# Negative temperature

SI temperature/coldness (1/kT) scale.

In physics, certain systems can achieve negative temperature; that is, their thermodynamic temperature can be expressed as a negative quantity on the Kelvin or Rankine scales.

In colloquial usage, "negative temperature" may refer to temperatures that are expressed as negative numbers on the more familiar Celsius or Fahrenheit scales, with values that are colder than the zero points of those scales but still warmer than absolute zero.

A system with a truly negative temperature on the Kelvin scale is hotter than any system with a positive temperature. If a negative-temperature system and a positive-temperature system come in contact, heat will flow from the negative- to the positive-temperature system.[1][2]

That a system at negative temperature is hotter than any system at positive temperature seems paradoxical if absolute temperature is interpreted as an average kinetic energy of the system. The paradox is resolved by understanding temperature through its more rigorous definition as the tradeoff between energy and entropy, with the reciprocal of the temperature, thermodynamic beta, as the more fundamental quantity. Systems with a positive temperature will increase in entropy as one adds energy to the system. Systems with a negative temperature will decrease in entropy as one adds energy to the system.[3]

Most familiar systems cannot achieve negative temperatures, because adding energy always increases their entropy. The possibility of decreasing in entropy with increasing energy requires the system to "saturate" in entropy, with the number of high energy states being small. These kinds of systems, bounded by a maximum amount of energy, are generally forbidden classically. Thus, negative temperature is a strictly quantum phenomenon. Some systems, however (see the examples below), have a maximum amount of energy that they can hold, and as they approach that maximum energy their entropy actually begins to decrease.[4]

## Clarification on different definitions of temperature and entropyEdit

Temperature is defined by the relationship between entropy and energy. The negative temperatures discussed here arise from statistical mechanics using the Boltzmann definition of entropy. Entropy is also independently defined in thermodynamics, and in the thermodynamic limit (i.e. many degrees of freedom) these definitions are generally consistent with each other. However, for small systems and systems where the number of states decreases with energy, the Boltzmann entropy and the thermodynamic entropy are not consistent, and the temperatures derived from these entropies are different. Some theorists have proposed using an alternate definition of entropy originally proposed by Gibbs as a way to resolve these inconsistencies,[5] although this new definition would create other inconsistencies.[6] Regardless of how we choose to define entropy and temperature, the physical behavior of a negative temperature system is the same.

## Heat and molecular energy distributionEdit

Negative temperatures can only exist in a system where there are a limited number of energy states (see below). As the temperature is increased on such a system, particles move into higher and higher energy states, and as the temperature increases, the number of particles in the lower energy states and in the higher energy states approaches equality. (This is a consequence of the definition of temperature in statistical mechanics for systems with limited states.) By injecting energy into these systems in the right fashion, it is possible to create a system in which there are more particles in the higher energy states than in the lower ones. The system can then be characterised as having a negative temperature.

A substance with a negative temperature is not colder than absolute zero, but rather it is hotter than infinite temperature. As Kittel and Kroemer (p. 462) put it, "The temperature scale from cold to hot runs:

+0 K, … , +300 K, … , +∞ K, −∞ K, … , −300 K, … , −0 K."

The corresponding inverse temperature scale, for the quantity β = 1/kT (where k is Boltzmann's constant), runs continuously from low energy to high as +∞, … , 0, …, −∞. Because it avoids the abrupt jump from +∞ to −∞, β is considered more natural than T.

In many familiar physical systems, temperature is associated to the kinetic energy of atoms. Since there is no upper bound on the momentum of an atom, there is no upper bound to the number of energy states available when more energy is added, and therefore no way to get to a negative temperature. However, in statistical mechanics, temperature can correspond to other degrees of freedom than just kinetic energy (see below).

## Temperature and disorderEdit

The distribution of energy among the various translational, vibrational, rotational, electronic, and nuclear modes of a system determines the macroscopic temperature. In a "normal" system, thermal energy is constantly being exchanged between the various modes.

However, in some situations, it is possible to isolate one or more of the modes. In practice, the isolated modes still exchange energy with the other modes, but the time scale of this exchange is much slower than for the exchanges within the isolated mode. One example is the case of nuclear spins in a strong external magnetic field. In this case, energy flows fairly rapidly among the spin states of interacting atoms, but energy transfer between the nuclear spins and other modes is relatively slow. Since the energy flow is predominantly within the spin system, it makes sense to think of a spin temperature that is distinct from the temperature associated to other modes.

A definition of temperature can be based on the relationship:

${\displaystyle T={\frac {dq_{\mathrm {rev} }}{dS}}}$

The relationship suggests that a positive temperature corresponds to the condition where entropy, S, increases as thermal energy, qrev, is added to the system. This is the "normal" condition in the macroscopic world, and is always the case for the translational, vibrational, rotational, and non-spin related electronic and nuclear modes. The reason for this is that there are an infinite number of these types of modes, and adding more heat to the system increases the number of modes that are energetically accessible, and thus increases the entropy.

