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The standard Gibbs free energy of formation of a compound is the change of Gibbs free energy that accompanies the formation of 1 mole of that substance from its component elements, in their standard states (the most stable form of the element at 25 °C and 100 kPa).
Historically, the term 'free energy' has been used for either quantity. In physics, free energy most often refers to the Helmholtz free energy, denoted by A (or F), while in chemistry, free energy most often refers to the Gibbs free energy. The values of the two free energies are usually quite similar and the intended free energy function is ...
When both temperature and pressure are held constant, and the number of particles is expressed in moles, the chemical potential is the partial molar Gibbs free energy. [1] [2] At chemical equilibrium or in phase equilibrium, the total sum of the product of chemical potentials and stoichiometric coefficients is zero, as the free energy is at a ...
The definition of the Gibbs function is = + where H is the enthalpy defined by: = +. Taking differentials of each definition to find dH and dG, then using the fundamental thermodynamic relation (always true for reversible or irreversible processes): = where S is the entropy, V is volume, (minus sign due to reversibility, in which dU = 0: work other than pressure-volume may be done and is equal ...
When the Gibbs free energy for a chemical reaction is negative, the reaction will proceed spontaneously. When a chemical system is at equilibrium, the change in Gibbs free energy is zero. An equilibrium constant is simply related to the free energy change when the reactants are in their standard states:
In solution chemistry and biochemistry, the Gibbs free energy decrease (∂G/∂ξ, in molar units, denoted cryptically by ΔG) is commonly used as a surrogate for (−T times) the global entropy produced by spontaneous chemical reactions in situations where no work is being done; or at least no "useful" work; i.e., other than perhaps ± P dV.
Molar Gibbs free energy is commonly referred to as chemical potential, symbolized by , particularly when discussing a partial molar Gibbs free energy for a component in a mixture. For the characterization of substances or reactions, tables usually report the molar properties referred to a standard state .
Another way of looking at the theorem is to start with the definition of the Gibbs free energy (G), G = H - TS, where H stands for enthalpy. For a change from reactants to products at constant temperature and pressure the equation becomes Δ G = Δ H − T Δ S {\displaystyle \Delta G=\Delta H-T\Delta S} .