Holmium is a chemical element; it has symbol Ho and atomic number 67. It is a rare-earth element and the eleventh member of the lanthanide series. It is a relatively soft, silvery, fairly corrosion-resistant and malleable metal. Like many other lanthanides, holmium is too reactive to be found in native form, as pure holmium slowly forms a yellowish oxide coating when exposed to air. When isolated, holmium is relatively stable in dry air at room temperature. However, it reacts with water and corrodes readily, and also burns in air when heated.

Holmium, 67Ho
Pronunciation/ˈhlmiəm/ (HOHL-mee-əm)
Appearancesilvery white
Standard atomic weight Ar°(Ho)
Holmium in the periodic table
Hydrogen Helium
Lithium Beryllium Boron Carbon Nitrogen Oxygen Fluorine Neon
Sodium Magnesium Aluminium Silicon Phosphorus Sulfur Chlorine Argon
Potassium Calcium Scandium Titanium Vanadium Chromium Manganese Iron Cobalt Nickel Copper Zinc Gallium Germanium Arsenic Selenium Bromine Krypton
Rubidium Strontium Yttrium Zirconium Niobium Molybdenum Technetium Ruthenium Rhodium Palladium Silver Cadmium Indium Tin Antimony Tellurium Iodine Xenon
Caesium Barium Lanthanum Cerium Praseodymium Neodymium Promethium Samarium Europium Gadolinium Terbium Dysprosium Holmium Erbium Thulium Ytterbium Lutetium Hafnium Tantalum Tungsten Rhenium Osmium Iridium Platinum Gold Mercury (element) Thallium Lead Bismuth Polonium Astatine Radon
Francium Radium Actinium Thorium Protactinium Uranium Neptunium Plutonium Americium Curium Berkelium Californium Einsteinium Fermium Mendelevium Nobelium Lawrencium Rutherfordium Dubnium Seaborgium Bohrium Hassium Meitnerium Darmstadtium Roentgenium Copernicium Nihonium Flerovium Moscovium Livermorium Tennessine Oganesson


Atomic number (Z)67
Groupf-block groups (no number)
Periodperiod 6
Block  f-block
Electron configuration[Xe] 4f11 6s2
Electrons per shell2, 8, 18, 29, 8, 2
Physical properties
Phase at STPsolid
Melting point1734 K ​(1461 °C, ​2662 °F)
Boiling point2873 K ​(2600 °C, ​4712 °F)
Density (at 20° C)8.795 g/cm3[3]
when liquid (at m.p.)8.34 g/cm3
Heat of fusion17.0 kJ/mol
Heat of vaporization251 kJ/mol
Molar heat capacity27.15 J/(mol·K)
Vapor pressure
P (Pa) 1 10 100 1 k 10 k 100 k
at T (K) 1432 1584 (1775) (2040) (2410) (2964)
Atomic properties
Oxidation states0,[4] +1, +2, +3 (a basic oxide)
ElectronegativityPauling scale: 1.23
Ionization energies
  • 1st: 581.0 kJ/mol
  • 2nd: 1140 kJ/mol
  • 3rd: 2204 kJ/mol
Atomic radiusempirical: 176 pm
Covalent radius192±7 pm
Color lines in a spectral range
Spectral lines of holmium
Other properties
Natural occurrenceprimordial
Crystal structurehexagonal close-packed (hcp) (hP2)
Lattice constants
Hexagonal close packed crystal structure for holmium
a = 357.80 pm
c = 561.77 pm (at 20 °C)[3]
Thermal expansionpoly: 11.2 µm/(m⋅K) (at r.t.)
Thermal conductivity16.2 W/(m⋅K)
Electrical resistivitypoly: 814 nΩ⋅m (at r.t.)
Magnetic orderingparamagnetic
Young's modulus64.8 GPa
Shear modulus26.3 GPa
Bulk modulus40.2 GPa
Speed of sound thin rod2760 m/s (at 20 °C)
Poisson ratio0.231
Vickers hardness410–600 MPa
Brinell hardness500–1250 MPa
CAS Number7440-60-0
DiscoveryPer Theodor Cleve, Jacques-Louis Soret and Marc Delafontaine (1878)
Isotopes of holmium
Main isotopes[5] Decay
abun­dance half-life (t1/2) mode pro­duct
163Ho synth 4570 y ε 163Dy
164Ho synth 28.8 min ε 164Dy
β 164Er
165Ho 100% stable
166Ho synth 26.812 h β 166Er
166m1Ho synth 1132.6 y β 166Er
167Ho synth 3.1 h β 167Er
 Category: Holmium
| references

