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Satoru Matsuishi

Bio: Satoru Matsuishi is an academic researcher from Tokyo Institute of Technology. The author has contributed to research in topics: Electride & Superconductivity. The author has an hindex of 37, co-authored 180 publications receiving 6361 citations.


Papers
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Journal ArticleDOI
TL;DR: Kinetic analysis with infrared spectroscopy reveals that C12A7:e(-) markedly enhances N(2) dissociation on Ru by the back donation of electrons and that the poisoning of ruthenium surfaces by hydrogen adatoms can be suppressed effectively because of the ability of C12 a7: e(-) to store hydrogen reversibly.
Abstract: Methods that fix atmospheric nitrogen to ammonia under mild conditions could offer a more environmentally benign alternative to the Haber–Bosch process. Now, a Ru-loaded electride, [Ca24Al28O64]4+(e−)4, is reported that acts as an efficient electron donor and reversible hydrogen store, and is demonstrated to function as an efficient catalyst for ammonia synthesis.

997 citations

Journal ArticleDOI
01 Aug 2003-Science
TL;DR: The removal of clathrated oxygen ions from the crystallographic cages in a single crystal of 12CaO·7Al2O3, leading to the formation of high-density electrons highly localized in the cages, may be regarded as a thermally and chemically stable single crystalline “electride.”
Abstract: We removed approximately 100% of clathrated oxygen ions from the crystallographic cages in a single crystal of 12CaO.7Al2O3, leading to the formation of high-density (approximately 2 x 10(21) cm-3) electrons highly localized in the cages. The resulting electron forms a structure that we interpret as an F+ center and migrates throughout the crystal by hopping to a neighboring cage with conductivity approximately 100 siemens per centimeter, demonstrating that the encaged electron behaves as an anion. The electron anions couple antiferromagnetically with each other, forming a diamagnetic pair or singlet bipolaron. The resulting [Ca24Al28O64]4+(4e-) may be regarded as a thermally and chemically stable single crystalline "electride."

719 citations

Journal ArticleDOI
03 Oct 2002-Nature
TL;DR: Here it is demonstrated a process by which the transparent insulating oxide 12CaO·7Al2O3 (refs 7–13) can be converted into an electrical conductor and suggested that this concept can be applied to other main-group metal oxides, for the direct optical writing of conducting wires in insulating transparent media and the formation of a high-density optical memory.
Abstract: Materials that are good electrical conductors are not in general optically transparent, yet a combination of high conductivity and transparency is desirable for many emerging opto-electronic applications1,2,3,4,5,6. To this end, various transparent oxides composed of transition or post-transition metals (such as indium tin oxide) are rendered electrically conducting by ion doping1,2,3,4,5,6. But such an approach does not work for the abundant transparent oxides of the main-group metals. Here we demonstrate a process by which the transparent insulating oxide 12CaO·7Al2O3 (refs 7–13) can be converted into an electrical conductor. H- ions are incorporated into the subnanometre-sized cages of the oxide by a thermal treatment in a hydrogen atmosphere; subsequent irradiation of the material with ultraviolet light results in a conductive state that persists after irradiation ceases. The photo-activated material exhibits moderate electrical conductivity (∼0.3 S cm-1) at room temperature, with visible light absorption losses of only one per cent for 200-nm-thick films. We suggest that this concept can be applied to other main-group metal oxides, for the direct optical writing of conducting wires in insulating transparent media and the formation of a high-density optical memory.

413 citations

Journal ArticleDOI
21 Feb 2013-Nature
TL;DR: A layered-structure electride of dicalcium nitride, Ca2N, is reported, which possesses two-dimensionally confined anionic electrons whose concentration agrees well with that for the chemical formula of [Ca2N]+·e−.
Abstract: The ionic crystal Ca2N is shown to be an electride in terms of [Ca2N]+·e−, with diffusive two-dimensional transport in dense electron layers. The physical properties of electrides — ionic crystals in which electrons behave as anions — significantly depend on the topology of the confining cavity for anionic electrons. Thus, an essential step towards practical electride applications is to discover new confinement spaces with unique topologies. Confined two-dimensional electron layers have previously been achieved by artificially fabricating hetero-interface structures usually of semiconducting materials. Here the authors extend the range of materials demonstrating such behaviour to an electride, dicalcium nitride (Ca2N). This compound has ideal properties for electron confinement: a layered structure with appropriate interlayer spacing and a chemistry that allows for loosely bound electron layers without electron trapping. By providing a new material image for electrides, this work should lead to a series of two-dimensional electrides with unique physical properties. Recent studies suggest that electrides—ionic crystals in which electrons serve as anions—are not exceptional materials but rather a generalized form, particularly under high pressure1,2,3. The topology of the cavities confining anionic electrons determines their physical properties4. At present, reported confining sites consist only of zero-dimensional cavities or weakly linked channels4. Here we report a layered-structure electride of dicalcium nitride, Ca2N, which possesses two-dimensionally confined anionic electrons whose concentration agrees well with that for the chemical formula of [Ca2N]+·e−. Two-dimensional transport characteristics are demonstrated by a high electron mobility (520 cm2 V−1 s−1) and long mean scattering time (0.6 picoseconds) with a mean free path of 0.12 micrometres. The quadratic temperature dependence of the resistivity up to 120 Kelvin indicates the presence of an electron–electron interaction. A striking anisotropic magnetoresistance behaviour with respect to the direction of magnetic field (negative for the field perpendicular to the conducting plane and positive for the field parallel to it) is observed, confirming diffusive two-dimensional transport in dense electron layers. Additionally, band calculations support confinement of anionic electrons within the interlayer space, and photoemission measurements confirm anisotropic low work functions of 3.5 and 2.6 electronvolts, revealing the loosely bound nature of the anionic electrons. We conclude that Ca2N is a two-dimensional electride in terms of [Ca2N]+·e−.

