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Liquid helium
View on WikipediaLiquid helium in a transparent bowl, cooled below the Lambda point, where it exhibits properties of superfluidity
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| Properties | |
|---|---|
| He | |
| Molar mass | 4.002602 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Liquid helium is a physical state of helium at very low temperatures at standard atmospheric pressures. Liquid helium may show superfluidity.
At standard pressure, the chemical element helium exists in a liquid form only at the extremely low temperature of −269 °C (−452.20 °F; 4.15 K). Its boiling point and critical point depend on the isotope of helium present: the common isotope helium-4 or the rare isotope helium-3. These are the only two stable isotopes of helium. See the table below for the values of these physical quantities. The density of liquid helium-4 at its boiling point and a pressure of one atmosphere (101.3 kilopascals) is about 125 g/L (0.125 g/ml), or about one-eighth the density of liquid water.[1]
Liquefaction
[edit]Helium was first liquefied on July 10, 1908, by the Dutch physicist Heike Kamerlingh Onnes at the University of Leiden in the Netherlands.[2] At that time, helium-3 was unknown because the mass spectrometer had not yet been invented. In more recent decades, liquid helium has been used as a cryogenic refrigerant (which is used in cryocoolers), and liquid helium is produced commercially for use in superconducting magnets such as those used in magnetic resonance imaging (MRI), nuclear magnetic resonance (NMR), magnetoencephalography (MEG), and experiments in physics, such as low temperature Mössbauer spectroscopy. The Large Hadron Collider contains superconducting magnets that are cooled with 120 tonnes of liquid helium.[3]
Liquified helium-3
[edit]A helium-3 atom is a fermion and at very low temperatures, they form two-atom Cooper pairs which are bosonic and condense into a superfluid. These Cooper pairs are substantially larger than the interatomic separation.
Characteristics
[edit]

The temperature required to produce liquid helium is low because of the weakness of the attractions between the helium atoms. These interatomic forces in helium are weak to begin with because helium is a noble gas, but the interatomic attractions are reduced even more by the effects of quantum mechanics. These are significant in helium because of its low atomic mass of about four daltons. The zero-point energy of liquid helium is less if its atoms are less confined by their neighbors. Hence in liquid helium, its ground state energy can decrease by a naturally occurring increase in its average interatomic distance. However at greater distances, the effects of the interatomic forces in helium are even weaker.[4]
Because of the very weak interatomic forces in helium, the element remains a liquid at atmospheric pressure all the way from its liquefaction point down to absolute zero. At temperatures below their liquefaction points, both helium-4 and helium-3 undergo transitions to superfluids. (See the table below.)[4] Liquid helium can be solidified only under very low temperatures and high pressures.[5]
Liquid helium-4 and the rare helium-3 are not completely miscible.[6] Below 0.9 kelvin at their saturated vapor pressure, a mixture of the two isotopes undergoes a phase separation into a normal fluid (mostly helium-3) that floats on a denser superfluid consisting mostly of helium-4.[7] This phase separation happens because the overall mass of liquid helium can reduce its thermodynamic enthalpy by separating.
At extremely low temperatures, the superfluid phase, rich in helium-4, can contain up to 6% helium-3 in solution. This makes the small-scale use of the dilution refrigerator possible, which is capable of reaching temperatures of a few millikelvins.[6][8]
Superfluid helium-4 has substantially different properties from ordinary liquid helium.
History
[edit]In 1908, Kamerlingh-Onnes succeeded in liquifying a small quantity of helium. In 1923, he provided advice to the Canadian physicist John Cunningham McLennan, who was the first to produce quantities of liquid helium almost on demand.[9]
Important early work on the characteristics of liquid helium was done by the Soviet physicist Lev Landau, later extended by the American physicist Richard Feynman.
In 1961, Vignos and Fairbank reported the existence of a different phase of solid helium-4, designated the gamma-phase. It exists for a narrow range of pressure between 1.45 and 1.78 K.[10]
Data
[edit]| Properties of liquid helium | Helium-4 | Helium-3 |
|---|---|---|
| Critical temperature[4] | 5.2 K (−267.95 °C) | 3.3 K (−269.85 °C) |
| Boiling point at one atmosphere[4] | 4.2 K (−268.95 °C) | 3.2 K (−269.95 °C) |
| Minimum melting pressure[11] | 25 bar (360 psi) | 29 bar (420 psi) at 0.3 K (−272.850 °C) |
| Superfluid transition temperature at saturated vapor pressure | 2.17 K (−270.98 °C)[12] | 1 mK in the absence of a magnetic field[13] |
Gallery
[edit]-
Liquid helium (in a vacuum bottle) at 4.2 K (−268.95 °C) and 1 bar (15 psi) boiling slowly.
