Boltzmann constant

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Boltzmann constant

Ludwig Boltzmann
Definition:	The proportionality factor that relates the average relative kinetic energy of particles in a gas with the thermodynamic temperature of the gas
Symbol:	kB
Value in joules per kelvin:	1.380649×10−23 J⋅K−1

The Boltzmann constant (k_B or k) is the proportionality factor that relates the average relative kinetic energy of particles in a gas with the thermodynamic temperature of the gas. It occurs in the definitions of the kelvin and the gas constant, and in Planck's law of black-body radiation and Boltzmann's entropy formula, and is used in calculating thermal noise in resistors. The Boltzmann constant has dimensions of energy divided by temperature, the same as entropy. It is named after the Austrian scientist Ludwig Boltzmann.

As part of the 2019 redefinition of SI base units, the Boltzmann constant is one of the seven "defining constants" that have been given exact definitions. They are used in various combinations to define the seven SI base units. The Boltzmann constant is defined to be exactly 1.380649×10⁻²³ J⋅K⁻¹.

Roles of the Boltzmann constant

Relationships between Boyle's, Charles's, Gay-Lussac's, Avogadro's, combined and ideal gas laws, with the Boltzmann constant k_B = R/N_A = n R/N  (in each law, properties circled are variable and properties not circled are held constant)

Macroscopically, the ideal gas law states that, for an ideal gas, the product of pressure p and volume V is proportional to the product of amount of substance n (in moles) and absolute temperature T:

${\displaystyle pV=nRT,}$

where R is the molar gas constant (8.31446261815324 J⋅K⁻¹⋅mol⁻¹). Introducing the Boltzmann constant as the gas constant per molecule k = R/N_A transforms the ideal gas law into an alternative form:

${\displaystyle pV=NkT,}$

where N is the number of molecules of gas. For n = 1 mol, N is equal to the number of particles in one mole (the Avogadro number).

Role in the equipartition of energy

Main article: Equipartition of energy

Given a thermodynamic system at an absolute temperature T, the average thermal energy carried by each microscopic degree of freedom in the system is 1/2kT (i.e., about 2.07×10⁻²¹ J, or 0.013 eV, at room temperature). It's important to note that this is generally true only for classical systems with a large number of particles, and in which quantum effects are negligible.

In classical statistical mechanics, this average is predicted to hold exactly for homogeneous ideal gases. Monatomic ideal gases (the six noble gases) possess three degrees of freedom per atom, corresponding to the three spatial directions. According to the equipartition of energy this means that there is a thermal energy of 3/2kT per atom. This corresponds very well with experimental data. The thermal energy can be used to calculate the root-mean-square speed of the atoms, which turns out to be inversely proportional to the square root of the atomic mass. The root mean square speeds found at room temperature accurately reflect this, ranging from 1370 m/s for helium, down to 240 m/s for xenon.

Kinetic theory gives the average pressure p for an ideal gas as

${\displaystyle p={\frac {1}{3}}{\frac {N}{V}}m{\overline {v^{2}}}.}$

Combination with the ideal gas law

${\displaystyle pV=NkT}$

shows that the average translational kinetic energy is

${\displaystyle {\tfrac {1}{2}}m{\overline {v^{2}}}={\tfrac {3}{2}}kT.}$

Considering that the translational motion velocity vector v has three degrees of freedom (one for each dimension) gives the average energy per degree of freedom equal to one third of that, i.e. 1/2kT.

The ideal gas equation is also obeyed closely by molecular gases; but the form for the heat capacity is more complicated, because the molecules possess additional internal degrees of freedom, as well as the three degrees of freedom for movement of the molecule as a whole. Diatomic gases, for example, possess a total of six degrees of simple freedom per molecule that are related to atomic motion (three translational, two rotational, and one vibrational). At lower temperatures, not all these degrees of freedom may fully participate in the gas heat capacity, due to quantum mechanical limits on the availability of excited states at the relevant thermal energy per molecule.

