A comparative study of ferroelectric and non-ferroelectric-gated organic field-effect transistors (FETs) have been carried out by using a small molecule semiconductor 6,13 bis(triisopropylsilylethynyl) pentacene (TIPS-pentacene) to understand the fundamental aspects of carrier transport in FET architectures. Temperature-dependent current-voltage characteristics from non-ferroelectric dielectric-gated FETs show a clear activated transport, independent of the dielectric constant. While using the ferroelectric dielectric polymer poly(vinylidene fluoride-trifluoroethylene) (PVDF-TrFE), where the dielectric constant may be tuned by changing the temperature, a negative temperature coefficient of the carrier mobility is observed beyond 200 K. The polarization fluctuation dominant transport inherent to a ferroelectric dielectric in conjunction with the discrete nature of traps in TIPS-pentacene results in an effective de-trapping of the shallow trap states into more mobile states.

Highly efficient Pt-TiO2 composite photoelectrodes were synthesized by combining two novel deposition methods: ACVD and a room temperature RF (radio frequency) magnetron sputtering method. A room temperature RF magnetron sputtering method allowed uniform deposition of Pt nanoparticles (NPs) onto the as-synthesized nanostructured columnar TiO2 films by ACVD. Pt NP sizes from 0.5 to 3 nm demonstrating a high particle density (>1012 cm−2) could be achieved by varying deposition time with constant pressure and power intensity. As-synthesized Pt-TiO2 films were used as photoanodes for water photolysis. Pt nanoparticles deposited onto the TiO2 film for 20s produced the highest photocurrent (7.92 mA/cm2 to 9.49 mA/cm2) and maximized the energy conversion efficiency (16.2 % to 21.2 %) under UV illumination. However, as the size of Pt particles increased, more trapping sites for photogenerated electron-hole pairs decreased photoreaction.

Burn rates of various nano-energetic composites were measured by two techniques; on-chip method and conventional optical method. A comparison is presented to confirm the validity of on-chip method. On-chip initiators were prepared using platinum heater films and nanoenergetic composites. Thin film Pt heaters were fabricated with different dimensions and ignition delay was studied using a nano-energetic composite of CuO nano-rods and Al-nano-particles. The ignition delay as a function of electrical power is presented for the same energetic composite. Heater with smaller surface area is found to be more efficient, which may be due to the lower heat losses.

Current approaches of mixing fuel and oxidizer nanoparticles or adding fuel nanoparticles to oxidizer gel lead to an overall reduced interfacial area of contact between them and thus, limit their burn rates severely. We have developed an approach of self-assembling fuel nanoparticles around an oxidizer matrix using a monofunctional polymer, poly(4)-vinyl pyridine (P4VP). The polymer has been used to accomplish binding of fuel and oxidizer in a molecularly engineered manner. We use composite of Al-nanoparticles and CuO nanorods for executing this self-assembly. TEM images of this composite confirms the self-assembly of Al-nanoparticles around the oxidizer nanorods. The burn rate of self-assembled composite has been found significantly higher than that of the composite prepared by simple mixing.