Phases of ice

Log-lin pressure-temperature phase diagram of water. The Roman numerals correspond to some ice phases listed below.

An alternative formulation of the phase diagram for certain ices and other phases of water

Pressure dependence of ice melting

Currently, 19 solid phases of water (both crystalline and amorphous) have been observed at various densities, along with hypothetical proposed phases of ice that have not been observed.

Theory

Most liquids under increased pressure freeze at higher temperatures because the pressure helps to hold the molecules together. However, the strong hydrogen bonds in water make it different: for some pressures higher than 1 atm (0.10 MPa), water freezes at a temperature below 0 °C, as shown in the phase diagram below. The melting of ice under high pressures is thought to contribute to the movement of glaciers.

Ice, water, and water vapour can coexist at the triple point, which is exactly 273.16 K (0.01 °C) at a pressure of 611.657 Pa. The kelvin was defined as ⁠1/273.16⁠ of the difference between this triple point and absolute zero, though this definition changed in May 2019. Unlike most other solids, ice is difficult to superheat. In an experiment, ice at −3 °C was superheated to about 17 °C for about 250 picoseconds.

Subjected to higher pressures and varying temperatures, ice can form in nineteen separate known crystalline phases. With care, at least fifteen of these phases (one of the known exceptions being ice X) can be recovered at ambient pressure and low temperature in metastable form. The types are differentiated by their crystalline structure, proton ordering, and density. There are also two metastable phases of ice under pressure, both fully hydrogen-disordered; these are IV and XII. Ice XII was discovered in 1996. In 2006, XIII and XIV were discovered. Ices XI, XIII, and XIV are hydrogen-ordered forms of ices I_h, V, and XII respectively. In 2009, ice XV was found at extremely high pressures and −143 °C. At even higher pressures, ice is predicted to become a metal; this has been variously estimated to occur at 1.55 TPa or 5.62 TPa.

Non-crystalline ice

As well as crystalline forms, solid water can exist in amorphous states as amorphous solid water (ASW) of varying densities. Water in the interstellar medium is dominated by amorphous ice, making it likely the most common form of water in the universe. Low-density ASW (LDA), also known as hyperquenched glassy water, may be responsible for noctilucent clouds on Earth and is usually formed by deposition of water vapor in cold or vacuum conditions. High-density ASW (HDA) is formed by compression of ordinary ice I_h or LDA at GPa pressures. Very-high-density ASW (VHDA) is HDA slightly warmed to 160 K under 1–2 GPa pressures.

In outer space, hexagonal crystalline ice (the predominant form found on Earth) is extremely rare. Amorphous ice is more common; however, hexagonal crystalline ice can be formed by volcanic action.

Ice from a theorized superionic water may possess two crystalline structures. At pressures in excess of 500,000 bars (7,300,000 psi) such superionic ice would take on a body-centered cubic structure. However, at pressures in excess of 1,000,000 bars (15,000,000 psi) the structure may shift to a more stable face-centered cubic lattice. It is speculated that superionic ice could compose the interior of ice giants such as Uranus and Neptune.

Known phases

Phase	Characteristics
Amorphous ice	Amorphous ice is ice lacking crystal structure. Amorphous ice exists in four forms: low-density (LDA) formed at atmospheric pressure, or below, medium-density (MDA), high-density (HDA) and very-high-density amorphous ice (VHDA), forming at higher pressures. LDA forms by extremely quick cooling of liquid water ("hyperquenched glassy water", HGW), by depositing water vapour on very cold substrates ("amorphous solid water", ASW) or by heating high density forms of ice at ambient pressure ("LDA"). Recently, a medium-density amorphous form ("MDA") has been shown to exist, created by ball-milling ice Ih at low temperatures.
Ice Ih	Normal hexagonal crystalline ice. Virtually all ice in the biosphere is ice Ih, with the exception only of a small amount of ice Ic.
Ice Ic	A metastable cubic crystalline variant of ice. The oxygen atoms are arranged in a diamond structure. It is produced at temperatures between 130 and 220 K, and can exist up to 240 K, when it transforms into ice Ih. It may occasionally be present in the upper atmosphere. More recently, it has been shown that many samples which were described as cubic ice were actually stacking disordered ice with trigonal symmetry. The first samples of ice I with cubic symmetry (i.e. cubic ice) were only reported in 2020.
Ice II	A rhombohedral crystalline form with highly ordered structure. Formed from ice Ih by compressing it at temperature of 190–210 K. When heated, it undergoes transformation to ice III.
Ice III	A tetragonal crystalline ice, formed by cooling water down to 250 K at 300 MPa. Least dense of the high-pressure phases. Denser than water.
Ice IV	A metastable rhombohedral phase. It can be formed by heating high-density amorphous ice slowly at a pressure of 810 MPa. It does not form easily without a nucleating agent.
Ice V	A monoclinic crystalline phase. Formed by cooling water to 253 K at 500 MPa. Most complicated structure of all the phases.
Ice VI	A tetragonal crystalline phase. Formed by cooling water to 270 K at 1.1 GPa. Exhibits Debye relaxation.
Ice VII	A cubic phase. The hydrogen atoms' positions are disordered. Exhibits Debye relaxation. The hydrogen bonds form two interpenetrating lattices.
Ice VIIt	Forms at around 5 GPa, when Ice VII becomes tetragonal.
Ice VIII	A more ordered version of ice VII, where the hydrogen atoms assume fixed positions. It is formed from ice VII, by cooling it below 5 °C (278 K) at 2.1 GPa.
Ice IX	A tetragonal phase. Formed gradually from ice III by cooling it from 208 K to 165 K, stable below 140 K and pressures between 200 MPa and 400 MPa. It has density of 1.16 g/cm3, slightly higher than ordinary ice.
Ice X	Proton-ordered symmetric ice. Forms at pressures around 70 GPa, or perhaps as low as 30 GPa.
Ice XI	An orthorhombic, low-temperature equilibrium form of hexagonal ice. It is ferroelectric. Ice XI is considered the most stable configuration of ice Ih.
Ice XII	A tetragonal, metastable, dense crystalline phase. It is observed in the phase space of ice V and ice VI. It can be prepared by heating high-density amorphous ice from 77 K to about 183 K at 810 MPa. It has a density of 1.3 g·cm−3 at 127 K (i.e., approximately 1.3 times denser than water).
Ice XIII	A monoclinic crystalline phase. Formed by cooling water to below 130 K at 500 MPa. The proton-ordered form of ice V.
Ice XIV	An orthorhombic crystalline phase. Formed below 118 K at 1.2 GPa. The proton-ordered form of ice XII.
Ice XV	A proton-ordered form of ice VI formed by cooling water to around 80–108 K at 1.1 GPa.
Ice XVI	The least dense crystalline form of water, topologically equivalent to the empty structure of sII clathrate hydrates.
Square ice	Square ice crystals form at room temperature when squeezed between two layers of graphene. The material was a new crystalline phase of ice when it was first reported in 2014. The research derived from the earlier discovery that water vapor and liquid water could pass through laminated sheets of graphene oxide, unlike smaller molecules such as helium. The effect is thought to be driven by the van der Waals force, which may involve more than 10,000 atmospheres of pressure.
Ice XVII	A porous hexagonal crystalline phase with helical channels, with density near that of ice XVI. Formed by placing hydrogen-filled ice in a vacuum and increasing the temperature until the hydrogen molecules escape.
Ice XVIII	A form of water also known as superionic water or superionic ice in which oxygen ions develop a crystalline structure while hydrogen ions move freely.
Ice XIX	Another phase related to ice VI formed by cooling water to around 100 K at approximately 2 GPa.

