Manganese monosilicide

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Manganese monosilicide
MnSi-ingot.jpg
MnSi prepared by zone melting
MnSi lattice.png
Structures of left-handed and right-handed MnSi crystals (3 presentations, with different numbers of atoms per unit cell)
Names
IUPAC name
Manganese silicide
Identifiers
3D model (JSmol)
PubChem CID
  • InChI=1S/Mn.Si
    Key: PYLLWONICXJARP-UHFFFAOYSA-N
  • [Si].[Mn]
Properties
MnSi
Molar mass 83.023 g/mol
Melting point 1,280 °C (2,340 °F; 1,550 K) [1]
31.3×10−6 emu/g [2]
Thermal conductivity 0.1 W/(cm·K) [1]
Structure
Cubic [3]
P213 (No. 198), cP8
a = 0.45598(2) nm
4
Hazards
Flash point Non-flammable
Related compounds
Other anions
Manganese germanide
Other cations
Iron silicide
Cobalt silicide
Related compounds
Manganese disilicide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Manganese monosilicide (MnSi) is an intermetallic compound, a silicide of manganese. It occurs in cosmic dust as the mineral brownleeite. MnSi has a cubic crystal lattice with no inversion center; therefore its crystal structure is helical, with right-hand and left-hand chiralities.

Contents

MnSi is a paramagnetic metal that turns into a ferromagnet at cryogenic temperatures below 29 K. In the ferromagnetic state, the spatial arrangement of electron spins in MnSi changes with magnetic field, forming helical, conical, skyrmion, and regular ferromagnetic phases.

Crystal structure and magnetism

Magnetic phase diagram of MnSi. At low temperatures, with increasing magnetic field, spins in MnSi form helical, conical, skyrmion (SkS) and regular ferromagnetic spatial structures. At high temperatures the spin orientation is random (paramagnetic) MnSi magnetic phase diagram.png
Magnetic phase diagram of MnSi. At low temperatures, with increasing magnetic field, spins in MnSi form helical, conical, skyrmion (SkS) and regular ferromagnetic spatial structures. At high temperatures the spin orientation is random (paramagnetic)
Simulated and measured (by STXM) images of helical, skyrmion and conical phases in FeGe. All magnetic properties are very similar in FeGe and MnSi, except for Tc values. FeGe magnetic phase diagram2a.png
Simulated and measured (by STXM) images of helical, skyrmion and conical phases in FeGe. All magnetic properties are very similar in FeGe and MnSi, except for Tc values.

Manganese monosilicide is a non-stoichiometric compound, meaning that the 1:1 Mn:Si composition, lattice constant and many other properties vary depending on the synthesis and processing history of the crystal. [3]

MnSi has a cubic crystal lattice with no inversion center; therefore its crystal structure is helical, with right-hand and left-hand chiralities. At low temperatures and magnetic fields, the magnetic structure of MnSi can be described as a stack of ferromagnetically ordered layers lying parallel to the (111) crystallographic planes. The direction of magnetic moment varies from layer to layer by a small angle due to the antisymmetric exchange. [3]

Upon cooling to temperatures below Tc = 29 K, MnSi changes from a paramagnetic into a ferromagnetic state; the transition temperature Tc decreases with increasing pressure, vanishing at 1.4 GPa. [3]

Electron spins in MnSi show dissimilar, yet regular spatial arrangements at different values of applied magnetic field. Those arrangements are named helical, skyrmion, conical, and regular ferromagnetic. They can be controlled not only by temperature and magnetic field, but also by electric current, and the current density required for manipulating skyrmions (~106 A/m2) is approximately one million times smaller than that needed for moving magnetic domains in traditional ferromagnets. As a result, skyrmions in MnSi have potential application in ultrahigh-density magnetic storage devices. [4]

Synthesis

Centimeter-scale single crystals of MnSi can be prepared by direct crystallization from the melt using the Bridgman, zone melting or Czochralski methods. [3]

Related Research Articles

<span class="mw-page-title-main">Ferromagnetism</span> Mechanism by which materials form into and are attracted to magnets

Ferromagnetism is a property of certain materials that results in a significant, observable magnetic permeability, and in many cases, a significant magnetic coercivity, allowing the material to form a permanent magnet. Ferromagnetic materials are familiar metals that are noticeably attracted to a magnet, a consequence of their substantial magnetic permeability. Magnetic permeability describes the induced magnetization of a material due to the presence of an external magnetic field. This temporarily induced magnetization, for example, inside a steel plate, accounts for its attraction to the permanent magnet. Whether or not that steel plate acquires a permanent magnetization itself depends not only on the strength of the applied field but on the so-called coercivity of the ferromagnetic material, which can vary greatly.

