Effect of topography-dependent light coupling through a near-field aperture on the local photocurrent of a solar cell.

An aperture-type scanning near-field optical microscope (a-SNOM) is readily used for the optical and optoelectronic characterizations of a wide variety of chemical, biological and optoelectronic samples with sub-wavelength optical resolution. These samples mostly exhibit nanoscale topographic variations, which are related to local material inhomogeneity probed either by an optical contrast or by secondary effects such as photoconductivity or photoluminescence. To date, in the interpretation and evaluation of the measurement results from a-SNOM or derived methods, often only the local material inhomogeneity is taken into account. A possible influence of the optical interaction between the scanning probe and the surface topography is rarely discussed. In this paper, we present experimental and theoretical investigation of the effects of nanoscale topographic features on a-SNOM measurement results. We conduct local photocurrent measurements on a thin-film solar cell with an a-SNOM as the illumination source. A clear correlation between the photocurrent response and local topography is observed in all measurements with a signal contrast of up to ∼30%, although the sample features homogeneous permittivity and electrical properties. With the help of finite-difference time-domain (FDTD) simulations, this correlation is reproduced and local light coupling is identified as the mechanism which determines the local photocurrent response. Our results suggest that a-SNOM-based measurements of any sample with material inhomogeneity will be superimposed by the local light-coupling effect if surface topography variation exists. This effect should always be taken into consideration for an accurate interpretation of the measurement results.

Sonochemical synthesis of hydrogenated amorphous silicon nanoparticles from liquid trisilane at ambient temperature and pressure.

Silicon nanoparticles (Si-NPs) are increasing in relevance in diverse fields of scientific and nanotechnological inquiry, where currently some of the most important areas of research involve energy storage and biomedical applications. The present article is concerned with a curious and scalable method for the preparation of discrete, unoxidized, hydrogenated, and amorphous Si-NPs of tunable size in the range of 1.5-50nm. Using ultrasound generated with a conventional ultrasonic horn, the "fusion" of Si-NPs is demonstrated at ambient temperature and pressure by sonicating solutions containing readily available, semiconductor-grade purity trisilane (Si3H8). The only requirement for the synthesis is that it be carried out in an inert atmosphere such as that of a N2-filled glove box. Various spectroscopic techniques and electron microscopy images are used to show that the size of the Si-NPs can be controlled by varying the amplitude of the ultrasonic waves or the concentration of trisilane in the solution. Moreover, sustained ultrasonic irradiation is found to yield highly porous Si-NP agglomerates that may find use in applications requiring non-crystalline nanoscopic high specific surface area morphologies.

Angular dependence of light trapping in nanophotonic thin-film solar cells.

The angular dependence of light-trapping in nanophotonic thin-film solar cells is inherent due to the wavelength-scale dimensions of the periodic nanopatterns. In this paper, we experimentally investigate the dependence of light coupling to waveguide modes for light trapping in a-Si:H solar cells deposited on nanopatterned back contacts. First, we accurately determine the spectral positions of individual waveguide modes in thin-film solar cells in external quantum efficiency and absorptance. Second, we demonstrate the strong angular dependence of this spectral position for our solar cells. Third, a moderate level of disorder is introduced to the initially periodic nanopattern of the back contacts. As a result, the angular dependence is reduced. Last, we experimentally compare this dependence on the angle of incidence for randomly textured, 2D periodically nanopatterned and 2D disordered back contacts in external quantum efficiency and short-circuit current density.

Nanoscale observation of waveguide modes enhancing the efficiency of solar cells.

Nanophotonic light management concepts are on the way to advance photovoltaic technologies and accelerate their economical breakthrough. Most of these concepts make use of the coupling of incident sunlight to waveguide modes via nanophotonic structures such as photonic crystals, nanowires, or plasmonic gratings. Experimentally, light coupling to these modes was so far exclusively investigated with indirect and macroscopic methods, and thus, the nanoscale physics of light coupling and propagation of waveguide modes remain vague. In this contribution, we present a nanoscopic observation of light coupling to waveguide modes in a nanophotonic thin-film silicon solar cell. Making use of the subwavelength resolution of the scanning near-field optical microscopy, we resolve the electric field intensities of a propagating waveguide mode at the surface of a state-of-the-art nanophotonic thin-film solar cell. We identify the resonance condition for light coupling to this individual waveguide mode and associate it to a pronounced resonance in the external quantum efficiency that is found to increase significantly the power conversion efficiency of the device. We show that a maximum of the incident light couples to the investigated waveguide mode if the period of the electric field intensity of the waveguide mode matches the periodicity of the nanophotonic two-dimensional grating. Our novel experimental approach establishes experimental access to the local analysis of light coupling to waveguide modes in a number of optoelectronic devices concerned with nanophotonic light-trapping as well as nanophotonic light emission.

Design of nanostructured plasmonic back contacts for thin-film silicon solar cells.

We report on a plasmonic light-trapping concept based on localized surface plasmon polariton induced light scattering at nanostructured Ag back contacts of thin-film silicon solar cells. The electromagnetic interaction between incident light and localized surface plasmon polariton resonances in nanostructured Ag back contacts was simulated with a three-dimensional numerical solver of Maxwell's equations. Geometrical parameters as well as the embedding material of single and periodic nanostructures on Ag layers were varied. The design of the nanostructures was analyzed regarding their ability to scatter incident light at low optical losses into large angles in the silicon absorber layers of the thin-film silicon solar cells.

Capillary zone electrophoresis of amino acids on a hybrid poly(dimethylsiloxane)-glass chip.

Poly(dimethylsiloxane) (PDMS)-PDMS and hybrid PDMS-glass devices have been characterized and compared in terms of current-voltage linearity, contact angle, electroosmotic velocity, electroosmotic mobility, and electrokinetic potential in dependence on the surface treatment. The hybrid PDMS-glass microfluidic devices have further been tested as on-chip capillary electrophoresis systems for the separation of fluorescently labeled amino acids. It has been demonstrated that different methods of surface pretreatment of the PDMS-glass devices result in significantly different separation performance, with plate numbers varying from 650 to 57 000 in dependence on the surface state and the nature of the amino acids. Electrophoretic separations of amino acids have been achieved within tens of seconds with detection limits of less than 2 microM (approximately 2 x 10(-16) to 2.5 x 10(-16) mol quantities at injection volumes of 110-120 pL). The detected amounts of fluorescein isothiocyante (FITC)-amino acids are at least ten times lower, since the amino acid:FITC ratio is 10:1 mol. The results demonstrate the perspective of such hybrid PDMS-glass microfluidic systems and the methods to modify their surfaces for on-chip separation methods for biomolecules.