Our group explores light-matter interactions in organic optical materials.
In particular, we are interested in:
Experimental set-ups that are currently under development in our lab utilize ultrafast time-resolved spectroscopy, ultrafast and cw photoconductivity techniques, luminescence spectroscopy, and single-molecule fluorescence microscopy.
Organic optical materials have been extensively studied as an alternative to inorganic materials due to their low cost, easy fabrication, and tunable properties. Applications of organic optical materials include xerography, thin-film transistors, light-emitting diodes, solar cells, photorefractive devices, and many others [1-4]. By slight synthetic modifications or doping, it is possible to vary optical properties (such as absorption and fluorescence spectra), thermal and structural properties (such as phase transition temperatures and a type of packing in a crystallographic unit cell), and electronic properties (such as charge carrier mobility) of organic materials and therefore, tailor them for specific applications [5-7]. In spite of many demonstrated and even commercialized applications of organic materials, a number of issues, both fundamental and applied, remain. For example, basic physics of light-induced charge carrier generation and subsequent transport, the processes that lay foundation for most of the applications of organic optical materials, is not understood [8,9]. On the applied side, it is often challenging to make a series of organic thin films with exactly reproducible properties. Indeed, the dependence of the thin film structure on the fabrication methods and conditions and the relationship between the structure and optical and electronic properties of the film are not straightforward. Therefore, systematic comprehensive studies are needed to reveal the physical nature of all processes contributing to the device performance and understand structure-property relationships [5,6,7,10,11].
As the technology develops towards nanoscales, organic molecules attract more and more attention as potential nano-devices. Studies that utilize single-molecule fluorescence spectroscopy revealed that individual organic molecules are promising candidates for nanoscale optical switches, probes of nanoenvironment, nanomotors, and so forth [12-16]. Both the physical description of the stochastic behavior of single-molecule devices and the development of the actual nanoscale electronic and all-optical devices are at their initial stages – they represent exciting opportunities for persistent and creative individuals !