Third Law of Thermodynamics – 3rd Law

The entropy of a system approaches a constant value as the temperature approaches absolute zero.

Based on empirical evidence, this law states that the entropy of a pure crystalline substance is zero at the absolute zero of temperature, 0 K and that it is impossible by means of any process, no matter how idealized, to reduce the temperature of a system to absolute zero in a finite number of steps. This allows us to define a zero point for the thermal energy of a body.


The third law of thermodynamics was developed by the German chemist Walther Nernst during the years 1906–12. For this research Walther Nernst won the 1920 Nobel Prize in chemistry. Therefore the third law of thermodynamics is often referred to as Nernst’s theorem or Nernst’s postulate. As can be seen, the third law of thermodynamics states that the entropy of a system in thermodynamic equilibrium approaches zero as the temperature approaches zero. Or conversely the absolute temperature of any pure crystalline substance in thermodynamic equilibrium approaches zero when the entropy approaches zero.

Nernst Heat Theorem (a consequence of the Third Law) is:

It is impossible for any process, no matter how idealized, to reduce the entropy of a system to its absolute-zero value in a finite number of operations.


nernst theorem

The Nernst heat theorem was later used by a German physicist Max Planck to define the third law of thermodynamics in terms of entropy and absolute zero.

Some materials (e.g. any amorphous solid) do not have a well-defined order at absolute zero. In these materials (e.g. glass) some finite entropy remains also at absolute zero, because the system’s microscopic structure (atom by atom) can be arranged in a different ways (W ≠ 1). This constant entropy is known as the residual entropy, which is the difference between a non-equilibrium state and crystal state of a substance close to absolute zero.

Note that the exact definition of entropy is:

Entropy = (Boltzmann’s constant k) x logarithm of number of possible states

S = kB logW

This equation, which relates the microscopic details, or microstates, of the system (via W) to its macroscopic state (via the entropy S), is the key idea of statistical mechanics.

Absolute Zero

Absolute zero is the coldest theoretical temperature, at which the thermal motion of atoms and molecules reaches its minimum.  This is a state at which the enthalpy and entropy of a cooled ideal gas reaches its minimum value, taken as 0.


lim ST→0 = 0  


S = entropy (J/K)

T = absolute temperature (K)

Classically, this would be a state of motionlessness, but quantum uncertainty dictates that the particles still possess a finite zero-point energy. Absolute zero is denoted as 0 K on the Kelvin scale, −273.15 °C on the Celsius scale, and −459.67 °F on the Fahrenheit scale.

Relation to Heat Engines

According to the Carnot’s principle, that specifies limits on the maximum efficiency any heat engine can have is the Carnot efficiency.This principle also states that the efficiency of a Carnot cycle depends solely on the difference between the hot and cold temperature reservoirs.

Carnot Efficiency Formula


  • is the efficiency of Carnot cycle, i.e. it is the ratio = W/QH of the work done by the engine to the heat energy entering the system from the hot reservoir.
  • TC is the absolute temperature (Kelvins) of the cold reservoir,
  • TH is the absolute temperature (Kelvins) of the hot reservoir,

The third law dictates that TC can never be zero, therefore we see that a 100% efficient heat engine is not possible.

Nuclear and Reactor Physics:

  1. J. R. Lamarsh, Introduction to Nuclear Reactor Theory, 2nd ed., Addison-Wesley, Reading, MA (1983).
  2. J. R. Lamarsh, A. J. Baratta, Introduction to Nuclear Engineering, 3d ed., Prentice-Hall, 2001, ISBN: 0-201-82498-1.
  3. W. M. Stacey, Nuclear Reactor Physics, John Wiley & Sons, 2001, ISBN: 0- 471-39127-1.
  4. Glasstone, Sesonske. Nuclear Reactor Engineering: Reactor Systems Engineering, Springer; 4th edition, 1994, ISBN: 978-0412985317
  5. W.S.C. Williams. Nuclear and Particle Physics. Clarendon Press; 1 edition, 1991, ISBN: 978-0198520467
  6. Kenneth S. Krane. Introductory Nuclear Physics, 3rd Edition, Wiley, 1987, ISBN 978-0471805533
  7. G.R.Keepin. Physics of Nuclear Kinetics. Addison-Wesley Pub. Co; 1st edition, 1965
  8. Robert Reed Burn, Introduction to Nuclear Reactor Operation, 1988.
  9. U.S. Department of Energy, Nuclear Physics and Reactor Theory. DOE Fundamentals Handbook, Volume 1 and 2. January 1993.

Advanced Reactor Physics:

  1. K. O. Ott, W. A. Bezella, Introductory Nuclear Reactor Statics, American Nuclear Society, Revised edition (1989), 1989, ISBN: 0-894-48033-2.
  2. K. O. Ott, R. J. Neuhold, Introductory Nuclear Reactor Dynamics, American Nuclear Society, 1985, ISBN: 0-894-48029-4.
  3. D. L. Hetrick, Dynamics of Nuclear Reactors, American Nuclear Society, 1993, ISBN: 0-894-48453-2. 
  4. E. E. Lewis, W. F. Miller, Computational Methods of Neutron Transport, American Nuclear Society, 1993, ISBN: 0-894-48452-4.