Ice Ih

Photograph showing details of an ice cube under magnification. Ice I_h is the form of ice commonly seen on Earth.

Phase space of ice I_h with respect to other ice phases.

Ice I_h (hexagonal ice crystal) (pronounced: ice one h, also known as ice-phase-one) is the hexagonal crystal form of ordinary ice, or frozen water. Virtually all ice in the biosphere is ice I_h, with the exception only of a small amount of ice I_c that is occasionally present in the upper atmosphere. Ice I_h exhibits many peculiar properties that are relevant to the existence of life and regulation of global climate. For a description of these properties, see Ice, which deals primarily with ice I_h.

The crystal structure is characterized by the oxygen atoms forming hexagonal symmetry with near tetrahedral bonding angles. Ice I_h is stable down to −268 °C (5 K; −450 °F), as evidenced by x-ray diffraction and extremely high resolution thermal expansion measurements. Ice I_h is also stable under applied pressures of up to about 210 megapascals (2,100 atm) where it transitions into ice III or ice II.

Physical properties

The density of ice I_h is 0.917 g/cm³ which is less than that of liquid water. This is attributed to the presence of hydrogen bonds which causes atoms to become closer in the liquid phase. Because of this, ice I_h floats on water, which is highly unusual when compared to other materials. The solid phase of materials is usually more closely and neatly packed and has a higher density than the liquid phase. When lakes freeze, they do so only at the surface while the bottom of the lake remains near 4 °C (277 K; 39 °F) because water is densest at this temperature. No matter how cold the surface becomes, there is always a layer at the bottom of the lake that is 4 °C (277 K; 39 °F). This anomalous behavior of water and ice is what allows fish to survive harsh winters. The density of ice I_h increases when cooled, down to about −211 °C (62 K; −348 °F); below that temperature, the ice expands again (negative thermal expansion).

The latent heat of melting is 5987 J/mol, and its latent heat of sublimation is 50911 J/mol. The high latent heat of sublimation is principally indicative of the strength of the hydrogen bonds in the crystal lattice. The latent heat of melting is much smaller, partly because liquid water near 0 °C also contains a significant number of hydrogen bonds. The refractive index of ice I_h is 1.31.

Crystal structure

Crystal structure of ice I_h. Dashed lines represent hydrogen bonds

The accepted crystal structure of ordinary ice was first proposed by Linus Pauling in 1935. The structure of ice I_h is the wurtzite lattice, roughly one of crinkled planes composed of tessellating hexagonal rings, with an oxygen atom on each vertex, and the edges of the rings formed by hydrogen bonds. The planes alternate in an ABAB pattern, with B planes being reflections of the A planes along the same axes as the planes themselves. The distance between oxygen atoms along each bond is about 275 pm and is the same between any two bonded oxygen atoms in the lattice. The angle between bonds in the crystal lattice is very close to the tetrahedral angle of 109.5°, which is also quite close to the angle between hydrogen atoms in the water molecule (in the gas phase), which is 105°. This tetrahedral bonding angle of the water molecule essentially accounts for the unusually low density of the crystal lattice – it is beneficial for the lattice to be arranged with tetrahedral angles even though there is an energy penalty in the increased volume of the crystal lattice. As a result, the large hexagonal rings leave almost enough room for another water molecule to exist inside. This gives naturally occurring ice its rare property of being less dense than its liquid form. The tetrahedral-angled hydrogen-bonded hexagonal rings are also the mechanism that causes liquid water to be densest at 4 °C. Close to 0 °C, tiny hexagonal ice I_h-like lattices form in liquid water, with greater frequency closer to 0 °C. This effect decreases the density of the water, causing it to be densest at 4 °C when the structures form infrequently.

Hydrogen disorder

See also: Ice rules and Geometrical frustration § Water ice

The Wurtzite structure. In Ice I_h, the oxygen atoms are arranged on the lattice points, and the hydrogen atoms are on the bonds between lattice points. Each oxygen atom has 4 neighboring ones. Note that the lattice bipartites into two subsets, here colored black and white.

The hydrogen atoms in the crystal lattice lie very nearly along the hydrogen bonds, and in such a way that each water molecule is preserved. This means that each oxygen atom in the lattice has two hydrogens adjacent to it, at about 101 pm along the 275 pm length of the bond. The crystal lattice allows a substantial amount of disorder in the positions of the hydrogen atoms frozen into the structure as it cools to absolute zero. As a result, the crystal structure contains some residual entropy inherent to the lattice and determined by the number of possible configurations of hydrogen positions that can be formed while still maintaining the requirement for each oxygen atom to have only two hydrogens in closest proximity, and each H-bond joining two oxygen atoms having only one hydrogen atom. This residual entropy S₀ is equal to 3.4±0.1 J mol⁻¹ K⁻¹ $=R\ln(1.50\pm 0.02)$.

By contrast, the structure of ice II is hydrogen-ordered, which helps to explain the entropy change of 3.22 J/mol when the crystal structure changes to that of ice I. Also, ice XI, an orthorhombic, hydrogen-ordered form of ice I_h, is considered the most stable form at low temperatures.

Theoretical calculation

There are various ways of approximating this number from first principles. The following is the one used by Linus Pauling.

Suppose there are a given number N of water molecules in an ice lattice. To compute its residual entropy, we need to count the number of configurations that the lattice can assume. The oxygen atoms are fixed at the lattice points, but the hydrogen atoms are located on the lattice edges. The problem is to pick one end of each lattice edge for the hydrogen to bond to, in a way that still makes sure each oxygen atom is bond to two hydrogen atoms.

