Interchain Interactions in Organic π‐Conjugated Materials: Impact on Electronic Structure, Optical Response, and Charge TransportCornil, J.; Beljonne, D.; Calbert, J.‐P.; Brédas, J.‐L.
doi: 10.1002/1521-4095(200107)13:14<1053::AID-ADMA1053>3.0.CO;2-7pmid: N/A
The pioneering work of Heeger, MacDiarmid, and Shirakawa, rewarded by the 2000 Nobel Prize in Chemistry, has paved the way for the development of the fields of plastic electronics and photonics. Functional organic molecular materials and conjugated oligomers or polymers now allow the low‐cost fabrication of thin films for insertion into new generations of electronic and optoelectronic devices. The performance of these devices relies on the understanding and optimization of several complementary processes (see sketch). Our goal is to discuss, from a theoretical standpoint, the electronic structure characteristics and interfacial properties that are of importance in all these areas. The concept of interface should be taken here in the microscopic sense, i.e., molecular interactions among two or several chains/molecules (of the same or of a different nature). Specifically, we will address the impact of interchain interactions within an organic layer on the transport and optical properties. These issues will therefore be more directly related to transistor and light‐emitting diode applications; however, in all instances, the aspects related to interfacial charge or energy transfer processes will dictate the ultimate performance of a material in a given device.
Highly Organized Mesoporous Titania Thin Films Showing Mono‐Oriented 2D Hexagonal ChannelsGrosso, D.; de A. A. Soler‐Illia, G. J.; Babonneau, F.; Sanchez, C.; Albouy, P.‐A.; Brunet‐Bruneau, A.; Balkenende, A. R.
doi: 10.1002/1521-4095(200107)13:14<1085::AID-ADMA1085>3.0.CO;2-Qpmid: N/A
Structure‐directing agents that aid in the formation of ordered, mesostructured titania have been found in poly(ethylene oxide) surfactants. Thermal treatment of the films results in stiffening of the titania network, thereby providing straight channels with elliptical pore cross sections (see Figure). The preparation, characterization, and properties of these films are thoroughly discussed, as well as the possibility of extending the technique for the preparation of 3D structures.
Poly‐2,8‐(indenofluorene‐co‐anthracene)—A Colorfast Blue‐Light‐Emitting Random CopolymerMarsitzky, D.; Scott, J. C.; Chen, J.‐P.; Lee, V. Y.; Miller, R. D.; Setayesh, S.; Müllen, K.
doi: 10.1002/1521-4095(200107)13:14<1096::AID-ADMA1096>3.0.CO;2-Ipmid: N/A
The incorporation of anthracene monomers in fluorene polymers (see Figure) suppresses the formation of aggregates severely thereby increasing the electroluminescence quantum efficiency. The spectral properties of these new polymers, their preparation, and applications are discussed.