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Lambda point transition: as the liquid is cooled down through 2.17 K (−270.98 °C), the boiling suddenly becomes violent for a moment.
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Superfluid phase at temperature below 2.17 K (−270.98 °C). In this state, the thermal conductivity is extremely high. This causes heat in the body of the liquid to be transferred to its surface so quickly that vaporization takes place only at the free surface of the liquid. Thus, there are no gas bubbles in the body of the liquid.
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The liquid helium is in the superfluid phase. A thin invisible film creeps up the inside wall of the bowl and down on the outside. A drop forms. It will fall off into the liquid helium below. This will repeat until the cup is empty—provided the liquid remains superfluid.
See also
[edit]References
[edit]- ^ "The Observed Properties of Liquid Helium at the Saturated Vapor Pressure". University of Oregon. 2004.
- ^ Wilks (1967), p. 7.
- ^ "Cryogenics: Low temperatures, high performance". CERN. 28 June 2023.
- ^ a b c d Wilks (1967), p. 1.
- ^ Horbaniuc, Bogdan D. (2004). "Refrigeration and Air-Conditioning". Encyclopedia of Energy: 261–289. doi:10.1016/B0-12-176480-X/00085-1. ISBN 9780121764807.
- ^ a b D. O. Edwards; D. F. Brewer; P. Seligman; M. Skertic & M. Yaqub (1965). "Solubility of He3 in Liquid He4 at 0K". Phys. Rev. Lett. 15 (20): 773. Bibcode:1965PhRvL..15..773E. doi:10.1103/PhysRevLett.15.773.
- ^ Pricaupenko, L; Triener, J. (16 January 1995). "Phase Separation of Liquid 3He–4He Mixtures: Effect of Confinement". Physical Review Letters. 74 (3): 430–433. Bibcode:1995PhRvL..74..430P. doi:10.1103/PhysRevLett.74.430. PMID 10058756.
- ^ Wilks (1967), p. 244.
- ^ "THE LIFE OF SIR JOHN CUNNINGHAM McLENNAN Ph.D, F.R.S.C, F.R.S., O.B.E., K.B.E. (1867 - 1935)". University of Toronto Physics. Archived from the original on 2006-05-05.
- ^ Vignos, James H.; Fairbank, Henry A. (1961-03-15). "New Solid Phase in H4". Physical Review Letters. 6 (6): 265–267. Bibcode:1961PhRvL...6..265V. doi:10.1103/PhysRevLett.6.265.
- ^ Wilks (1967), pp. 474–478.
- ^ Wilks (1967), p. 289.
- ^ Dieter Vollhart & Peter Wölfle (1990). The Superfluid Phases of Helium 3. Taylor and Francis. p. 3.
- General
- VanSciver, Steven W. (2012). Helium cryogenics. International cryogenics monograph series (2. ed.). New York, NY: Springer. ISBN 978-1-4419-9978-8.
- Wilks, J. (1967). The Properties of Liquid and Solid Helium. Oxford: Clarendon Press. ISBN 0-19-851245-7.
- Freezing Physics: Heike Kamerlingh Onnes and the Quest for Cold, Van Delft Dirk (2007). Edita - The Publishing House Of The Royal Netherlands Academy of Arts and Sciences. ISBN 978-90-6984-519-7.
External links
[edit]- He-3 and He-4 phase diagrams, etc.
- Helium-3 phase diagram, etc.
- Onnes's liquifaction of helium
- Kamerlingh Onnes's 1908 article, online and analyzed on BibNum Archived 2018-02-18 at the Wayback Machine [for English analysis, click 'à télécharger']
- CERN's cryogenic systems.
