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In thermodynamics, the Gibbs free energy (or Gibbs energy as the recommended name; symbol ) is a thermodynamic potential that can be used to calculate the maximum amount of work, other than pressure–volume work, that may be performed by a thermodynamically closed system at constant temperature and pressure.
The standard Gibbs free energy of formation (G f °) of a compound is the change of Gibbs free energy that accompanies the formation of 1 mole of a substance in its standard state from its constituent elements in their standard states (the most stable form of the element at 1 bar of pressure and the specified temperature, usually 298.15 K or 25 °C).
Several free energy functions may be formulated based on system criteria. Free energy functions are Legendre transforms of the internal energy. The Gibbs free energy is given by G = H − TS, where H is the enthalpy, T is the absolute temperature, and S is the entropy. H = U + pV, where U is the internal energy, p is the pressure, and V is the ...
Thermodynamic databases contain information about thermodynamic properties for substances, the most important being enthalpy, entropy, and Gibbs free energy.Numerical values of these thermodynamic properties are collected as tables or are calculated from thermodynamic datafiles.
The energy is replaced by the characteristic potential of that ensemble, the Gibbs Free Energy. The letter Z stands for the German word Zustandssumme , "sum over states". The usefulness of the partition function stems from the fact that the macroscopic thermodynamic quantities of a system can be related to its microscopic details through the ...
It describes how the Gibbs free energy, which was presented originally by Josiah Willard Gibbs, varies with temperature. [1] It was derived by Helmholtz first, and Gibbs derived it only 6 years later. [2] The attribution to Gibbs goes back to Wilhelm Ostwald, who first translated Gibbs' monograph into German and promoted it in Europe. [3] [4]
The locus of these points (the inflection point within a G-x or G-c curve, Gibbs free energy as a function of composition) is known as the spinodal curve. [1] [2] [3] For compositions within this curve, infinitesimally small fluctuations in composition and density will lead to phase separation via spinodal decomposition.
The green curve is the total (Gibbs if this is at constant pressure) free energy as a function of radius. Shown is the free energy barrier, , and radius at the top of the barrier, . This total free energy is a sum of two terms. The first is a bulk term, which is plotted in red.