Polymer donor–polymer acceptor (all-polymer) solar cells

Facchetti, Antonio

doi:10.1016/j.mattod.2013.04.005

Cited by 661 publications

(598 citation statements)

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“…[1][2][3][4] A range of new NFAs with different building blocks and geometrical dimensions has been designed to boost the power conversion efficiency (PCE) of OSCs. Among the highest performing NFAs, linear rod-like acceptor-donor-acceptor (A-D-A) structures incorporating fused ladder-type aromatics have attracted much interest.…”

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confidence: 99%

An Alkylated Indacenodithieno[3,2‐b]thiophene‐Based Nonfullerene Acceptor with High Crystallinity Exhibiting Single Junction Solar Cell Efficiencies Greater than 13% with Low Voltage Losses

et al. 2018

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The development of nonfullerene acceptors (NFAs), which are used to replace fullerene derivatives in organic solar cells (OSCs) due to their extended light absorption and tunable energy levels, has seen impressive progress in the past few years. [1][2][3][4] A range of new NFAs with different building blocks and geometrical dimensions has been designed to boost the power conversion efficiency (PCE) of OSCs. Among the highest performing NFAs, linear rod-like acceptor-donor-acceptor (A-D-A) structures incorporating fused ladder-type aromatics have attracted much interest. Common donor units include 4,9-dihydro-s-indaceno[1,2-b:5,6-b′]dithiophene (IDT) [5][6][7][8][9] and 6,12-dihydro-dithienoindeno [10][11][12][13][14][15][16][17][18] In both cases, the fused core facilitates π-electron delocalization and improves the π-π stacking between molecules, hence enhancing the intrinsic charge carrier mobility.In 2015, Zhan and coworkers reported a new NFA, 3,9-bis(2-methylene-(3-(1,1-dicyanomethylene)-indanone))-5,5,11,11--b′]dithiophene (ITIC) (Scheme 1), which is comprised an electron-donating IDTT-based core flanked by two electron-withdrawing units of 1,1-dicyanomethylene-3-indanone (IC), that exhibited a promising PCE of 6.8% at that time. [10] Since then, many strategies have been applied to modify the structure of ITIC in order to adjust the absorption spectra and energy levels to further improve the PCE, for example, by changing the side chains, [17,18] extending the conjugation length, [19][20][21][22] and substituting the end acceptor groups. [13][14][15][16] To date, a few systems based on these NFAs have achieved a PCE of over 10%. [5,[13][14][15]18,20,22] However, it is noticeable that in all cases these NFAs incorporate phenylalkyl or thienylalkyl side chains as the solubilizing groups on the fused core. These aryl-based side chains facilitate the synthesis of the IDTT core under Friedel-Crafts conditions via the formation of stable triaryl cations. However, since the nature of the side chains has a

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An Alkylated Indacenodithieno[3,2‐b]thiophene‐Based Nonfullerene Acceptor with High Crystallinity Exhibiting Single Junction Solar Cell Efficiencies Greater than 13% with Low Voltage Losses

et al. 2018

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“…1−3 In all-polymer BHJ solar cells (PSCs), both components of the active layer, i.e., electron donor and acceptor, are polymeric semiconductors which have potential advantages over the extensively studied donor polymer/acceptor fullerene composite solar cells. 4,5 Although significant progress has been made in the development of polymer/fullerene composite solar cell in terms of their high device efficiency over >9%, the use of fullerene acceptor (PC 61 BM and PC 71 BM) has some disadvantages like relatively weak absorption ability in the visible region, high cost of synthesis, and morphological instability of polymer/fullerene blend over time and temperature that limits the performance of the solar cell. 6−9 On the other hand, non-fullerene n-type polymeric acceptors have promising features such as high absorption in visible-infrared region, low cost, high thermal and photochemical stability, mechanical flexibility, and synthetic adaptability.…”

