Acta Phys. -Chim. Sin. ›› 2024, Vol. 40 ›› Issue (6): 2306050.doi: 10.3866/PKU.WHXB202306050
• REVIEW • Previous Articles Next Articles
Yawen Guo, Dawei Li, Yang Gao, Cuihong Li*(
)
Received:2023-06-28
Revised:2023-08-08
Accepted:2023-08-09
Published:2023-11-29
Contact:
Email: licuihong@bnu.edu.cn (Cuihong Li)
Supported by:Yawen Guo, Dawei Li, Yang Gao, Cuihong Li. Recent Progress on Stability of Organic Solar Cells Based on Non-Fullerene Acceptors[J]. Acta Phys. -Chim. Sin. 2024, 40(6), 2306050. doi: 10.3866/PKU.WHXB202306050
Fig 1
(a) Jablonski diagram of the PBDB-T: ITIC blend. Reproduced with permission 42. Copyright 2020, The Royal Society of Chemistry. (b) The primary photo-oxidation reaction sites of ITIC. Reproduced with permission 43. Copyright 2019, The Royal Society of Chemistry. (c) The DFT simulation of structures of O-IDTBR and IDFBR. Reproduced with permission 44. Copyright 2019, WILEY-VCH. (d) Photochemical reaction between ITIC and DIO additives under UV light, and product analysis by MALDI-TOF mass spectroscopy. Reproduced with permission 45. Copyright 2019, WILEY-VCH."
Fig 3
(a) A typical device structure of inverted OSCs. (b) Photographs of photo-oxidized ITIC and PC71BM pristine films upon different times of exposure. (c) MS spectra of pristine non-fullerene acceptor IT-4F, pristine acceptor moiety EG-2F and photo-degraded IT-4F. Reproduced with permission 60. Copyright 2019, The Royal Society of Chemistry. (d) MALDI-TOF mass spectra and (e) chemical structures of ZnO induced photo-degradation products of ITIC. Reproduced with permission 73. Copyright 2019, The Royal Society of Chemistry."
Fig 4
(a) Mass spectra and chemical structures of degradation products of acceptors and monoethanolamine. Reproduced with permission 59. Copyright 2020, American Chemical Society. (b) The amine group would attack the C=C linker of the A-D-A structure of NFAs through an addition reaction as a nucleophile. Reproduced with permission 57. Copyright 2020, Nature Publishing Group."
Fig 6
(a) Chemical structure of IDTT-CR; normalized UV-Vis absorption spectra of (b) IDTT-CR before and after adding ethanolamine in THF : H2O mixtures (96 : 4, v/v); (c) IDTT-CR in THF solutions in air under different irradiation times (100 mW∙cm−2). Reproduced with permission 94. Copyright 2021, The Royal Society of Chemistry."
Fig 7
(a) A new all-fused-ring NFA without the C=C linker (ITYM); (b) time-dependent absorption decays of ITYM and the control NFAs at the corresponding maximum absorptions upon the ethanolamine treatment; (c) AM1.5 G illumination. Reproduced with permission 95. Copyright 2021, Chinese Chemistry Society."
Fig 8
TEM images of (a) pristine PBTIBDTT: ITIC blend film, annealed for (b) 48 h and (c) 96 h; (d) pristine PBTIBDTT: oF-ITIC blend film, annealed for (e) 48 h and (f) 96 h; (g) pristine PBTIBDTT: mF-ITIC blend film, annealed for (h) 48 h and (i) 96 h. The insets show wider views of the films. The scale bar of the insets is 1 μm. Reproduced with permission 98. Copyright 2019, The Royal Society of Chemistry."
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