Fidelity of quantum states 2026-10-14
For density operators on the same finite-dimensional Hilbert space, quantum fidelity measures how close their quantum states are. This article uses the unsquared convention:Each square root is the positive square root of an operator, and is the trace norm. Quantum fidelity is symmetric in its inputs; it is one exactly when , and zero exactly when , meaning that the support of a positive operator for one state is orthogonal to that for the other. Larger quantum fidelity means greater similarity. The separate squared quantum fidelity is . [ref]
https://jhwatrous.github.io/TQI.3.pdf#page=16. Watrous, The Theory of Quantum Information, Definition 3.11 and Proposition 3.12
For two normalized pure states, quantum fidelity is the magnitude of their inner product, . Thus compared with itself has , while and have . For , comparison with gives , , and trace distance by the pure-state trace distance and fidelity identity.
Why compare density operators rather than their entries? A change of coordinates should not make the same physical preparations look more or less alike. Unitary invariance of trace distance and fidelity makes quantum fidelity independent of a common basis choice. Multiplying a pure state vector by a global phase leaves its density operator unchanged, so its quantum fidelity with the original state is one. These features make quantum fidelity useful for checking whether quantum channels, state preparations, and Schumacher compression preserve a target quantum state.
The connection to Uhlmann's theorem supplies another beautiful interpretation: quantum fidelity is the largest absolute inner product between pure vectors obtained from a purification of a density operator for each state, using a sufficiently large common reference space. Uhlmann's 1976 paper extended transition probability to algebraic states, including those of a C-star algebra; for density operators its transition probability corresponds to our squared quantum fidelity. The measurement characterization of quantum fidelity gives a complementary description directly in terms of observable outcome statistics. [ref]
https://www.physik.uni-leipzig.de/~uhlmann/PDF/Uh76a.pdf. Uhlmann, The transition probability in the state space of a star-algebra, Reports on Mathematical Physics 9, 273–279, 1976
Past exam of the mathematics course of the University of Cambridge 2005 iii Paper 58 4 ii Solution Created 2026-10-03 Updated 2026-10-14
Write and . A pure-state density matrix is a rank-one orthogonal projector, so andTaking its square root and trace yields the unsquared quantum fidelityUse unitary invariance of trace distance and fidelity to choose a basis of the span of the two quantum states in which and , with and . Choosing state-vector phases to make the coefficients nonnegative does not change either density matrix. On that span,Its eigenvalues are and , with zero eigenvalues on the orthogonal complement. The positive square root of therefore has two eigenvalues , so the trace distance is . Thus the pure-state trace distance and fidelity identity isIdentical pure quantum states give ; orthogonal pure quantum states give . If the span is one-dimensional, the identical-state result follows directly, so no second basis vector is required. This formula uses the unsquared fidelity convention in the paper; if fidelity denotes squared overlap instead, the square inside the formula is omitted.
Past exam of the mathematics course of the University of Cambridge 2005 iii Paper 58 4 i Solution Created 2026-10-03 Updated 2026-10-14
For a positive operator , the spectral theorem writes with . Hence its unique positive square root of an operator is . Conjugating this spectral decomposition shows for a unitary operator .
Let and . Then and . The square-root covariance and the cyclic property of the trace giveFor the quantum fidelity, covariance first gives . ThereforeApply the same square-root identity and the cyclic property of the trace to obtainThus unitary invariance of trace distance and fidelity givesThe same acts on both quantum states: these quantities depend on the relative distinguishability of the quantum states, not on a choice of basis.