Liquid helium
View on GrokipediaFundamental Properties
Phase Behavior and Diagram
Liquid helium-4 exhibits a distinctive phase diagram characterized by the absence of a solid-liquid-gas triple point, a feature unique among quantum fluids due to helium's weak interatomic forces and significant zero-point energy. At atmospheric pressure, helium-4 does not solidify even at absolute zero; instead, it remains in the liquid state down to 0 K under its saturated vapor pressure, with solidification requiring external pressures exceeding approximately 25 bar. This behavior arises because the zero-point motion of helium atoms dominates, preventing the lattice formation necessary for a solid phase at low pressures. The phase diagram thus features a liquid region extending from the critical point to absolute zero along the vapor pressure curve, without the typical triple point intersection found in classical substances.[9] The liquid-vapor critical point of helium-4 occurs at a temperature of 5.2 K and a pressure of 2.27 atm, marking the end of the liquid-vapor coexistence curve. Below the normal boiling point of 4.2 K at 1 atm, the liquid phase splits into two distinct regions separated by the lambda line: the normal liquid phase, denoted He I, exists above this line, while below it lies the superfluid phase, He II. The lambda transition, a second-order phase change, takes place at 2.17 K under saturated vapor pressure, where He I transforms into He II, accompanied by the onset of superfluid density ρ_s > 0 in the lower phase. The lambda line traces a steep path in the pressure-temperature (P-T) diagram at low pressures with a positive slope of approximately 30 bar/K near the lambda point, extending to higher pressures and lower temperatures up to about 1.8 K and 29 bar before terminating at the tricritical point with the solid phase.[10][11] The phase boundaries in the helium-4 diagram, including the vapor pressure curve and melting curve, follow the Clausius-Clapeyron relation, which describes the slope of first-order transition lines based on the enthalpy change ΔH and volume change ΔV across the boundary. For the lambda transition, as a second-order process with ΔH = 0 and ΔV ≈ 0, the relation adapts through Ehrenfest equations to yield the observed slope via differences in specific heat and thermal expansion: , where is the molar volume. At higher pressures, the solid phases (body-centered cubic and hexagonal close-packed) emerge along the melting curve, which exhibits a minimum pressure of about 25 bar at absolute zero (0 K).[12]Thermodynamic Characteristics
Liquid helium-4 displays distinctive thermodynamic properties influenced by quantum effects, particularly below the lambda transition temperature of approximately 2.17 K at saturated vapor pressure. The specific heat capacity exhibits a pronounced lambda-shaped anomaly at this transition, with a sharp peak in the helium-I phase just above the lambda point, followed by a rapid decrease in the superfluid helium-II phase. This behavior arises from the onset of long-range order in the superfluid state, where excitations such as phonons and rotons contribute less to heat capacity compared to the disordered helium-I phase. Measurements confirm that the specific heat drops by nearly a factor of two immediately below the lambda point, deviating from classical expectations for a simple fluid.[13] In the superfluid helium-II phase, thermal conductivity reaches extraordinarily high values, often exceeding that of high-purity copper by factors of up to at temperatures around 1 K, due to efficient heat transport via counterflow of the normal and superfluid components involving phonons and rotons. This quantum-enhanced conduction allows superfluid helium to maintain near-uniform temperatures over macroscopic distances without significant gradients, contrasting sharply with the relatively low thermal conductivity of helium-I, which is about times poorer than copper. The mechanism relies on the collisionless propagation of excitations in the dilute normal fluid, enabling effective heat transfer rates on the order of watts per square centimeter in confined geometries.[14] Viscosity in superfluid helium-II is described by the two-fluid model, which posits the liquid as a mixture of a viscous normal fluid component with density and a frictionless superfluid component with density , such that the total density . The superfluid component exhibits zero shear viscosity, allowing dissipationless flow, while the normal component carries finite viscosity akin to a classical fluid and is responsible for entropy transport. Above the lambda point, and , recovering normal liquid behavior; below it, increases with decreasing temperature, reaching nearly the full density at millikelvin temperatures. This model, originally formulated by Landau, quantitatively accounts for observed flow and dissipation phenomena in helium-II.[15] For liquid helium-3, which remains normal down to much lower temperatures due to its fermionic nature, the specific heat at very low temperatures (below ~0.1 K) follows a linear dependence , characteristic of a degenerate Fermi liquid, where is the Sommerfeld coefficient enhanced by strong interactions compared to the free Fermi gas value. This linear term dominates over a weaker phonon contribution proportional to , reflecting the excitation of quasiparticles near the Fermi surface.[16]Superfluidity and Quantum Phenomena
