Quantum Mechanics – Pure and Mixed Density Operators of a Schmidt Decomposition

density-operatorlinear algebraquantum mechanics

Suppose we have Hilbert space factorisable in to K subsystems
$$
\mathcal{H} = \mathcal{H}_1\otimes…\otimes\mathcal{H}_K
$$

in which we can express a pure state as the Schmidt decomposition
$$
|\psi\rangle=\displaystyle\sum_{i_1…i_K} c_{i_1…i_K}|i_1\rangle^{(1)}\otimes…\otimes|i_K\rangle^{(K)} = \displaystyle\sum_{i_1…i_K} c_{i_1…i_K}|i_1,…,i_K\rangle = \sum_I c_I |I\rangle
$$

The density operator for a pure state is then

$$
\rho = \sum_{I,J} c_{I}c_J^* |I\rangle\langle J| = \sum_{I,J} a_{IJ} |I\rangle\langle J|
$$

Suppose we then use our Schmidt decomposition to form the eigenstates

$$
|\psi_n\rangle = \sum_{I} c_{I,n}|I\rangle
$$

From the spectral theorem we can then form a mixed density operator as

$$
\rho = \sum_n \lambda_n |\psi_n\rangle\langle\psi_n| = \sum_{n,I} \lambda_n c_{I,n}c^*_{I,n} |I\rangle\langle I| = \sum_I b_I |I\rangle\langle I|
$$

Suppose now I consider the following composition in to a bipartite system
$$
\mathcal{H} = (\mathcal{H}_1\otimes…\otimes\mathcal{H}_{J-1})\otimes(\mathcal{H}_J\otimes…\otimes\mathcal{H}_K) = \mathcal{H}_A\otimes\mathcal{H}_B
$$

and I wish to consider a reduced density operator $\rho_A$, so I wish to write a general density operator as
$$
\rho_{AB} = \sum_{n,m} p_{nm} (\rho_A^n \otimes \rho_B^m)
$$

I would therefore like as general a choice of $\rho_A^n$,$\rho_B^m$ as possible and my intuition tells me to choose mixed density operators but how I am reading it, I would think the pure state density operators are "more general" for perhaps the very naive reason that there are more indices giving more possible choices?

Hopefully this clarifies my overall question: can either pure or mixed states be seen as "more general" than one or the other in some sense, specifically with how many coefficients there are for each state represented?

Best Answer

The Schmidt decomposition is just a confusing red herring here.

Given a basis $\lvert \psi_i\rangle$ of our Hilbert space, we may expand any vector in that basis, and hence a normalized state is $\lvert \psi\rangle = \sum c_i\lvert \psi_i\rangle$ with $\sum_i \lvert c_i\rvert^2 = 1$. So its associated density matrix is

$$ \rho_\psi = \lvert \psi\rangle\langle \psi\rvert = \sum_{i,j} c_ic^\ast_j \lvert \psi_i\rangle\langle \psi_i\rvert = \sum_{i,j} \rho_{ij}\lvert \psi_i\rangle\langle \psi_j\rvert. \tag{1}$$

You seem to be confused because this "looks" as if there is more freedom here in the $\rho_{ij}$ than in the $\lambda_i$ when we write a generic mixed state as $$ \rho = \sum_i \lambda_i \lvert \phi_i\rangle \langle \phi_i\rvert,\tag{2}$$ in terms of its eigenstates $\lvert \phi_i\rangle$ - after all there are $n^2$ of the $\rho_{ij}$ and only $n$ of the $\lambda_i$.

There are a few different ways to note that eq. (2) defines a more general class of operators than eq. (1):

  • Eq. (1) is an expansion of an arbitrary $\rho_\psi$ in a fixed basis $\lvert \psi_i\rangle$, something that works for all pure state matrices, while eq. (2) is specifically in the eigenbasis of $\rho$ - some other $\rho'$ would not have the same form in that same basis in general.

  • There isn't actually more independent parameters in eq. (1) because there are only as much of the $c_i$ as there are of the $\lambda_i$ in eq. (2), and while the $\lambda_i$ are constrained by $\sum_i \lambda_i = 1$, the $c_i$ are constrained by $\sum_i \lvert c_i\rvert^2 = 1$, so in both cases you essentially have $n-1$ independent parameters, but in eq. (2) you can additionally choose the basis differently and this gives you different $\rho$s (see the first point again), so there is more freedom in eq. (2) than in eq. (1).

  • A very "manifest" difference is simply that the pure state matrix fulfills the purity condition $\rho_\psi^2 = \rho_\psi$ by construction, while the mixed state matrix does not - it does not follow from eq. (2) and $\sum_i \lambda_i = 1$, while it does follow from eq. (1) and $\sum_i \lvert c_i\rvert^2 = 1$, so that alone shows you the second equation is more general.

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