Two-dimensional gas
A two-dimensional gas is a collection of objects constrained to move in a planar or other two-dimensional space in a gaseous state. The objects can be: classical ideal gas elements such as rigid disks undergoing elastic collisions; elementary particles, or any ensemble of individual objects in physics which obeys laws of motion without binding interactions. The concept of a two-dimensional gas is used either because:
- the issue being studied actually takes place in two dimensions (as certain surface molecular phenomena); or,
- the two-dimensional form of the problem is more tractable than the analogous mathematically more complex three-dimensional problem.
While physicists have studied simple two body interactions on a plane for centuries, the attention given to the two-dimensional gas (having many bodies in motion) is a 20th-century pursuit. Applications have led to better understanding of superconductivity,[1] gas thermodynamics, certain solid state problems and several questions in quantum mechanics.
Classical mechanics
[edit]Research at Princeton University in the early 1960s[2] posed the question of whether the Maxwell–Boltzmann statistics and other thermodynamic laws could be derived from Newtonian laws applied to multi-body systems rather than through the conventional methods of statistical mechanics. While this question appears intractable from a three-dimensional closed form solution, the problem behaves differently in two-dimensional space. In particular an ideal two-dimensional gas was examined from the standpoint of relaxation time to equilibrium velocity distribution given several arbitrary initial conditions of the ideal gas. Relaxation times were shown to be very fast: on the order of mean free time .
In 1996 a computational approach was taken to the classical mechanics non-equilibrium problem of heat flow within a two-dimensional gas.[3] This simulation work showed that for N>1500, good agreement with continuous systems is obtained.
Electron gas
[edit]While the principle of the cyclotron to create a two-dimensional array of electrons has existed since 1934, the tool was originally not really used to analyze interactions among the electrons (e.g. two-dimensional gas dynamics). An early research investigation explored cyclotron resonance behavior and the de Haas–van Alphen effect in a two-dimensional electron gas.[4] The investigator was able to demonstrate that for a two-dimensional gas, the de Haas–van Alphen oscillation period is independent of the short-range electron interactions.
Later applications to Bose gas
[edit]In 1991 a theoretical proof was made that a Bose gas can exist in two dimensions.[5] In the same work an experimental recommendation was made that could verify the hypothesis.
Experimental research with a molecular gas
[edit]In general, 2D molecular gases are experimentally observed on weakly interacting surfaces such as metals, graphene etc. at a non-cryogenic temperature and a low surface coverage. As a direct observation of individual molecules is not possible due to fast diffusion of molecules on a surface, experiments are either indirect (observing an interaction of a 2D gas with surroundings, e.g. condensation of a 2D gas) or integral (measuring integral properties of 2D gases, e.g. by diffraction methods).
An example of the indirect observation of a 2D gas is the study of Stranick et al. who used a scanning tunnelling microscope in ultrahigh vacuum (UHV) to image an interaction of a two-dimensional benzene gas layer in contact with a planar solid interface at 77 kelvins.[6] The experimenters were able to observe mobile benzene molecules on the surface of Cu(111), to which a planar monomolecular film of solid benzene adhered. Thus the scientists could witness the equilibrium of the gas in contact with its solid state.
Integral methods that are able to characterize a 2D gas usually fall into a category of diffraction (see for example study of Kroger et al.[7]). The exception is the work of Matvija et al. who used a scanning tunneling microscope to directly visualize a local time-averaged density of molecules on a surface.[8] This method is of special importance as it provides an opportunity to probe local properties of 2D gases; for instance it enables to directly visualize a pair correlation function of a 2D molecular gas in a real space.
If the surface coverage of adsorbates is increased, a 2D liquid is formed,[9] followed by a 2D solid. It was shown that the transition from a 2D gas to a 2D solid state can be controlled by a scanning tunneling microscope which can affect the local density of molecules via an electric field.[10]
Implications for future research
[edit]A multiplicity of theoretical physics research directions exist for study via a two-dimensional gas, such as:[citation needed]
- Complex quantum mechanics phenomena, whose solutions may be more appropriate in a two-dimensional environment;
- Studies of phase transitions (e.g. melting phenomena at a planar surface);
- Thin film phenomena such as chemical vapor deposition;
- Surface excitations of a solid.
See also
[edit]References
[edit]- ^ Feld; et al. (2011). "Observation of a pairing pseudogap in a two-dimensional gas". Nature. 480 (7375): 75–78. arXiv:1110.2418. Bibcode:2011Natur.480...75F. doi:10.1038/nature10627. PMID 22129727. S2CID 4425050.
- ^ C.M.Hogan, Non-equilibrium statistical mechanics of a two-dimensional gas, Dissertation, Princeton University, Department of Physics, May 4, 1964
- ^ D. Risso and P. Cordero, Two-Dimensional Gas of Disks: Thermal Conductivity, Journal of Statistical Physics, volume 82, pages 1453–1466, (1996)
- ^ Kohn, Walter (1961). "Cyclotron Resonance and de Haas–van Alphen Oscillations of an Interacting Electron Gas". Physical Review. 123 (4): 1242–1244. Bibcode:1961PhRv..123.1242K. doi:10.1103/physrev.123.1242.
- ^ Vanderlei Bagnato and Daniel Kleppner. Bose–Einstein condensation in low-dimensional traps, American Physical Society, 8 April 1991
- ^ Stranick, S. J.; Kamna, M. M.; Weiss, P. S, Atomic Scale Dynamics of a Two-Dimensional Gas-Solid Interface, Pennsylvania State University, Park Dept. of Chemistry, 3 June 1994
- ^ Kroger, I. (2009). "Tuning intermolecular interaction in long-range-ordered submonolayer organic films". Nature Physics. 5 (2): 153–158. Bibcode:2009NatPh...5..153S. doi:10.1038/nphys1176.
- ^ Matvija, Peter; Rozbořil, Filip; Sobotík, Pavel; Ošťádal, Ivan; Kocán, Pavel (2017). "Pair correlation function of a 2D molecular gas directly visualized by scanning tunneling microscopy". The Journal of Physical Chemistry Letters. 8 (17): 4268–4272. doi:10.1021/acs.jpclett.7b01965. PMID 28830146.
- ^ Thomas Waldmann; Jens Klein; Harry E. Hoster; R. Jürgen Behm (2012), "Stabilization of Large Adsorbates by Rotational Entropy: A Time-Resolved Variable-Temperature STM Study", ChemPhysChem (in German), vol. 14, no. 1, pp. 162–169, doi:10.1002/cphc.201200531, PMID 23047526, S2CID 36848079
- ^ Matvija, Peter; Rozbořil, Filip; Sobotík, Pavel; Ošťádal, Ivan; Pieczyrak, Barbara; Jurczyszyn, Leszek; Kocán, Pavel (2017). "Electric-field-controlled phase transition in a 2D molecular layer". Scientific Reports. 7 (1): 7357. Bibcode:2017NatSR...7.7357M. doi:10.1038/s41598-017-07277-7. PMC 5544747. PMID 28779091.