Role in Boltzmann factors

More generally, systems in equilibrium at temperature T have probability P_i of occupying a state i with energy E weighted by the corresponding Boltzmann factor:

${\displaystyle P_{i}\propto {\frac {\exp \left(-{\frac {E}{kT}}\right)}{Z}},}$

where Z is the partition function. Again, it is the energy-like quantity kT that takes central importance.

Consequences of this include (in addition to the results for ideal gases above) the Arrhenius equation in chemical kinetics.

Role in the statistical definition of entropy

Further information: Entropy (statistical thermodynamics)

 

Boltzmann's grave in the Zentralfriedhof, Vienna, with bust and entropy formula.

In statistical mechanics, the entropy S of an isolated system at thermodynamic equilibrium is defined as the natural logarithm of W, the number of distinct microscopic states available to the system given the macroscopic constraints (such as a fixed total energy E):

${\displaystyle S=k\,\ln W.}$

This equation, which relates the microscopic details, or microstates, of the system (via W) to its macroscopic state (via the entropy S), is the central idea of statistical mechanics. Such is its importance that it is inscribed on Boltzmann's tombstone.

The constant of proportionality k serves to make the statistical mechanical entropy equal to the classical thermodynamic entropy of Clausius:

${\displaystyle \Delta S=\int {\frac {{\rm {d}}Q}{T}}.}$

One could choose instead a rescaled dimensionless entropy in microscopic terms such that

${\displaystyle {S'=\ln W},\quad \Delta S'=\int {\frac {\mathrm {d} Q}{kT}}.}$

This is a more natural form and this rescaled entropy exactly corresponds to Shannon's subsequent information entropy.

The characteristic energy kT is thus the energy required to increase the rescaled entropy by one nat.

The thermal voltage

In semiconductors, the Shockley diode equation—the relationship between the flow of electric current and the electrostatic potential across a p–n junction—depends on a characteristic voltage called the thermal voltage, denoted by V_T. The thermal voltage depends on absolute temperature T as

$${\displaystyle V_{\mathrm {T} }={kT \over q},}$$

where q is the magnitude of the electrical charge on the electron with a value 1.602176634×10⁻¹⁹ C Equivalently,

$${\displaystyle {V_{\mathrm {T} } \over T}={k \over q}\approx 8.61733034\times 10^{-5}\ \mathrm {V/K} .}$$

At room temperature 300 K (27 °C; 80 °F), V_T is approximately 25.85 mV which can be derived by plugging in the values as follows:

$${\displaystyle V_{\mathrm {T} }={kT \over q}={\frac {1.38\times 10^{-23}\ \mathrm {J} \cdot k^{-1}\times 300\ \mathrm {K} }{1.6\times 10^{-19}\ \mathrm {C} }}\simeq 25.85\ \mathrm {mV} }$$

At the standard state temperature of 298.15 K (25.00 °C; 77.00 °F), it is approximately 25.69 mV. The thermal voltage is also important in plasmas and electrolyte solutions (e.g. the Nernst equation); in both cases it provides a measure of how much the spatial distribution of electrons or ions is affected by a boundary held at a fixed voltage.

History

The Boltzmann constant is named after its 19th century Austrian discoverer, Ludwig Boltzmann. Although Boltzmann first linked entropy and probability in 1877, the relation was never expressed with a specific constant until Max Planck first introduced k, and gave a more precise value for it (1.346×10⁻²³ J/K, about 2.5% lower than today's figure), in his derivation of the law of black-body radiation in 1900–1901. Before 1900, equations involving Boltzmann factors were not written using the energies per molecule and the Boltzmann constant, but rather using a form of the gas constant R, and macroscopic energies for macroscopic quantities of the substance. The iconic terse form of the equation S = k ln W on Boltzmann's tombstone is in fact due to Planck, not Boltzmann. Planck actually introduced it in the same work as his eponymous h.

