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      A polymer tandem solar cell with 10.6% power conversion efficiency

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          Abstract

          An effective way to improve polymer solar cell efficiency is to use a tandem structure, as a broader part of the spectrum of solar radiation is used and the thermalization loss of photon energy is minimized. In the past, the lack of high-performance low-bandgap polymers was the major limiting factor for achieving high-performance tandem solar cell. Here we report the development of a high-performance low bandgap polymer (bandgap <1.4 eV), poly[2,7-(5,5-bis-(3,7-dimethyloctyl)-5H-dithieno[3,2-b:2′,3′-d]pyran)-alt-4,7-(5,6-difluoro-2,1,3-benzothia diazole)] with a bandgap of 1.38 eV, high mobility, deep highest occupied molecular orbital. As a result, a single-junction device shows high external quantum efficiency of >60% and spectral response that extends to 900 nm, with a power conversion efficiency of 7.9%. The polymer enables a solution processed tandem solar cell with certified 10.6% power conversion efficiency under standard reporting conditions (25 °C, 1,000 Wm −2, IEC 60904-3 global), which is the first certified polymer solar cell efficiency over 10%.

          Abstract

          Tandem solar cell structures combine high- and low-bandgap materials, allowing a broader spectral absorption of solar radiation. The authors report the synthesis of a high performance low-bandgap polymer which enables fabrication of a tandem solar cell with a certified power conversion efficiency of 10.6%.

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          Most cited references16

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          Simultaneous enhancement of open-circuit voltage, short-circuit current density, and fill factor in polymer solar cells.

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            Fluorine substituted conjugated polymer of medium band gap yields 7% efficiency in polymer-fullerene solar cells.

            Recent research advances on conjugated polymers for photovoltaic devices have focused on creating low band gap materials, but a suitable band gap is only one of many performance criteria required for a successful conjugated polymer. This work focuses on the design of two medium band gap (~2.0 eV) copolymers for use in photovoltaic cells which are designed to possess a high hole mobility and low highest occupied molecular orbital and lowest unoccupied molecular orbital energy levels. The resulting fluorinated polymer PBnDT-FTAZ exhibits efficiencies above 7% when blended with [6,6]-phenyl C(61)-butyric acid methyl ester in a typical bulk heterojunction, and efficiencies above 6% are still maintained at an active layer thicknesses of 1 μm. PBnDT-FTAZ outperforms poly(3-hexylthiophene), the current medium band gap polymer of choice, and thus is a viable candidate for use in highly efficient tandem cells. PBnDT-FTAZ also highlights other performance criteria which contribute to high photovoltaic efficiency, besides a low band gap.
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              Inverted polymer solar cells integrated with a low-temperature-annealed sol-gel-derived ZnO Film as an electron transport layer.

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                Author and article information

                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Pub. Group
                2041-1723
                05 February 2013
                : 4
                : 1446
                Affiliations
                [1 ]Department of Material Science and Engineering, University of California, Los Angeles , Los Angeles, California 90095, USA
                [2 ]Tsukuba Material Development Laboratory, Sumitomo Chemical Co., Ltd. 6 , Kitahara, Tsukuba City, Ibaraki 300-3294, Japan
                [3 ]National Renewable Energy Laboratory , Golden, Colorado 80401, USA
                [4 ]California NanoSystems Institute, University of California, Los Angeles , Los Angeles, California 90095, USA
                [5 ]These authors contributed equally to this work
                [6 ]Present address: Department of Mechanical Engineering, Oyama National College of Technology, 771 Nakakuki, Oyama 323-0806, Japan
                Author notes
                Article
                ncomms2411
                10.1038/ncomms2411
                3660643
                23385590
                85b50b99-05ab-406a-8c25-bcc946a192ed
                Copyright © 2013, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/

                History
                : 06 June 2012
                : 20 December 2012
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