Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep34319
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dc.titleEfficiency enhancement of hybrid perovskite solar cells with MEH-PPV hole-transporting layers
dc.contributor.authorChen, H.-W
dc.contributor.authorHuang, T.-Y
dc.contributor.authorChang, T.-H
dc.contributor.authorSanehira, Y
dc.contributor.authorKung, C.-W
dc.contributor.authorChu, C.-W
dc.contributor.authorIkegami, M
dc.contributor.authorMiyasaka, T
dc.contributor.authorHo, K.-C
dc.date.accessioned2020-10-31T11:25:49Z
dc.date.available2020-10-31T11:25:49Z
dc.date.issued2016
dc.identifier.citationChen, H.-W, Huang, T.-Y, Chang, T.-H, Sanehira, Y, Kung, C.-W, Chu, C.-W, Ikegami, M, Miyasaka, T, Ho, K.-C (2016). Efficiency enhancement of hybrid perovskite solar cells with MEH-PPV hole-transporting layers. Scientific Reports 6 : 34319. ScholarBank@NUS Repository. https://doi.org/10.1038/srep34319
dc.identifier.issn2045-2322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/182422
dc.description.abstractIn this study, hybrid perovskite solar cells are fabricated using poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV) and poly(3-hexylthiophene-2,5-diyl) (P3HT) as dopant-free hole-transporting materials (HTMs), and two solution processes (one- and two-step methods, respectively) for preparing methylammonium lead iodide perovskite. By optimizing the concentrations and solvents of MEH-PPV solutions, a power conversion efficiency of 9.65% with hysteresis-less performance is achieved, while the device with 2,2?,7,7?-tetrakis(N,N-di-p-methoxyphenylamine)-9,9?spirobifluorene (Spiro-OMeTAD) doped with lithium salts and tert-butylpyridine (TBP) exhibits an efficiency of 13.38%. This result shows that non-doped MEH-PPV is a suitable, low-cost HTM for efficient polymer-based perovskite solar cells. The effect of different morphologies of methylammonium lead iodide perovskite on conversion efficiency is also investigated by incident photon-to-electron conversion efficiency (IPCE) curves and electrochemical impedance spectroscopy (EIS). © The Author(s) 2016.
dc.publisherNature Publishing Group
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1038/srep34319
dc.description.sourcetitleScientific Reports
dc.description.volume6
dc.description.page34319
dc.published.statepublished
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