Flexible Catalysis
Máté Weisz, Sergii Strelchuk
TL;DR
The paper introduces flexible catalysis, a generalization of quantum state catalysis where a set of catalyst states can be used such that catalysts may transform among themselves while enabling the desired transformation. It formalizes transformation theories (TTs) and catalytic classes, then specializes to multisets over groups to analyze how translation, torsion, and group structure affect catalytic power. The main results show that flexible catalysis strictly extends standard catalysis and multicopy in several quantum-information channels (notably LU and LOCC for extraction) while sometimes yielding no advantage in others (e.g., PM with finite flexibility). Across LOCC, LU, and PM, flexible catalysis provides a richer framework that can enable state transformations and extractions unattainable by traditional catalytic methods, with implications for resource theories and space-bounded quantum computation. The work also outlines several open questions and potential directions, including infinite-catalyst regimes and extensions to mixed states and additional channels.
Abstract
In quantum information and computation, a central challenge is to determine which quantum states can be transformed into one another under restricted sets of free operations. While many transformations are impossible directly, catalytic processes can enable otherwise forbidden conversions: an auxiliary quantum state (the catalyst) facilitates the transformation while remaining unchanged. In this work, we introduce flexible catalysis, a generalization in which the catalyst is allowed to transform into a different auxiliary state, provided it remains a valid catalyst. We show that this framework subsumes both standard catalytic and multicopy transformations, and we analyze its advantages across several classes of free operations. In particular, we prove that when the free operations are local unitaries or permutation matrices, flexible catalysis enables state extractions that are unattainable with standard catalysis alone.