## ExamplesEdit

### Noninteracting two–level particlesEdit

Entropy, thermodynamic beta, and temperature as a function of the energy for a system of N noninteracting two–level particles.

The simplest example, albeit a rather nonphysical one, is to consider a system of N particles, each of which can take an energy of either or but are otherwise noninteracting. This can be understood as a limit of the Ising model in which the interaction term becomes negligible. The total energy of the system is

${\displaystyle E=\epsilon \sum _{i=1}^{N}\sigma _{i}=\epsilon \cdot j}$

where σi is the sign of the ith particle and j is the number of particles with positive energy minus the number of particles with negative energy. From elementary combinatorics, the total number of microstates with this amount of energy is a binomial coefficient:

${\displaystyle \Omega _{E}={\binom {N}{(N+j)/2}}={\frac {N!}{\left({\frac {N+j}{2}}\right)!\left({\frac {N-j}{2}}\right)!}}.}$

By the fundamental assumption of statistical mechanics, the entropy of this microcanonical ensemble is

${\displaystyle S=k_{B}\ln \Omega _{E}}$

We can solve for thermodynamic beta (β = 1/kBT) by considering it as a central difference without taking the continuum limit:

${\displaystyle \beta ={\frac {1}{k_{B}}}{\frac {\delta _{2\epsilon }[S]}{2\epsilon }}}$
${\displaystyle \beta ={\frac {1}{2\epsilon }}(\ln \Omega _{E+\epsilon }-\ln \Omega _{E-\epsilon })}$
${\displaystyle \beta ={\frac {1}{2\epsilon }}\ln \left({\frac {\left({\frac {N+j-1}{2}}\right)!\left({\frac {N-j+1}{2}}\right)!}{\left({\frac {N+j+1}{2}}\right)!\left({\frac {N-j-1}{2}}\right)!}}\right)}$
${\displaystyle \beta ={\frac {1}{2\epsilon }}\ln \left({\frac {N-j+1}{N+j+1}}\right).}$

hence the temperature

${\displaystyle T(E)={\frac {2\epsilon }{k_{B}}}\left[\ln \left({\frac {(N+1)\epsilon -E}{(N+1)\epsilon +E}}\right)\right]^{-1}.}$

### Nuclear spinsEdit

The previous example is approximately realized by a system of nuclear spins in an external magnetic field.[7][8] This allows the experiment to be run as a variation of nuclear magnetic resonance spectroscopy. In the case of electronic and nuclear spin systems, there are only a finite number of modes available, often just two, corresponding to spin up and spin down. In the absence of a magnetic field, these spin states are degenerate, meaning that they correspond to the same energy. When an external magnetic field is applied, the energy levels are split, since those spin states that are aligned with the magnetic field will have a different energy from those that are anti-parallel to it.

In the absence of a magnetic field, such a two-spin system would have maximum entropy when half the atoms are in the spin-up state and half are in the spin-down state, and so one would expect to find the system with close to an equal distribution of spins. Upon application of a magnetic field, some of the atoms will tend to align so as to minimize the energy of the system, thus slightly more atoms should be in the lower-energy state (for the purposes of this example we will assume the spin-down state is the lower-energy state). It is possible to add energy to the spin system using radio frequency (RF) techniques.[9] This causes atoms to flip from spin-down to spin-up.

Since we started with over half the atoms in the spin-down state, this initially drives the system towards a 50/50 mixture, so the entropy is increasing, corresponding to a positive temperature. However, at some point, more than half of the spins are in the spin-up position.[10] In this case, adding additional energy reduces the entropy, since it moves the system further from a 50/50 mixture. This reduction in entropy with the addition of energy corresponds to a negative temperature.[11] In NMR spectroscopy, this corresponds to pulses with a pulse width of over 180° (for a given spin). While relaxation is fast in solids, it can take several seconds in solutions and even longer in gases and in ultracold systems; several hours were reported for silver and rhodium at picokelvin temperatures.[11] It is still important to understand that the temperature is negative only with respect to nuclear spins. Other degrees of freedom, such as molecular vibrational, electronic and electron spin levels are at a positive temperature, so the object still has positive sensible heat. Relaxation actually happens by exchange of energy between the nuclear spin states and other states (e.g. through the nuclear Overhauser effect with other spins).

### LasersEdit

This phenomenon can also be observed in many lasing systems, wherein a large fraction of the system's atoms (for chemical and gas lasers) or electrons (in semiconductor lasers) are in excited states. This is referred to as a population inversion.