In 1920, Planck wrote in his Nobel Prize lecture:

This constant is often referred to as Boltzmann's constant, although, to my knowledge, Boltzmann himself never introduced it — a peculiar state of affairs, which can be explained by the fact that Boltzmann, as appears from his occasional utterances, never gave thought to the possibility of carrying out an exact measurement of the constant.

This "peculiar state of affairs" is illustrated by reference to one of the great scientific debates of the time. There was considerable disagreement in the second half of the nineteenth century as to whether atoms and molecules were real or whether they were simply a heuristic tool for solving problems. There was no agreement whether chemical molecules, as measured by atomic weights, were the same as physical molecules, as measured by kinetic theory. Planck's 1920 lecture continued:

Nothing can better illustrate the positive and hectic pace of progress which the art of experimenters has made over the past twenty years, than the fact that since that time, not only one, but a great number of methods have been discovered for measuring the mass of a molecule with practically the same accuracy as that attained for a planet.

In versions of SI prior to the 2019 redefinition of the SI base units, the Boltzmann constant was a measured quantity rather than a fixed value. Its exact definition also varied over the years due to redefinitions of the kelvin (see Kelvin § History) and other SI base units (see Joule § History).

In 2017, the most accurate measures of the Boltzmann constant were obtained by acoustic gas thermometry, which determines the speed of sound of a monatomic gas in a triaxial ellipsoid chamber using microwave and acoustic resonances. This decade-long effort was undertaken with different techniques by several laboratories; it is one of the cornerstones of the 2019 redefinition of SI base units. Based on these measurements, the CODATA recommended 1.380649×10⁻²³ J/K to be the final fixed value of the Boltzmann constant to be used for the International System of Units.

Value in different units

Values of kB	Units	Comments
1.380649×10−23	J/K	SI by definition, J/K = m2⋅kg/(s2⋅K) in SI base units
8.617333262×10−5	eV/K
2.083661912×1010	Hz/K	(k/h)
1.380649×10−16	erg/K	CGS system, 1 erg = 1×10−7 J
3.297623483×10−24	cal/K	1 calorie = 4.1868 J
1.832013046×10−24	cal/°R
5.657302466×10−24	ft lb/°R
0.695034800	cm−1/K	(k/(hc))
3.166811563×10−6	Eh/K	(Eh = Hartree)
1.987204259×10−3	kcal/(mol⋅K)	(kNA)
8.314462618×10−3	kJ/(mol⋅K)	(kNA)
−228.5991672	dB(W/K/Hz)	10 log10(k/(1 W/K/Hz)), used for thermal noise calculations

Since k is a proportionality factor between temperature and energy, its numerical value depends on the choice of units for energy and temperature. The small numerical value of the Boltzmann constant in SI units means a change in temperature by 1 K only changes a particle's energy by a small amount. A change of 1 °C is defined to be the same as a change of 1 K. The characteristic energy kT is a term encountered in many physical relationships.

The Boltzmann constant sets up a relationship between wavelength and temperature (dividing hc/k by a wavelength gives a temperature) with one micrometer being related to 14387.777 K, and also a relationship between voltage and temperature (multiplying the voltage by k in units of eV/K) with one volt being related to 11604.518 K. The ratio of these two temperatures, 14387.777 K / 11604.518 K ≈ 1.239842, is the numerical value of hc in units of eV⋅μm.

Natural units

The Boltzmann constant provides a mapping from this characteristic microscopic energy E to the macroscopic temperature scale T = E/k. In physics research another definition is often encountered in setting k to unity, resulting in temperature and energy quantities of the same type. In this context temperature is measured effectively in units of energy and the Boltzmann constant is not explicitly needed.

The equipartition formula for the energy associated with each classical degree of freedom then becomes

${\displaystyle E_{\mathrm {dof} }={\tfrac {1}{2}}T}$

The use of natural units simplifies many physical relationships; in this form the definition of thermodynamic entropy coincides with the form of information entropy:

${\displaystyle S=-\sum _{i}P_{i}\ln P_{i}.}$

where P_i is the probability of each microstate.