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Dive into the research topics where Hiroyuki Nojiri is active.

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Featured researches published by Hiroyuki Nojiri.


Proceedings of the National Academy of Sciences of the United States of America | 2016

Ideal charge-density-wave order in the high-field state of superconducting YBCO

H. Jang; W. S. Lee; Hiroyuki Nojiri; S. Matsuzawa; H. Yasumura; Laimei Nie; Akash V. Maharaj; Simon Gerber; Yijin Liu; Apurva Mehta; D. A. Bonn; Ruixing Liang; W. N. Hardy; C. A. Burns; Zahirul Islam; Sanghoon Song; J. B. Hastings; T. P. Devereaux; Zhi-Xun Shen; Steven A. Kivelson; Chi-Chang Kao; Diling Zhu; J.-S. Lee

Significance Compelling evidence of various forms of nonsuperconducting electronic order in the cuprate high-temperature superconductors has fundamentally altered our understanding of the essential physics of these materials. However, it has been difficult to establish the nature of the quantum (zero-temperature) phases that compete and/or coexist with superconductivity. By studying high-quality crystals of YBCO using an X-ray laser and pulsed magnetic fields, we have established that the field induced charge-density-wave (CDW) order that arises when superconductivity is suppressed at low temperatures is incommensurate, unidirectional, and 3D-ordered. While disorder ultimately precludes true CDW long-range order, there does appear to be a sharply defined crossover field, which we associate with a transition to a nematic state with long-range orientational order. The existence of charge-density-wave (CDW) correlations in cuprate superconductors has now been established. However, the nature of the CDW ground state has remained uncertain because disorder and the presence of superconductivity typically limit the CDW correlation lengths to only a dozen unit cells or less. Here we explore the field-induced 3D CDW correlations in extremely pure detwinned crystals of YBa2Cu3O2 (YBCO) ortho-II and ortho-VIII at magnetic fields in excess of the resistive upper critical field (Hc2) where superconductivity is heavily suppressed. We observe that the 3D CDW is unidirectional and possesses a long in-plane correlation length as well as significant correlations between neighboring CuO2 planes. It is significant that we observe only a single sharply defined transition at a critical field proportional to Hc2, given that the field range used in this investigation overlaps with other high-field experiments including quantum oscillation measurements. The correlation volume is at least two to three orders of magnitude larger than that of the zero-field CDW. This is by far the largest CDW correlation volume observed in any cuprate crystal and so is presumably representative of the high-field ground state of an “ideal” disorder-free cuprate.


European Physical Journal D | 2017

The OVAL experiment: A new experiment to measure vacuum magnetic birefringence using high repetition pulsed magnets

Xing Fan; Shusei Kamioka; Toshiaki Inada; Takayuki Yamazaki; T. Namba; S. Asai; Junko Omachi; Kosuke Yoshioka; Makoto Kuwata-Gonokami; Akira Matsuo; K. Kawaguchi; Koichi Kindo; Hiroyuki Nojiri

AbstractnA new experiment to measure vacuum magnetic birefringence (VMB), the OVAL experiment, is reported. We developed an original pulsed magnet that has a high repetition rate and applies the strongest magnetic field among VMB experiments online. The vibration isolation design and feedback system enable the direct combination of the magnet with a Fabry-Pérot cavity. To demonstrate and benchmark the searching potential, a calibration measurement with dilute nitrogen gas and a prototype search for VMB are performed. Based on the results, a strategy to observe VMB is reported.nGraphical abstract


Journal of the American Chemical Society | 2017

Topological Self-Assembly of Highly Symmetric Lanthanide Clusters: A Magnetic Study of Exchange-Coupling “Fingerprints” in Giant Gadolinium(III) Cages

Lei Qin; Guo-Jun Zhou; You-Zhu Yu; Hiroyuki Nojiri; Christian Schröder; Richard E. P. Winpenny; Yan-Zhen Zheng

The creation of a perfect hollow nanoscopic sphere of metal centers is clearly an unrealizable synthetic challenge. It is, however, an inspirational challenge from the viewpoint of chemical architecture and also as finite molecular species may provide unique microscopic insight into the origin and onset of phenomena such as topological spin-frustration effects found in infinite 2D and 3D systems. Herein, we report a series of high-symmetry gadolinium(III) (S = 7/2) polyhedra, Gd20, Gd32, Gd50, and Gd60, to test an approach based on assembling polymetallic fragments that contain different polygons. Structural analysis reveals that the Gd20 cage resembles a dodecahedron; the vertices of the Gd32 polyhedron exactly reveal symmetry Oh; Gd50 displays an unprecedented polyhedron in which an icosidodecahedron Gd30 core is encapsulated by an outer Gd20 dodecahedral shell with approximate Ih symmetry; and the Gd60 shows a truncated octahedron geometry. Experimental and theoretical magnetic studies show that this series produces the expected antiferromagnetic interaction that can be modeled based on classical spins at the Gd sites. From the magnetization analyses, we can roughly correlate the derivative bands to the Gd-O-Gd angles. Such a magneto-structural correlation may be used as fingerprints to identify these cages.


