Andrew A. R. Watt

Biomolecule-assisted synthesis of water-soluble silver nanoparticles and their biomedical applications.

The application of nanoparticles in the biomedical field is an exciting interdisciplinary research area in current materials science. In the present study, size-tunable and water-soluble noble metal silver nanoparticles (Ag NPs) have been successfully synthesized with the assistance of glutathione (GSH). The as-synthesized Ag NPs are ready to bind covalently with a model protein (bovine serum albumin) in mild conditions. The optical property of surface-modifiable Ag NPs was extremely sensitive to their size and the surface modification, suggesting a potential in the biomedical analysis and detection. Furthermore, Ag NPs with an average diameter of ca. 6 nm effectively suppress the proliferation of human leukemic K562 cells in the dose- and time-dependent manners, suggesting the promising potential of Ag NPs in cancer therapy.

High-performance, single-layer antireflective optical coatings comprising mesoporous silica nanoparticles.

Mesoporous silica nanoparticles are used to fabricate antireflectance coatings on glass substrates. The combination of mesoporous silica nanoparticles in conjunction with a suitable binder material allows mechanically robust single layer coatings with a reflectance <0.1% to be produced by simple wet processing techniques. Further advantages of these films is that their structure results in broadband antireflective properties with a reflection minimum that can tuned between 400 nm and 1900 nm. The ratio of binder material to mesoporous nanoparticles allows control of the refractive index. In this report, we discuss how control of the structural properties of the coatings allows optimization of the optical properties.

The transitional heterojunction behavior of PbS/ZnO colloidal quantum dot solar cells.

The nature of charge separation at the heterojunction interface of solution processed lead sulphide-zinc oxide colloidal quantum dot solar cells is investigated using impedance spectroscopy and external quantum efficiency measurements to examine the effect of varying the zinc oxide doping density. Without doping, the device behaves excitonically with no depletion region in the PbS layer such that only charge carriers generated within a diffusion length of the PbS/ZnO interface have a good probability of being harvested. After the ZnO is photodoped such that the doping density is near or greater than that of the PbS, a significant portion of the depletion region is found to lie within the PbS layer increasing charge extraction (p-n operation).

Carrier transport in PbS nanocrystal conducting polymer composites

In this letter we report the carrier mobilities in an inorganic nanocrystal: conducting polymer composite. The composite material in question (lead sulphide nanocrystals in the conducting polymer poly [2-methoxy-5-(2′-ethyl-hexyloxy)-p-phenylene vinylene] (MEH-PPV) was made using a single-pot, surfactant-free synthesis. Mobilties were measured using time of flight techniques. We have found that the inclusion of PbS nanocrystals in MEH-PPV both balances and markedly increases the hole and electron mobilities—the hole mobility is increased by a factor of ∼105 and the electron mobility increased by ∼107 under an applied bias of 5kVcm−1. These results explain why dramatic improvements in electrical conductivity and photovoltaic performance are seen in devices fabricated from these composites.

SnS/PbS nanocrystal heterojunction photovoltaics.

We report advances in the growth, characterization and photovoltaic properties of SnS nanocrystals, with controlled < 10 nm size, and their inclusion into a lead chalcogenide solar cell. The SnS/PbS nanocrystalline film heterojunction is shown to display a type II band alignment, in which the direction of flow of the photocurrent depends on the order of the layers and not the relative work functions of the contacts. On placing the SnS layer next to the indium tin oxide (ITO) cathode we observe a dramatic increase in V(oc) to as much as 0.45 V. Our results suggest that SnS nanocrystal films can be used in multi-junction solar cells, that a SnS/PbS heterojunction on its own shows photovoltaic behaviour, and that a SnS layer in an ITO/SnS/PbS/Al device is acting to suppress the flow of an electron injection current.

