Detailed Summary
The specific heat capacity of solids can be effectively derived using the law of equipartition of energy from kinetic theory. When analyzing a solid, assume it is composed of N atoms, each of which vibrates around a mean position. In such oscillations, the average energy associated with a single dimension is given by 2 × ½ kBT = kBT. Consequently, for three-dimensional vibrations, the total average energy becomes 3kBT. For one mole of a solid, where N = NA (Avogadro's number), the total energy is expressed as:
U = 3kBT × NA = 3RT.
Since we consider a solid, the volume change (∆V) is negligible, thus we can employ the relationship ΔQ = ΔU, resulting in the expression for heat (
ΔQ) related to temperature change as:
3Q = UΔT.
This established relationship implies that the molar heat capacity of solids can generally be approximated as:
C = 3R,
where R is the universal gas constant. Empirical data shows that this theoretical model aligns well with experimental values at standard conditions, with carbon being an exception due to its unique structure (graphene, diamond, etc.). In summary, the specific heat capacity of solids is effectively examined through their atomic vibrations and energy distribution as described by the kinetic theory.