Transition to Superfluid State
Liquid helium-4, composed of bosonic atoms with zero spin due to the helium-4 nucleus having zero spin, obeys Bose-Einstein statistics.[17] Below the critical temperature of approximately 2.17 K, known as the lambda point, a macroscopic fraction of these atoms occupies the ground state, forming a Bose-Einstein condensate that underlies the superfluid transition.[17] This condensation arises because, for non-interacting bosons, the occupation of the lowest energy state becomes macroscopic when the thermal de Broglie wavelength exceeds the interparticle spacing, a condition met in liquid helium-4 at low temperatures.[18] Landau developed the two-fluid model to describe the superfluid state, positing that liquid helium-II consists of two interpenetrating components: a normal fluid with density that carries viscosity and entropy, and a superfluid component with density that flows without friction.[15] The normal fluid arises from thermal excitations in the system, specifically phonons at low energies and rotons at higher energies near the minimum of the excitation spectrum, while the superfluid component represents the condensate.[15] The total density is , and the model's derivation relies on the Galilean invariance of the excitation spectrum, ensuring no entropy in the superfluid part.[18] This framework explains the thermodynamic anomalies at the lambda transition, such as the divergence in specific heat.[19] In the Ginzburg-Landau phenomenological theory, the superfluid transition is characterized by an order parameter , a complex scalar field representing the macroscopic wavefunction of the condensate.[19] Near the lambda point, the free energy expansion in powers of and its gradient captures the second-order phase transition, with the coefficient of changing sign at 2.17 K.[19] The phase of determines the superfluid velocity through the relation where is the mass of a helium-4 atom and is the reduced Planck's constant; this expression follows from the hydrodynamic form of the Schrödinger equation for the condensate.[18] The irrotational nature of (except at singularities like vortices) ensures quantized circulation in multiples of , with as Planck's constant.[18]Behaviors in Superfluid Helium-II
Superfluid helium-II exhibits remarkable macroscopic quantum behaviors, including the formation of thin films that enable frictionless flow over surfaces. The Rollin film, a layer approximately 30 nm thick, forms on solid surfaces in contact with helium-II and creeps along them due to zero viscosity, allowing the superfluid to transfer without resistance even against gravity.[20] This creeping motion is observed as the film climbs container walls and flows over edges, with transfer rates reaching up to several centimeters per second near the lambda point, decreasing at lower temperatures.[21] The Rollin film facilitates the thermomechanical effect, commonly known as the fountain effect, where a temperature gradient across a narrow channel causes superfluid helium to flow from the colder to the warmer side, building pressure that can eject helium as a fountain. This counterintuitive flow arises because the chemical potential difference drives the superfluid component, with no entropy carried by the flow, leading to a pressure rise proportional to the temperature difference. Experiments demonstrate this effect in setups with fine capillaries, where heating one reservoir results in helium squirting from the other, highlighting the irreversible nature of heat transport in helium-II. Another key behavior is the quantization of circulation in superfluid flow, where vortices form with discrete circulation values predicted by Onsager and elaborated by Feynman. The circulation κ around a closed path enclosing a vortex core is quantized as κ = n (h / m), where n is an integer, h is Planck's constant, and m is the mass of a helium-4 atom.[22] In rotating helium-II, these quantized vortices arrange into tangles or lattices to mimic solid-body rotation, with vortex density proportional to the rotation rate, enabling the superfluid to achieve angular momentum without classical vorticity.[22] The core radius of these vortices is on the order of angstroms, comparable to interatomic spacing, underscoring the atomic-scale quantum coherence.[22] Superfluid flow remains dissipationless only below a critical velocity, typically around 1 cm/s, beyond which quantized vortices are created, leading to energy dissipation through vortex motion and reconnection.[23] This critical velocity marks the onset of quantum turbulence, where vortex creation at obstacles or boundaries causes a sudden drop in superflow conductivity, with the value depending on geometry and temperature but generally scaling inversely with channel size.