2021
DOI: 10.1002/adfm.202102413
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A Chlorinated Donor Polymer Achieving High‐Performance Organic Solar Cells with a Wide Range of Polymer Molecular Weight

Abstract: In the field of non‐fullerene organic solar cells (OSCs), compared to the rapid development of non‐fullerene acceptors, the progress of high‐performance donor polymers is relatively slow. The property and performance of donor polymers in OSCs are often sensitive to the molecular weight of the polymers. In this study, a chlorinated donor polymer named D18‐Cl is reported, which can achieve high performance with a wide range of polymer molecular weight. The devices based on D18‐Cl show a higher open‐circuit volta… Show more

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Cited by 73 publications
(73 citation statements)
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“…The neat D18-Cl film shows a strong (010) 𝜋-𝜋 stacking peak in the OOP direction at q = 1.63 Å −1 and a (100) lamellar peak in the IP direction at q = 0.32 Å −1 , suggesting its preferential face-on orientation. [20] The neat N3 film also adopts the dominant face-on orientation with an obvious 𝜋-𝜋 stacking peak in the OOP direction at q = 1.73 Å −1 and a (100) lamellar peak in the IP direction at q = 0.30 Å −1 . [12] To explore the vertical phase separation differences among the three blend systems, angle-dependent GIWAXS measurement was performed with the incident angle varied from 0.08°to 0.16°(Figure 4a and Figure S7, Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The neat D18-Cl film shows a strong (010) 𝜋-𝜋 stacking peak in the OOP direction at q = 1.63 Å −1 and a (100) lamellar peak in the IP direction at q = 0.32 Å −1 , suggesting its preferential face-on orientation. [20] The neat N3 film also adopts the dominant face-on orientation with an obvious 𝜋-𝜋 stacking peak in the OOP direction at q = 1.73 Å −1 and a (100) lamellar peak in the IP direction at q = 0.30 Å −1 . [12] To explore the vertical phase separation differences among the three blend systems, angle-dependent GIWAXS measurement was performed with the incident angle varied from 0.08°to 0.16°(Figure 4a and Figure S7, Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…The neat D18‐Cl film shows a strong (010) π – π stacking peak in the OOP direction at q = 1.63 Å −1 and a (100) lamellar peak in the IP direction at q = 0.32 Å −1 , suggesting its preferential face‐on orientation. [ 20 ] The neat N3 film also adopts the dominant face‐on orientation with an obvious π – π stacking peak in the OOP direction at q = 1.73 Å −1 and a (100) lamellar peak in the IP direction at q = 0.30 Å −1 . [ 12 ]…”
Section: Resultsmentioning
confidence: 99%
“…Herein, we introduced the volatile solid additive DIB into a binary system comprised of a polymer donor, D18‐Cl, [ 54 ] and a small‐molecule acceptor, L8‐BO. [ 12 ] The chemical structures of D18‐Cl, L8‐BO, and DIB are shown in Figure a.…”
Section: Introductionmentioning
confidence: 99%
“…The previously reported HOMO/LUMO of D18‐Cl and L8‐BO are summarized in Figure S1 (Supporting Information). [ 12,54 ] The donor D18‐Cl has a deep HOMO energy level of −5.49 eV, whereas the acceptor, L8‐BO, as a Y6 derivative, adopts a relatively shallower LUMO energy level of −3.90 eV. [ 15 ] Therefore, the binary D18‐Cl/L8‐BO system has a higher theoretical V OC limit than conventional Y6‐based binary systems.…”
Section: Introductionmentioning
confidence: 99%
“…Dithieno[3',2':3,4;2'',3'':5,6]benzo[1,2-c][1,2,5]thiadiazole (DTBT) is an outstanding electron-withdrawing acceptor unit. Due to its electron-deficiency and good planarity, it has been widely adopted in high-performance donors such as D18, [30][31][32] but the incorporation of the DTBT unit in UFAs has not been reported yet. We believe that the DTBT unit would be a promising candidate in the design of UFAs.…”
Section: Introductionmentioning
confidence: 99%