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Suppressed Degradation Process of PBDB-TF-T1:BTP-4F-12-Based Organic Solar Cells with Solid Additive Atums Green

  • Technische Universität München
  • Chinese Academy of Sciences
  • Humanoid Technologies Lab (H2T)
  • Deutsches Elektronen-Synchrotron (DESY)

Publikation: Beitrag in FachzeitschriftArtikelBegutachtung

3 Zitate (Scopus)

Abstract

Solid additives have garnered significant attention due to their numerous advantages over liquid additives. This study explores the potential of the green-fluorescent conjugated polymer denoted Atums Green as a solid additive in green-solvent-based PBDB-TF-T1:BTP-4F-12 solar cells. Even tiny amounts of Atums Green doping significantly improve the device performance. For the reference solar cell without any additive, we find that device degradation is not caused by chemical redox reactions but by changes in crystallinity and microstructure evolution during aging in air under illumination. Operando GIWAXS and GISAXS are used to investigate the structure evolution. We discover a four-stage degradation process for the reference cell. In general, the lattice spacing and crystallite coherence length decrease, while the domain sizes increase, which causes the loss of shirt-circuit current JSC and fill factor FF. Furthermore, a decomposition component is detected in GIWAXS and GISAXS, corresponding to the loss of the open-circuit voltage VOC. Atums Green doping effectively suppresses the evolution of crystallinity and domain sizes as well as the continuous decomposition, thereby enhancing the device stability under illumination in air. This finding reveals the kinetic degradation process of organic solar cells, establishes a correlation between the morphological properties and device performance, and further demonstrates the promising potential of Atums Green doping in organic solar cells.

OriginalspracheEnglisch
Seiten (von - bis)9475-9484
Seitenumfang10
FachzeitschriftACS Applied Materials and Interfaces
Jahrgang17
Ausgabenummer6
DOIs
PublikationsstatusVeröffentlicht - 12 Feb. 2025

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