The oxygen atoms can be divided into two sets in a checkerboard pattern, shown in the picture as black and white balls. Focus attention on the oxygen atoms in one set: there are N/2 of them. Each has four hydrogen bonds, with two hydrogens close to it and two far away. This means there are ${\textstyle {\tbinom {4}{2}}=6}$ allowed configurations of hydrogens for this oxygen atom (see Binomial coefficient). Thus, there are 6^N/2 configurations that satisfy these N/2 atoms. But now, consider the remaining N/2 oxygen atoms: in general they won't be satisfied (i.e., they will not have precisely two hydrogen atoms near them). For each of those, there are 2⁴ = 16 possible placements of the hydrogen atoms along their hydrogen bonds, of which 6 are allowed. So, naively, we would expect the total number of configurations to be

$$6^{N/2}(6/16)^{N/2}=(3/2)^{N}.$$

Using Boltzmann's entropy formula, we conclude that

$$S_{0}=k\ln(3/2)^{N}=nR\ln(3/2),$$where k is the Boltzmann constant and R is the molar gas constant. So, the molar residual entropy is $R\ln(3/2)=3.37\mathrm {J} \cdot \mathrm {mol} ^{-1}\mathrm {K} ^{-1}$.

The same answer can be found in another way. First orient each water molecule randomly in each of the 6 possible configurations, then check that each lattice edge contains exactly one hydrogen atom. Assuming that the lattice edges are independent, then the probability that a single edge contains exactly one hydrogen atom is 1/2, and since there are 2N edges in total, we obtain a total configuration count $6^{N}\times (1/2)^{2N}=(3/2)^{N}$, as before.

Refinements

This estimate is 'naive', as it assumes the six out of 16 hydrogen configurations for oxygen atoms in the second set can be independently chosen, which is false. More complex methods can be employed to better approximate the exact number of possible configurations, and achieve results closer to measured values. Nagle (1966) used a series summation to obtain $R\ln(1.50685\pm 0.00015)$.

As an illustrative example of refinement, consider the following way to refine the second estimation method given above. According to it, six water molecules in a hexagonal ring would allow $6^{6}\times (1/2)^{6}=729$ configurations. However, by explicit enumeration, there are actually 730 configurations. Now in the lattice, each oxygen atom participates in 12 hexagonal rings, so there are 2N rings in total for N oxygen atoms, or 2 rings for each oxygen atom, giving a refined result of $R\ln(1.5\times (730/729)^{2})=R\ln(1.504)$.

Ice Ic

Ice I_c (pronounced "ice one c" or "ice I c") is a metastable cubic crystalline variant of ice. Hans König was the first to identify and deduce the structure of ice I_c. The oxygen atoms in ice I_c are arranged in a diamond structure and is extremely similar to ice I_h having nearly identical densities and the same lattice constant along the hexagonal puckered-planes. It forms at temperatures between 130 and 220 kelvins (−143 and −53 degrees Celsius) upon cooling, and can exist up to 240 K (−33 °C) upon warming, when it transforms into ice I_h.

Phase diagram of water

Apart from forming from supercooled water, ice I_c has also been reported to form from amorphous ice as well as from the high-pressure ices II, III and V. It can form in and is occasionally present in the upper atmosphere and is believed to be responsible for the observation of Scheiner's halo, a rare ring that occurs near 28 degrees from the Sun or the Moon.

Ordinary water ice is known as ice I_h (in the Bridgman nomenclature). Different types of ice, from ice II to ice XIX, have been created in the laboratory at different temperatures and pressures.

Some authors have expressed doubts whether ice I_c really has a cubic crystal system, claiming that it is merely stacking-disordered ice I (“ice I_sd”), and it has been dubbed the ″most faceted ice phase in a literal and a more general sense.″

However, in 2020, two research groups individually prepared ice I_c without stacking disorder. Komatsu et al. prepared C₂ hydrate at high pressure and decompressed it at 100 K to make hydrogen molecules extracted from the structure, resulting in ice I_c without stacking disorder. Del Rosso et al. prepared ice XVII from C₀ hydrate and heated it at 0 GPa to obtain pure ice I_c without stacking disorder. Pure ice I_c prepared in the latter method transforms into ice I_h at 226 K with an enthalpy change of -37.7 J/mol.

Ice II

Ice II is a rhombohedral crystalline form of ice with a highly ordered structure. It is formed from ice I_h by compressing it at a temperature of 198 K at 300 MPa or by decompressing ice V. When heated it undergoes transformation to ice III. Ordinary water ice is known as ice I_h, (in the Bridgman nomenclature). Different types of ice, from ice II to ice XIX, have been created in the laboratory at different temperatures and pressures. It is thought that the cores of icy moons like Jupiter's Ganymede may be made of ice II.

History

The properties of ice II were first described and recorded by Gustav Heinrich Johann Apollon Tammann in 1900 during his experiments with ice under high pressure and low temperatures. Having produced ice III, Tammann then tried condensing the ice at a temperature between −70 and −80 °C (203 and 193 K; −94 and −112 °F) under 200 MPa (2,000 atm) of pressure. Tammann noted that in this state ice II was denser than he had observed ice III to be. He also found that both types of ice can be kept at normal atmospheric pressure in a stable condition so long as the temperature is kept at that of liquid air, which slows the change in conformation back to ice I_h.

In later experiments by Bridgman in 1912, it was shown that the difference in volume between ice II and ice III was in the range of 0.0001 m³/kg (2.8 cu in/lb). This difference hadn't been discovered by Tammann due to the small change and was why he had been unable to determine an equilibrium curve between the two. The curve showed that the structural change from ice III to ice II was more likely to happen if the medium had previously been in the structural conformation of ice II. However, if a sample of ice III that had never been in the ice II state was obtained, it could be supercooled even below −70 °C without it changing into ice II. Conversely, however, any superheating of ice II was not possible in regards to retaining the same form. Bridgman found that the equilibrium curve between ice II and ice IV was much the same as with ice III, having the same stability properties and small volume change. The curve between ice II and ice V was extremely different, however, with the curve's bubble being essentially a straight line and the volume difference being almost always 0.0000545 m³/kg (1.51 cu in/lb).

Quest for a hydrogen-disordered counterpart of ice II

As ice II is completely hydrogen ordered, the presence of its disordered counterpart is a great matter of interest. Shephard et al. investigated the phase boundaries of NH₄F-doped ices because NH₄F has been reported to be a hydrogen disordering reagent. However, adding 2.5 mol% of NH₄F resulted in the disappearance of ice II instead of the formation of a disordered ice II. According to the DFC calculation by Nakamura et al., the phase boundary between ice II and its disordered counterpart is estimated to be in the stability region of liquid water.

