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      Efficient ternary blend all-polymer solar cells with a polythiophene derivative as a hole-cascade material

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          Abstract

          Efficient ternary all polymer solar cells (all-PSCs) based on PTB7-Th: PBDD-ff4T: N2200 were reported, where PTB7-Th and PBDD-ff4T were two polymer donors and N2200 was a polymer acceptor. The all-PSCs showed an optimized PCE of up to 7.2% which is superior to those of the binary all-PSCs based on PTB7-Th: N2200 and PBDD-ff4T: N2200.

          Abstract

          Ternary blending is one of the effective strategies to broaden the complementary absorption range and smooth the energy level at the donor/acceptor interface for achieving high efficiency bulk heterojunction (BHJ) polymer solar cells (PSCs). In this study, we report efficient ternary blend all-polymer solar cells (all-PSCs) with complementary absorption bands based on two polymer donors PTB7-Th and PBDD-ff4T and one polymer acceptor N2200. The polythiophene derivative PBDD-ff4T as a hole-cascade material plays a bridging role in energy levels between PTB7-Th and N2200, and thus provides more efficient channels for charge transfer. The ternary all-PSCs with 10 wt% PBDD-ff4T content show efficient photon harvesting, enhanced charge mobility and better active layer morphology due to the induced crystallization of PTB7-Th by the inserted PBDD-ff4T in the donor domains. As a result, the device without any extra treatments exhibits an optimized power conversion efficiency (PCE) of 7.2% with an open circuit voltage ( V oc) of 0.82 V, a short circuit current density ( J sc) of 15.7 mA cm −2, and a fill factor (FF) of 56%. While the PCEs are 5.9% and 4.2% for the all-PSCs based on the binary blends PTB7-Th: N2200 and PBDD-ff4T: N2200, respectively. This PCE of 7.2% is one of the highest values reported in the literature so far for ternary all-PSCs and polythiophene derivative-based all-PSCs.

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          Molecular design of photovoltaic materials for polymer solar cells: toward suitable electronic energy levels and broad absorption.

          Bulk heterojunction (BHJ) polymer solar cells (PSCs) sandwich a blend layer of conjugated polymer donor and fullerene derivative acceptor between a transparent ITO positive electrode and a low work function metal negative electrode. In comparison with traditional inorganic semiconductor solar cells, PSCs offer a simpler device structure, easier fabrication, lower cost, and lighter weight, and these structures can be fabricated into flexible devices. But currently the power conversion efficiency (PCE) of the PSCs is not sufficient for future commercialization. The polymer donors and fullerene derivative acceptors are the key photovoltaic materials that will need to be optimized for high-performance PSCs. In this Account, I discuss the basic requirements and scientific issues in the molecular design of high efficiency photovoltaic molecules. I also summarize recent progress in electronic energy level engineering and absorption spectral broadening of the donor and acceptor photovoltaic materials by my research group and others. For high-efficiency conjugated polymer donors, key requirements are a narrower energy bandgap (E(g)) and broad absorption, relatively lower-lying HOMO (the highest occupied molecular orbital) level, and higher hole mobility. There are three strategies to meet these requirements: D-A copolymerization for narrower E(g) and lower-lying HOMO, substitution with electron-withdrawing groups for lower-lying HOMO, and two-dimensional conjugation for broad absorption and higher hole mobility. Moreover, better main chain planarity and less side chain steric hindrance could strengthen π-π stacking and increase hole mobility. Furthermore, the molecular weight of the polymers also influences their photovoltaic performance. To produce high efficiency photovoltaic polymers, researchers should attempt to increase molecular weight while maintaining solubility. High-efficiency D-A copolymers have been obtained by using benzodithiophene (BDT), dithienosilole (DTS), or indacenodithiophene (IDT) donor unit and benzothiadiazole (BT), thienopyrrole-dione (TPD), or thiazolothiazole (TTz) acceptor units. The BDT unit with two thienyl conjugated side chains is a highly promising unit in constructing high-efficiency copolymer donor materials. The electron-withdrawing groups of ester, ketone, fluorine, or sulfonyl can effectively tune the HOMO energy levels downward. To improve the performance of fullerene derivative acceptors, researchers will need to strengthen absorption in the visible spectrum, upshift the LUMO (the lowest unoccupied molecular orbital) energy level, and increase the electron mobility. [6,6]-Phenyl-C(71)-butyric acid methyl ester (PC(70)BM) is superior to [6,6]-phenyl-C(61)-butyric acid methyl ester (PCBM) because C(70) absorbs visible light more efficiently. Indene-C(60) bisadduct (ICBA) and Indene-C(70) bisadduct (IC(70)BA) show 0.17 and 0.19 eV higher LUMO energy levels, respectively, than PCBM, due to the electron-rich character of indene and the effect of bisadduct. ICBA and IC(70)BA are excellent acceptors for the P3HT-based PSCs.
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            Efficient organic solar cells processed from hydrocarbon solvents

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              Recent Advances in Bulk Heterojunction Polymer Solar Cells.

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                Author and article information

                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                2016
                2016
                : 4
                : 38
                : 14752-14760
                Affiliations
                [1 ]Laboratory of Advanced Optoelectronic Materials
                [2 ]College of Chemistry
                [3 ]Chemical Engineering and Materials Science
                [4 ]Soochow University
                [5 ]Suzhou 215123
                Article
                10.1039/C6TA05932E
                53c5ca8f-8c16-4e89-af55-9b20b0e51e3d
                © 2016
                History

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