Enhancing Two-Photon Excited Fluorescence of Metal-Organic Framework Single Crystals through Modulation of Inorganic Nodes

被引:0
|
作者
Meng, Ya-Ru [1 ]
Xu, Min-Jie [1 ]
Li, Shu-Fan [1 ]
Li, Bo-Cong [1 ]
Zhang, Gen [1 ]
Su, Jian [1 ,2 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Chem & Chem Engn, Nanjing 210094, Peoples R China
[2] Nanjing Univ, State Key Lab Coordinat Chem, Nanjing 210023, Peoples R China
基金
中国国家自然科学基金;
关键词
ABSORPTION; DESIGN; SITES;
D O I
10.1021/acs.inorgchem.4c02941
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Regulation of the two-photon excited fluorescence (TPEF) emission intensity and wavelength of metal-organic framework (MOF) crystals with similar constitutions presents a significant challenge. In this study, two MOFs, Zn-BTPPA and Cd-3-BTPPA, were constructed using tetrakis(1,1 '-biphenyl-4-carboxylic acid)-1,4-benzenediamine (H(4)BTPPA) as the organic ligand and mononuclear Zn and trinuclear Cd-3 inorganic nodes, respectively. The incorporation of H(4)BTPPA within the MOF structures enables effective TPEF emission in both Zn-BTPPA and Cd-3-BTPPA. The TPEF results show that Zn-BTPPA and Cd-3-BTPPA exhibited strong emissions at 523 and 463 nm, respectively, when excited with a 780 nm laser. Moreover, Zn-BTPPA and Cd-3-BTPPA exhibited much higher two-photon absorption cross sections, approximately 4.9 and 5.2 times higher than that of the reported dinuclear MOF, Cd-2-BTPPA, with a similar composition, respectively. With different inorganic nodes, the stacking of chromophores, pi<middle dot><middle dot><middle dot>pi interactions, and ligand geometry were found to correlate with the enhanced TPEF in Cd-3-BTPPA and the blue-shifted TPEF in Zn-BTPPA. This work serves as an inspiration for designing efficient TPEF MOF materials based on the structure-property relationship.
引用
收藏
页码:17856 / 17863
页数:8
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