Ice III

"the form of water" redirects here. For the German high-speed train, see ICE 3.

Phase diagram of water, showing the region where ice III is stable.

Ice III is a form of solid matter that consists of tetragonal crystalline ice formed by cooling water to 250 K (about -10 °C) at 300 MPa. It is the least dense of the high-pressure water phases, with a density of 1160 kg/m³ (at 350 MPa). It has a very high relative permittivity at 117 and has a specific gravity of 1.16 with respect to water.

Ordinary water ice is known as ice I_h (in the Bridgman nomenclature). Different types of ice, from Ice II to Ice XIX, have been created in the laboratory at different temperatures and pressures.

Ice IV

For the high speed train, see ICE 4.

Ice IV is a metastable high-pressure phase of ice. It is formed when liquid water is compressed with an immense force.

Preparation

Several organic nucleating reagents had been proposed to selectively crystallize ice IV from liquid water, but even with such reagents, the crystallization of ice IV from liquid water was very difficult and seemed to be a random event.

In 2001, Salzmann and his coworkers reported a whole new method to prepare ice IV reproducibly; when high-density amorphous ice (HDA) is heated at a rate of 0.4 K/min and a pressure of 0.81 GPa, ice IV is crystallized at about 165 K. What governs the crystallization products is the heating rate; fast heating (over 10 K/min) results in the formation of single-phase ice XII.

Crystal structure

The crystal structure of ice IV was elucidated by Engelhardt and Kamb in 1981 by low-temperature single-crystal X-ray diffraction. Its structure is described by a rhombohedral unit cell with a space group of R-3c. The hydrogen geometry had been suggested to be completely disordered as IR and Raman spectra consist only of broad peaks, and the disordered nature was confirmed by neutron powder diffraction studies by Lobban (1998) and Klotz et al. (2003). In addition, the entropy difference between ice VI (disordered phase) and ice IV is very small, according to Bridgman's measurement.

Engelhardt–Kamb Collapse (EKC)

Engelhardt and Kamb mentioned in the paper in 1981 that the structure of ice IV could be derived from the structure of ice Ic by cutting and forming some hydrogen bondings and adding subtle structural distortions. Shephard et al. compressed the ambient phase of NH₄F, an isostructural material of ice, to obtain NH₄F II, whose hydrogen-bonded network is similar to ice IV. As the compression of ice Ih results in the formation of high-density amorphous ice (HDA), not ice IV, they claimed that the compression-induced conversion of ice I into ice IV is important, naming it "Engelhardt–Kamb collapse" (EKC). They suggested that the reason why we cannot obtain ice IV directly from ice Ih is that ice Ih is hydrogen-disordered; if oxygen atoms are arranged in the ice IV structure, hydrogen bonding may not be formed due to the donor-acceptor mismatch.

Quest for hydrogen ordering

As discussed above, ice IV is a hydrogen-disordered phase. Its ordered counterpart, however, has never been reported yet. Salzmann et al. (2011) reported the DSC thermograms of HCl-doped ice IV finding an endothermic feature at about 120 K. Ten years later, Rosu-Finsen and Salzmann (2021) reported more detailed DSC data where the endothermic feature becomes larger as the sample is quench-recovered at higher pressure. They proposed three scenarios to explain the experimental results: weak hydrogen-ordering, orientational glass transition, and mechanical distortions.

Ice V

This article is about the form of water ice. For the high-speed train, see ICE V. For internal combustion engine vehicle, see ICEV. For the King Gizzard & the Lizard Wizard song, see Ice V (song).

"Ice 5" redirects here. For the ice hockey series, see Freeway Face-Off.

Ice V, pronounced "ice five", is a monoclinic crystalline phase of water, formed by cooling water to 253 K at 500 MPa. It has a density of 1.24 g cm³ (at 350 MPa).

Ice V has a complicated structure, including 4-membered, 5-membered, 6-membered, and 8-membered rings and a total of 28 molecules in the unit cell. Ganymede's interior probably includes a liquid water ocean with tens to hundreds of kilometers of ice V at its base.

Ice VI

Ice VI is a form of ice that exists at high pressure at the order of about 1 GPa (= 10 000 bar) and temperatures ranging from 130 up to 355 Kelvin (−143 °C up to 82 °C); see also the phase diagram of water. Its discovery and the discovery of other high-pressure forms of water were published by P.W. Bridgman in January 1912.

It is part of one of the inner layers of Titan.

Properties

Ice VI has a density of 1.31 g/cm³ and a tetragonal crystal system with the space group P4₂/nmc; its unit cell contains 10 water molecules and has the dimensions a=6.27 Å and c=5.79 Å. The triple point of ice VI with ice VII and liquid water is at about 82 °C and 2.22 GPa and its triple point with ice V and liquid water is at 0.16 °C and 0.6324 GPa = 6324 bar.

Ice VI undergoes phase transitions into ices XV and XIX upon cooling depending on pressure as hydrochloric acid is doped.

Ice VII

The crystal structure of Ice VII. The red atoms are oxygen while the pink atoms are hydrogen. Image generated using CrystalMaker®.

Ice VII is a cubic crystalline form of ice. It can be formed from liquid water above 3 GPa (30,000 atmospheres) by lowering its temperature to room temperature, or by decompressing heavy water (D₂O) ice VI below 95 K. (Different types of ice, from ice II to ice XVIII, have been created in the laboratory at different temperatures and pressures. Ordinary water ice is known as ice I_h in the Bridgman nomenclature.) Ice VII is metastable over a wide range of temperatures and pressures and transforms into low-density amorphous ice (LDA) above 120 K (−153 °C). Ice VII has a triple point with liquid water and ice VI at 355 K and 2.216 GPa, with the melt line extending to at least 715 K (442 °C) and 10 GPa. Ice VII can be formed within nanoseconds by rapid compression via shock-waves. It can also be created by increasing the pressure on ice VI at ambient temperature. At around 5 GPa, Ice VII becomes the tetragonal Ice VII_t.

Like the majority of ice phases (including ice I_h), the hydrogen atom positions are disordered. In addition, the oxygen atoms are disordered over multiple sites. The structure of ice VII comprises a hydrogen bond framework in the form of two interpenetrating (but non-bonded) sublattices. Hydrogen bonds pass through the center of the water hexamers and thus do not connect the two lattices. Ice VII has a density of about 1.65 g cm⁻³ (at 2.5 GPa and 25 °C (77 °F; 298 K)), which is less than twice the cubic ice density as the intra-network O–O distances are 8% longer (at 0.1 MPa) to allow for interpenetration. The cubic unit cell has a side length of 3.3501 Å (for D₂O, at 2.6 GPa and 22 °C (72 °F; 295 K)) and contains two water molecules.

