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

Bekcy Joseph; Shivam Singh; Nathaniel P. Gallop; Fabian Eller; Alexander Ehm; Julius Brunner; Dietrich R. T. Zahn; Eva Herzig; Boris Rivkin; Yana Vaynzof

arXiv · 2604.05883

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

Bekcy Joseph·Shivam Singh·Nathaniel P. Gallop·Fabian Eller·Alexander Ehm·Julius Brunner·Dietrich R. T. Zahn·Eva Herzig·Boris Rivkin·Yana Vaynzof

View original source ↗Read source document ↗Export metadata ↓

Abstract

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.

Explore related subjects

cond-mat.mtrl-sci

Keep this discovery

BibTeX RIS

Bekcy Joseph, Shivam Singh, Nathaniel P. Gallop, Fabian Eller, Alexander Ehm, Julius Brunner, Dietrich R. T. Zahn, Eva Herzig, Boris Rivkin, Yana Vaynzof. 2026-04-07. Additive-Induced Stabilization of the Energetic Landscape of PM6:Y12 Organic Solar Cells. https://arxiv.org/abs/2604.05883

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

arXiv2026

Measuring chiral phonons

Chiral phonons are quantized vibrations where the atomic motion in a solid breaks improper rotation symmetries. In many cases, chiral phonons possess angular momenta and are therefore selective to circularly polarized light. Both fundamental and applied research efforts on chiral phonons have been gaining increasing attention owing to their importance in a variety of fields including spintronics, spin-selective chemical reactions, thermal transport, quantum information processing and biosensing, where the bi-directional spin-lattice coupling enabled by chiral phonons can be harnessed in new ways, and potentially lead to new functionalities. Thus far, the studies of chiral phonons across diverse materials platforms have evolved largely independently within these fields, but the experimental techniques are often interrelated. In this perspective, we present a detailed description, as well as advantages and disadvantages of the current approaches for experimentally measuring chiral phonons in chiral and achiral materials. We conclude with a discussion of new methods for measuring chiral phonons. Ultimately, this work seeks to offer an experimental guide for systematically investigating the properties of chiral phonons in various materials systems and applications.

cond-mat.mtrl-sci↗

arXiv2026

A model of grain growth in UN integrating molecular dynamics, phase-field modeling, and uncertainty quantification

Grain growth kinetics and grain-boundary (GB) properties in uranium mononitride (UN) are investigated through an integrated multiscale framework combining molecular dynamics (MD), phase-field modeling, and surrogate-assisted uncertainty quantification. MD simulations yield GB energies for 27 symmetric tilt boundaries from 0--2000~K, which are consistent with available DFT values. The average GB energy is nearly temperature-independent below 1000~K and increases at higher temperatures. A mechanistic pore-drag model applied to the only available grain growth dataset for actinide nitrides yields a mobility reduction factor of $s \approx 0.93$--$0.99$, statistically indistinguishable from unity, confirming that pore drag is negligible under the experimental conditions. The intrinsic GB mobility is therefore extracted directly from the effective mobility, yielding $M_0 = 2.05\times10^{-15}$~m$^4$/(J$\cdot$s) and $Q_M = 0.89$~eV. Phase-field simulations conducted from 1500--2000~K confirm normal curvature-driven grain growth, with grain size distributions converging to the Hillert-like form. A surrogate-assisted global sensitivity analysis---combining principal component analysis, Gaussian process regression, and Sobol decomposition---reveals that the mobility prefactor $M_0$ dominates output variance at all times, followed by the activation energy $Q_M$, while the GB energy $\gamma$ contributes minimally. These results establish the first quantitative grain growth framework for UN and identify the reduction of uncertainty in $M_0$ and $Q_M$ as the highest-priority target for future experimental efforts.

cond-mat.mtrl-sci↗

arXiv2026

Silicon Solar Cell Design for >30% Efficiency via Singlet Fission

Singlet fission (SF) materials convert high-energy photons into multiple charge carriers, providing a route to exceed the efficiency limits of single-junction silicon solar cells without many of the complexities of multi-junction tandem designs. Following the first demonstration of an SF-enhanced silicon solar cell in 2025, there is a need to understand how SF materials can be effectively integrated into high-efficiency industrial silicon devices and translated from proof of concept to a manufacturable technology. Using coupled optical and electrical simulations, we assess the efficiency potential of several industrially relevant silicon cell architectures combined with SF materials. Interdigitated back-contact (IBC) cells offer the greatest potential for improvement due to unrestricted front-surface access and can achieve efficiencies exceeding 33%. However, performance is highly sensitive to front-surface passivation quality. Appropriate silicon design, particularly controlled surface doping and fixed interfacial charge, can mitigate recombination losses and relax passivation requirements for ultra-thin exciton-transfer layers.

cond-mat.mtrl-sci↗