[24] In ion-trapping experiments, positive ions accelerate to this threshold before nucleating vortex rings, confirming the mechanism involves quantum tunneling or thermal activation for vortex formation.[25] Superfluidity persists in confined geometries, such as the porous Vycor glass with pore diameters around 4 nm, where helium fills the nanopores and exhibits a shifted superfluid transition.[26] In these restrictions, the superfluid fraction emerges below approximately 1.95 K, lower than the bulk lambda point of 2.17 K, due to dimensional crossover effects, yet the helium maintains coherent flow with reduced but finite superfluid density. Path-integral Monte Carlo simulations reveal that superfluidity localizes in adsorbed layers near pore walls, with the response robust even at high pressures up to 62 bar.[27]Production Methods
Liquefaction Processes for Helium-4
Gaseous helium, primarily extracted from natural gas deposits via cryogenic distillation or pressure swing adsorption processes, is purified to high purity before liquefaction.[3] Liquid helium-4 is produced by cooling gaseous helium through a series of thermodynamic processes that exploit its unique properties, primarily using the Collins cycle, a modified Claude refrigeration cycle developed in the mid-20th century. This cycle involves compressing helium gas to moderate pressures (typically around 15-20 bar), followed by precooling with liquid nitrogen to approximately 80 K, and then employing multiple heat exchangers and expansion stages to progressively lower the temperature to the liquefaction point. The key innovation lies in the use of expansion turbines—either reciprocating pistons or centrifugal turbines—for isentropic expansion, which provides more efficient cooling than purely isenthalpic processes, allowing the system to reach temperatures below 4.2 K from ambient gaseous helium.[28][29] The normal boiling point of helium-4 is 4.222 K at 1 atm, where it condenses into a liquid under saturated vapor pressure conditions. To achieve liquefaction, the Collins cycle incorporates counterflow heat exchangers that transfer heat from the high-pressure incoming stream to the low-pressure returning vapor, maximizing thermal efficiency. The final stage employs a Joule-Thomson (JT) valve for isenthalpic expansion, where the gas cools upon throttling due to the positive JT coefficient for helium below its inversion temperature of approximately 40 K. The JT coefficient is defined as , which quantifies the temperature change with pressure at constant enthalpy and enables the necessary cooling for phase transition when pre-cooled sufficiently.[30] Achieving the superfluid transition at the lambda point (2.17 K at saturated vapor pressure) requires additional cooling beyond simple liquefaction, typically via evaporative pumping under reduced pressure, which lowers the boiling point by decreasing the vapor pressure over the liquid. While dilution refrigeration using helium-3 mixtures can extend cooling further, for pure helium-4, evaporation suffices to cross the lambda line. This process demands precise control to avoid excessive boil-off and maintain system integrity. Liquefaction efficiency is inherently limited by the low critical temperature of helium-4 (5.2 K), resulting in a small Carnot coefficient of performance (COP) of about 0.014 for cooling from 300 K to 4.2 K, calculated as . Actual systems achieve a figure of merit (FOM) of 0.25–0.32 relative to Carnot, translating to a specific liquefaction work of approximately 200 kJ/mol, far exceeding the thermodynamic ideal of around 27 kJ/mol due to irreversibilities in compression, heat transfer, and expansion. These metrics highlight the energy-intensive nature of helium-4 production, with modern Collins-based plants requiring roughly 2–5 kW of electrical input per liter of liquid produced per hour.[29][31]Handling Liquid Helium-3
Liquid helium-3 (³He) consists of fermionic atoms with nuclear spin 1/2, subjecting it to Fermi-Dirac statistics that inhibit Bose-Einstein condensation and thus prevent superfluidity through bosonic mechanisms observed in helium-4.[32] Instead, superfluidity in ³He emerges only at ultralow temperatures below approximately 2.6 mK, facilitated by p-wave spin-triplet pairing of Cooper pairs, as first observed in the A and B phases.[32] This fermionic behavior dominates its thermodynamic properties, with the liquid remaining in a normal Fermi-liquid state down to the superfluid transition. The boiling point of liquid ³He at standard atmospheric pressure is 3.19 K, significantly lower than that of helium-4 due to its lighter mass and weaker interatomic interactions.[33] Its scarcity contributes to high production costs; ³He constitutes only about 1 in 10⁶ atoms in natural helium deposits, primarily extracted as a byproduct from tritium decay in nuclear facilities.