Ultrafast charge-generation dynamics through interfacial energetic modulation for high-performance single-component organic photovoltaics with 14.8% efficiency.
Yao Li, Yongmin Luo, Yulong Hai, Xinkang Wang, Lunbi Wu, Ruijie Ma, Kezhou Fan, Top Archie Dela Peña, Sha Liu, He Yan, Kam Sing Wong, Gang Li, Tao Jia, Junwu Chen, Jiaying Wu
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引用次数: 0
Abstract
Bulk heterojunction (BHJ) organic solar cells (OSCs) have achieved high efficiencies but suffer from poor morphological stability due to phase separation after long-term operation. Single-component OSCs (SCOSCs) based on double-cable polymers (DCP), offer improved stability through covalently linked donor and acceptor units. However, their efficiency remains limited by inefficient charge generation arising from extensive intermixed morphologies. Here, we report a fluorinated double-cable polymer, DCPY2-F, which achieves an outstanding efficiency of 14.8% with high short-circuit current density of 26.83 mA cm-2. Ultrafast pump-probe transient absorption spectroscopy reveals that fluorination of DCPY2 into DCPY2-F accelerates interfacial charge transfer and long-range charge separation dynamics. The pump-push-probe transient absorption spectroscopy and steady-state electroluminescence show that the faster interfacial charge transfer arises from a reduced reorganization energy and a correspondingly accelerated molecular reorganization process (2.5 ps vs. 0.8 ps). Despite comparable acceptor aggregate sizes with DCPY2, DCPY2-F also shows faster long-range charge separation dynamics, which we attribute to a narrower charge transfer states (CTs) energetic distribution. Molecular dynamics simulations further reveal that fluorination strengthens non-covalent interactions, promoting well-aligned intermolecular donor-acceptor interfaces. These structurally and energetically ordered interfacial CT states enable ultrafast and efficient charge generation. In corresponding binary blends, fluorination similarly enhances charge-transfer dynamics and photocurrent. These findings establish a unified fluorination strategy for accelerating charge generation dynamics in both SCOSCs and blends, and provide a mechanistic understanding for improving charge generation for high-performance single-component systems.
块状异质结有机太阳能电池(osc)具有较高的效率,但由于长期运行导致相分离,其形态稳定性较差。基于双缆聚合物(DCP)的单组分OSCs (SCOSCs)通过共价连接的供体和受体单元提供了更好的稳定性。然而,它们的效率仍然受到广泛的混合形态引起的低效率电荷产生的限制。在这里,我们报道了一种氟化双电缆聚合物DCPY2-F,它在26.83 mA cm-2的高短路电流密度下实现了14.8%的卓越效率。超快泵浦-探针瞬态吸收光谱揭示DCPY2氟化成DCPY2- f加速了界面电荷转移和远程电荷分离动力学。泵-推-探针瞬态吸收光谱和稳态电致发光表明,界面电荷转移速度更快是由于重组能的降低和相应的分子重组过程的加速(2.5 ps vs 0.8 ps)。尽管与DCPY2的受体聚集大小相当,但DCPY2- f也表现出更快的远程电荷分离动力学,我们将其归因于更窄的电荷转移态(ct)能量分布。分子动力学模拟进一步揭示了氟化增强非共价相互作用,促进分子间供体-受体界面排列良好。这些结构上和能量上有序的界面CT态使得超快速和高效的电荷产生成为可能。在相应的二元共混物中,氟化同样增强了电荷转移动力学和光电流。这些发现建立了统一的氟化策略,以加速SCOSCs和共混物中的电荷生成动力学,并为改善高性能单组分体系的电荷生成提供了机制理解。
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.