<span class="mw-page-title-main">Crystal structure</span> Ordered arrangement of atoms, ions, or molecules in a crystalline material

In crystallography, crystal structure is a description of the ordered arrangement of atoms, ions, or molecules in a crystalline material. Ordered structures occur from the intrinsic nature of the constituent particles to form symmetric patterns that repeat along the principal directions of three-dimensional space in matter.

<span class="mw-page-title-main">Antiferromagnetism</span> Regular pattern of magnetic moment ordering

In materials that exhibit antiferromagnetism, the magnetic moments of atoms or molecules, usually related to the spins of electrons, align in a regular pattern with neighboring spins pointing in opposite directions. This is, like ferromagnetism and ferrimagnetism, a manifestation of ordered magnetism. The phenomenon of antiferromagnetism was first introduced by Lev Landau in 1933.

<span class="mw-page-title-main">Curie temperature</span> Temperature above which magnetic properties change

In physics and materials science, the Curie temperature (TC), or Curie point, is the temperature above which certain materials lose their permanent magnetic properties, which can (in most cases) be replaced by induced magnetism. The Curie temperature is named after Pierre Curie, who showed that magnetism was lost at a critical temperature.

<span class="mw-page-title-main">Heusler compound</span>

Heusler compounds are magnetic intermetallics with face-centered cubic crystal structure and a composition of XYZ (half-Heuslers) or X2YZ (full-Heuslers), where X and Y are transition metals and Z is in the p-block. The term derives from the name of German mining engineer and chemist Friedrich Heusler, who studied such a compound (Cu2MnAl) in 1903. Many of these compounds exhibit properties relevant to spintronics, such as magnetoresistance, variations of the Hall effect, ferro-, antiferro-, and ferrimagnetism, half- and semimetallicity, semiconductivity with spin filter ability, superconductivity, topological band structure and are actively studied as Thermoelectric materials. Their magnetism results from a double-exchange mechanism between neighboring magnetic ions. Manganese, which sits at the body centers of the cubic structure, was the magnetic ion in the first Heusler compound discovered. (See the Bethe–Slater curve for details of why this happens.)

<span class="mw-page-title-main">Helimagnetism</span>

Helimagnetism is a form of magnetic ordering where spins of neighbouring magnetic moments arrange themselves in a spiral or helical pattern, with a characteristic turn angle of somewhere between 0 and 180 degrees. It results from the competition between ferromagnetic and antiferromagnetic exchange interactions. It is possible to view ferromagnetism and antiferromagnetism as helimagnetic structures with characteristic turn angles of 0 and 180 degrees respectively. Helimagnetic order breaks spatial inversion symmetry, as it can be either left-handed or right-handed in nature.

<span class="mw-page-title-main">Lanthanum strontium manganite</span>

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<span class="mw-page-title-main">Magnetic structure</span>

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<span class="mw-page-title-main">Magnetic skyrmion</span> Condensed matter phenomenon; vortex-like magnetic quasiparticle

In physics, magnetic skyrmions are statically stable soliton which have been predicted theoretically and observed experimentally in condensed matter systems. Magnetic skyrmions can be formed in magnetic materials in their 'bulk' such as in manganese monosilicide (MnSi), or in magnetic thin films. They can be achiral, or chiral in nature, and may exist both as dynamic excitations or stable or metastable states. Although the broad lines defining magnetic skyrmions have been established de facto, there exist a variety of interpretations with subtle differences.

<span class="mw-page-title-main">Iron monosilicide</span> Chemical compound

Iron monosilicide (FeSi) is an intermetallic compound, a silicide of iron that occurs in nature as the rare mineral naquite. It is a narrow-bandgap semiconductor with a room-temperature electrical resistivity of around 10 kΩ·cm and unusual magnetic properties at low temperatures. FeSi has a cubic crystal lattice with no inversion center; therefore its magnetic structure is helical, with right-hand and left-handed chiralities.

