⁶Se, 9.37%), selenium-77 (⁷⁷Se, 7.63%), selenium-78 (⁷⁸Se, 23.77%), selenium-80 (⁸⁰Se, 49.61%) and selenium-82 (⁸²Se, 8.73%). The most abundant is ⁸⁰Se. The first three are stable, the last three are stable as well; ⁸²Se has an extremely long effective half-life (~10²⁰ years). There are no environmentally relevant radioactive isotopes; its constant abundance makes it a stable reference in quantitative analyses by mass spectrometry.
Selenium is relatively rare in the Earth's crust, with a concentration of about 0.05 ppm. It occurs mainly combined in copper selenide (Cu₂Se) and in selenious anhydride (SeO₃). It is obtained as a byproduct of copper refining, in Mining. The main reserves are in the Russian Union, Canada, the United States, Zimbabwe and Chile. Selenium never appears free in nature: it is always combined with other elements in minerals. Selenium-enriched plants accumulate selenium in large volumes in soils with high selenium content (zones of China, South Dakota, Zimbabwe).
Selenium was discovered in 1817 by the Swedish chemist Jöns Jacob Berzelius, who identified it accidentally in the sugar industry of Humboldt, Sweden. Berzelius noted that the substance shared properties of metals and non-metals; he baptised it 'selenium', from the Greek 'selene' (the moon), in reference to its similarity with sulfur. Its discovery is considered one of the first applications of analytical chemistry in the chemical industry.
Selenium is used in semiconductor materials for photoconductive devices, photocells and image reproduction devices. It is also incorporated into certain alloys to improve conductivity and resistance to corrosion, and in some industrial formulations where a material with special optical and electrical properties is needed.
Selenium compounds are used in the manufacture of colour glass (red tones or neutralising greenish tints), in high-efficiency photovoltaic panels, in photoconductive photocells for light sensors and in some components of electroluminescence. Cadmium selenides (CdSe, together with CdTe) are used in thin-film solar cells.
Selenium is an essential element in trace amounts for living things. It is part of selenoproteins, a group of proteins that incorporate the amino acid selenocysteine. Some of them participate in the regulation of the cell's oxidation state and in protection against certain oxidative damage. Others intervene in thyroid hormone metabolism. The presence of selenium modifies the chemical properties of the active centre of these proteins, allowing certain biological reactions. Its function depends on incorporation into specific chemical forms, not simply on being present as an element. Selenium deficiency can cause health problems, while in excess it is toxic.
Selenium is toxic in high doses, especially in the form of inorganic compounds. Exposure to selenium vapours can irritate the eyes, respiratory tract and digestive system. Metallic selenium is stable and does not react easily, but inorganic compounds are toxic. Tellurium and selenium are mainly excreted through metabolism, but exposure habits must be controlled through adequate ventilation, respiratory protection and gloves. Selenium must be handled in well-ventilated areas, with appropriate personal protective equipment and rigorous control of environmental exposure.
Selenium does not degrade in the environment and its accumulation can affect soils and surface waters. Industrial discharges of selenium compounds can be dangerous for aquatic life. Appropriate filtration systems and waste management technologies are essential to prevent pollution. Selenium in metallic alloys is considered a stable and safe compound when used properly. Natural soils with high selenium content can be dangerous for ecosystems if vegetation absorbs too much selenium.
Some forms of selenium exhibit photoconductivity, a property by which its electrical conductivity increases upon receiving light. The light energy facilitates the generation of charge carriers capable of transporting current. This phenomenon aroused interest in the development of photocells, light sensors and image reproduction devices. Although many of these applications have been replaced by more modern technologies, the photoconductivity of selenium remains a notable example of the relationship between light and electricity.
Selenium presents several structural forms, known as allotropes, whose optical properties are different. Some amorphous varieties show reddish tones, while crystalline grey selenium has a dark appearance and semiconductor behaviour. These differences are due to the organisation of their atoms and the way their electronic structure interacts with light. That is why selenium's colour is not unique: it depends on the specific form of the material and the conditions in which it is found.
Certain selenium compounds are incorporated into glass to modify its colour and optical properties. Depending on the composition and manufacturing conditions, they can contribute to red tones or neutralise greenish tints caused by other impurities. The effect depends not exclusively on the amount of selenium, but also on its chemical form and the rest of the components present. That is why manufacturers carefully adjust the formulation to achieve a uniform appearance and the required visual characteristics.
Selenium exhibits photoconductive properties that allow transforming changes in illumination into variations of an electric signal. This feature was exploited in historic image reproduction technologies and continues to be relevant in certain specialised detection systems. In some digital radiography devices, for example, an amorphous selenium layer can directly convert X-rays into electric charges, without the need for first converting to visible light. This mechanism is known as direct conversion and allows recording images with detectors designed for this purpose.
Selenium is part of selenoproteins, a group of proteins that incorporate the amino acid selenocysteine. Some of them participate in the regulation of the cell's oxidation state and in protection against certain oxidative damage. Others intervene in the metabolism of thyroid hormones. The presence of selenium modifies the chemical properties of the active centre of these proteins, allowing certain biological reactions. Its function depends on incorporation into specific chemical forms, not simply on being present as an element.
Selenium and sulfur belong to the same group of the periodic table and share some chemical characteristics, but they do not behave identically. Selenium is more polarisable and its bonds exhibit different properties, which influences the stability and reactivity of its compounds. In addition, selenium can incorporate into proteins in the form of selenocysteine, while sulfur appears in amino acids such as cysteine and methionine. These differences affect both inorganic chemistry and biological processes.
Selenocysteine is an amino acid that contains selenium instead of the sulfur present in cysteine. It is incorporated into certain proteins through a specialised cellular mechanism, different from the one used for most amino acids. Its selenium atom can facilitate important chemical reactions, especially those related to electron transfer. Although it is structurally similar to cysteine, its chemical properties are different. This difference allows certain enzymes to perform functions that depend on the characteristic reactivity of selenium.
Main sources consulted: PubChem, Royal Society of Chemistry, NIST, IUPAC. Last revision: November 2026.