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dc.contributor.authorCorrea, LA
dc.contributor.authorXu, B
dc.contributor.authorMorris, B
dc.contributor.authorAdesso, G
dc.date.accessioned2019-09-17T11:13:07Z
dc.date.issued2019-09-06
dc.description.abstractThe reaction-coordinate mapping is a useful technique to study complex quantum dissipative dynamics into structured environments. In essence, it aims to mimic the original problem by means of an 'augmented system', which includes a suitably chosen collective environmental coordinate---the 'reaction coordinate'. This composite then couples to a simpler 'residual reservoir' with short-lived correlations. If, in addition, the residual coupling is weak, a simple quantum master equation can be rigorously applied to the augmented system, and the solution of the original problem just follows from tracing out the reaction coordinate. But, what if the residual dissipation is strong? Here we consider an exactly solvable model for heat transport---a two-node linear "quantum wire" connecting two baths at different temperatures. We allow for a structured spectral density at the interface with one of the reservoirs and perform the reaction-coordinate mapping, writing a perturbative master equation for the augmented system. We find that: (a) strikingly, the stationary state of the original problem can be reproduced accurately by a weak-coupling treatment even when the residual dissipation on the augmented system is very strong; (b) the agreement holds throughout the entire dynamics under large residual dissipation in the overdamped regime; (c) and that such master equation can grossly overestimate the stationary heat current across the wire, even when its non-equilibrium steady state is captured faithfully. These observations can be crucial when using the reaction-coordinate mapping to study the largely unexplored strong-coupling regime in quantum thermodynamics.en_GB
dc.description.sponsorshipEuropean Research Council (ERC)en_GB
dc.description.sponsorshipLondon Mathematical Societyen_GB
dc.description.sponsorshipUS National Science Foundationen_GB
dc.identifier.citationVol. 151 (9), article 094107en_GB
dc.identifier.doi10.1063/1.5114690
dc.identifier.grantnumber637352en_GB
dc.identifier.grantnumber31826en_GB
dc.identifier.grantnumberNSF PHY1748958en_GB
dc.identifier.urihttp://hdl.handle.net/10871/38776
dc.language.isoenen_GB
dc.publisherAIP Publishingen_GB
dc.rights© 2019 Author(s). Published under license by AIP Publishingen_GB
dc.titlePushing the limits of the reaction-coordinate mappingen_GB
dc.typeArticleen_GB
dc.date.available2019-09-17T11:13:07Z
dc.descriptionThis is the author accepted manuscript. The final version is available from AIP Publishing via the DOI in this recorden_GB
dc.identifier.eissn1089-7690
dc.identifier.journalJournal of Chemical Physicsen_GB
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserveden_GB
dcterms.dateAccepted2019-08-11
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2019-08-11
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2019-09-17T11:10:44Z
refterms.versionFCDAM
refterms.dateFOA2019-09-17T11:13:10Z
refterms.panelBen_GB


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