Inorganic Chemistry | 2017

Giant Exchange Coupling Evidenced with a Magnetization Jump at 52 T for a Gadolinium-Nitroxide Chelate

Takuya Kanetomo; Takumi Kihara; Atsushi Miyake; Akira Matsuo; Masashi Tokunaga; Koichi Kindo; Hiroyuki Nojiri; Takayuki Ishida

The Gd-radical complex [GdIII(hfac)3(6bpyNO)] (6bpyNO = 2,2-bipyridin-6-yl tert-butyl nitroxide; Hhfac = 1,1,1,5,5,5-hexafluoropentane-2,4-dione) showed a magnetization jump at 52 T observed in a pulsed-field facility, corresponding to an exchange coupling constant of -17.4 K. Furthermore, hysteretic behavior due to a relatively slow magnetization reversal was recorded around 2 T. From the high-frequency EPR study, the exchange coupling between Gd and radical spins accompanies an anisotropic character, which is responsible for both the broad jump and the slow magnetization reversal.


Inorganic Chemistry | 2017

Design of a Family of Ln3 Triangles with the HAT Ligand (1,4,5,8,9,12-Hexaazatriphenylene): Single-Molecule Magnetism

Ismael F. Díaz-Ortega; Juan Manuel Herrera; Tulika Gupta; Gopalan Rajaraman; Hiroyuki Nojiri; Enrique Colacio

A series of trinuclear Ln3 complexes (LnIII = Yb (1), Er (2), Dy (3) and Gd (4)) were prepared from the tris-chelate bidentate ligand 1,4,5,8,9,12-hexaazatriphenylene (HAT). 1 and 2 exhibited field-induced single-molecule-magnet (SMM) behavior with estimated Ueff values of 21.30 and 13.86 K, respectively. Complex 3 behaved as a SMM even at zero field, and two different thermally assisted relaxation processes were detected with Ueff values of 29.6 K (fast relaxation process, FR) and 69 K (slow relaxation process, SR) due to the existence of two magnetically different DyIII centers in the molecule. Ab initio studies reveal that all the Dy3+ centers have almost an Ising ground state. The local anisotropy axes are not coplanar but form angles with the Dy3 plane in the range 58-78°. The magnetic interaction between the anisotropic Dy3+ ions is antiferromagnetic in nature and very weak in magnitude. However, due to the extreme feebleness of the magnetic interaction with regard to the local excitation energies, the magnetization blockade is most probably of single-ion origin. Calculations support the existence of two relaxation processes, which take place through the first excited state following an Orbach/Raman mechanism. Finally, for complex 4, the magnetocaloric effect was simulated using the magnetic parameters extracted from the fit of the magnetization and susceptibility data and demonstrated that the simulated -ΔSm values were almost coincident with those extracted from the integration of the field dependence of the magnetization. The simulated MCE value at 2 K and 5 T (20.46 J kg-1 K-1) makes complex 4 an attractive candidate for cryogenic magnetization.


Angewandte Chemie | 2017

Quantum Monte Carlo Simulations and High-Field Magnetization Studies of Antiferromagnetic Interactions in a Giant Hetero-Spin Ring

Lei Qin; Jared Singleton; Wei-Peng Chen; Hiroyuki Nojiri; Larry Engelhardt; Richard E. P. Winpenny; Yan-Zhen Zheng

Chromium lanthanide heterometallic wheel complexes {Cr8 Ln8 } (Ln=Gd, Dy and Y) with alternating metal centres are presented. Quantum Monte Carlo simulations reveal antiferromagnetic exchange-coupling constants with an average of 2.1u2005K within the {Cr8 Gd8 } wheel, which leads to a large ground spin state (ST =16) that is confirmed by magnetization studies up to 20u2005Tesla. The {Cr8 Dy8 } wheel is a single-molecule magnet.


Physical Review Letters | 2017

Search for Two-Photon Interaction with Axionlike Particles Using High-Repetition Pulsed Magnets and Synchrotron X Rays

Toshiaki Inada; T. Yamazaki; T. Namba; S. Asai; T. Kobayashi; Kenji Tamasaku; Yoshikazu Tanaka; Yuichi Inubushi; Kei Sawada; Makina Yabashi; Tetsuya Ishikawa; Akira Matsuo; K. Kawaguchi; Koichi Kindo; Hiroyuki Nojiri

We report on new results of a search for a two-photon interaction with axionlike particles (ALPs). The experiment is carried out at a synchrotron radiation facility using a light shining through a wall (LSW) technique. For this purpose, we develop a novel pulsed-magnet system, composed of multiple racetrack magnets and a transportable power supply. It produces fields of about 10xa0T over 0.8xa0m with a high repetition rate of 0.2xa0Hz and yields a new method of probing a vacuum with high intensity fields. The data obtained with a total of 27u2009676 pulses provide a limit on the ALP-two-photon coupling constant that is more stringent by a factor of 5.2 compared to a previous x-ray LSW limit for the ALP mass ≲0.1u2009u2009eV.


