Yuri S. Kivshar

Bio: Yuri S. Kivshar is an academic researcher from Australian National University. The author has contributed to research in topics: Metamaterial & Soliton. The author has an hindex of 126, co-authored 1845 publications receiving 79415 citations. Previous affiliations of Yuri S. Kivshar include Technische Universität Darmstadt & Los Alamos National Laboratory.

Polarization properties of optical metasurfaces of different symmetries

Abstract: Optical metasurfaces have become a new paradigm for creating flat optical devices. While being typically an order of magnitude thinner than the wavelength of light, metasurfaces allow control of the phase of propagating light waves across the full $2\ensuremath{\pi}$ range and therefore enable the realization of optical elements such as lenses, waveplates, and beam converters. Currently one of the limiting factors of functional metasurfaces is their small range of operational angles. Here we demonstrate both theoretically and experimentally that the angular range can be broadened by increasing the rotational symmetry of metasurfaces. We develop an analytical model based on the discrete dipole approximation that quantitatively describes the response of metasurfaces under oblique excitation. It shows that the effective optical symmetry is doubled for structures with odd rotational symmetry, increasing the angular range correspondingly. We apply and experimentally verify our model for metasurfaces consisting of identical meta-atoms, arranged into square lattices, hexagonal lattices, and on the vertices of a Penrose tiling. The results demonstrate the increasing angular performance with increasing rotational symmetry.

The role of ferroelectric domain structure in second harmonic generation in random quadratic media

Abstract: We study theoretically and numerically the second harmonic generation in a nonlinear crystal with random distribution of ferroelectric domains. We show that the specific features of disordered domain structure greatly affect the emission pattern of the generated harmonics. This phenomena can be used to characterize the degree of disorder in nonlinear photonic structures.

Nonlinear localized modes at phase-slip defects in waveguide arrays.

Abstract: We study light localization at a phase-slip defect created by two semi-infinite mismatched identical arrays of coupled optical waveguides. We demonstrate that the nonlinear defect modes possess the specific properties of both nonlinear surface modes and discrete solitons. We analyze the stability of the localized modes and their generation in both linear and nonlinear regimes.

Nonlinear multicore waveguiding structures with balanced gain and loss

Abstract: We study existence, stability, and dynamics of linear and nonlinear stationary modes propagating in radially symmetric multicore waveguides with balanced gain and loss. We demonstrate that, in general, the system can be reduced to an effective PT-symmetric dimer with asymmetric coupling. In the linear case, we find that there exist two modes with real propagation constants before an onset of the PT-symmetry breaking while other modes have always the propagation constants with nonzero imaginary parts. This leads to a stable (unstable) propagation of the modes when gain is localized in the core (ring) of the waveguiding structure. In the case of nonlinear response, we show that an interplay between nonlinearity, gain, and loss induces a high degree of instability, with only small windows in the parameter space where quasistable propagation is observed. We propose a novel stabilization mechanism based on a periodic modulation of both gain and loss along the propagation direction that allows bounded light propagation in the multicore waveguiding structures.

Snake instability of one-dimensional parametric spatial solitons.

Abstract: We show that one-dimensional parametric spatial solitons undergo temporal instability that leads to their breakup into spatiotemporal patterns with a characteristic snakelike shape.

I and i

Abstract: There is, I think, something ethereal about i —the square root of minus one. I remember first hearing about it at school. It seemed an odd beast at that time—an intruder hovering on the edge of reality. Usually familiarity dulls this sense of the bizarre, but in the case of i it was the reverse: over the years the sense of its surreal nature intensified. It seemed that it was impossible to write mathematics that described the real world in …

Fast parallel algorithms for short-range molecular dynamics

Abstract: Three parallel algorithms for classical molecular dynamics are presented. The first assigns each processor a fixed subset of atoms; the second assigns each a fixed subset of inter-atomic forces to compute; the third assigns each a fixed spatial region. The algorithms are suitable for molecular dynamics models which can be difficult to parallelize efficiently—those with short-range forces where the neighbors of each atom change rapidly. They can be implemented on any distributed-memory parallel machine which allows for message-passing of data between independently executing processors. The algorithms are tested on a standard Lennard-Jones benchmark problem for system sizes ranging from 500 to 100,000,000 atoms on several parallel supercomputers--the nCUBE 2, Intel iPSC/860 and Paragon, and Cray T3D. Comparing the results to the fastest reported vectorized Cray Y-MP and C90 algorithm shows that the current generation of parallel machines is competitive with conventional vector supercomputers even for small problems. For large problems, the spatial algorithm achieves parallel efficiencies of 90% and a 1840-node Intel Paragon performs up to 165 faster than a single Cray C9O processor. Trade-offs between the three algorithms and guidelines for adapting them to more complex molecular dynamics simulations are also discussed.

疟原虫var基因转换速率变化导致抗原变异[英]／Paul H, Robert P, Christodoulou Z, et al//Proc Natl Acad Sci U S A

Abstract: 抗原变异可使得多种致病微生物易于逃避宿主免疫应答。表达在感染红细胞表面的恶性疟原虫红细胞表面蛋白1（PfPMP1）与感染红细胞、内皮细胞、树突状细胞以及胎盘的单个或多个受体作用，在黏附及免疫逃避中起关键的作用。每个单倍体基因组var基因家族编码约60种成员，通过启动转录不同的var基因变异体为抗原变异提供了分子基础。