Ice VII is the only disordered phase of ice that can be ordered by simple cooling, and it forms (ordered) ice VIII below 273 K up to ~8 GPa. Above this pressure, the VII–VIII transition temperature drops rapidly, reaching 0 K at ~60 GPa. Thus, ice VII has the largest stability field of all of the molecular phases of ice. The cubic oxygen sub-lattices that form the backbone of the ice VII structure persist to pressures of at least 128 GPa; this pressure is substantially higher than that at which water loses its molecular character entirely, forming ice X. In high pressure ices, protonic diffusion (movement of protons around the oxygen lattice) dominates molecular diffusion, an effect which has been measured directly.

Natural occurrence

Scientists hypothesize that ice VII may comprise the ocean floor of Europa as well as extrasolar planets (such as Awohali, and Enaiposha) that are largely made of water.

In 2018, ice VII was identified among inclusions found in natural diamonds. Due to this demonstration that ice VII exists in nature, the International Mineralogical Association duly classified ice VII as a distinct mineral. The ice VII was presumably formed when water trapped inside the diamonds retained the high pressure of the deep mantle due to the strength and rigidity of the diamond lattice, but cooled down to surface temperatures, producing the required environment of high pressure without high temperature.

Ice VIII

The crystal structure of ice VIII

Ice VIII is a tetragonal crystalline form of ice formed from ice VII by cooling it below 5 °C. It is more ordered than ice VII, since the hydrogen atoms assume fixed positions.

This article is about a real form of solid water. For the fictional material called Ice-nine that appears in the Kurt Vonnegut novel, see Ice-nine.

For other uses, see Ice-nine (disambiguation).

Ice IX

Ice IX is a form of solid water stable at temperatures below 140 K or –133.15 C and pressures between 200 and 400 MPa. It has a tetragonal crystal lattice and a density of 1.16 g/cm³, 26% higher than ordinary ice. It is formed by cooling ice III from 208 K to 165 K (rapidly—to avoid forming ice II). Its structure is identical to ice III other than being completely proton-ordered.

Ice X

Ice X, within physical chemistry, is a cubic crystalline form of ice formed in the same manner as ice VII, but at pressures as high as about 70 GPa. It has symmetrized hydrogen bonds, where a hydrogen atom is found at the center of two oxygen atoms.

Ice XI

Crystal structure of Ice XI viewed along the c-axis

Ice XI is the hydrogen-ordered form of the ordinary form of ice. The total internal energy of ice XI is about one sixth lower than ice I_h, so in principle it should naturally form when ice I_h is cooled to below 72 K. The low temperature required to achieve this transition is correlated with the relatively low energy difference between the two structures. Water molecules in ice I_h are surrounded by four semi-randomly directed hydrogen bonds. Such arrangements should change to the more ordered arrangement of hydrogen bonds found in ice XI at low temperatures, so long as localized proton hopping is sufficiently enabled; a process that becomes easier with increasing pressure. Correspondingly, ice XI is believed to have a triple point with hexagonal ice and gaseous water at (~72 K, ~0 Pa).

Properties

Crystal structure of ice XI (c-axis in the vertical direction)

Ice XI has an orthorhombic structure with space group Cmc2₁ containing eight molecules per unit cell. Its lattice parameters are a=4.465(3) Å, b=7.859(4) Å, and c=7.292(2) Å at 5 K. There are actually 16 crystallographically inequivalent hydrogen-ordered configurations of ice with an orthorhombic structure of eight atoms per unit cell, but electronic structure calculations show Cmc2₁ to be the most stable. Another possible configuration, with space group Pna2₁ is also of interest, as it is an antiferroelectric crystal, which Davidson and Morokuma incorrectly suggested as the most stable structure in 1984.

In practice, ice XI is most easily prepared from a dilute (10 mM) KOH solution kept just below 72 K for about a week (for D₂O a temperature just below 76 K will suffice). The hydroxide ions create defects in the hexagonal ice, allowing protons to jump more freely between the oxygen atoms (and so this structure of ice XI breaks the 'ice rules'). More specifically, each hydroxide ion creates a Bjerrum L defect and an ionized vertex. Both the defect and the ion can move throughout the lattice and 'assist' with proton reordering. The positive K⁺ ion may also play a role because it is found that KOH works better than other alkali hydroxides. The exact details of these ordering mechanisms are still poorly understood and under question because experimentally the mobility of the hydroxide and K⁺ ions appear to be very low around 72 K. The current belief is that KOH acts only to assist with the hydrogen reordering and is not required for the lower-energy stability of ice XI. However, calculations by Toshiaki Iitaka in 2010 call this into question. Iitaka argues that the KOH ions compensate for the large net electric dipole moment of the crystal lattice along the c-axis. The aforementioned electronic structure calculations are done assuming an infinite lattice and ignore the effects of macroscopic electric fields created by surface charges. Because such fields are present in any finite size crystal, in non-doped ice XI, domains of alternating dipole moment should form as in conventional ferroelectrics. It has also been suggested that the ice I_h => ice XI transition is enabled by the tunneling of protons.

Although ice XI is thought to be a more stable conformation than ice I_h, the transformation is very slow. According to one report, in Antarctic conditions it is estimated to take at least 100,000 years to form without the assistance of catalysts. Ice XI was sought and found in Antarctic ice that was about 100 years old in 1998. A further study in 2004 was not able to reproduce this finding, however, after studying Antarctic ice which was around 3000 years old. The 1998 Antarctic study also claimed that the transformation temperature (ice XI => ice I_h) is −36 °C (237 K), which is far higher than the temperature of the expected triple point mentioned above (72 K, ~0 Pa). Ice XI was also found in experiments using pure water at very low temperature (~10 K) and low pressure – conditions thought to be present in the upper atmosphere. Recently, small domains of ice XI were found to form in pure water; its phase transition back to ice I_h occurred at 72 K while under hydrostatic pressure conditions of up to 70 MPa.

Ice I_h that has been transformed to ice XI and then back to ice I_h, on raising the temperature, retains some hydrogen-ordered domains and more easily transforms back to ice XI again. A neutron powder diffraction study found that small hydrogen-ordered domains can exist up to 111 K.

There are distinct differences in the Raman spectra between ices I_h and XI, with ice XI showing much stronger peaks in the translational (~230 cm⁻¹), librational (~630 cm⁻¹) and in-phase asymmetric stretch (~3200 cm⁻¹) regions.

