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Updated: Jul 8, 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
"Steric-Locking" Polymer Acceptor Enabled 20.53% Efficiency With Suppressed Energetic Disorder and Enhanced
Yanna Sun1, Huanhuan Gao2, Yuanyuan Kan1
1Shandong Provincial Key Laboratory for Science of Material Creation and Energy Conversion, Science Center for Material Creation and Energy Conversion, Institute of Frontier Chemistry, School of Chemistry and Chemical Engineering, Shandong University, Qingdao, China.
None:
The realization of high-performance organic photovoltaics via environmentally benign manufacturing is pivotal for sustainable energy. While all-polymer solar cells (all-PSCs) offer superior stability and mechanical resilience, achieving high efficiencies in nonhalogenated green solvents remains a formidable challenge. Here, we report a "steric-locking" strategy for polymer acceptor design that enables a record-breaking power conversion efficiency of 20.53% (certified 19.79%) in o-xylene-processed all-PSCs. The introduction of a steric-locking guest polymer acceptor (PY-IDT) into the PM6:PYF-T-o host matrix profoundly regulates the crystallization kinetics and suppresses the excessive self-aggregation of the host acceptor. This molecular-level structural refinement significantly reduces energetic disorder and minimizes non-radiative voltage loss. Consequently, the suppressed energetic disorder and refined nanostructured domains yielded a concurrent leap in open-circuit voltage (0.942 V) and fill factor (82.11%). Furthermore, the steric-locked morphology demonstrates exceptional mechanical robustness, maintaining 92.6% of its initial efficiency after 1000 bending cycles. This work establishes a new efficiency benchmark and provides a universal chemical framework for developing high-performance, sustainable, and flexible optoelectronics.
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