Inorganic surface passivation of PbS nanocrystals resulting in strong photoluminescent emission

Strong photoluminescent emission has been obtained from 3 nm PbS nanocrystals in aqueous colloidal solution, following treatment with CdS precursors. The observed emission can extend across the entire visible spectrum and usually includes a peak near 1.95 eV. We show that much of the visible emission results from absorption by higher-lying excited states above 3.0 eV with subsequent relaxation to and emission from states lying above the observed band-edge of the PbS nanocrystals. The fluorescent lifetimes for this emission are in the nanosecond regime, characteristic of exciton recombination.

Rotating fullerene chains in carbon nanopeapods.

The rotation of fullerene chains in SWNT peapods is studied using low-voltage high resolution transmission electron microscopy. Anisotropic fullerene chain structures (i.e., C300) are formed in situ in carbon nanopeapods via electron beam induced coalescence of individual fullerenes (i.e., C60). A low electron accelerating voltage of 80 kV is used to prevent damage to the SWNT. The large asymmetric C300 fullerene structure exhibits translational motion inside the SWNT and unique corkscrew like rotation motion. Another asymmetric fullerene chain containing mixed fullerene species is prepared by fusing smaller C60 fullerenes to a larger Sc@C82 fullerene, and this also exhibits corkscrew rotational motion. Chains of Sc3C2@C80 in SWNT peapods adopt a zigzag packing structure, and the entire zigzag chain rotates inside the SWNT to induce structural modifications to the SWNT diameter and cross-sectional shape of the SWNT. The expansion and contraction of the diameter of the SWNT is measured as 17%, demonstrating nanoactuation behavior in carbon nanopeapods.

Dynamics of Paramagnetic Metallofullerenes in Carbon Nanotube Peapods

We filled SWNTs with the paramagnetic fullerene Sc@C82 to form peapods. The interfullerene 1D packing distance measured using TEM is d = 1.1 +/- 0.02 nm. The Sc@C82 in SWNT peapods continuously rotated during the 2 s TEM exposure time, and we did not see the Sc atoms. However, Sc@C82 metallofullerenes in MWNT peapods have periods of fixed orientation, indicated by the brief observation of Sc atoms. La@C82 peapods were also prepared and their rotational behavior examined. The interfullerene 1D packing of both La@C82 and Sc@C82 peapods is identical and thus independent of the charge transfer state for these paramagnetic fullerenes. The La@C82 metallofullerenes in the peapods have fixed orientations for extended periods of time, up to 50 s in some cases. The La@C82 spontaneously rotates rapidly between fixed orientations.

Improved performance of multilayer InAs/GaAs quantum-dot solar cells using a high-growth-temperature GaAs spacer layer

The use of high-growth-temperature GaAs spacer layers is demonstrated to significantly enhance the performance of multilayer InAs/GaAs quantum-dot solar cells. Threading dislocations are observed for a 30-layer quantum-dot structure with GaAs spacer layers grown at low temperature (510 °C). The formation of threading dislocations is suppressed by growing the GaAs spacer layer at high temperature (580 °C), leading to enhanced quantum-dot optical and structural characteristics. Incorporation of the high-growth-temperature GaAs spacer layers into a 30-layer InAs/GaAs quantum-dot solar cell results in a dramatic increase in the short-circuit current compared to the one without the high-growth-temperature spacer layers and an increase in the short-circuit current compared to the reference GaAs solar cell.

Amino-acid-assisted synthesis and size-dependent magnetic behaviors of hematite nanocubes

This article reports the amino-acid-assisted synthesis and size-dependent magnetic properties of hematite nanocubes. The products were characterized using x-ray diffraction, Raman spectroscopy, transmission electron microscopy (TEM), and high-resolution TEM. The magnetic behavior of hematite nanocubes was studied using a vibrating sample magnetometer at room temperature. The sizes of hematite nanocubes were controlled by tuning the reaction parameters. The amino acid has double-hydrophilic functional groups, –NH2 and –COOH, which are utilized to control the growth and final size of hematite nanocubes. We show that utilizing biomolecules in chemical synthesis is a useful method for tailoring the physical properties of nanomaterials.