Ice I_c also has a proton-ordered form. The total internal energy of ice XIc was predicted as similar as ice XIh

History

Hints of hydrogen-ordering in ice had been observed as early as 1964, when Dengel et al. attributed a peak in thermo-stimulated depolarization (TSD) current to the existence of a proton-ordered ferroelectric phase. However, they could not conclusively prove that a phase transition had taken place, and Onsager pointed out that the peak could also arise from the movement of defects and lattice imperfections. Onsager suggested that experimentalists look for a dramatic change in heat capacity by performing a careful calorimetric experiment. A phase transition to ice XI was first identified experimentally in 1972 by Shuji Kawada and others.

Ferroelectric properties

Ice XI is ferroelectric, meaning that it has an intrinsic polarization. To qualify as a ferroelectric it must also exhibit polarization switching under an electric field, which has not been conclusively demonstrated but which is implicitly assumed to be possible. Cubic ice also has a ferrolectric phase and in this case the ferroelectric properties of the ice have been experimentally demonstrated on monolayer thin films. In a similar experiment, ferroelectric layers of hexagonal ice were grown on a platinum (111) surface. The material had a polarization that had a decay length of 30 monolayers suggesting that thin layers of ice XI can be grown on substrates at low temperature without the use of dopants. One-dimensional nano-confined ferroelectric ice XI was created in 2010.

Astrophysical implications

As was mentioned, ice XI can theoretically form at low pressures at temperatures between 50–70 K – temperatures present in astrophysical environments of the outer solar system and within permanently shaded polar craters on the Moon and Mercury. Ice XI forms most easily around 70 K – paradoxically, it takes longer to form at lower temperatures. Extrapolating from experimental measurements, it is estimated to take ~50 years to form at 70 K and ~300 million years at 50 K. It is theorized to be present in places like the upper atmospheres of Uranus and Neptune and on Pluto and Charon.

Small domains of ice XI could exist in the atmospheres of Jupiter and Saturn as well. The fact that small domains of ice XI can exist at temperatures up to 111 K has some scientists speculating that it may be fairly common in interstellar space, with small 'nucleation seeds' spreading through space and converting regular ice, much like the fabled ice-nine mentioned in Vonnegut's Cat's Cradle. The possible roles of ice XI in interstellar space and planet formation have been the subject of several research papers. Until observational confirmation of ice XI in outer space is made, the presence of ice XI in space remains controversial owing to the aforementioned criticism raised by Iitaka. The infrared absorption spectra of ice XI was studied in 2009 in preparation for searches for ice XI in space.

Ice XII

The crystal structure of ice XII

Ice XII is a metastable, dense, crystalline phase of solid water, a type of ice. Ice XII was first reported in 1996 by C. Lobban, J.L. Finney and W.F. Kuhs and, after initial caution, was properly identified in 1998.

It was first obtained by cooling liquid water to 260 K (−13 °C; 8 °F) at a pressure of 0.55 gigapascals (5,400 atm). Ice XII was discovered existing within the phase stability region of ice V. Later research showed that ice XII could be created outside that range. Pure ice XII can be created from ice I_h at 77 K (−196.2 °C; −321.1 °F) by rapid compression (0.81-1.00 GPa/min) or by warming high density amorphous ice at pressures between 0.8 to 1.6 gigapascals (7,900 to 15,800 atm).

While it is similar in density (1.29 g/cm³ at 127 K (−146 °C; −231 °F)) to ice IV (also found in the ice V space) it exists as a tetragonal crystal. Topologically it is a mix of seven- and eight-membered rings, a 4-connected net (4-coordinate sphere packing)—the densest possible arrangement without hydrogen bond interpenetration.

Ice XIV

When hydrochloric-acid-doped ice XII is cooled down to about 110 K, it undergoes a phase transition into a partially hydrogen-ordered phase, namely ice XIV. The transition entropy from ice XIV to ice XII is estimated to be 60% of Pauling entropy based on DSC measurements. The formation of ice XIV from ice XII is more favoured at high pressure.

Ice XV

Ice XV is a crystalline form of ice, a partially proton-ordered form of ice VI. It is created by cooling hydrochloric-acid-doped ice VI to around 130 K at 1 GPa (9820 atm).

Predictions and the experimental discovery

Although the parent phase ice VI was discovered in 1935, corresponding proton-ordered forms (ice XV) had not been observed until 2009. Theoretically, the proton ordering in ice VI was predicted several times; for example, density functional theory calculations predicted the phase transition temperature is 108 K and the most stable ordered structure is antiferroelectric in the space group Cc, while an antiferroelectric P2₁2₁2₁ structure were found 4 K per water molecule higher in energy.

On 14 June 2009, Christoph Salzmann and colleagues at the University of Oxford reported having experimentally reported an ordered phase of ice VI, named ice XV, and say that its properties differ significantly from those predicted. In particular, ice XV is antiferroelectric rather than ferroelectric as had been predicted.

Phase transition mechanism and crystal structure

In detail, ice XV has a smaller density (larger unit-cell volume) than ice VI. This makes the VI-to-XV disorder-to-order transition much favoured at low pressures. Indeed, differential scanning calorimetry by Shephard and Salzmann revealed that reheating quench-recovered HCl-doped ice XV at ambient pressure even produces exotherms originating from transient ordering, i.e. more ordered ice XV is obtained at ambient pressure. Being consistent with this, the ice VI-XV transition is reversible at ambient pressure. It was also shown that HCl-doping is selectively effective in producing ice XV while other acids and bases (HF, LiOH, HClO₄, HBr) do not significantly enhance ice XV formations.

Based on powder neutron diffraction, the crystal structure of ice XV has been investigated in detail. Komatsu et al. suggested that, in combination with density functional theory calculations, none of the possible perfectly ordered orientational configurations are energetically favoured, suggesting that there are several energetically close configurations that coexist in ice XV. They proposed 'the orthorhombic Pmmn space group as a plausible space group to describe the time-space averaged structure of ice XV. Salzmann et al. argued that P-1 model is still the best (with the second best candidate of P2₁), whereas Rietveld refinement using the Pmmn space group only works well for poorly ordered samples. The lattice parameters, in particular b and c, are good indicators of the ice XV formation. Combining density functional theory calculations, they successfully constructed fully ordered model in P-1 and showed that experimental diffraction data should be analysed using space groups that permit full hydrogen order while the Pmmn model only accepts partially ordered structures.

Ice XVI

Ice XVI. White edges mark the unit cell (~17 Å).

