Efficient, thermally stable, second order nonlinear optical response in organic hybrid covalent/ionic self-assembled films.

A covalent/electrostatic layer-by-layer self-assembly method was used to achieve polar ordering of a water soluble, reactive dye in the fabrication of nonlinear optical (NLO) films. We observed a quadratic relationship between the second harmonic intensity I2(omega) and bilayer number for all films made with Procion Brown MX-GRN, demonstrating that the polar ordering of the chromophores is consistent in each successive bilayer. As the ionic strength of the dye deposition solution was increased to 0.5 M NaCl, the of the films increased by approximately 250% to 50 x 10(-9) esu, with a corresponding average chromophore tilt angle of 38 degrees . This was attributed to increased shielding of the dye charges which led to higher chromophore density in the bilayers. The electrooptic coefficient for films of 50 bilayers fabricated at 0.5 M NaCl was 14 +/- 2 pm/V. Importantly, these films exhibited excellent thermal stability, with only a 10% decrease in (I2(omega))(1/2) after 36 h at 85 degrees C and then 24 h at 150 degrees C. Furthermore, the (I2(omega))(1/2) recovered completely upon cooling to room temperature. These results with a commodity textile dye point to the potential value of this class of reactive chromophores and this self-assembly method for fabrication of electrooptic materials at ambient conditions from aqueous solutions.