Either you get a simple tapering off, or there were cases where sometimes when you're dealing with material interfaces you get a a rapid depletion from the interfaces
Where the time evolution is given by hopping terms?
When talking about condensed matter, you usually are talking about electronic band structure, you are not asking exactly the same type of questions and I want to be sure what you want...
those are the two ways I could see this system diffusing
where you just gradually diffuse to a stead concentration, or you deplete rapidly at interfaces due to a high chemical potential, then eventually reach the same $t -> \infinity$ final state
Something like this, I think: If the diffusion on a timescale where the system can reach local equilibrium, then it's the first, otherwise, it's the second
Your system is globally not equilibrium, so the scale would be much smaller than the scale of a significant variation in the concentration (macro variable) but much bigger than the lattice scale.
@Skyler Not necessarily... Suppose a gas is expended slowly (because of diffusion limits or a wall) then the final state is not the same as explosive decompression
Because you extracted work instead of dumping it in heat
Oh, but I guess in your case it could be the same though, as nothing is working on anything...
But maybe just keep that in mind. If there is something else then an adiabatic evolution, then your thermodynamic evolution cannot only be described by a potential and the path to reach a particular state is important!
@Skyler Just convolute the heat kernel with step functions