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Simultaneously Enhancing Exciton/Charge Transport in Organic Solar Cells by an Organoboron Additive.
Lu, Heng; Chen, Kai; Bobba, Raja Sekhar; Shi, Jiangjian; Li, Mengyang; Wang, Yilin; Xue, Jingwei; Xue, Peiyao; Zheng, Xiaojian; Thorn, Karen E; Wagner, Isabella; Lin, Chao-Yang; Song, Yin; Ma, Wei; Tang, Zheng; Meng, Qingbo; Qiao, Quinn; Hodgkiss, Justin M; Zhan, Xiaowei.
Affiliation
  • Lu H; School of Materials Science and Engineering, Peking University, Beijing, 100871, China.
  • Chen K; MacDiarmid Institute for Advanced Materials and Nanotechnology, School of Chemical and Physical Sciences, Victoria University of Wellington, Wellington, 6010, New Zealand.
  • Bobba RS; Robinson Research Institute, Faculty of Engineering, Victoria University of Wellington, Wellington, 6010, New Zealand.
  • Shi J; Department of Mechanical and Aerospace Engineering, Syracuse University, Syracuse, NY, 13244, USA.
  • Li M; CAS Key Laboratory for Renewable Energy, Beijing Key Laboratory for New Energy Materials and Devices, Institute of Physics, Chinese Academy of Sciences, Beijing, 100190, China.
  • Wang Y; Center for Advanced Low-Dimension Materials, State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai, 201620, China.
  • Xue J; State Key Laboratory for Mechanical Behavior of Materials, Xi'an Jiaotong University, Xi'an, 710049, China.
  • Xue P; State Key Laboratory for Mechanical Behavior of Materials, Xi'an Jiaotong University, Xi'an, 710049, China.
  • Zheng X; School of Materials Science and Engineering, Peking University, Beijing, 100871, China.
  • Thorn KE; School of Materials Science and Engineering, Peking University, Beijing, 100871, China.
  • Wagner I; MacDiarmid Institute for Advanced Materials and Nanotechnology, School of Chemical and Physical Sciences, Victoria University of Wellington, Wellington, 6010, New Zealand.
  • Lin CY; MacDiarmid Institute for Advanced Materials and Nanotechnology, School of Chemical and Physical Sciences, Victoria University of Wellington, Wellington, 6010, New Zealand.
  • Song Y; Robinson Research Institute, Faculty of Engineering, Victoria University of Wellington, Wellington, 6010, New Zealand.
  • Ma W; School of Optics and Photonics, Beijing Institute of Technology, Beijing, 100081, China.
  • Tang Z; State Key Laboratory for Mechanical Behavior of Materials, Xi'an Jiaotong University, Xi'an, 710049, China.
  • Meng Q; Center for Advanced Low-Dimension Materials, State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Donghua University, Shanghai, 201620, China.
  • Qiao Q; CAS Key Laboratory for Renewable Energy, Beijing Key Laboratory for New Energy Materials and Devices, Institute of Physics, Chinese Academy of Sciences, Beijing, 100190, China.
  • Hodgkiss JM; Department of Mechanical and Aerospace Engineering, Syracuse University, Syracuse, NY, 13244, USA.
  • Zhan X; MacDiarmid Institute for Advanced Materials and Nanotechnology, School of Chemical and Physical Sciences, Victoria University of Wellington, Wellington, 6010, New Zealand.
Adv Mater ; 34(42): e2205926, 2022 Oct.
Article in En | MEDLINE | ID: mdl-36027579
ABSTRACT
Efficient exciton diffusion and charge transport play a vital role in advancing the power conversion efficiency (PCE) of organic solar cells (OSCs). Here, a facile strategy is presented to simultaneously enhance exciton/charge transport of the widely studied PM6Y6-based OSCs by employing highly emissive trans-bis(dimesitylboron)stilbene (BBS) as a solid additive. BBS transforms the emissive sites from a more H-type aggregate into a more J-type aggregate, which benefits the resonance energy transfer for PM6 exciton diffusion and energy transfer from PM6 to Y6. Transient gated photoluminescence spectroscopy measurements indicate that addition of BBS improves the exciton diffusion coefficient of PM6 and the dissociation of PM6 excitons in the PM6Y6BBS film. Transient absorption spectroscopy measurements confirm faster charge generation in PM6Y6BBS. Moreover, BBS helps improve Y6 crystallization, and current-sensing atomic force microscopy characterization reveals an improved charge-carrier diffusion length in PM6Y6BBS. Owing to the enhanced exciton diffusion, exciton dissociation, charge generation, and charge transport, as well as reduced charge recombination and energy loss, a higher PCE of 17.6% with simultaneously improved open-circuit voltage, short-circuit current density, and fill factor is achieved for the PM6Y6BBS devices compared to the devices without BBS (16.2%).
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Adv Mater Journal subject: BIOFISICA / QUIMICA Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Adv Mater Journal subject: BIOFISICA / QUIMICA Year: 2022 Document type: Article Affiliation country: