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Bilayer–Ternary Polymer Solar Cells Fabricated Using Spontaneous Spreading on Water.

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Title: Bilayer–Ternary Polymer Solar Cells Fabricated Using Spontaneous Spreading on Water.
Authors: Colberts, Fallon J. M.1, Wienk, Martijn M.1, Heuvel, Ruurd1, Li, Weiwei2, Le Corre, Vincent M.3, Koster, L. Jan Anton3, Janssen, René A. J.1,4 r.a.j.janssen@tue.nl
Source: Advanced Energy Materials. Nov2018, Vol. 8 Issue 32, pN.PAG-N.PAG. 1p.
Subject Terms: *Solar cells, *Ternary system, *Organic compounds, *Electric fields, *Electron transport
Abstract: A new method is presented to fabricate bilayer organic solar cells via sequential deposition of bulk‐heterojunction layers obtained using spontaneous spreading of polymer–fullerene blends on a water surface. Using two layers of a small bandgap diketopyrrolopyrrole polymer–fullerene blend, a small improvement in power conversion efficiency (PCE) from 4.9% to 5.1% is obtained compared to spin‐coated devices of similar thickness. Next, bilayer–ternary cells are fabricated by first spin coating a wide bandgap thiophene polymer–fullerene blend, followed by depositing a small bandgap diketopyrrolopyrrole polymer–fullerene layer by transfer from a water surface. These novel bilayer–ternary devices feature a PCE of 5.9%, higher than that of the individual layers. Remarkable, external quantum efficiencies (EQEs) over 100% are measured for the wide bandgap layer under near‐infrared bias light illumination. Drift‐diffusion calculations confirm that near‐infrared bias illumination can result in a significant increase in EQE as a result of a change in the internal electric field in the device, but cannot yet account for the magnitude of the effect. The experimental results indicate that the high EQEs over 100% under bias illumination are related to a barrier for electron transport over the interface between the two blends. Polymer–fullerene bulk‐heterojunction layers made by spontaneous spreading on a water surface and subsequently transferred to glass substrates are used to fabricate unique bilayer–ternary solar cells that possess two complementary absorber layers stacked on top of each other. Surprisingly, these novel devices can exhibit external quantum efficiencies exceeding 100% under bias illumination. [ABSTRACT FROM AUTHOR]
Database: Energy & Power Source
Description
Abstract:A new method is presented to fabricate bilayer organic solar cells via sequential deposition of bulk‐heterojunction layers obtained using spontaneous spreading of polymer–fullerene blends on a water surface. Using two layers of a small bandgap diketopyrrolopyrrole polymer–fullerene blend, a small improvement in power conversion efficiency (PCE) from 4.9% to 5.1% is obtained compared to spin‐coated devices of similar thickness. Next, bilayer–ternary cells are fabricated by first spin coating a wide bandgap thiophene polymer–fullerene blend, followed by depositing a small bandgap diketopyrrolopyrrole polymer–fullerene layer by transfer from a water surface. These novel bilayer–ternary devices feature a PCE of 5.9%, higher than that of the individual layers. Remarkable, external quantum efficiencies (EQEs) over 100% are measured for the wide bandgap layer under near‐infrared bias light illumination. Drift‐diffusion calculations confirm that near‐infrared bias illumination can result in a significant increase in EQE as a result of a change in the internal electric field in the device, but cannot yet account for the magnitude of the effect. The experimental results indicate that the high EQEs over 100% under bias illumination are related to a barrier for electron transport over the interface between the two blends. Polymer–fullerene bulk‐heterojunction layers made by spontaneous spreading on a water surface and subsequently transferred to glass substrates are used to fabricate unique bilayer–ternary solar cells that possess two complementary absorber layers stacked on top of each other. Surprisingly, these novel devices can exhibit external quantum efficiencies exceeding 100% under bias illumination. [ABSTRACT FROM AUTHOR]
ISSN:16146832
DOI:10.1002/aenm.201802197