Dual?Fibril Network Engineering for Scalable and Sustainable Organic Photovoltaics

By employing a multifunctional additive strategy, high?quality films with a dual?fibril network morphology are successfully printed, achieving a remarkable PCE of 20.23% for the device and 17.26% in the module.Green?printed, high?efficiency organic photovoltaics modules are critical to the commercial expansion and practical deployment of organic photovoltaics. Since the emergence of Y6?based non?fullerene acceptors (NFAs), the power conversion efficiency (PCE) of OSCs is remarkable progress. However, a considerable performance gap remains between devices processed with halogenated versus non?halogenated (green) solvents, primarily due to difficulties in controlling molecular aggregation. Here, hydroxyl?rich cellulose acetate butyrate (CAB) is introduced as a multifunctional additive to enhance the morphology and performance of modules fabricated via large?area green printing. CAB suppresses excessive molecular aggregation and modulates the film?formation dynamics. Crucially, its hydroxyl side groups interact synergistically with both donor and acceptor materials to induce a dual?fibril network, providing abundant interfacial area for exciton dissociation and continuous pathways for efficient charge transport. As a result, green?printed PM6:PTP?eC9 devices achieve PCE of 19.04%. Moreover, ternary PM6:PTQ?10:PTP?eC9 devices and modules with an active area of 16.94 cm2 exhibit PCEs of 20.23% and 17.26%, respectively. This work demonstrates a viable additive engineering strategy for realizing scalable, environmentally benign, and high?performance organic photovoltaics.

» Publication Date: 19/09/2025

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This project has received funding from the European Union's Horizon 2020 research and innovation programme under grant agreement Nº 768737


                   




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