<span class="mw-page-title-main">Iron germanide</span> Chemical compound

Iron germanide (FeGe) is an intermetallic compound, a germanide of iron. At ambient conditions it crystallizes in three polymorphs with monoclinic, hexagonal and cubic structures. The cubic polymorph has no inversion center, it is therefore helical, with right-hand and left-handed chiralities.

<span class="mw-page-title-main">Manganese germanide</span> Chemical compound

Manganese germanide (MnGe) is an intermetallic compound, a germanide of manganese. Its crystals have a cubic symmetry with no inversion center, they are therefore helical, with right-hand and left-handed chiralities.

<span class="mw-page-title-main">Cobalt germanide</span> Chemical compound

Cobalt germanide (CoGe) is an intermetallic compound, a germanide of cobalt.

<span class="mw-page-title-main">Cobalt monosilicide</span> Chemical compound

Cobalt monosilicide (CoSi) is an intermetallic compound, a silicide of cobalt. It is a diamagnetic semimetal with an electrical resistivity of around 1 mΩ·cm.

<span class="mw-page-title-main">Manganese disilicide</span> Chemical compound

Manganese disilicide (MnSi2) is an intermetallic compound, a silicide of manganese. It is a non-stoichiometric compound, with a silicon deficiency expressed as MnSi2–x. Crystal structures of many MnSi2–x compounds resemble a chimney ladder and are called Nowotny phases. They include MnSi2 (x=0), Mn4Si7 (x=0.250), Mn11Si19 (x=0.273), Mn15Si26 (x=0.267) and Mn27Si47 (x=0.259). These phases have very similar unit cells whose length varies from 1.75 nm for MnSi2 or Mn4Si7, which have almost the same structures, to 11.8 nm for Mn27Si47.

Copper oxide selenite is an inorganic compound with the chemical formula Cu2OSeO3. It is an electrically insulating, piezoelectric and piezomagnetic material, which becomes a ferrimagnet upon cooling below 58 K. As of 2021, Cu2OSeO3 is the only insulating material that hosts magnetic skyrmions.

Chromium(IV) silicide or chromium monosilicide is an inorganic compound of chromium and silicon with a chemical formula of CrSi. It is a metal with an electrical resistivity of ca. 2×10−4 Ω·cm.

<span class="mw-page-title-main">Manganese arsenide</span> Chemical compound

Manganese arsenide (MnAs) is an intermetallic compound, an arsenide of manganese. It forms ferromagnetic crystals with hexagonal (NiAs-type) crystal structure, which convert to the paramagnetic orthorhombic β-phase upon heating to 45 °C (113 °F). MnAs has potential applications in spintronics, for electrical spin injection into GaAs and Si based devices.

Mavlyanovite is a manganese-silicon mineral with formula Mn5Si3. It was named after Gani Mavlyanov, an Uzbek geologist who lived from 1910 to 1988.

References

  1. 1 2 Levinson, Lionel M. (1973). "Investigation of the defect manganese silicide MnnSi2n−m". Journal of Solid State Chemistry. 6 (1): 126–135. Bibcode:1973JSSCh...6..126L. doi:10.1016/0022-4596(73)90212-0.
  2. Shinoda, Daizaburo; Asanabe, Sizuo (1966). "Magnetic Properties of Silicides of Iron Group Transition Elements". Journal of the Physical Society of Japan. 21 (3): 555. Bibcode:1966JPSJ...21..555S. doi:10.1143/JPSJ.21.555.
  3. 1 2 3 4 5 Stishov, Sergei M.; Petrova, Alla E. (2011). "Itinerant helimagnetic compound MnSi". Uspekhi Fizicheskikh Nauk. 181 (11): 1157. doi:10.3367/UFNr.0181.201111b.1157.
  4. Nagaosa, Naoto; Tokura, Yoshinori (2013). "Topological properties and dynamics of magnetic skyrmions". Nature Nanotechnology. 8 (12): 899–911. Bibcode:2013NatNa...8..899N. doi:10.1038/nnano.2013.243. PMID   24302027.