Density Operator is a generalization of the more usual state vectors or wavefunctions: while those can only represent pure states, density matrices can also represent mixed states. Mixed states arise in quantum mechanics in two different situations: first when the preparation of the system is not fully known, and thus one must deal with a statistical ensemble of possible preparations, and second when one wants to describe a physical system which is entangled with another, without describing their combined state.
Density Operator
Pure states and Mixed states
Pure state A pure state is a quantum state that could be represented by a ket in state space.
Mixed state A mixed state is a physical state not coherently but statistically composed of many pure states.
If a group of pure states are denoted by ∣ψi⟩, with probability pi , the mixed state it represents is then written as {pi,∣ψi⟩}.
Density Operator
Density operator The density operator of a system in the mixed state {pi,∣ψi⟩} is defined as
ρ=i∑pi∣ψi⟩⟨ψi∣
If we define the density operator of a pure state system ρi=∣ψi⟩⟨ψi∣, then ρ=∑piρi.
Density Matrix If the state space has a pre-selected basis ∣ui⟩, the density matrix element is
ρmn=⟨ui∣ρ∣uj⟩=i∑pi⟨um∣ψi⟩⟨ψi∣un⟩
Corollary: The trace of density operator is 1. Trρ=1 .
Expectation Value The expectation value of an observation operator O is Tr{ρO}.
⟨O⟩(t)=Tr{ρ(t)O(t)}
Hermite The density matrix is a Hermite, positive semidefinite matrix.
ρ=P†ΛP⟹(ρ)†ρ=ρ=P†ΛP
Evolution
Schrodinger Picture
Since pure states ∣ψi⟩ are independent from each other and evolve respectively
{iℏdtd∣ψi(t)⟩=H(t)∣ψi(t)⟩∣ψi(t0)⟩=∣ψi⟩
and at time t the density operator is ρ(t)=∑ipiρi(t)=∑ipi∣ψi(t)⟩⟨ψi(t)∣, thus we can derive
iℏdtdρ(t)=[H(t),ρ(t)]
and dtdρS=∂t∂ρS.
Relaxation
If, in addition, the system undergoes at random instants a succession of brief, weak collisions with other systems and decays due to the environment, their average effect can be represented by the addition to iℏdtdρ(t)=[H(t),ρ(t)] of a relaxation operator.
(dtdρii)rel=−j=i∑Γi→jρii+j=i∑Γj→iρjj
(dtdρij)rel=−γijρij
in which the off-diagonal elements of the density matrix ρij termed coherences since they depend on the relative phases of the ∣i⟩ and ∣j⟩ components of the system wavefunction.
If we only consider the spontaneous emission, the relaxation rates are
Γe→g=−Γg→e=Γγij=2Γ+γc
which could be proved in quantum theory of damping.