In nature, holmium occurs together with the other rare-earth metals (like thulium). It is a relatively rare lanthanide, making up 1.4 parts per million of the Earth's crust, an abundance similar to tungsten. Holmium was discovered through isolation by Swedish chemist Per Theodor Cleve. It was also independently discovered by Jacques-Louis Soret and Marc Delafontaine, who together observed it spectroscopically in 1878. Its oxide was first isolated from rare-earth ores by Cleve in 1878. The element's name comes from Holmia, the Latin name for the city of Stockholm.[6][7][8]

Like many other lanthanides, holmium is found in the minerals monazite and gadolinite and is usually commercially extracted from monazite using ion-exchange techniques. Its compounds in nature and in nearly all of its laboratory chemistry are trivalently oxidized, containing Ho(III) ions. Trivalent holmium ions have fluorescent properties similar to many other rare-earth ions (while yielding their own set of unique emission light lines), and thus are used in the same way as some other rare earths in certain laser and glass-colorant applications.

Holmium has the highest magnetic permeability and magnetic saturation of any element and is thus used for the pole pieces of the strongest static magnets. Because holmium strongly absorbs neutrons, it is also used as a burnable poison in nuclear reactors.



Holmium is the eleventh member of the lanthanide series. In the periodic table, it appears in period 6, between the lanthanides dysprosium to its left and erbium to its right, and above the actinide einsteinium.

Physical properties


With a boiling point of 3,000 K (2,730 °C), holmium is the sixth most volatile lanthanide after ytterbium, europium, samarium, thulium and dysprosium. At standard temperature and pressure, holmium, like many of the second half of the lanthanides, normally assumes a hexagonally close-packed (hcp) structure.[9] Its 67 electrons are arranged in the configuration [Xe] 4f11 6s2, so that it has thirteen valence electrons filling the 4f and 6s subshells.[10]

Holmium, like all of the lanthanides, is paramagnetic at standard temperature and pressure.[11] However, holmium is ferromagnetic at temperatures below 19 K (−254.2 °C; −425.5 °F).[12] It has the highest magnetic moment (10.6 μB) of any naturally occurring element[13] and possesses other unusual magnetic properties. When combined with yttrium, it forms highly magnetic compounds.[14]

Chemical properties


Holmium metal tarnishes slowly in air, forming a yellowish oxide layer that has an appearance similar to that of iron rust. It burns readily to form holmium(III) oxide:[15]

4 Ho + 3 O2 → 2 Ho2O3

It is a relatively soft and malleable element that is fairly corrosion-resistant and chemically stable in dry air at standard temperature and pressure. In moist air and at higher temperatures, however, it quickly oxidizes, forming a yellowish oxide.[16] In pure form, holmium possesses a metallic, bright silvery luster.

Holmium is quite electropositive: on the Pauling electronegativity scale, it has an electronegativity of 1.23.[17] It is generally trivalent. It reacts slowly with cold water and quickly with hot water to form holmium(III) hydroxide:[18]

2 Ho (s) + 6 H2O (l) → 2 Ho(OH)3 (aq) + 3 H2 (g)

Holmium metal reacts with all the stable halogens:[19]

2 Ho (s) + 3 F2 (g) → 2 HoF3 (s) [pink]
2 Ho (s) + 3 Cl2 (g) → 2 HoCl3 (s) [yellow]
2 Ho (s) + 3 Br2 (g) → 2 HoBr3 (s) [yellow]
2 Ho (s) + 3 I2 (g) → 2 HoI3 (s) [yellow]

Holmium dissolves readily in dilute sulfuric acid to form solutions containing the yellow Ho(III) ions, which exist as a [Ho(OH2)9]3+ complexes:[19]

2 Ho (s) + 3 H2SO4 (aq) → 2 Ho3+ (aq) + 3 SO2−
(aq) + 3 H2 (g)

Oxidation states


As with many lanthanides, holmium is usually found in the +3 oxidation state, forming compounds such as holmium(III) fluoride (HoF3) and holmium(III) chloride (HoCl3). Holmium in solution is in the form of Ho3+ surrounded by nine molecules of water. Holmium dissolves in acids.[13] However, holmium is also found to exist in +2, +1 and 0 oxidation states.[20][10]



