材料科学
卟啉
飞秒
吸收(声学)
激光器
光电子学
沉积(地质)
复合数
共轭体系
薄膜
双光子吸收
纳米技术
光化学
化学工程
光学
聚合物
复合材料
化学
古生物学
生物
沉积物
工程类
物理
作者
Yuting Ke,Hui Li,Mark G. Humphrey,Qian Zhang,Jun Wang,Yanliang Liu,Ridong Cong,Chi Zhang,Zhipeng Huang
标识
DOI:10.1002/adom.202401286
摘要
Abstract Constructing organic‐inorganic composites presents a promising approach to enhance the nonlinear optical (NLO) response of materials. However, the effectiveness of this approach is impeded by the complexity of synthesis procedures and challenges in controlling the loading amount. Herein, a convenient and controllable electrodeposition method to non‐covalently combine SnS 2 with tetracationic porphyrin (TMPyP) and the remarkable enhancement in NLO absorption of the resultant composite, are introduced. Through this method, a series of SnS 2 /TMPyP thin films are synthesized, allowing for the regulation of porphyrin loading via varying the deposition time. These resultant SnS 2 /TMPyP composites exhibit prominent nonlinear absorption coefficients when subjected to femtosecond laser irradiation of varying wavelengths. Notably, the compound with an electrochemical deposition time of 30 s achieves the largest third‐order nonlinear absorption coefficient of 6155 ± 243 cm GW −1 under 800 nm laser excitation, marking an 8.9‐fold increase compared to pristine SnS 2 nanosheets. Based on the staggered energy level structure between TMPyP and SnS 2 , effective enhancement of charge separation/transfer is achieved by leveraging the unique π‐conjugated groups of porphyrins, which facilitates the NLO process and improves the NLO performance of films.
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