Ice XVI is the least dense (0.81 g/cm³) experimentally obtained crystalline form of ice. It is topologically equivalent to the empty structure of sII clathrate hydrates. It was first obtained in 2014 by removing gas molecules from a neon clathrate under vacuum at temperatures below 147 K. The resulting empty water frame, ice XVI, is thermodynamically unstable at the experimental conditions, yet it can be preserved at cryogenic temperatures. Above 145–147 K at positive pressures ice XVI transforms into the stacking-faulty ice I_c and further into ordinary ice I_h. Theoretical studies predict ice XVI to be thermodynamically stable at negative pressures (that is under tension).

Water phase diagram extended to negative pressures calculated with TIP4P/2005 model.

Ice XVII

Crystal structure of ice XVII

Ice XVII is a metastable form of ice with a hexagonal structure and helical channels that was discovered in 2016. It can be formed by freezing water with hydrogen molecules at high pressure to form a filled ice, and then removing the hydrogen molecules from the structure. The form has potential for being used in hydrogen storage. Ice XVII made from heavy water can also be reduced to pure cubic ice.

Discovery

In 2016, the discovery of a new form of ice was announced. Characterized as a "porous water ice metastable at atmospheric temperatures", this new form was discovered by taking a filled ice and removing the non-water components, leaving the crystal structure behind, similar to how ice XVI, another porous form of ice, was synthesized from a clathrate hydrate.

To create ice XVII, the researchers first produced filled ice in a stable phase named C₀ from a mixture of hydrogen (H₂) and water (H₂O), using temperatures from 100 to 270 K (−173 to −3 °C; −280 to 26 °F) and pressures from 360 to 700 MPa (52,000 to 102,000 psi; 3,600 to 6,900 atm). The filled ice is then placed in a vacuum, and the temperature gradually increased until the hydrogen frees itself from the crystal structure. The resulting form is metastable at room pressure while under 120 K (−153 °C; −244 °F), but collapses into ice I_h (ordinary ice) when brought above 130 K (−143 °C; −226 °F). The crystal structure is hexagonal in nature, and the pores are helical channels with a diameter of about 6.10 Å (6.10×10⁻¹⁰ m; 2.40×10⁻⁸ in).

Hydrogen storage

The discovery announcement also mentioned that ice XVII could repeatedly adsorb and release hydrogen molecules without degrading its structure. The total amount of hydrogen that ice XVII can adsorb depends on the amount of pressure applied, but hydrogen molecules can be adsorbed by ice XVII even at pressures as low as a few millibars if the temperature is under 40 K (−233.2 °C; −387.7 °F). The adsorbed hydrogen molecules can then be released, or desorbed, through the application of heat. This was an unexpected property of ice XVII, and could allow it to be used for hydrogen storage, an issue often mentioned in environmental technology.

Aside from storing hydrogen via compression or liquification, it can also be stored within a solid substance, either via a reversible chemical process (chemisorption) or by having the hydrogen molecules attach to the substance via the van der Waals force (physisorption). The storage method used by ice XVII falls in the latter category, physisorption. In physisorption, there is no chemical reaction, and the chemical bond between the two atoms within a hydrogen molecule remains intact. Because of this, the number of adsorption–desorption cycles ice XVII can withstand is "theoretically infinite".

One significant advantage of using ice XVII as a hydrogen storage medium is the low cost of the only two chemicals involved: hydrogen and water. In addition, ice XVII has shown the ability to store hydrogen at an H₂ to H₂O molar ratio above 40%, higher than the theoretical maximum ratio for sII clathrate hydrates, another potential storage medium. However, if ice XVII is used as a storage medium, it must be kept under a temperature of 130 K (−143 °C; −226 °F) or risk being destabilized.

Cubic ice

It was reported in 2020 that cubic ice based on heavy water (D₂O) can be formed from ice XVII. This was done by heating specially prepared D₂O ice XVII powder. The result was free of structural deformities compared to standard cubic ice, or ice I_sd. This discovery was reported around the same time another research group announced that they were able to obtain pure D₂O cubic ice by first synthesizing filled ice in the C₂ phase, and then decompressing it.

In the absence of an applied electric field, H⁺ ions diffuse in the O²⁻ lattice.

When an electric field is applied, H⁺ ions migrate towards the anode.

A remarkable characteristic of superionic ice is its ability to act as a conductor.

Ice XVIII (superionic water)

Superionic water, also called superionic ice or ice XVIII, is a phase of water that exists at extremely high temperatures and pressures. In superionic water, water molecules break apart and the oxygen ions crystallize into an evenly spaced lattice while the hydrogen ions float around freely within the oxygen lattice. The freely mobile hydrogen ions make superionic water almost as conductive as typical metals, making it a superionic conductor. It is one of the 19 known crystalline phases of ice. Superionic water is distinct from ionic water, which is a hypothetical liquid state characterized by a disordered soup of hydrogen and oxygen ions.

While theorized for decades, it was not until the 1990s that the first experimental evidence emerged for superionic water. Initial evidence came from optical measurements of laser-heated water in a diamond anvil cell, and from optical measurements of water shocked by extremely powerful lasers. The first definitive evidence for the crystal structure of the oxygen lattice in superionic water came from x-ray measurements on laser-shocked water which were reported in 2019.

If it were present on the surface of the Earth, superionic ice would rapidly decompress. In May 2019, scientists at the Lawrence Livermore National Laboratory (LLNL) were able to synthesize superionic ice, confirming it to be almost four times as dense as normal ice and black in color.

Superionic water is theorized to be present in the mantles of giant planets such as Uranus and Neptune.

Properties

As of 2013, it is theorized that superionic ice can possess two crystalline structures. At pressures in excess of 50 GPa (7,300,000 psi) it is predicted that superionic ice would take on a body-centered cubic structure. However, at pressures in excess of 100 GPa, and temperatures above 2000 K, it is predicted that the structure would shift to a more stable face-centered cubic lattice. The ice appears black in color.

History of theoretical and experimental evidence

Demontis et al. made the first prediction for superionic water using classical molecular dynamics simulations in 1988. In 1999, Cavazzoni et al. predicted that such a state would exist for ammonia and water in conditions such as those existing on Uranus and Neptune. In 2005 Laurence Fried led a team at Lawrence Livermore National Laboratory to recreate the formative conditions of superionic water. Using a technique involving smashing water molecules between diamonds and super heating it with lasers they observed frequency shifts which indicated that a phase transition had taken place. The team also created computer models which indicated that they had indeed created superionic water. In 2013 Hugh F. Wilson, Michael L. Wong, and Burkhard Militzer at the University of California, Berkeley published a paper predicting the face-centered cubic lattice structure that would emerge at higher pressures.

