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Institution

National Institute of Advanced Industrial Science and Technology

GovernmentTsukuba, Ibaraki, Japan
About: National Institute of Advanced Industrial Science and Technology is a government organization based out in Tsukuba, Ibaraki, Japan. It is known for research contribution in the topics: Catalysis & Thin film. The organization has 22114 authors who have published 65856 publications receiving 1669827 citations. The organization is also known as: Sangyō Gijutsu Sōgō Kenkyū-sho.
Topics: Catalysis, Thin film, Carbon nanotube, Hydrogen, Laser


Papers
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Journal ArticleDOI
TL;DR: Exclusively in regions exhibiting this new spectrum, local "checkerboard" charge ordering of high energy states coexists harmoniously with the low energy Bogoliubov quasiparticle states.
Abstract: The doping dependence of nanoscale electronic structure in superconducting ${\mathrm{Bi}}_{2}{\mathrm{Sr}}_{2}\mathrm{Ca}{\mathrm{Cu}}_{2}{\mathrm{O}}_{8+\ensuremath{\delta}}$ is studied by scanning tunneling microscopy. At all dopings, the low energy density-of-states modulations are analyzed according to a simple model of quasiparticle interference and found to be consistent with Fermi-arc superconductivity. The superconducting coherence peaks, ubiquitous in near-optimal tunneling spectra, are destroyed with strong underdoping and a new spectral type appears. Exclusively in regions exhibiting this new spectrum, we find local ``checkerboard'' charge ordering of high energy states, with a wave vector of $\stackrel{\ensuremath{\rightarrow}}{Q}=(\ifmmode\pm\else\textpm\fi{}2\ensuremath{\pi}/4.5{a}_{0},0)$; $(0,\ifmmode\pm\else\textpm\fi{}2\ensuremath{\pi}/4.5{a}_{0})\ifmmode\pm\else\textpm\fi{}15%$. Surprisingly, this spatial ordering of high energy states coexists harmoniously with the low energy Bogoliubov quasiparticle states.

344 citations

Journal ArticleDOI
TL;DR: In this paper, four types of orthorhombic olivine LiMPO4 (M:Co, Fe, Ni and Mn) were investigated as highvoltage cathode active materials for lithium secondary batteries.

343 citations

Journal ArticleDOI
TL;DR: TheTRPC3-selective inhibitor Pyr3 is a powerful tool to study in vivo function of TRPC3, suggesting a pharmaceutical potential of Pyr3 in treatments of TR PC3-related diseases such as cardiac hypertrophy.
Abstract: Canonical transient receptor potential (TRPC) channels control influxes of Ca2+ and other cations that induce diverse cellular processes upon stimulation of plasma membrane receptors coupled to phospholipase C (PLC). Invention of subtype-specific inhibitors for TRPCs is crucial for distinction of respective TRPC channels that play particular physiological roles in native systems. Here, we identify a pyrazole compound (Pyr3), which selectively inhibits TRPC3 channels. Structure-function relationship studies of pyrazole compounds showed that the trichloroacrylic amide group is important for the TRPC3 selectivity of Pyr3. Electrophysiological and photoaffinity labeling experiments reveal a direct action of Pyr3 on the TRPC3 protein. In DT40 B lymphocytes, Pyr3 potently eliminated the Ca2+ influx-dependent PLC translocation to the plasma membrane and late oscillatory phase of B cell receptor-induced Ca2+ response. Moreover, Pyr3 attenuated activation of nuclear factor of activated T cells, a Ca2+-dependent transcription factor, and hypertrophic growth in rat neonatal cardiomyocytes, and in vivo pressure overload-induced cardiac hypertrophy in mice. These findings on important roles of native TRPC3 channels are strikingly consistent with previous genetic studies. Thus, the TRPC3-selective inhibitor Pyr3 is a powerful tool to study in vivo function of TRPC3, suggesting a pharmaceutical potential of Pyr3 in treatments of TRPC3-related diseases such as cardiac hypertrophy.

343 citations

Journal ArticleDOI
TL;DR: This work replaces easily decomposable liquid electrolytes with a solid Li-ion conductor, which acts as both a catholyte and a Li protector, and replaces conventional solid air cathodes with a gel cathode, which contacts directly with the solid catholytes to form a closed and sustainable gel/solid interface.
Abstract: Electrolyte degradation, Li dendrite formation and parasitic reactions with H₂O and CO₂ are all directly correlated to reversibility and cycleability of Li-air batteries when operated in ambient air. Here we replace easily decomposable liquid electrolytes with a solid Li-ion conductor, which acts as both a catholyte and a Li protector. Meanwhile, the conventional solid air cathodes are replaced with a gel cathode, which contacts directly with the solid catholyte to form a closed and sustainable gel/solid interface. The proposed Li-air cell has sustained repeated cycling in ambient air for 100 cycles (~78 days), with discharge capacity of 2,000 mAh g(-1). The recharging is based largely on the reversible reactions of Li₂CO₃ product, originating from the initial discharge product of Li₂O₂ instead of electrolyte degradation. Our results demonstrate that a reversible long-life Li-air battery is attainable by coordinated approaches towards the focal issues of electrolytes and Li metal.

342 citations

Journal ArticleDOI
TL;DR: A perovskite heterojunction consisting of SrRuO3 (SRO) film epitaxially grown on SrTi0.99 Nb0.01 O3 (Nb:STO) substrate was studied in this article.
Abstract: Transport properties have been studied for a perovskite heterojunction consisting of SrRuO3 (SRO) film epitaxially grown on SrTi0.99Nb0.01O3 (Nb:STO) substrate. The SRO/Nb:STO interface exhibits rectifying current–voltage (I–V) characteristics agreeing with those of a Schottky junction composed of a deep work-function metal (SRO) and an n-type semiconductor (Nb:STO). A hysteresis appears in the I–V characteristics, where high resistance and low resistance states are induced by reverse and forward bias stresses, respectively. The resistance switching is also triggered by applying short voltage pulses of 1μs–10ms duration.

342 citations


Authors

Showing all 22289 results

NameH-indexPapersCitations
Takeo Kanade147799103237
Ferenc A. Jolesz14363166198
Michele Parrinello13363794674
Kazunari Domen13090877964
Hideo Hosono1281549100279
Hideyuki Okano128116967148
Kurunthachalam Kannan12682059886
Shaobin Wang12687252463
Ajit Varki12454258772
Tao Zhang123277283866
Ramamoorthy Ramesh12264967418
Kazuhito Hashimoto12078161195
Katsuhiko Mikoshiba12086662394
Qiang Xu11758550151
Yoshinori Tokura11785870258
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202367
2022265
20213,064
20203,389
20193,257
20183,181