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dc.contributor.authorYoo, Jason Jungwan
dc.contributor.authorWieghold, Sarah
dc.contributor.authorSponseller, Melany C.
dc.contributor.authorChua, Matthew R.
dc.contributor.authorBertram, Sophie N.
dc.contributor.authorHartono, Noor Titan Putri
dc.contributor.authorTresback, Jason S.
dc.contributor.authorHansen, Eric C.
dc.contributor.authorCorrea-Baena, Juan-Pablo
dc.contributor.authorBulovic, Vladimir
dc.contributor.authorBuonassisi, Tonio
dc.contributor.authorShin, Seong Sik
dc.contributor.authorBawendi, Moungi G.
dc.date.accessioned2020-04-24T19:42:56Z
dc.date.available2020-04-24T19:42:56Z
dc.date.issued2019-06
dc.date.submitted2019-03
dc.identifier.issn1754-5692
dc.identifier.issn1754-5706
dc.identifier.urihttps://hdl.handle.net/1721.1/124871
dc.description.abstractStabilization of the crystal phase of inorganic/organic lead halide perovskites is critical for their high performance optoelectronic devices. However, due to the highly ionic nature of perovskite crystals, even phase stabilized polycrystalline perovskites can undergo undesirable phase transitions when exposed to a destabilizing environment. While various surface passivating agents have been developed to improve the device performance of perovskite solar cells, conventional deposition methods using a protic polar solvent, mainly isopropyl alcohol (IPA), results in a destabilization of the underlying perovskite layer and an undesirable degradation of device properties. We demonstrate the hidden role of IPA in surface treatments and develop a strategy in which the passivating agent is deposited without destabilizing the high quality perovskite underlayer. This strategy maximizes and stabilizes device performance by suppressing the formation of the perovskite δ-phase and amorphous phase during surface treatment, which is observed using conventional methods. Our strategy also effectively passivates surface and grain boundary defects, minimizing non-radiative recombination sites, and preventing carrier quenching at the perovskite interface. This results in an open-circuit-voltage loss of only ∼340 mV, a champion device with a power conversion efficiency of 23.4% from a reverse current–voltage scan, a device with a record certified stabilized PCE of 22.6%, and enhanced operational stability. In addition, our perovskite solar cell exhibits an electroluminescence external quantum efficiency up to 8.9%. ©2019en_US
dc.description.sponsorshipInstitute for Soldier Nanotechnology (Grant W911NF-13-D-0001)en_US
dc.description.sponsorshipNASA (Grant NNX16AM70H)en_US
dc.description.sponsorshipDOE Division of Materials Sciences and Engineering (Award DE-FG02-07ER46454)en_US
dc.description.sponsorshipNSF (Grant CBET-1605495)en_US
dc.publisherRoyal Society of Chemistry (RSC)en_US
dc.relation.isversionof10.1039/c9ee00751ben_US
dc.rightsCreative Commons Attribution Noncommercial 3.0 unported licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc/3.0/en_US
dc.sourceRoyal Society of Chemistry (RSC)en_US
dc.subjectRenewable Energy, Sustainability and the Environmenten_US
dc.subjectNuclear Energy and Engineeringen_US
dc.subjectPollutionen_US
dc.subjectEnvironmental Chemistryen_US
dc.titleAn interface stabilized perovskite solar cell with high stabilized efficiency and low voltage lossen_US
dc.typeArticleen_US
dc.identifier.citationYoo, Jason J. et al. "An interface stabilized perovskite solar cell with high stabilized efficiency and low voltage loss." Energy & Environmental Science, 12, 7 (June 2019): 2192--2199 © 2019 Royal Society of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.relation.journalEnergy & environmental scienceen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.date.submission2019-07-18T12:58:10Z
mit.journal.volume12en_US
mit.journal.issue7en_US
mit.metadata.statusComplete


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