[34] Handling ³He requires specialized cryogenic infrastructure to maintain it in the liquid phase, often involving mixtures with helium-4 to leverage phase separation for cooling. To achieve the millikelvin temperatures essential for studying ³He's quantum properties, the dilution refrigerator exploits the phase separation in ³He/⁴He mixtures. In this device, ³He dissolves into the ⁴He superfluid at higher temperatures but separates into a concentrated ³He-rich phase and a dilute phase below ~0.8 K; continuous circulation of ³He from the concentrated to the dilute phase absorbs heat via the endothermic mixing enthalpy, providing cooling power on the order of 1 μW at 15 mK.[35] This method enables sustained temperatures down to ~10 mK without solidification, critical for probing ³He's Fermi-liquid regime. In the normal liquid state above the superfluid transition, ³He exhibits degenerate Fermi behavior characterized by the Fermi temperature K, below which quantum effects like Pauli exclusion become prominent and Pauli blocking suppresses scattering.[36] The low-temperature specific heat follows the linear form , where the Sommerfeld coefficient mJ/mol·K² reflects the enhanced effective mass of quasiparticles due to strong interactions in this dilute Fermi liquid.[37] These properties underscore ³He's role as a model system for correlated fermionic matter, distinct from the bosonic helium-4.Historical Development
Initial Discovery and Early Studies
The liquefaction of helium was first achieved by Dutch physicist Heike Kamerlingh Onnes on July 10, 1908, at the University of Leiden, marking a pivotal advancement in low-temperature physics.[38] Onnes employed a closed-cycle process inspired by Carl von Linde's method for air liquefaction, involving the compression of helium gas, its pre-cooling to approximately 20 K using liquid hydrogen, and subsequent expansion through a throttle valve in a vacuum-insulated vessel.[39] This apparatus also utilized liquid air for initial cooling stages, yielding about 60 milliliters of liquid helium on the first successful run, with a measured boiling point of 4.25 K at atmospheric pressure and a critical temperature slightly above 5 K.[40] The achievement, detailed in Onnes' contemporaneous communications from the Leiden laboratory, enabled systematic exploration of phenomena below 4.2 K, previously inaccessible.[38] Early investigations revealed striking anomalies in liquid helium's behavior. Onnes noted the absence of a solid phase under atmospheric pressure even at temperatures as low as 1.15 K, achieved through rapid evaporation in vacuum vessels equipped with high-capacity pumps; no intermediate liquid-to-solid transition was observed, unlike other substances.[39] Thermal expansion measurements, conducted via dilatometry shortly after liquefaction, showed an unusual density maximum around 2.2 K, implying negative expansion coefficients below this point—a deviation from classical expectations governed by the Grüneisen parameter, which typically predicts positive expansion for most materials.[40] These findings, reported in Onnes' 1909-1910 publications, highlighted helium's non-classical liquid properties and spurred theoretical interest in quantum effects at low temperatures.[38] In 1911, Onnes' access to liquid helium facilitated the serendipitous discovery of superconductivity during resistance measurements on pure mercury wires immersed in the cryogen. At 4.2 K, the electrical resistance dropped abruptly to nearly zero, a phenomenon initially attributed to the extreme low temperatures enabled by helium but later recognized as distinct from helium's own quantum behaviors.[39] This observation, replicated in tin and lead, underscored helium's role in probing metallic properties but was not immediately connected to liquid helium's intrinsic anomalies.[41] By the early 1920s, foundational thermodynamic studies further illuminated liquid helium's peculiarities. In 1922, Onnes and visiting researcher L.I. Dana conducted preliminary specific heat measurements using calorimetric techniques on samples at saturated vapor pressure, revealing a heat capacity that did not conform to the classical Dulong-Petit limit of approximately 3R per mole expected for monatomic systems at higher temperatures; instead, it exhibited a marked increase toward the boiling point without saturating classically at low temperatures.[42] These results, published in Leiden communications, indicated quantum deviations in helium's thermal properties, setting the stage for deeper investigations into its low-temperature phase behavior up to the mid-1920s.[42]Key Milestones in Superfluidity Research
