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  • Li, Suhan  (4)
  • Zhang, Lianjie  (4)
  • 1
    In: Chinese Journal of Chemistry, Wiley, Vol. 36, No. 6 ( 2018-06), p. 495-501
    Abstract: In this work, a new A‐D‐A type nonfullerene small molecular acceptor SiIDT‐IC, with a fused‐ring silaindacenodithiophene (SiIDT) as D unit and 2‐(3‐oxo‐2,3‐dihydroinden‐1‐ylidene)malononitrile (INCN) as the end A unit, was design and synthesized. The SiIDT‐IC film shows absorption peak and edge at 695 and 733 nm, respectively. The HOMO and LUMO of SiIDT‐IC are of −5.47 and −3.78 eV, respectively. Compared with carbon‐bridging, the Si‐bridging can result in an upper‐lying LUMO level of an acceptor, which is benefit to achieve a higher open‐circuit voltage in polymer solar cells (PSCs). Complementary absorption and suitable energy level alignment between SiIDT‐IC and wide bandgap polymer donor PBDB‐T were found. For the PBDB‐T:SiIDT‐IC based inverted PSCs, a D/A ratio of 1: 1 was optimal to achieve a power conversion efficiency (PCE) of 7.27%. With thermal annealing (TA) of the blend film, a higher PCE of 8.16% could be realized due to increasing of both short‐circuit current density and fill factor. After the TA treatment, hole and electron mobilities were elevated to 3.42 × 10 −4 and 1.02 × 10 −4 cm 2 ·V −1 ·s −1 , respectively. The results suggest that the SiIDT, a Si‐bridged fused ring, is a valuable D unit to construct efficient nonfullerene acceptors for PSCs.
    Type of Medium: Online Resource
    ISSN: 1001-604X , 1614-7065
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2018
    detail.hit.zdb_id: 2144352-X
    SSG: 6,25
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  • 2
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2023
    In:  Energy & Environmental Science Vol. 16, No. 8 ( 2023), p. 3474-3485
    In: Energy & Environmental Science, Royal Society of Chemistry (RSC), Vol. 16, No. 8 ( 2023), p. 3474-3485
    Abstract: Solution processing of a bulk-heterojunction (BHJ) active layer in air with high relative humidity (RH) usually results in an inferior power conversion efficiency (PCE) of organic solar cells (OSCs). In this work, we demonstrate that such a challenge also exists in the state-of-the-art Y-series non-fullerene acceptor (NFA) based active layers such as PM6:Y6, PM6:L8-BO, and PM6:BTP-eC9. Moisture condensation during processing in high RH air should be the crucial factor that deteriorates the BHJ morphology. It was found that polymers PQSi705 and PTQ10, both comprising a quinoxaline–thiophene conjugated skeleton but with/without the 5% siloxane-terminated side chain, respectively, showed quite different humidity tolerance when casting the active layer. The PTQ10:Y6 active layer processed in a N 2 glovebox, air with 65% RH, and air with 93% RH exhibited PCEs of 14.82%, 13.43%, and 12.22%, respectively, whereas the resulting PQSi705:Y6 active layers displayed almost identical PCEs of ∼16.1%, suggesting that PQSi705 with a siloxane-terminated side chain decoration afforded high humidity endurance in air-processing. The robustness of the PQSi705:Y6 active layer against moisture or water was also supported by investigations such as long-term storage (306 days) of OSCs in air, water immersion on the active layer surface, and exposing the active layer to boiling water vapor, all showing superior PCE retention. With m -TEH as the NFA, the PQSi705: m -TEH active layers processed in the N 2 glovebox and 90% RH air exhibited almost identical PCEs of ∼18%. This is the highest efficiency so far reported for BHJ active layers fabricated in high RH air. Moreover, strong humidity tolerance in the air-processing was also achieved by more polymer donors or non-fullerene acceptors with siloxane-terminated side chains, suggesting certain universality. This work indicates that attaching a siloxane-terminated side chain on photoactive materials is a valuable chemical countermeasure to allow air-processing and withstand large variations in humidity.
    Type of Medium: Online Resource
    ISSN: 1754-5692 , 1754-5706
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 2439879-2
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  • 3
    In: Science China Chemistry, Springer Science and Business Media LLC, Vol. 64, No. 7 ( 2021-07), p. 1208-1218
    Type of Medium: Online Resource
    ISSN: 1674-7291 , 1869-1870
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2021
    detail.hit.zdb_id: 2546722-0
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  • 4
    In: Asian Journal of Organic Chemistry, Wiley, Vol. 7, No. 11 ( 2018-11), p. 2285-2293
    Abstract: Fused‐ring electron acceptors with acceptor‐donor‐acceptor (A‐D‐A) structure have become a hot research field in recent years. In this work, 2,1,3‐benzoxadiazole (BO) and 2,1,3‐benzoselenadiazole (BS) were introduced as π‐bridges between indaceno [1,2‐ b  : 5,6‐ b ′] dithiophene (IDT) cores and rhodanine termini for two nonfullerene acceptors IDTBOR and IDTBSR, to compare the structure‐property relationship. Inserting BO as the π‐bridge afforded IDTBOR with deeper LUMO and HOMO levels, whereas BS‐based IDTBSR possessed a smaller optical band gap. With PBDB‐T as polymer donor, IDTBOR‐ and IDTBSR‐based solar cells showed power conversion efficiencies of 7.74 and 6.95%, respectively. A higher open‐circuit voltage of 0.95 V was found for IDTBSR, owing to its up‐lying LUMO level. A higher short‐circuit current density of 15.98 mA/cm 2 and fill factor of 54.67% were achieved for IDTBOR, mainly because of the higher electron mobility and better structure order in the blend film. The results suggest that BO and BS units are valuable π‐bridges to construct efficient nonfullerene acceptors.
    Type of Medium: Online Resource
    ISSN: 2193-5807 , 2193-5815
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2018
    detail.hit.zdb_id: 2679333-7
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