The isotopes of holmium range from 140Ho to 175Ho. The primary decay mode before the most abundant stable isotope, 165Ho, is positron emission, and the primary mode after is beta minus decay. The primary decay products before 165Ho are terbium and dysprosium isotopes, and the primary products after are erbium isotopes.[21]

Natural holmium consists of one primordial isotope, holmium-165;[13] it is the only isotope of holmium that is thought to be stable, although it is predicted to undergo alpha decay to terbium-161 with a very long half-life.[22] Of the 35 synthetic radioactive isotopes that are known, the most stable one is holmium-163 (163Ho), with a half-life of 4570 years.[23] All other radioisotopes have ground-state half-lives not greater than 1.117 days, with the longest, holmium-166 (166Ho) having a half-life of 26.83 hours,[24] and most have half-lives under 3 hours.

166m1Ho has a half-life of around 1200 years.[25] The high excitation energy, resulting in a particularly rich spectrum of decay gamma rays produced when the metastable state de-excites, makes this isotope useful as a means for calibrating gamma ray spectrometers.[26]



Oxides and chalcogenides

Ho2O3, left: natural light, right: under a cold-cathode fluorescent lamp

Holmium(III) oxide is the only oxide of holmium. It changes its color depending on the lighting conditions. In daylight, it has a yellowish color. Under trichromatic light, it appears orange red, almost indistinguishable from the appearance of erbium oxide under the same lighting conditions.[27] The color change is related to the sharp emission lines of trivalent holmium ions acting as red phosphors.[28] Holmium(III) oxide appears pink under a cold-cathode fluorescent lamp.

Other chalcogenides are known for holmium. Holmium(III) sulfide has orange-yellow crystals in the monoclinic crystal system,[21] with the space group P21/m (No. 11).[29] Under high pressure, holmium(III) sulfide can form in the cubic and orthorhombic crystal systems.[30] It can be obtained by the reaction of holmium(III) oxide and hydrogen sulfide at 1,598 K (1,325 °C; 2,417 °F).[31] Holmium(III) selenide is also known. It is antiferromagnetic below 6 K.[32]



All four trihalides of holmium are known. Holmium(III) fluoride is a yellowish powder that can be produced by reacting holmium(III) oxide and ammonium fluoride, then crystallising it from the ammonium salt formed in solution.[33] Holmium(III) chloride can be prepared in a similar way, with ammonium chloride instead of ammonium fluoride.[34] It has the YCl3 layer structure in the solid state.[35] These compounds, as well as holmium(III) bromide and holmium(III) iodide, can be obtained by the direct reaction of the elements:[19]

2 Ho + 3 X2 → 2 HoX3

In addition, holmium(III) iodide can be obtained by the direct reaction of holmium and mercury(II) iodide, then removing the mercury by distillation.[36]

Organoholmium compounds


Organoholmium compounds are very similar to those of the other lanthanides, as they all share an inability to undergo π backbonding. They are thus mostly restricted to the mostly ionic cyclopentadienides (isostructural with those of lanthanum) and the σ-bonded simple alkyls and aryls, some of which may be polymeric.[37]



Holmium (Holmia, Latin name for Stockholm) was discovered by the Swiss chemists Jacques-Louis Soret and Marc Delafontaine in 1878 who noticed the aberrant spectrographic emission spectrum of the then-unknown element (they called it "Element X").[38][39]

The Swedish chemist Per Teodor Cleve also independently discovered the element while he was working on erbia earth (erbium oxide). He was the first to isolate the new element.[7][6][40] Using the method developed by the Swedish chemist Carl Gustaf Mosander, Cleve first removed all of the known contaminants from erbia. The result of that effort was two new materials, one brown and one green. He named the brown substance holmia (after the Latin name for Cleve's home town, Stockholm) and the green one thulia. Holmia was later found to be the holmium oxide, and thulia was thulium oxide.[41]

In the English physicist Henry Moseley's classic paper on atomic numbers, holmium was assigned the value 66. The holmium preparation he had been given to investigate had been impure, dominated by neighboring (at the time undiscovered) dysprosium. He would have seen x-ray emission lines for both elements, but assumed that the dominant ones belonged to holmium, instead of the dysprosium impurity.[42]

Occurrence and production

A specimen of gadolinite - holmium is the black part of it.

