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Layer-by-Layer Deposited Organic/Inorganic Hybrid Multilayer Films Containing Noncentrosymmetrically Orientated Azobenzene Chromophores

Year: 2007

Journal: Langmuir, 2007, 23 (14), pp 7594–7601, 20111221

Authors: En-Hua Kang, Tianjia Bu, Pengcheng Jin, Junqi Sun, Yanqiang Yang, and Jiacong Shen

Organizations: Key Lab of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, P. R. China 130012, and Center for Condensed Matter Science and Technology, Department of Physics, Harbin Institute of Technology, Harbin, P. R. China 150001

Organic/inorganic hybrid multilayer films with noncentrosymmetrically orientated azobenzene chromophores were fabricated by the sequential deposition of ZrO2 layers by a surface sol−gel process and subsequent layer-by-layer (LbL) adsorption of the nonlinear optical (NLO)-active azobenzene-containing polyanion PAC-azoBNS and poly(diallyldimethylammonium chloride) (PDDA). Noncentrosymmetric orientation of the NLO-active azobenzene chromophores was achieved because of the strong repulsion between the negatively charged ZrO2 and the sulfonate groups of the azobenzene chromophore in PAC-azoBNS. Regular deposition of ZrO2/PAC-azoBNS/PDDA multilayer films was verified by UV−vis absorption spectroscopy and quartz crystal microbalance measurements. Both UV−vis absorption spectroscopy and transmission second harmonic generation (SHG) measurements confirmed the noncentrosymmetric orientation of the azobenzene chromophores in the as-prepared ZrO2/PAC-azoBNS/PDDA multilayer films. The square root of the SHG signal (I2ω1/2) increases with the increase of the azobenzene graft ratio in PAC-azoBNS as the number of deposition cycles of the ZrO2/PAC-azoBNS/PDDA films remains the same, while the second-order susceptibility of the film decreases with the increase of the azobenzene graft ratio. Furthermore, the present method was successfully extended to realize the noncentrosymmetric orientation of azobenzene chromophores in multilayer films when small organic azobenzene compounds with carboxylic acid and/or hydroxyl groups at one end and sulfonate groups at the other end were used. The present method was characterized by its simplicity and flexibility in film preparation, and it is anticipated to be a facile way to fabricate second-order nonlinear optical film materials.