Second-Order Nonlinear Optical Susceptibilities of Metal–Organic Frameworks Using a Combined Local Field Theory/Charge Embedding Electrostatic Scheme

2016 ◽  
Vol 120 (12) ◽  
pp. 6741-6749 ◽  
Author(s):  
Tomasz Seidler ◽  
Benoît Champagne
2017 ◽  
Vol 46 (43) ◽  
pp. 14779-14784 ◽  
Author(s):  
Ming-Dao Zhang ◽  
Yan-Le Li ◽  
Zhen-Zhen Shi ◽  
He-Gen Zheng ◽  
Jing Ma

Two 3D enantiotopic chiral metal–organic frameworks, with ferroelectric behaviors and second-order nonlinear optical effects, were constructed based on achiral ligands in one pot with high enantiomeric excess owing to the hydrogen bonds.


2016 ◽  
Vol 45 (10) ◽  
pp. 4218-4223 ◽  
Author(s):  
Tao Song ◽  
Jiancan Yu ◽  
Yuanjing Cui ◽  
Yu Yang ◽  
Guodong Qian

Two series of cationic dyes have been encapsulated in the 1D channel of MOFs, and the tunable second order nonlinear optical properties of these MOF⊃dye materials were observed.


2019 ◽  
Author(s):  
javier enriquez ◽  
Ignacio Chi-Duran ◽  
Carolina Manquian ◽  
Felipe Herrera ◽  
Ruben Fritz ◽  
...  

Non-centrosymmetric single-crystal metal-organic frameworks (MOF) are promising candidates for phase-matched nonlinear optical communication, but typical hydrothermal synthesis produces small crystals with relatively low transmittance and poor phase matching. We study the effect of the metal-to-ligand molar ratio and reaction pH on the hydro-thermal synthesis of the non-centrosymmetric Zn(3-ptz)<sub>2</sub> and Zn(OH)(3-ptz) MOFs with <i>in-situ </i>ligand formation. In acidic environments, we find that decreasing the amount of ligand below the stoichiometric molar ratio 1:2 also produces highly transparent single-crystal octahedrons of <b>Zn(3-ptz)<sub>2</sub></b>. In alkaline environments, we obtain long rod-like <b>Zn(OH)(3-ptz) </b>crystals whose length exceeds previous reports by up to four orders of magnitude. Potential applications of these results in the development of MOF-based nonlinear optical devices are discussed.


1979 ◽  
Vol 19 (8) ◽  
pp. 2357-2366 ◽  
Author(s):  
K. Bardakci

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