363 citations

Journal ArticleDOI
TL;DR: A yellow-emitting phosphor, the Eu(2+)-doped chlorometasilicate (Ca(1-x-y,)Sr(x,)Eu(y))(7)(SiO(3))(6)Cl(2), which can be used to create glareless white light-emitter diodes, and phosphors based on this host material have much less blue absorption than other phosphors.
Abstract: The luminous efficiency of white light-emitting diodes, which are used as light sources for next-generation illumination, is continuously improving. Presently available white light-emitting diodes emit with extremely high luminance because their emission areas are much smaller than those of conventional light sources. Consequently, white light-emitting diodes produce a glare that is uncomfortable to the human eye. Here we report a yellow-emitting phosphor, the Eu(2+)-doped chlorometasilicate (Ca(1-x-y,)Sr(x,)Eu(y))(7)(SiO(3))(6)Cl(2), which can be used to create glareless white light-emitting diodes. The (Ca(1-x-y,)Sr(x,)Eu(y))(7)(SiO(3))(6)Cl(2) exhibits a large Stokes shift, efficiently converting violet excitation light to yellow luminescence, and phosphors based on this host material have much less blue absorption than other phosphors. We used crystal structure analysis to determine the origin of the desired luminescence, and we used (Ca(1-x-y,)Sr(x,)Eu(y))(7)(SiO(3))(6)Cl(2) and a blue-emitting phosphor in combination with a violet chip to fabricate glareless white light-emitting diodes that have large emission areas and are suitable for general illumination.

300 citations


Cited by
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Journal ArticleDOI
TL;DR: This Review will compare the results obtained from different systems and try to give a picture on how different types of metal species work in different reactions and give perspectives on the future directions toward better understanding of the catalytic behavior of different metal entities in a unifying manner.
Abstract: Metal species with different size (single atoms, nanoclusters, and nanoparticles) show different catalytic behavior for various heterogeneous catalytic reactions. It has been shown in the literature that many factors including the particle size, shape, chemical composition, metal–support interaction, and metal–reactant/solvent interaction can have significant influences on the catalytic properties of metal catalysts. The recent developments of well-controlled synthesis methodologies and advanced characterization tools allow one to correlate the relationships at the molecular level. In this Review, the electronic and geometric structures of single atoms, nanoclusters, and nanoparticles will be discussed. Furthermore, we will summarize the catalytic applications of single atoms, nanoclusters, and nanoparticles for different types of reactions, including CO oxidation, selective oxidation, selective hydrogenation, organic reactions, electrocatalytic, and photocatalytic reactions. We will compare the results o...

2,700 citations

Journal ArticleDOI
TL;DR: Transparent conductors (TCs) have a multitude of applications for solar energy utilization and for energy savings, especially in buildings as discussed by the authors, which leads naturally to considerations of spectral selectivity, angular selectivity, and temporal variability of TCs, as covered in three subsequent sections.

1,471 citations

Journal ArticleDOI
TL;DR: The response of the worldwide scientific community to the discovery in 2008 of superconductivity at T c'='26'K in the Fe-based compound LaFeAsO1−x F x has been very enthusiastic.
Abstract: The response of the worldwide scientific community to the discovery in 2008 of superconductivity at T c = 26 K in the Fe-based compound LaFeAsO1−x F x has been very enthusiastic. In short order, ot...

1,373 citations

Journal ArticleDOI
TL;DR: The fundamental relationships between electronic structure, adsorption energy, and apparent activity for a wide variety of 2D electrocatalysts are described with the goal of providing a better understanding of these emerging nanomaterials at the atomic level.
Abstract: Over the past few decades, the design and development of advanced electrocatalysts for efficient energy conversion technologies have been subjects of extensive study. With the discovery of graphene, two-dimensional (2D) nanomaterials have emerged as some of the most promising candidates for heterogeneous electrocatalysts due to their unique physical, chemical, and electronic properties. Here, we review 2D-nanomaterial-based electrocatalysts for selected electrocatalytic processes. We first discuss the unique advances in 2D electrocatalysts based on different compositions and functions followed by specific design principles. Following this overview, we discuss various 2D electrocatalysts for electrocatalytic processes involved in the water cycle, carbon cycle, and nitrogen cycle from their fundamental conception to their functional application. We place a significant emphasis on different engineering strategies for 2D nanomaterials and the influence these strategies have on intrinsic material performance, ...

1,363 citations

Journal ArticleDOI
TL;DR: A detailed review of the superconductivity of FePnictide and chalcogenide (FePn/Ch) superconductors can be found in this paper.
Abstract: Kamihara and coworkers' report of superconductivity at ${T}_{c}=26\text{ }\text{ }\mathrm{K}$ in fluorine-doped LaFeAsO inspired a worldwide effort to understand the nature of the superconductivity in this new class of compounds. These iron pnictide and chalcogenide (FePn/Ch) superconductors have Fe electrons at the Fermi surface, plus an unusual Fermiology that can change rapidly with doping, which lead to normal and superconducting state properties very different from those in standard electron-phonon coupled ``conventional'' superconductors. Clearly, superconductivity and magnetism or magnetic fluctuations are intimately related in the FePn/Ch, and even coexist in some. Open questions, including the superconducting nodal structure in a number of compounds, abound and are often dependent on improved sample quality for their solution. With ${T}_{c}$ values up to 56 K, the six distinct Fe-containing superconducting structures exhibit complex but often comparable behaviors. The search for correlations and explanations in this fascinating field of research would benefit from an organization of the large, seemingly disparate data set. This review provides an overview, using numerous references, with a focus on the materials and their superconductivity.

1,349 citations