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confidence: 99%

Improved All-Polymer Solar Cell Performance of n-Type Naphthalene Diimide–Bithiophene P(NDI2OD-T2) Copolymer by Incorporation of Perylene Diimide as Coacceptor

et al. 2016

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Naphthalene diimide−bithiophene P(NDI2OD-T2) is a well-known donor−acceptor polymer, previously explored as n-type material in all-polymer solar cells (all-PSCs) and organic field effect transistor (OFETs) applications. The optical, bulk, electrochemical, and semiconducting properties of P(NDI2OD-T2) polymer were tuned via random incorporation of perylene diimide (PDI) as coacceptor with naphthalene diimide (NDI). Three random copolymers containing 2,2′-bithiophene as donor unit and varying compositions of naphthalene diimide (NDI) and perylene diimide (xPDI, x = 15, 30, and 50 mol % of PDI) as two mixed acceptors were synthesized by Stille coupling copolymerization. Proton NMR spectra recorded in CDCl 3 showed that the π−π stacking induced aggregation among the naphthalene units could be successfully disrupted by the random incorporation of bulky PDI units. The newly synthesized random copolymers were investigated as electron acceptors in BHJ all-PSCs, and their performance was compared with P(NDI2OD-T2) as reference polymer. An enhanced PCE of 5.03% was observed for BHJ all-PSCs (all-polymer solar cells) fabricated using NDI-Th-PDI30 as acceptor and PTB7-Th as donor, while the reference polymer blend with the same donor polymer exhibited PCE of 2.97% efficiency under similar conditions. SCLC bulk carrier mobility measured for blend devices showed improved charge mobility compared to reference polymer, with PTB7-Th:NDI-Th-PDI30 blend device exhibiting the high hole and electron mobility of 4.2 × 10 −4 and 1.5 × 10 −4 cm 2 /(V s), respectively. This work demonstrates the importance of molecular design via random copolymer strategy to control the bulk crystallinity, compatibility, blend morphology, and solar cell performance of n-type copolymers.

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“…1 for chemical structures) [32] and also extended the measurements to polymer:polymer blends, which have attracted significant attention recently due to much improved performance [33]. We employed P3HT∶F8TBT as an example for polymer:polymer blends.…”

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Temperature Dependence of Charge Carrier Generation in Organic Photovoltaics

et al. 2015

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The charge generation mechanism in organic photovoltaics is a fundamental yet heavily debated issue. All the generated charges recombine at the open-circuit voltage (VOC), so that investigation of recombined charges at VOC provides a unique approach to understanding charge generation. At low temperatures, we observe a decrease of VOC, which is attributed to reduced charge separation. Comparison between benchmark polymer: fullerene and polymer: polymer blends highlights the critical role of charge delocalization in charge separation and emphasizes the importance of entropy in charge generation.

Funding Agencies|National Basic Research Program of China [2015CB932200]; Natural Science Foundation of Jiangsu [BK20131413]; National Natural Science Foundation of China [11474164]; Swedish Research Council (VR); European Commission Marie Sklodowska-Curie actions; Swedish Energy Agency; Knut and AliceWallenberg foundation (KAW)

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Polymer donor–polymer acceptor (all-polymer) solar cells

Cited by 661 publications

References 93 publications

An Alkylated Indacenodithieno[3,2‐b]thiophene‐Based Nonfullerene Acceptor with High Crystallinity Exhibiting Single Junction Solar Cell Efficiencies Greater than 13% with Low Voltage Losses

An Alkylated Indacenodithieno[3,2‐b]thiophene‐Based Nonfullerene Acceptor with High Crystallinity Exhibiting Single Junction Solar Cell Efficiencies Greater than 13% with Low Voltage Losses

Improved All-Polymer Solar Cell Performance of n-Type Naphthalene Diimide–Bithiophene P(NDI2OD-T2) Copolymer by Incorporation of Perylene Diimide as Coacceptor

Temperature Dependence of Charge Carrier Generation in Organic Photovoltaics

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