Non-resonant terahertz field enhancement in periodically arranged nanoslits

We analyze ultra strong non-resonant field enhancement of THz field in periodic arrays of nanoslits cut in ultrathin metal films. The main feature of our approach is that the slit size and metal film thickness are several orders of magnitude smaller than the wavelength k of the impinging radiation. Two regimes of operation are found. First, when the grating period, frequency-independent enhancement is observed, accompanied by a very high transmission approaching unity. With high accuracy, this enhancement equals the ratio of P to the slit width w. Second, when the grating period approaches the THz wavelength but before entering the Raleigh-Wood anomaly, the field enhancement in nanoslit stays close to that in a single isolated slit, i.e., the well-known inversefrequency dependence. Both regimes are non-resonant and thus extremely broadband. The results are obtained by the microscopic Drude-Lorentz model taking into account retardation processes in the metal film and validated by the finite difference frequency domain method. We expect sensor and modulation applications of the predicted giant broadband field enhancement

Microscopic model of the THz field enhancement in a metal nanoslit

We discuss the strong THz-field enhancement effect in a metal slit of dozens of nanometers sizes reported recently. Proposed simple microscopic model considers electric charges induced at the edges of the slit by a polarized incident wave. These charges contribute then to the field in the slit. The model is capable of explaining peculiarities of the field enhancement phenomenon such as an inverse frequency dependence of the enhancement factor. It provides closed-form expressions for the enhancement factor and field mapping inside the slit having only one fitting parameter. The model predicts influence of the slit shape on the field enhancement

Metamaterial Polarization Converter Analysis: Limits of Performance

In this paper we analyze the theoretical limits of a metamaterial converter that allows for linear-to- elliptical polarization transformation with any desired ellipticity and ellipse orientation. We employ the transmission line approach providing a needed level of the design generalization. Our analysis reveals that the maximal conversion efficiency for transmission through a single metamaterial layer is 50%, while the realistic re ection configuration can give the conversion efficiency up to 90%. We show that a double layer transmission converter and a single layer with a ground plane can have 100% polarization conversion efficiency. We tested our conclusions numerically reaching the designated limits of efficiency using a simple metamaterial design. Our general analysis provides useful guidelines for the metamaterial polarization converter design for virtually any frequency range of the electromagnetic waves.Comment: 10 pages, 11 figures, 2 table

Single-molecule DNA-mapping and whole-genome sequencing of individual cells

To elucidate cellular diversity and clonal evolution in tissues and tumors, one must resolve genomic heterogeneity in single cells. To this end, we have developed low-cost, mass-producible micro-/nanofluidic chips for DNA extraction from individual cells. These chips have modules that collect genomic DNA for sequencing or map genomic structure directly, on-chip, with denaturation-renaturation (D-R) optical mapping [Marie R, et al. (2013) Proc Natl Acad Sci USA 110:4893-4898]. Processing of single cells from the LS174T colorectal cancer cell line showed that D-R mapping of single molecules can reveal structural variation (SV) in the genome of single cells. In one experiment, we processed 17 fragments covering 19.8 Mb of the cell's genome. One megabase-large fragment aligned well to chromosome 19 with half its length, while the other half showed variable alignment. Paired-end single-cell sequencing supported this finding, revealing a region of complexity and a 50-kb deletion. Sequencing struggled, however, to detect a 20-kb gap that D-R mapping showed clearly in a megabase fragment that otherwise mapped well to the reference at the pericentromeric region of chromosome 4. Pericentromeric regions are complex and show substantial sequence homology between different chromosomes, making mapping of sequence reads ambiguous. Thus, D-R mapping directly, from a single molecule, revealed characteristics of the single-cell genome that were challenging for short-read sequencing