Prof Michael Johnston

Abstract:

We have used optical-pump terahertz-probe spectroscopy to explore the photoinduced conductivity dynamics in mesoporous anatase TiO2 films, commonly employed as the electron-transporting electrode in dye-sensitized solar cells. We find an intrinsic mobility value of 0.1 cm²/(V s) and diffusion length of ∼20 nm for electron motion through the TiO2 matrix. The photoconductivity dynamics in TiO2 films, both before and after sensitization with a ruthenium bypyridyl complex termed Z907, were examined in order to study the charge injection, trapping, and recombination time scales. We observe a biphasic charge injection from Z907, with a fast sub-500 fs component, followed by a slower 70-200 ps component. This is followed by photoconductivity decay over the first few nanoseconds, predominantly reflecting charge carrier trapping. In addition, we have utilized terahertz spectroscopy to investigate the influence of treating the titania surface with TiCl4 on early-time charge dynamics. In the solar cells, surface treatment of the mesoporous TiO2 with TiCl4 is critical to enable efficient operation. Here, we find that neither early-time charge mobility nor charge injection rate or decay times are significantly affected by the treatment, which suggests that it may, instead, have an impact on phenomena occurring on longer time scales. © 2010 American Chemical Society.

Abstract:

We demonstrate a new scheme for generating THz radiation based on the photo-Dember effect in lateral geometry. By micro-structuring a semiconductor surface we achieve strongly enhanced THz emission comparable to high-efficiency externally biased photoconductive emitters. © 2010 Optical Society of America.

Abstract:

We investigate a novel method to generate intense THz radiation by multiplexing coherent photo-Dember currents in a lateral geometry. These THz emitters are passive devices with a peak frequency at about 1.5 THz. © OSA / UP 2010.

Abstract:

We have investigated the ultrafast far-infrared transmission of isolated single-walled carbon nanotubes using optical-pump THz-probe spectroscopy. The THz dielectric response is dominated by excitons with an initial, rapid decay due to Auger recombination followed by a slow decay of isolated single excitons. Frequencydependent analysis of the photomduced dielectric function suggest an internal excitonic excitation at ∼11 meV with further low-frequency (∼0.6 and 1.4 THz) absorption features at high densities ascribed to exciton complexes. A featureless conductivity bleaching is attributed to an exciton-induced reduction in the mobility of free carriers caused by phase-space filling. © 2009 American Chemical Society.