828 research outputs found
Helicity Dependent Directional Surface Plasmon Polariton Excitation Using A Metasurface with Interfacial Phase Discontinuity
Surface plasmon polaritons (SPPs) have been widely exploited in various
scientific communities, ranging from physics, chemistry to biology, due to the
strong confinement of light to the metal surface. For many applications it is
important that the free space photon can be coupled to SPPs in a controllable
manner. In this Letter, we apply the concept of interfacial phase discontinuity
for circularly polarizations on a metasurface to the design of a novel type of
polarization dependent SPP unidirectional excitation at normal incidence.
Selective unidirectional excitation of SPPs along opposite directions is
experimentally demonstrated at optical frequencies by simply switching the
helicity of the incident light. This approach, in conjunction with dynamic
polarization modulation techniques, opens gateway towards integrated plasmonic
circuits with electrically reconfigurable functionalities.Comment: 17 pages, 5 figures. Published on <Light:Science & Applications
Towards using concurrent Java API correctly
Concurrent Programs are hard to analyze or debug due to the complex program logic and unpredictable execution environment. In practice, ordinary programmers often adopt existing well-designed concurrency related API (e.g., those in java.util.concurrent) so as to avoid dealing with these issues. These API can however often be used incorrectly, which results in hardto-debug concurrent bugs. In this work, we propose an approach for enforcing the correct usage of concurrency-related Java API. Our idea is to annotate concurrency-related Java classes with annotations related to misuse of these API and develop lightweight type checker to detect concurrent API misuse based on the annotations. To automate this process, we need to solve two problems: (1) how do we obtain annotations of the relevant API; and (2) how do we systematically detect concurrent API misuse based on the annotations? We solve the first problem by extracting annotations from the API documentation using natural language processing techniques. We solve the second problem by implementing our type checkers in the Checker Framework to detect concurrent API misuse. We apply our approach to extract annotations for all classes in the Java standard library and use them to detect concurrent API misuse in open source projects on GitHub. We confirm that concurrent API misuse is common and often results in bugs or inefficiency.No Full Tex
Highly sensitive magnetic properties and large linear magnetoresistance in antiferromagnetic CrxSe(0.875\lex\le1)single crystals
CrxSe (x\le1) is a class of quasi-layered binary compounds with potential
applications in spintronics due to its intriguing antiferromagnetic properties.
In this work, CrxSe single crystals with high Cr content (x=0.87, 0.91 and
0.95) were grown, and their magnetic and transport properties were investigated
in detail. It is found that with small increase of Cr content, the N\'eel
temperature (TN) of the samples can dramatically increase from 147 K to 257 K,
accompanied with obvious changes in the magnetic anisotropy and hysteresis. The
phenomena of field-induced spin-flop transitions were unveiled in these alloys,
indicating their comparatively low anisotropy. The magnetoresistance (MR) of
the three compounds showed positive dependence at low temperatures and
particularly, non-saturated linear positive MR was observed in Cr0.91Se and
Cr0.95Se, with a large value of 16.2% achieved in Cr0.91Se (10K, 9T). The
calculated Fermi surface and MR showed that the quasi-linear MR is a product of
carrier compensation. Our work revealed highly sensitive magnetic and transport
properties in the Cr-Se compounds, which can lay foundation when constructing
further antiferromagnetic spintronic devices based on them
Growth of high-quality CrI3 single crystals and engineering of its magnetic properties via V and Mn doping
CrI3, as a soft van der Waals layered magnetic material, has been widely
concerned and explored for its magnetic complexity and tunability. In this
work, high quality and large size thin CrI3, V and Mn doped single crystals
were prepared by chemical vapor transfer method. A remarkable irreversible
Barkhausen effect was observed in CrI3 and CrMn0.06I3, which can be attributed
to the low dislocation density that facilitates movement of the domain walls.
In addition, the introduction of the doping element Mn allows higher saturation
magnetization intensity. Cr0.5V0.5I3 exhibits substantially increased
coercivity force and larger magnetocrystalline anisotropy compared to CrI3,
while kept similar Curie temperature and good environmental stability. The
first principles calculations suggest direct and narrowed band gaps in
Cr0.5V0.5I3 and VI3 comparing to CrI3. The smaller band gaps and good hard
magnetic property make Cr0.5V0.5I3 an alternative choice to future research of
spintronic devices
M2-like macrophages in the fibrotic liver protect mice against lethal insults through conferring apoptosis resistance to hepatocytes.
Acute injury in the setting of liver fibrosis is an interesting and still unsettled issue. Most recently, several prominent studies have indicated the favourable effects of liver fibrosis against acute insults. Nevertheless, the underlying mechanisms governing this hepatoprotection remain obscure. In the present study, we hypothesized that macrophages and their M1/M2 activation critically involve in the hepatoprotection conferred by liver fibrosis. Our findings demonstrated that liver fibrosis manifested a beneficial role for host survival and apoptosis resistance. Hepatoprotection in the fibrotic liver was tightly related to innate immune tolerance. Macrophages undertook crucial but divergent roles in homeostasis and fibrosis: depleting macrophages in control mice protected from acute insult; conversely, depleting macrophages in fibrotic liver weakened the hepatoprotection and gave rise to exacerbated liver injury upon insult. The contradictory effects of macrophages can be ascribed, to a great extent, to the heterogeneity in macrophage activation. Macrophages in fibrotic mice exhibited M2-preponderant activation, which was not the case in acutely injured liver. Adoptive transfer of M2-like macrophages conferred control mice conspicuous protection against insult. In vitro, M2-polarized macrophages protected hepatocytes against apoptosis. Together, M2-like macrophages in fibrotic liver exert the protective effects against lethal insults through conferring apoptosis resistance to hepatocytes
Identification and functional characterization of an N-terminal oligomerization domain for polycystin-2*
Autosomal dominant polycystic kidney disease (ADPKD), the most common inherited cause of kidney failure, is caused by mutations in either PKD1 (85%) or PKD2 (15%). The PKD2 protein, polycystin-2 (PC2 or TRPP2), is a member of the transient receptor potential (TRP) superfamily and functions as a non-selective calcium channel. PC2 has been found to form oligomers in native tissues suggesting that it may form functional homo- or heterotetramers with other subunits, similar to other TRP channels. Our experiments unexpectedly revealed that PC2 mutant proteins lacking the known C-terminal dimerization domain were still able to form oligomers and co-immunoprecipitate full-length PC2, implying the possible existence of a proximal dimerization domain. Using yeast two-hybrid and biochemical assays, we have mapped an alternative dimerization domain to the N terminus of PC2 (NT2-1-223, L224X). Functional characterization of this domain demonstrated that it was sufficient to induce cyst formation in zebrafish embryos and inhibit PC2 surface currents in mIMCD3 cells probably by a dominant-negative mechanism. In summary, we propose a model for PC2 assembly as a functional tetramer which depends on both C- and N-terminal dimerization domains. These results have significant implications for our understanding of PC2 function and disease pathogenesis in ADPKD and provide a new strategy for studying PC2 function
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