材料科学
钙钛矿(结构)
结晶
光伏
化学工程
亚稳态
面(心理学)
能量转换效率
Crystal(编程语言)
纳米技术
聚合物结晶
相变
成核
纳米晶
聚合物
晶体结构
相(物质)
纤维素
晶体生长
动力学
纳米颗粒
离解(化学)
结晶度
高分子
离子
胶体
化学物理
作者
Yili Wang,K Wang,Peng Gao,Chunchun Yin,Jiandong He,Shuaiyuan Wang,Chao Luo,Yi Yuan,Yirong Wang,Qing Zhao,Jinfeng Wang,Jinming Zhang,Jinming Zhang,Jizheng Wang,Jun Zhang,Jun Zhang
摘要
Perovskite solar cells (PSCs) face a critical challenge in balancing high power conversion efficiency (PCE) with operational stability, largely governed by the crystallization kinetics and facet configuration of perovskite films. Here, we report a kinetically segmented crystallization strategy mediated by a conformationally preorganized macromolecular regulator, cellulose 2,4,6-trichlorophenylcarbamate (3Cl-NC). Through multidentate coordination, 3Cl-NC establishes localized precursor-rich microenvironments that promote heterogeneous nucleation. During thermal annealing, this association transitions into a thermally activated dynamic coordination state that retards long-range precursor transport while maintaining local availability for controlled crystal growth. This segmented regulation suppresses metastable δ-phase accumulation and facilitates photoactive α-phase formation. Furthermore, 3Cl-NC thermodynamically stabilizes the high-Miller-index (210) orientation, establishing a synergistic architecture that intrinsically enhances lattice structural stability. Consequently, the resulting perovskite films exhibit higher phase purity, relieved residual stress, and suppressed ion migration, enabling devices to achieve a champion PCE of 26.59% (certified 26.29%) with improved long-term stability.
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