Additional experimental evidence was found by Marius Millot and colleagues in 2018 by inducing high pressure on water between diamonds and then shocking the water using a laser pulse.

2018–2019 experiments

In 2018, researchers at LLNL squeezed water between two pieces of diamond with a pressure of 2,500 MPa (360,000 psi). The water was squeezed into type VII ice, which is 60 percent denser than normal water.

The compressed ice was then transported to the University of Rochester where it was blasted by a pulse of laser light. The reaction created conditions like those inside of ice giants such as Uranus and Neptune by heating up the ice thousands of degrees under a pressure a million times greater than the Earth's atmosphere in only 10 to 20 billionths of a second. The experiment concluded that the current in the conductive water was indeed carried by ions rather than electrons and thus pointed to the water being superionic. More recent experiments from the same Lawrence Livermore National Laboratory team used x-ray crystallography on laser-shocked water droplets to determine that the oxygen ions enter a face-centered-cubic phase, which was dubbed ice XVIII and reported in the journal Nature in May 2019.

Existence in ice giants

It is theorized that the ice giant planets Uranus and Neptune hold a layer of superionic water. Machine learning and free-energy methods predict close-packed superionic phases to be stable over a wide temperature and pressure range, and a body-centred cubic superionic phase to be kinetically favoured, but stable over a small window of parameters.

On the other hand, there are also studies that suggest that other elements present inside the interiors of these planets, particularly carbon, may prevent the formation of superionic water.

Ice XIX

Ice XIX is a proposed crystalline phase of water. Along with ice XV, it is one of two phases of ice directly related to ice VI. Ice XIX is prepared by cooling HCl-doped ice VI at a pressure above 1.6 GPa down to about 100 K. As of 2022, its crystal structure has not been elucidated.

Discovery

Initial report

The first report regarding ice XIX was published in 2018 by Thomas Loerting's group from Austria. They quenched HCl-doped ice VI to 77 K at different pressures between 1.0 and 1.8 GPa to collect differential scanning calorimetry (DSC) thermograms, dielectric spectrum, Raman spectrum, and X-ray diffraction patterns. In the DSC signals, there was an endothermic feature at about 110 K in addition to the endotherm corresponding to the ice XV-VI transition. Additionally, the Raman spectra, dielectric properties, and the ratio of the lattice parameters differed from those of ice XV. Based on these observations, they proposed the existence of a second hydrogen-ordered phase of ice VI, naming it ice beta-XV.

Alternative explanation

In 2019, Alexander Rosu-Finsen and Christoph Salzman argued that there was no need to consider this to be a new phase of ice, and proposed a "deep-glassy" state scenario. According to their DSC data, the size of the endothermic feature depends not only on quench-recovery pressure but also on the heating rate and annealing duration at 93 K. They also collected neutron diffraction profiles of quench-recovered deuterium chloride-doped, D₂O ice VI/XV prepared at different pressures of 1.0, 1.4 and 1.8 GPa, to show that there were no significant differences among them. They concluded that the low-temperature endotherm originated from kinetic features related to glass transitions of deep glassy states of disordered ice VI.

Further exploration

Distinguishing between the two scenarios (new hydrogen-ordered phase vs. deep-glassy disordered ice VI) became an open question and the debate between the two groups has continued. Thoeny et al. (Loerting's group) collected another series of Raman spectra of ice beta-XV, and reported that (i) ice XV prepared by the protocol reported previously contains both ice XV and ice beta-XV domains; (ii) upon heating, Raman spectra of ice beta-XV showed loss of H-order.

In contrast, Salzmann's group again argued for the plausibility of a 'deep-glassy state' scenario based on neutron diffraction and neutron inelastic scattering experiments. Based on their experimental results, ice VI and deep-glassy ice VI share very similar features based on both elastic (diffraction) scattering and inelastic scattering experiments, and are different from the properties of ice XV.

In 2021, further crystallographic evidence for a new phase (ice XIX) was individually reported by three groups: Yamane et al. (Hiroyuki Kagi and Kazuki Komatsu's group from Japan), Gasser et al. (Loerting's group), and Salzmann's group. Yamane et al. collected neutron diffraction profiles in situ (i.e. under high pressure) and found new Bragg features completely different from both ice VI and ice XV. They performed Rietveld refinement of the profiles based on the ${\sqrt {2}}\times {\sqrt {2}}\times 1$ supercell of ice XV and proposed some leading candidates for the space group of ice XIX: P-4, Pca21, Pcc2, P21/a, and P21/c. They also measured dielectric spectra in situ and determined phase boundaries of ices VI/XV/XIX. They found that the sign of the slope of the boundary turns negative from positive at 1.6 GPa indicating the existence of two different phases by the Clausius–Clapeyron relation.

Gasser et al. also collected powder neutron diffractograms of quench-recovered ices VI, XV, and XIX and found similar crystallographic features to those reported by Yamane et al., concluding that P-4 and Pcc2 are the plausible space group candidates. Both Yamane et al.'s and Gasser et al.'s results suggested a partially hydrogen-ordered structure. Gasser et al. also found an isotope effect using DSC; the low-temperature endotherm for DCl-doped D₂O ice XIX was significantly smaller than that of HCl-doped H₂O ice XIX, and that doping of 0.5% of H₂O into D₂O is sufficient for the ordering transition.

Several months later, Salzmann et al. published a paper based on in-situ powder neutron diffraction experiments of ice XIX. In a change from their previous reports, they accepted the idea of the new phase (ice XIX) as they observed similar features to the previous two reports. However, they refined their diffraction profiles based on a disordered structural model (Pbcn) and argued that new Bragg reflections can be explained by distortions of ice VI, so ice XIX may still be regarded as a deep-glassy state of ice VI.

The crystal structure of ice XIX including hydrogen order/disorder is still under debate as of 2022.

Further reading

• Ice phases (www.idc-online.com)
• Fletcher, N. H. (2009-06-04). The Chemical Physics of Ice. ISBN 9780521112307.
• Petrenko, Victor F.; Whitworth, Robert W. (1999-08-19). Physics of Ice. ISBN 9780191581342.
• Chaplin, Martin (2007-11-11). "Hexagonal ice structure". Water Structure and Science. Retrieved 2008-01-02.
• London South Bank University Report
• Physik des Eises (PDF in German, iktp.tu-dresden.de)

External links

• Hunsberger, Maren (September 21, 2018). "A New State of Water Reveals a Hidden Ocean in Earth's Mantle". Seeker. Archived from the original on 2021-12-21 – via YouTube.
• Woo, Marcus (July 11, 2018). "The Hunt for Earth's Deep Hidden Oceans". Quanta Magazine.