Like all the other rare-earth elements, holmium is not naturally found as a free element. It occurs combined with other elements in gadolinite, monazite and other rare-earth minerals. No holmium-dominant mineral has yet been found. The main mining areas are China, United States, Brazil, India, Sri Lanka, and Australia with reserves of holmium estimated as 400,000 tonnes.[41] The annual production of holmium metal is of about 10 tonnes per year.[43]

Holmium makes up 1.3 parts per million of the Earth's crust by mass.[44] Holmium makes up 1 part per million of the soils, 400 parts per quadrillion of seawater, and almost none of Earth's atmosphere, which is very rare for a lanthanide.[41] It makes up 500 parts per trillion of the universe by mass.[45]

Holmium is commercially extracted by ion exchange from monazite sand (0.05% holmium), but is still difficult to separate from other rare earths. The element has been isolated through the reduction of its anhydrous chloride or fluoride with metallic calcium.[21] Its estimated abundance in the Earth's crust is 1.3 mg/kg. Holmium obeys the Oddo–Harkins rule: as an odd-numbered element, it is less abundant than both dysprosium and erbium. However, it is the most abundant of the odd-numbered heavy lanthanides. Of the lanthanides, only promethium, thulium, lutetium and terbium are less abundant on Earth. The principal current source are some of the ion-adsorption clays of southern China. Some of these have a rare-earth composition similar to that found in xenotime or gadolinite. Yttrium makes up about two-thirds of the total by mass; holmium is around 1.5%.[46] Holmium is relatively inexpensive for a rare-earth metal with the price about 1000 USD/kg.[47]


A solution of 4% holmium oxide in 10% perchloric acid, permanently fused into a quartz cuvette as an optical calibration standard

Glass containing holmium oxide and holmium oxide solutions (usually in perchloric acid) have sharp optical absorption peaks in the spectral range 200 to 900 nm. They are therefore used as a calibration standard for optical spectrophotometers.[48][49][50] The radioactive but long-lived 166m1Ho is used in calibration of gamma-ray spectrometers.[51]

Holmium is used to create the strongest artificially generated magnetic fields, when placed within high-strength magnets as a magnetic pole piece (also called a magnetic flux concentrator).[52] Holmium is also used in the manufacture of some permanent magnets.

Holmium-doped yttrium iron garnet (YIG) and yttrium lithium fluoride have applications in solid-state lasers, and Ho-YIG has applications in optical isolators and in microwave equipment (e.g., YIG spheres). Holmium lasers emit at 2.1 micrometres.[53] They are used in medical, dental, and fiber-optical applications.[14] It is also being considered for usage in the enucleation of the prostate.[54]

Since holmium can absorb nuclear fission-bred neutrons, it is used as a burnable poison to regulate nuclear reactors.[41] It is used as a colorant for cubic zirconia, providing pink coloring,[55] and for glass, providing yellow-orange coloring.[56] In March 2017, IBM announced that they had developed a technique to store one bit of data on a single holmium atom set on a bed of magnesium oxide.[57] With sufficient quantum and classical control techniques, holmium may be a good candidate to make quantum computers.[58]

Biological role and precautions


Holmium plays no biological role in humans, but its salts are able to stimulate metabolism.[21] Humans typically consume about a milligram of holmium a year. Plants do not readily take up holmium from the soil. Some vegetables have had their holmium content measured, and it amounted to 100 parts per trillion.[59] Holmium and its soluble salts are slightly toxic if ingested, but insoluble holmium salts are nontoxic. Metallic holmium in dust form presents a fire and explosion hazard.[60][61][62] Large amounts of holmium salts can cause severe damage if inhaled, consumed orally, or injected. The biological effects of holmium over a long period of time are not known. Holmium has a low level of acute toxicity.[63]

See also



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  • Ganjali, Mohammad Reza; Gupta, Vinod Kumar; Faridbod, Farnoush; Norouzi, Parviz (2016-02-25). Lanthanides Series Determination by Various Analytical Methods. Elsevier. ISBN 978-0-12-420095-1.
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  • G. Meyer; Lester R. Morss, eds. (1991). Synthesis of Lanthanide and Actinide Compounds. Kluwer Academic Publishers. ISBN 0792310187.
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Further reading

  • R. J. Callow, The Industrial Chemistry of the Lanthanons, Yttrium, Thorium, and Uranium, Pergamon Press, 1967.