Angewandte Chemie | 2017

Anisotropic Change in the Magnetic Susceptibility of a Dynamic Single Crystal of a Cobalt(II) Complex

Zi Shuo Yao; Shu Qi Wu; Yasutaka Kitagawa; Sheng Qun Su; You-Gui Huang; Guo Ling Li; Zhong Hai Ni; Hiroyuki Nojiri; Yoshihito Shiota; Kazunari Yoshizawa; Soonchul Kang; Shinji Kanegawa; Osamu Sato

Atypically anisotropic and large changes in magnetic susceptibility, along with a change in crystalline shape, were observed in a CoII complex at near room temperature. This was achieved by combining oxalate molecules, acting as rotor, and a CoII ion with unquenched orbital angular momentum. A thermally controlled 90° rotation of the oxalate counter anion triggered a symmetry-breaking ferroelastic phase transition, accompanied by contraction-expansion behavior (ca. 4.5u2009%) along the long axis of a rod-like single crystal. The molecular rotation induced a minute variation in the coordination geometry around the CoII ion, resulting in an abrupt decrease and a remarkable increase in magnetic susceptibility along the direction perpendicular and parallel to the long axis of the crystal, respectively. Theoretical calculations suggested that such an unusual anisotropic change in magnetic susceptibility was due to a substantial reorientation of magnetic anisotropy induced by slight disruption in the ideal D3 coordination environment of the complex cation.


Optics Express | 2016

Single-shot terahertz time-domain spectroscopy in pulsed high magnetic fields

G. Timothy Noe; Ikufumi Katayama; Fumiya Katsutani; James J. Allred; Jeffrey A. Horowitz; David M. Sullivan; Qi Zhang; Fumiya Sekiguchi; Gary Woods; Matthias C. Hoffmann; Hiroyuki Nojiri; Jun Takeda; Junichiro Kono

We have developed a single-shot terahertz time-domain spectrometer to perform optical-pump/terahertz-probe experiments in pulsed, high magnetic fields up to 30 T. The single-shot detection scheme for measuring a terahertz waveform incorporates a reflective echelon to create time-delayed beamlets across the intensity profile of the optical gate beam before it spatially and temporally overlaps with the terahertz radiation in a ZnTe detection crystal. After imaging the gate beam onto a camera, we can retrieve the terahertz time-domain waveform by analyzing the resulting image. To demonstrate the utility of our technique, we measured cyclotron resonance absorption of optically excited carriers in the terahertz frequency range in intrinsic silicon at high magnetic fields, with results that agree well with published values.


Chemistry: A European Journal | 2018

Slow Magnetic Relaxation in a Palladium-Gadolinium Complex Induced by Electron Density Donation from the Palladium Ion

David Chukwuma Izuogu; Takefumi Yoshida; Haitao Zhang; Goulven Cosquer; Keiichi Katoh; Shuhei Ogata; Miki Hasegawa; Hiroyuki Nojiri; Marko Damjanović; Wolfgang Wernsdorfer; Tomoya Uruga; Toshiaki Ina; Brian K. Breedlove; Masahiro Yamashita

Incorporating palladium in the first coordination sphere of acetato-bridged lanthanoid complexes, [Pd2 Ln2 (H2 O)2 (AcO)10 ]⋅2u2009AcOH (Ln=Gd (1), Y (2), Gd0.4 Y1.6 (3), Eu (4)), led to significant bonding interactions between the palladium and the lanthanoid ions, which were demonstrated by experimental and theoretical methods. We found that electron density was donated from the d8 Pd2+ ion to Gd3+ ion in 1 and 3, leading to the observed slow magnetic relaxation by using local orbital locator (LOL) and X-ray absorption near-edge structure (XANES) analysis. Field-induced dual slow magnetic relaxation was observed for 1 up to 20u2005K. Complex 3 and frozen aqueous and acetonitrile solutions of 1 showed only one relaxation peak, which confirms the role of intermolecular dipolar interactions in slowing the magnetic relaxation of 1. The slow magnetic relaxation occurred through a combination of Orbach and Direct processes with the highest pre-exponential factor (τo =0.06u2005s) reported so far for a gadolinium complex exhibiting slow magnetic relaxation. The results revealed that transition metal-lanthanoid (TM-Ln) axial interactions indeed could lead to new physical properties by affecting both the electronic and magnetic states of the compounds.

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Takayuki Ishida

University of Electro-Communications

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F. Duc

Centre national de la recherche scientifique

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