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Phys. Rev. A 63, 042307 (2001) [29 pages]

Theory of decoherence-free fault-tolerant universal quantum computation

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J. Kempe1,3,4, D. Bacon1,2, D. A. Lidar1,*, and K. B. Whaley1
1Department of Chemistry, University of California, Berkeley, California 94720
2Department of Physics, University of California, Berkeley, California 94720
3Department of Mathematics, University of California, Berkeley, California 94720
4École Nationale Superieure des Télécommunications, Paris, France

Received 19 April 2000; revised 5 September 2000; published 20 March 2001

Universal quantum computation on decoherence-free subspaces and subsystems (DFSs) is examined with particular emphasis on using only physically relevant interactions. A necessary and sufficient condition for the existence of decoherence-free (noiseless) subsystems in the Markovian regime is derived here for the first time. A stabilizer formalism for DFSs is then developed which allows for the explicit understanding of these in their dual role as quantum error correcting codes. Conditions for the existence of Hamiltonians whose induced evolution always preserves a DFS are derived within this stabilizer formalism. Two possible collective decoherence mechanisms arising from permutation symmetries of the system-bath coupling are examined within this framework. It is shown that in both cases universal quantum computation which always preserves the DFS (natural fault-tolerant computation) can be performed using only two-body interactions. This is in marked contrast to standard error correcting codes, where all known constructions using one- or two-body interactions must leave the code space during the on-time of the fault-tolerant gates. A further consequence of our universality construction is that a single exchange Hamiltonian can be used to perform universal quantum computation on an encoded space whose asymptotic coding efficiency is unity. The exchange Hamiltonian, which is naturally present in many quantum systems, is thus asymptotically universal.

© 2001 The American Physical Society

URL:
http://link.aps.org/doi/10.1103/PhysRevA.63.042307
DOI:
10.1103/PhysRevA.63.042307
PACS:
03.67.Lx, 03.65.Ta, 03.65.Fd, 89.70.+c

*Present address: Chemistry Department, University of Toronto, 80 St. George St., Toronto, Ontario, Canada M55 3H6.