In 1938, the phenomenon of superfluidity in liquid helium-4 was independently discovered by Pyotr Kapitza at the Institute of Physical Problems in Moscow and by John F. Allen and Donald Misener at the Royal Society Mond Laboratory in Cambridge. Kapitza's experiments demonstrated that below the transition temperature of approximately 2.17 K, liquid helium-4 exhibited an extraordinarily low viscosity, effectively flowing without resistance through narrow capillaries, which he termed "superfluidity." Concurrently, Allen and Misener observed similar frictionless flow in helium passed through fine glass tubes, confirming the absence of viscous drag in this phase. These findings marked the onset of intensive research into the quantum mechanical nature of helium's low-temperature behavior. The lambda point at 2.17 K was first indicated by a characteristic lambda-shaped anomaly in the specific heat curve, observed in calorimetric studies by W. H. Keesom and K. Clusius in 1932, well before the discovery of superfluidity. This anomaly, observed years before the superfluidity discovery, was later explained in part by Fritz London's 1938 proposal linking superfluidity to Bose-Einstein condensation in helium-4 atoms.[43] In 1938, László Tisza proposed the initial conceptual framework for understanding superfluidity via a two-fluid model, suggesting that liquid helium-II consists of an inviscid superfluid component and a viscous normal fluid component, with their relative proportions varying with temperature. This idea was further developed in 1941 by Lev Landau, who provided a rigorous theoretical foundation, incorporating phonon and roton excitations to explain the model's hydrodynamics and predict phenomena like second sound. Landau's formulation reconciled experimental observations of thermal transport and flow properties, establishing the two-fluid model as a cornerstone of superfluidity theory. During the 1950s, experimental investigations into rotational motion in superfluid helium revealed the quantized nature of vorticity. H.E. Hall and W.F. Vinen conducted pioneering studies on rotating helium-II, demonstrating that circulation around closed paths is quantized in units of , where is Planck's constant and is the helium-4 mass, arising from the formation of discrete vortex lines. Their work on mutual friction between the superfluid vortices and the normal fluid component quantified interactions that dissipate energy in rotating systems, providing direct evidence for the microscopic quantum structure underlying macroscopic superfluid flow. Advancing into the 21st century, research on ultracold superfluid helium nanodroplets has enabled precise quantum simulations of nanoscale effects, such as vortex dynamics and molecular solvation in confined quantum environments. These droplets, maintained at temperatures below 0.4 K, serve as isolated nanolaboratories where superfluidity persists down to sizes of a few hundred atoms, allowing studies of finite-size quantum phase transitions and ultrafast relaxation processes triggered by extreme-ultraviolet pulses. Recent experiments up to 2025 have explored temporary capture and quantum tunneling of light atoms within these droplets, revealing universal laws in vortex reconnection and dissipation at the nanoscale, which inform broader quantum fluid simulations.Practical Applications
Cryogenic Cooling Systems
Liquid helium plays a critical role in cryogenic cooling systems by providing the low temperatures necessary for superconductivity in magnets used in medical imaging and high-energy physics. In magnetic resonance imaging (MRI) machines, liquid helium cools the superconducting coils to approximately 4 K, enabling the generation of strong, stable magnetic fields without electrical resistance.[44] Conventional MRI scanners typically require over 1,000 liters of liquid helium to maintain this state.[44] Similarly, in particle accelerators like the Large Hadron Collider (LHC) at CERN, liquid helium circulates in a closed system to cool superconducting magnets to 1.9 K, with an inventory of approximately 140 tons required for operation.[45][46] Dewar flasks and cryostats designed for liquid helium storage and transport feature vacuum jackets and multilayer insulation to minimize heat ingress and reduce boil-off rates at 4.2 K. The vacuum jacket creates a thermal barrier, while multilayer insulation—consisting of alternating layers of reflective foil and spacers—further suppresses radiative heat transfer, enabling storage durations of weeks with losses below 1% per day in optimized systems. These designs are essential for maintaining the cryogenic conditions in both laboratory and industrial settings. Helium recovery systems employ closed-loop recycling to capture and reliquefy boil-off gas, addressing supply constraints in cryogenic infrastructures. These systems purify evaporated helium through compression, cooling, and re-liquefaction, achieving recovery efficiencies up to 90% and converting open-cycle operations to zero-boil-off configurations. Global consumption of liquid helium for cryogenic applications is approximately 100,000 m³ per year, underscoring the importance of such recycling to sustain availability.[47] Helium scarcity intensified in the 2010s due to production disruptions and rising demand, driving prices up by as much as 400% between 2010 and 2013.[48] As of 2025, renewed shortages following the U.S. Federal Helium Reserve shutdown have further increased prices and supply constraints, emphasizing the need for conservation.[49] To mitigate these challenges, alternatives such as liquid nitrogen (LN₂) pre-cooling are integrated into helium systems, reducing the energy and helium volume needed for initial cooldown by lowering temperatures to around 80 K before final helium refrigeration. Recent innovations, including zero-boil-off cryostats and helium-efficient MRI systems using pulse-tube refrigerators, reduce helium use by up to 90% and are increasingly adopted as of 2025.[50]Use in Scientific Experiments
