Carbon nanotube-amorphous silicon hybrid solar cell with improved conversion efficiency.

We report a hybrid solar cell based on single walled carbon nanotubes (SWNTs) interfaced with amorphous silicon (a-Si). The high quality carbon nanotube network was dry transferred onto intrinsic a-Si forming Schottky junction for metallic SWNT bundles and heterojunctions for semiconducting SWNT bundles. The nanotube chemical doping and a-Si surface treatment minimized the hysteresis effect in current-voltage characteristics allowing an increase in the conversion efficiency to 1.5% under an air mass 1.5 solar spectrum simulator. We demonstrated that the thin SWNT film is able to replace a simultaneously p-doped a-Si layer and transparent conductive electrode in conventional amorphous silicon thin film photovoltaics.

Porous Silicon Structures as Optical Gas Sensors.

We present a short review of recent progress in the field of optical gas sensors based on porous silicon (PSi) and PSi composites, which are separate from PSi optochemical and biological sensors for a liquid medium. Different periodical and nonperiodical PSi photonic structures (bares, modified by functional groups or infiltrated with sensory polymers) are described for gas sensing with an emphasis on the device specificity, sensitivity and stability to the environment. Special attention is paid to multiparametric sensing and sensor array platforms as effective trends for the improvement of analyte classification and quantification. Mechanisms of gas physical and chemical sorption inside PSi mesopores and pores of PSi functional composites are discussed.

Highly efficient detection of hydrogen peroxide in solution and in the vapor phase via fluorescence quenching.

Herein we report the highly efficient and sensitive detection of hydrogen peroxide in both aqueous solution and in the vapor phase via fluorescence quenching (turn-off mechanism) of the amplified fluorescent conjugated polymer-titanium complex induced by hydrogen peroxide. Inter- and intra-polymer energy migration leads to extremely high sensitivity.

Excitonic energy transfer in polymer wrapped carbon nanotubes in gradually grown nanoassemblies.

We investigate the exciton energy transfer (ET) in nanoassemblies (nanotube based aggregates) formed by polymer wrapped single-walled carbon nanotubes (SWNTs) using photoluminescence (PL) spectroscopy and simulation. The distinctive feature of this study is the gradual growth of such nanostructures in aqueous medium induced by increasing the concentration of porphyrin molecules stitching nanotube-polymer complexes in densely packed assemblies. Experimental dependencies of PL intensity on the porphyrin concentration for different types of semiconducting SWNTs demonstrate step-like behavior controlled by the amount of bound nanotubes and are in good agreement with the simulating model. The simulation algorithm determines the criterion of the aggregate formation depending on the number of porphyrin molecules per tube and the cascade exciton energy transfer between neighboring semiconducting nanotubes of different chiralities. Aggregates of small sizes (up to six-eight individual tubes) contain mostly semiconducting species, while aggregates of a larger size (up to several tens of tubes) incorporate metallic SWNTs, inducing strong PL quenching. From the fitting procedure, an ET rate of 0.6 × 10(10) s(-1) has been determined which is consistent with the center to center distance (∼2.3 nm) between adjacent tubes separated by polymer and porphyrin molecules. The threshold of the dimer formation corresponds to one porphyrin molecule per ∼20 nm of tube lengths that was supported by molecular dynamics simulation. These findings provide insight into the ET mechanism in SWNT nanoassemblies of variable sizes, which can be gradually controlled by the external factor (the concentration of porphyrin molecules).

Selective response of mesoporous silicon to adsorbants with nitro groups.

We demonstrate that the electronic structure of mesoporous silicon is affected by adsorption of nitro-based explosive molecules in a compound-selective manner. This selective response is demonstrated by probing the adsorption of two nitro-based molecular explosives (trinitrotoluene and cyclotrimethylenetrinitramine) and a nonexplosive nitro-based aromatic molecule (nitrotoluene) on mesoporous silicon using soft X-ray spectroscopy. The Si atoms strongly interact with adsorbed molecules to form Si-O and Si-N bonds, as evident from the large shifts in emission energy present in the Si L(2,3) X-ray emission spectroscopy (XES) measurements. Furthermore, we find that the energy gap (band gap) of mesoporous silicon changes depending on the adsorbant, as estimated from the Si L(2,3) XES and 2p X-ray absorption spectroscopy (XAS) measurements. Our ab initio molecular dynamics calculations of model compounds suggest that these changes are due to spontaneous breaking of the nitro groups upon contacting surface Si atoms. This compound-selective change in electronic structure may provide a powerful tool for the detection and identification of trace quantities of airborne explosive molecules.

Hybrid solar cells based on single-walled carbon nanotubes/Si heterojunctions.

Photovoltaic devices based on single-walled carbon nanotubes (SWNTs) and n-silicon heterojunctions have been fabricated by a spray deposition process. We provide direct evidence that nanotubes serve as an active photosensing material involved directly in the photon absorption process as well as contributing to charge separation, transport and collection. The characteristic band of the SWNT band in the photoconductivity spectrum matches the S(11) absorption band of semiconducting SWNTs of 7,6 chirality. Centrifugation of the SWNTs provides two fractions. The sediment fraction exhibits a conversion efficiency ( approximately 1.7%) higher by a factor of eight compared to the supernatant fraction. SEM images and conductivity measurements show that the SWNT network morphology of the sediment fraction has longer and thicker nanotube bundles forming highly porous films, accounting for the enhanced conductivity and higher transparency.

Photoactuation from a carbon nanotube-nafion bilayer composite.

A bilayer composite of single walled carbon nanotubes (SWNTs) deposited onto Nafion exhibits substantial mechanical motion upon exposure to visible or near-infrared light. The magnitude of the actuation parallels the absorption spectrum of the SWNTs in the near-infrared, but the actuation diminishes in the visible and disappears in the UV portions of the spectrum. In the near-infrared region, the photoactuation is linear with respect to the light intensity. The photoactuation also appears to be associated with a photocurrent across the nanotube/Nafion interface. The proposed mechanism for the actuation is that band bending of the semiconducting SWNTs induces polarization of mobile hydrogen ions at the Nafion interface, which then causes swelling of the polymer.

Structural control in thin layers of poly(p-phenyleneethynylene)s: photophysical studies of Langmuir and Langmuir-Blodgett films.

We present the relationship between the spatial arrangement and the photophysical properties of fluorescent polymers in thin films with controlled structures. Eight surfactant poly(p-phenyleneethynylene)s were designed and studied. These detailed studies of the behavior of the polymers at the air-water interface, and of the photophysical properties of their transferred LB films, revealed key structure-property relationships. Some of the polymers displayed pi-aggregates that are characteristic of an edge-on structure at the air-water interface. Monolayer LB films of these polymers showed greatly reduced quantum yields relative to solution values. Other polymers exhibited a highly emissive face-on structure at the air-water interface, and did not form pi-aggregates. The combination of pressure-area isotherms and the surface pressure dependent in situ UV-vis spectra of the polymers at the air-water interface revealed different behavioral details. In addition, the UV-vis spectra, fluorescence spectra, and quantum yields of the LB films provide design principles for making highly emissive films.