材料科学
平面的
非线性光学
共价键
非线性系统
订单(交换)
非线性光学
共价有机骨架
纳米技术
光电子学
复合材料
有机化学
计算机科学
量子力学
业务
化学
物理
计算机图形学(图像)
财务
多孔性
作者
Yi Wei,Kangshuai Geng,Yupei Sun,Jing Huang,Zhichao Shao,Hongwei Hou
标识
DOI:10.1002/adom.202501751
摘要
Abstract The covalent linkages in covalent organic frameworks (COFs) extend π‐electron delocalization, providing an ideal platform for constructing materials with excellent third‐order nonlinear optical (NLO) properties. However, excessive π‐conjugation within COF planes leads to increased exciton generation, which weakens the NLO response of COFs. In this study, a chiral induction strategy is employed to effectively disrupt the planarity of the COF structure, resulting in chiral non‐planar COFs. The resulting chiral non‐planar R‐ TpPz exhibits a significant improvement in NLO performance compared to its planar counterpart, TpPz. Specifically, the third‐order nonlinear absorption coefficient ( β eff ) and refractive index ( n₂ ) of R‐ TpPz are −126 cm GW − ¹ and 1.74 × 10 −3 cm 2 GW − ¹, respectively. The improvement of third‐order NLO properties is attributed to the enhanced built‐in electric field and optimized charge transfer pathways caused by the disruption of planarity. This study provides a new approach for the development of high‐performance NLO COF materials.
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