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Updated: Aug 6, 2026

Morphology Control for Fully Printable Organic–Inorganic Bulk-heterojunction Solar Cells Based on a Ti-alkoxide and Semiconducting Polymer
Published on: January 10, 2017
Thermally Activated "Cold" Holes Overcome Recombination Limits in Single-Component Organic Solar Cells With 15.6%
Haisheng Fang1, Linhu Liu2, Chengyi Xiao1
1Beijing Advanced Innovation Center for Soft Matter Science and Engineering & State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing, P. R. China.
Abstract:
Single-component organic solar cells (SCOSCs) based on double-cable conjugated polymers offer unparalleled morphological stability compared to bulk-heterojunction systems, but their efficiencies are severely bottlenecked by rapid geminate recombination. While the intrinsic donor-acceptor proximity in these polymers generates ultralong-lived charge-transfer (CT) states (>5 ns), these "cold" carriers are traditionally viewed as an energetic trap. Here, we report a thermodynamic strategy that converts this extended temporal window into a resource for thermally activated charge extraction. By engineering an interfacial energy ladder using a D18 polymer layer with a precise 0.02 eV highest occupied molecular orbital (HOMO) offset, we demonstrate that long-lived holes can be thermally promoted and selectively harvested. This active energy management mechanism successfully outcompetes non-radiative recombination loss, simultaneously elevating the open-circuit voltage, short-circuit current, and fill factor. Consequently, the optimized devices achieve a record-breaking power conversion efficiency of 15.65%. This work establishes a new paradigm for organic photovoltaics: demonstrating that long-lived excited states, previously considered a fundamental limitation, can be strategically harnessed as a thermal activation reservoir to overcome thermodynamic recombination losses.
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