In Lecture 4 about the Sommerfield Model there is a piece about a useful trick of scaling the proportionality between C and T.
Two separate examples are given however I don’t see why we consider g(\varepsilon_f) as “roughly constant” in the 3D free electron example but we don’t do the same for the density of states in the graphene model. The only difference I can come up with is that:
- For free electrons in 3D g(\varepsilon) \propto \sqrt{\varepsilon} while for graphene we have g(\varepsilon) \propto \varepsilon.
But won’t both these densities of states be constant for some value \varepsilon_f? So how come one system has C_e \propto T and the other has C_g \propto T^2