Realization of expeditious layer-by-layer siloxane-based self-assembly as an efficient route to structurally regular acentric superlattices with large electro-optic responses

被引:67
作者
Zhu, PW
van der Boom, ME
Kang, H
Evmenenko, G
Dutta, P
Marks, TJ
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Mat Res Ctr, Evanston, IL 60208 USA
[3] Northwestern Univ, Dept Phys & Astron, Evanston, IL 60208 USA
关键词
D O I
10.1021/cm020438t
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A new, expeditious siloxane-based layer-by-layer assembly process for the formation of intrinsically polar organic electro-optic thin films is described using highly reactive -SiCl2I-functionalized, silyl-protected donor-acceptor azo-benzene chromophore derivatives and octachlorotrisiloxane as a deprotecting reagent/interlayer precursor. This all-"wet-chemical" two-step process can be efficiently implemented in a vertical dipping procedure to yield polar films consisting of 40 alternating chromophore and capping layers. Each nanoscale bilayer (chromophore + polysiloxane layer approximate to 3.26-nm thick) can be grown in approximate to40 min-at least 1 order of magnitude more rapidly than previous siloxane-based solution deposition methodologies. Chromophore monolayer deposition from solution reaches completion in approximate to15 min at 55 degreesC. The adherent, structurally regular assemblies exhibit appreciable electro-optic responses (chi((2)) similar to 180 pm/V and r(33) similar to 65 pm/V determined by SHG measurements at 1064 mn) and high chromophore surface densities (approximate to40 Angstrom(2)/chromophore) and have been characterized by a full complement of physicochemical techniques: optical spectroscopy, aqueous contact-angle measurements, specular X-ray reflectivity, atomic force microscopy, and angle-dependent polarized second-harmonic generation.
引用
收藏
页码:4982 / 4989
页数:8
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