The performance of organic solar cells (OSCs) is critically governed by the fibrillar organization of bulk-heterojunction active layers, yet controlling long-range, directional fibrillar morphology under nonequilibrium processing remains challenging. Here we report that two-dimensional cobalt phosphosulfide (CoPS3) nanocrystals act as kinetic templates that reprogram molecular self-assembly during film formation. Through collective electronic interactions with conjugated polymer donors and small-molecule acceptors, CoPS3 modulates molecular densification and phase separation pathways, enabling refined, long-range fibrillar networks without increasing crystallinity. The resulting morphology enhances exciton dissociation and charge transport, and inhibits recombination, delivering a power conversion efficiency of 21.0%. This templating strategy is effective across multiple OSC systems, simultaneously improving efficiency and storage stability, offering a promising route for kinetic morphology control in organic optoelectronics. Controlling long-range, directional fibrillar morphology is important for organic solar cells (OSC). Here, the authors show that cobalt phosphosulfide nanocrystals can template film formation in OSCs, improving charge generation and transport, and achieving a power conversion efficiency of 21.0%.
Fibrillar networks formed during solution processing play a key role in the high performance of modern organic solar cells (OSCs). Yet their formation is intrinsically non-equilibrium and largely stochastic, leading to discontinuous domains and mismatched donor/acceptor interfaces that limit charge transport. Here, we...
Controlling the morphology evolution of blade-coated bulk-heterojunction active layers is crucial for achieving high-efficiency organic solar cells (OSCs), yet remains challenging because rapid solvent evaporation and unbalanced donor-acceptor aggregation often lead to poorly regulated phase separation and disordered m...
Ji-Jing Ma, Shao-Jie Fu, Yilin Wang et al.· ACS Applied Materials and In...· 0 citations
Achieving an ideal bi-continuous network in organic solar cells requires balancing molecular self-assembly and film-formation kinetics. For strong-interaction polymers like D18, intense backbone interactions often lead to kinetically trapped, disordered states. Here, we present a molecular symmetry-breaking strategy...
Zhi-Chao Mao, Hao-Tian Hu, Jing Li et al.· ACS Energy Letters· 0 citations
Understanding how molecular design governs assembly kinetics during film formation is essential for optimizing bulk-heterojunction morphology in organic solar cells (OSCs), yet the molecular mechanism by which terminal-group engineering regulates this process remains poorly understood. Herein, a series of non-fullerene...
Shan-Shan Qin, Feng-Zhi Wang, Zhen-Yu Chen et al.· ACS Applied Materials and In...· 0 citations
Uncontrolled crystal growth and structural heterogeneity in solution-processed self-assembled molecules (SAMs) remain major limitations for efficient interfacial charge transport. Herein, we report a dipole-engineered molecular strategy to regulate SAMs crystallization through the rational design of fluorinated benzimi...
Qian-Nan Li, Fei Wang, Bao-Lei Tang et al.· Advances in Materials· 0 citations
In mixed-component wide bandgap (WBG) perovskites, the elusive (111) crystal orientation confers enhanced operational stability compared to the conventional (100) orientation, yet typically compromises photovoltaic performance, presenting a critical stability-efficiency trade-off that remains unresolved. We report a th...