The Hamiltonian for a single mode of a luminescent radiation field at frequency ν is

${\displaystyle H=(h\nu -\mu )a^{\dagger }a.\,}$

The density operator in the grand canonical ensemble is

${\displaystyle \rho ={\frac {\exp(-\beta H)}{\mathbf {Tr} (\exp(-\beta H))}}.}$

For the system to have a ground state, the trace to converge, and the density operator to be generally meaningful, βH must be positive semidefinite. So if  < μ, and H is negative semidefinite, then β must itself be negative, implying a negative temperature.[12]

### Two-dimensional vortex motionEdit

The two-dimensional systems can exist in negative temperature states.[13][14]

### Motional degrees of freedomEdit

Negative temperatures have also been achieved in motional degrees of freedom. Using an optical lattice, upper bounds were placed on the kinetic energy, interaction energy and potential energy of cold 39
K
atoms. This was done by tuning the interactions of the atoms from repulsive to attractive using a Feshbach resonance and changing the overall harmonic potential from trapping to anti-trapping, thus transforming the Bose-Hubbard Hamiltonian from ${\displaystyle {\hat {H}}\rightarrow -{\hat {H}}}$ . Performing this transformation adiabatically while keeping the atoms in the Mott insulator regime, it is possible to go from a low entropy positive temperature state to a low entropy negative temperature state. In the negative temperature state, the atoms macroscopically occupy the maximum momentum state of the lattice. The negative temperature ensembles equilibrated and showed long lifetimes in an anti-trapping harmonic potential.[15]

## ReferencesEdit

1. ^ Ramsey, Norman (1956-07-01). "Thermodynamics and Statistical Mechanics at Negative Absolute Temperatures". Physical Review. 103 (1): 20–28. Bibcode:1956PhRv..103...20R. doi:10.1103/PhysRev.103.20.
2. ^ Tremblay, André-Marie (1975-11-18). "Comment on: Negative Kelvin temperatures: some anomalies and a speculation" (PDF). American Journal of Physics. 44 (10): 994–995. Bibcode:1976AmJPh..44..994T. doi:10.1119/1.10248.
3. ^ Atkins, Peter W. (2010-03-25). The Laws of Thermodynamics: A Very Short Introduction. Oxford University Press. pp. 10–14. ISBN 978-0-19-957219-9. OCLC 467748903.
4. ^ Atkins, Peter W. (2010-03-25). The Laws of Thermodynamics: A Very Short Introduction. Oxford University Press. pp. 89–95. ISBN 978-0-19-957219-9. OCLC 467748903.
5. ^ Dunkel, Jorn; Hilbert, Stefan (2013). "Consistent thermostatistics forbids negative absolute temperatures". Nature Physics. 10 (1): 67. arXiv:. Bibcode:2014NatPh..10...67D. doi:10.1038/nphys2815.
6. ^ Frenkel, Daan; Warren, Patrick B. (2015-02-01). "Gibbs, Boltzmann, and negative temperatures". American Journal of Physics. 83 (2): 163–170. arXiv:. Bibcode:2015AmJPh..83..163F. doi:10.1119/1.4895828. ISSN 0002-9505.
7. ^ Purcell, E. M.; Pound, R. V. (1951-01-15). "A Nuclear Spin System at Negative Temperature". Physical Review. 81 (2): 279–280. Bibcode:1951PhRv...81..279P. doi:10.1103/PhysRev.81.279.
8. ^ Varga, Peter (1998). "Minimax games, spin glasses, and the polynomial-time hierarchy of complexity classes". Physical Review E. 57 (6): 6487–6492. arXiv:. Bibcode:1998PhRvE..57.6487V. doi:10.1103/PhysRevE.57.6487.
9. ^ Ramsey, Norman F. (1998). Spectroscopy with coherent radiation: selected papers of Norman F. Ramsey with commentary. World Scientific series in 20th century physics, v. 21. Singapore; River Edge, N.J.: World Scientific. p. 417. ISBN 9789810232504. OCLC 38753008.
10. ^ Levitt, Malcolm H. (2008). Spin Dynamics: Basics of Nuclear Magnetic Resonance. West Sussex, England: John Wiley & Sons Ltd. p. 273. ISBN 978-0-470-51117-6.
11. ^ a b
12. ^ Hsu, W.; Barakat, R. (1992). "Statistics and thermodynamics of luminescent radiation". Physical Review B. 46 (11): 6760–6767. Bibcode:1992PhRvB..46.6760H. doi:10.1103/PhysRevB.46.6760.
13. ^ Montgomery, D.C. (1972). "Two-dimensional vortex motion and "negative temperatures"". Physics Letters A. 39 (1): 7–8. Bibcode:1972PhLA...39....7M. doi:10.1016/0375-9601(72)90302-7.
14. ^ Edwards, S.F.; Taylor, J.B. (1974). "Negative Temperature States of Two-Dimensional Plasmas and Vortex Fluids". Proceedings of the Royal Society of London A. 336 (1606): 257–271. Bibcode:1974RSPSA.336..257E. doi:10.1098/rspa.1974.0018. JSTOR 78450.
15. ^ Braun, S.; Ronzheimer, J. P.; Schreiber, M.; Hodgman, S. S.; Rom, T.; Bloch, I.; Schneider, U. (2013). "Negative Absolute Temperature for Motional Degrees of Freedom". Science. 339 (6115): 52–55. arXiv:. Bibcode:2013Sci...339...52B. doi:10.1126/science.1227831. PMID 23288533.