281 research outputs found
Determination of Formation Rate Constant of Carrier-Free 111In(III) with EDTA
開始ページ、終了ページ: 冊子体のページ付
Direct Observation of Nonequivalent Fermi-Arc States of Opposite Surfaces in Noncentrosymmetric Weyl Semimetal NbP
We have performed high-resolution angle-resolved photoemission spectroscopy
(ARPES) on noncentrosymmetric Weyl semimetal candidate NbP, and determined the
electronic states of both Nb- and P-terminated surfaces corresponding to the
"opposite" surfaces of a polar crystal. We revealed a drastic difference in the
Fermi-surface topology between the opposite surfaces, whereas the Fermi arcs on
both surfaces are likely terminated at the surface projection of the same bulk
Weyl nodes. Comparison of the ARPES data with our first-principles band
calculations suggests notable difference in electronic structure at the
Nb-terminated surface between theory and experiment. The present result opens a
platform for realizing exotic quantum phenomena arising from unusual surface
properties of Weyl semimetals.Comment: 5 pages, 4 figure
Arg-gingipain A DNA Vaccine Prevents Alveolar Bone Loss in Mice
博士(歯学)・第1630号(甲第929号)・平成17年3月31日http://jdr.iadrjournals.org/cgi/content/full/86/5/44
Radiative pumping in a strongly coupled microcavity filled with a neat molecular film showing excimer emission
Strong light-matter interactions have attracted much attention as a means to control the physical/chemical properties of organic semiconducting materials with light-matter hybrids called polaritons. To unveil the processes under strong coupling, studies on the dynamics of polaritons are of particular importance. While highly condensed molecular materials with large dipole density are ideal to achieve strong coupling, the emission properties of such films often become a mixture of monomeric and excimeric components, making the role of excimers unclear. Here, we use amorphous neat films of a new bis(phenylethynyl anthracene) derivative showing only excimer emission and investigate the excited-state dynamics of a series of strongly coupled microcavities, with each cavity being characterised by a different exciton–photon detuning. A time-resolved photoluminescence study shows that the excimer radiatively pumps the lower polariton in the relaxation process and the decay profile reflects the density of states. The delayed emission derived from triplet–triplet annihilation is not sensitive to the cavity environment, possibly due to the rapid excimer formation. Our results highlight the importance of controlling intermolecular interactions towards rational design of organic exciton–polariton devices, whose performance depends on efficient polariton relaxation pathways
Photon Upconverting Solid Films with Improved Efficiency for Endowing Perovskite Solar Cells with Near‐Infrared Sensitivity
Perovskite solar cells have emerged as the next‐generation high‐efficiency solar cell, but their absorption is mostly limited to the visible (vis) range. One possible solution is to integrate near‐infrared (NIR)‐to‐vis photon upconversion (UC). Herein, we show the first example of endowing perovskite solar cells with NIR sensitivity by using solid films showing NIR‐to‐vis UC based on triplet‐triplet annihilation (TTA). A high TTA‐UC efficiency of 4.1±0.3 % at an excitation intensity of 125 W/cm² is achieved by sensitizing a rubrene (acceptor) triplet with an osmium (Os) complex donor having singlet‐to‐triplet (S−T) absorption in the NIR range, and by increasing the fluorescence quantum yield through energy harvesting to a highly fluorescent collector. In particular, our spectroscopic studies indicate that the upconverted acceptor singlet energy is almost selectively transferred to the collector rather than being quenched by the donor. By attaching the TTA‐UC film behind a semi‐transparent perovskite solar cell, a photocurrent generation is observed under excitation at 938 nm
An EST-SSR Linkage Map of Raphanus sativus and Comparative Genomics of the Brassicaceae†
Raphanus sativus (2n = 2x = 18) is a widely cultivated member of the family Brassicaceae, for which genomic resources are available only to a limited extent in comparison to many other members of the family. To promote more genetic and genomic studies and to enhance breeding programmes of R. sativus, we have prepared genetic resources such as complementary DNA libraries, expressed sequences tags (ESTs), simple sequence repeat (SSR) markers and a genetic linkage map. A total of 26 606 ESTs have been collected from seedlings, roots, leaves, and flowers, and clustered into 10 381 unigenes. Similarities were observed between the expression patterns of transcripts from R. sativus and those from representative members of the genera Arabidopsis and Brassica, indicating their functional relatedness. The EST sequence data were used to design 3800 SSR markers and consequently 630 polymorphic SSR loci and 213 reported marker loci have been mapped onto nine linkage groups, covering 1129.2 cM with an average distance of 1.3 cM between loci. Comparison of the mapped EST-SSR marker positions in R. sativus with the genome sequence of A. thaliana indicated that the Brassicaceae members have evolved from a common ancestor. It appears that genomic fragments corresponding to those of A. thaliana have been doubled and tripled in R. sativus. The genetic map developed here is expected to provide a standard map for the genetics, genomics, and molecular breeding of R. sativus as well as of related species. The resources are available at http://marker.kazusa.or.jp/Daikon
Synthesis, Infra-red, Raman, NMR and structural characterization by X-ray Diffraction of [C12H17N2]2CdCl4 and [C6H10N2]2Cd3Cl10 compounds
The synthesis, infra-red, Raman and NMR spectra and crystal structure of 2,
4, 4- trimethyl-4, 5- dihydro-3H-benzo[b] [1, 4] diazepin-1-ium
tetrachlorocadmate, [C12H17N2]2CdCl4 and benzene-1,2-diaminium
decachlorotricadmate(II) [C6H10N2]2Cd3Cl10 are reported.
The [C12H17N2]2CdCl4 compound crystallizes in the triclinic system (P-1 space
group) with Z = 2 and the following unit cell dimensions: a = 9.6653(8)
angstrom, b = 9.9081(9) angstrom, c = 15.3737(2) angstrom, alpha =
79.486(1)degrees, beta = 88.610(8)degrees and gamma = 77.550(7)degrees. The
structure was solved by using 4439 independent reflections down to R value of
0.029. In crystal structure, the tetrachlorocadmiate anion is connected to two
organic cations through N-H...Cl hydrogen bonds and Van Der Waals interaction
as to build cation-anion-cation cohesion. The [C6H10N2]2Cd3Cl10 crystallizes in
the triclinic system (P-1 space group). The unit cell dimensions are a = 6.826
(5)angstrom, b = 9.861 (7)angstrom, c = 10.344 (3)angstrom, alpha = 103.50
(1)degrees, beta = 96.34 (4)degrees and gamma = 109.45 (3)degrees, Z=2. The
final R value is 0.053 (Rw=0.128). Its crystal structure consists of organic
cations and polymeric chains of [Cd3Cl10]4- anions running along the [011]
direction, In The [C6H10N2]2Cd3Cl10 compounds hydrogen bond interactions
between the inorganic chains and the organic cations, contribute to the crystal
packing.
PACS Codes: 61.10.Nz, 61.18.Fs, 78.30.-jComment: 19 pages, 10 figure
Triangles and tetrahedra: metal directed self-assembly of metallo-supramolecular structures incorporating bis-b-diketonato ligands
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