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Fabian Eller

Publications and source records attributed to Fabian Eller.

2 recordsLinked to original sources

Mobility-lifetime relation links photodegradation in spin-coated and gravure-printed organic solar cells

The degradation mechanisms of organic solar cells (OSCs) have been studied primarily in spin-coated, laboratory-scale devices, whereas scalable processing modifies the device architecture, active-layer morphology, and underlying charge-transport and recombination properties. Whether these changes also alter how solar cells degrade remains unclear. Here, we compare spin-coated and fully roll-to-roll-compatible gravure-printed PM6:Y12 solar cells during $\sim$1000 h of continuous illumination. Despite distinct initial properties and degradation signatures, the loss of power-conversion efficiency systematically follows the mobility-lifetime product $μτ$. Remarkably, ageing of the printed devices increases the recombination lifetime while strongly reducing charge-carrier mobility, showing that a longer lifetime alone does not imply improved device performance. The mobility reduction is accompanied by decreased PM6 lamellar order, whereas the additional open-circuit voltage loss originates predominantly from increased non-radiative recombination. Dark recovery further reveals a metastable contribution specific to the printed architecture. These results identify the mobility-lifetime product as a unifying physical descriptor for photodegradation, linking ageing-induced microscopic changes to macroscopic performance loss across spin-coated and scalable printed OSCs.

cond-mat.mtrl-sci↗

Additive-Induced Stabilization of the Energetic Landscape of PM6:Y12 Organic Solar Cells

Solvent additive engineering is a common strategy in organic photovoltaic (OPV) fabrication to improve film morphology and enhance device performance by controlling phase-separation kinetics and crystallinity. However, its effect on photostability, particularly with respect to the evolution of the energetic landscape under operational stress, remains unclear. This study investigates the impact of the additive 1-chloronaphthalene (1-CN) on the evolution of the device's energetic landscape in PM6:Y12 bulk heterojunction organic solar cells upon photoaging. Ultraviolet photoemission spectroscopy combined with argon gas cluster ion beam depth profiling is employed to probe the depth-resolved evolution of donor (PM6) and acceptor (Y12) energy levels before and after photodegradation. Our findings show that in additive-free devices, photodegradation leads to a significant 200 meV downward shift in the PM6 highest occupied molecular orbital (HOMO) level, reducing the donor-acceptor HOMO offset and impairing the driving force for hole transfer. As a consequence, the device experiences substantial efficiency loss. On the other hand, the incorporation of 1-CN effectively stabilizes the PM6 HOMO level, preserving adequate driving force for efficient exciton dissociation. Advanced X-ray diffraction characterization reveals more pronounced nanostructural degradation in blends without 1-CN than those with 1-CN upon photoaging. Collectively, these findings identify PM6 as the primary degradation pathway in PM6:Y12 blends and demonstrate that 1-CN enhances device stability by stabilizing PM6 energetics and preserving the nanostructural integrity upon photoaging.

cond-mat.mtrl-sci↗