Liquid helium plays a pivotal role in low-temperature physics experiments, particularly through its superfluid phase (helium II), which enables the study of quantum excitations via neutron scattering techniques. In superfluid helium-4 (He II), neutron scattering has been instrumental in probing roton excitations, which are quantized quasiparticles representing local density fluctuations with a characteristic energy minimum around 8.65 K and momentum near 1.92 Å⁻¹.[51] These studies reveal that rotons behave as interstitial helium atoms, providing evidence for their atomic-scale structure through inelastic neutron scattering measurements that map the excitation spectrum.[52] Such experiments, conducted at facilities like the Institut Laue-Langevin, have confirmed the Landau dispersion relation for excitations in He II, offering insights into the microscopic origins of superfluidity.[53] Dilution refrigerators, which exploit the phase separation of liquid helium-3 (³He) and helium-4 (⁴He) mixtures, achieve millikelvin temperatures essential for quantum computing experiments with superconducting qubits. These devices cool samples to below 10 mK by leveraging the entropy-driven dilution process, where ³He atoms dissolve into ⁴He at low temperatures, enabling efficient heat extraction. In quantum computing setups, such as those at Fermilab, dilution refrigerators maintain the coherence of superconducting qubits by minimizing thermal noise, allowing for the operation of multi-qubit processors with gate fidelities exceeding 99%. Immersion in liquid ³He further suppresses qubit decoherence from environmental phonons, demonstrating prolonged coherence times exceeding 100 μs in transmon qubit arrays.[54] Superfluid helium serves as a medium for optical tweezers experiments that explore analogs to Bose-Einstein condensates (BECs) by trapping nanoparticles and observing quantum hydrodynamic effects. In these setups, a focused laser beam (optical tweezer) confines dielectric nanoparticles, such as gold particles of ~50–80 nm diameter, within superfluid He II at 1.4 K, where the superfluid's vanishing viscosity allows for frictionless motion and minimal damping.[55] This enables the study of quantized vortex dynamics and phonon-roton interactions as BEC-like analogs, with trapped particles exhibiting ballistic trajectories over microns before interacting with excitations.[55] Such techniques, pioneered in cryogenic optical systems, provide a platform for visualizing superfluid flow at the single-particle level, bridging atomic BECs and macroscopic quantum fluids.[56] In the 2020s, superfluid helium has emerged as a sensitive medium in quantum sensors for dark matter detection, particularly through bolometric configurations that detect sub-GeV particle interactions. Superfluid ⁴He targets, operated as calorimeters, convert dark matter-induced nuclear recoils into quasiparticle excitations, with energy thresholds around 150 eV due to the material's low heat capacity (~1.5 mJ/mol·K at 0.1 K).[57] The QUEST-DMC experiment employs superfluid ³He bolometers with nanomechanical resonators to amplify signals from dark matter scattering, achieving background rejection via quasiparticle dynamics in the B-phase.[58] These detectors target weakly interacting massive particles (WIMPs) and axions in the 10 MeV to 1 GeV mass range, with prototypes projecting sub-eV energy resolution at millikelvin temperatures.[59]Quantitative Data
Physical Constants and Tables
Liquid helium's physical properties are characterized by its low atomic mass and quantum effects, leading to unique constants that differ markedly from classical liquids. For the predominant isotope, helium-4 (^4He), the standard atomic mass is 4.002602 u. The density of liquid ^4He at absolute zero under saturated vapor pressure is 0.1453 g/cm³, increasing slightly with temperature to 0.125 g/cm³ at the normal boiling point. In the normal fluid phase (He I), the speed of first sound is approximately 230 m/s near 3 K. These values highlight the material's low density and high compressibility compared to other substances.[60][61][62] The phase behavior of liquid ^4He is summarized in the following table, including key transition points under saturated vapor pressure unless otherwise noted:| Phase Transition | Temperature (K) | Pressure (bar) | Density (g/cm³) | Notes |
|---|---|---|---|---|
| Normal boiling point | 4.222 | 1.01325 | 0.125 | Equilibrium with vapor at 1 atm. |
| Lambda point (He I to He II) | 2.1768 | 0.05 (saturated) | 0.146 | Superfluid transition at low pressure. |
| Critical point | 5.1953 | 2.2746 | 0.06964 | End of liquid-vapor coexistence. |
| Property | ^3He | ^4He |
|---|---|---|
| Superfluid transition temperature (maximum) | 0.002491 K (at ~3 bar) | 2.1768 K (at saturated vapor pressure) |
| Fermi energy (non-interacting gas model, E_F / k_B) | ~2.8 K | N/A (bosonic) |

