10 results on '"Terabe, Kazuya"'
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2. Solid polymer electrolyte-based atomic switches: from materials to mechanisms and applications.
- Author
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Tsuruoka, Tohru and Terabe, Kazuya
- Abstract
\nImpact of StatementAs miniaturization of semiconductor memory devices is reaching its physical and technological limits, there is a demand for memory technologies that operate on new principles. Atomic switches are nanoionic devices that show repeatable resistive switching between high-resistance and low-resistance states under bias voltage applications, based on the transport of metal ions and redox reactions in solids. Their essential structure consists of an ion conductor sandwiched between electrochemically active and inert electrodes. This review focuses on the resistive switching mechanism of atomic switches that utilize a solid polymer electrolyte (SPE) as the ion conductor. Owing to the superior properties of polymer materials such as mechanical flexibility, compatibility with various substrates, and low fabrication costs, SPE-based atomic switches are a promising candidate for the next-generation of volatile and nonvolatile memories. Herein, we describe their operating mechanisms and key factors for controlling the device performance with different polymer matrices. In particular, the effects of moisture absorption in the polymer matrix on the resistive switching behavior are addressed in detail. As potential applications, atomic switches with inkjet-printed SPE and quantum conductance behavior are described. SPE-based atomic switches also have great potential in use for neuromorphic devices. The development of these devices will be enhanced using nanoarchitectonics concepts, which integrates functional materials and devices.This article reviews a series of works starting with the author’s 2011 paper on solid polymer electrolyte-based atomic switches, and describes the current status and future prospects for this technology. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
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3. Control of local ion transport to create unique functional nanodevices based on ionic conductors
- Author
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Terabe, Kazuya, Hasegawa, Tsuyoshi, Liang, Changhao, and Aono, Masakazu
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SEMICONDUCTORS , *IONS , *SILVER sulfide , *ELECTROCHEMISTRY , *ELECTRICAL conductors - Abstract
Abstract: The development of nanometer-scale devices operating under a new principle that could overcome the limitations of current semiconductor devices has attracted interest in recent years. We propose that nanoionic devices that operate by controlling the local transport of ions are promising in this regard. It is possible to control the local transport of ions using the solid electrochemical properties of ionic and electronic mixed conductors. As an example of this concept, here, we report a method of controlling the transport of silver ions of the mixed-conductor silver sulfide (Ag2S) crystal and basic research on nanoionic devices based on this mixed conductor. These devices show unique functions such as atom deposition, resistance switching, and quantum point contact switching. The switches operate through the formation and dissolution of an atomic bridge between the electrodes, and the behavior is realized by control of the local solid-state electrochemical reaction. Potential nanoionic devices utilizing the unique functions and characters that do not exist in conventional semiconductor devices are discussed. [Copyright &y& Elsevier]
- Published
- 2007
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4. Atomic switches: atomic-movement-controlled nanodevices for new types of computing.
- Author
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Hino, Takami, Hasegawa, Tsuyoshi, Terabe, Kazuya, Tsuruoka, Tohru, Nayak, Alpana, Ohno, Takeo, and Aono, Masakazu
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SWITCHING circuits , *ELECTROLYTIC oxidation , *ELECTRODES , *METAL oxide semiconductors , *NANOSTRUCTURED materials - Abstract
Atomic switches are nanoionic devices that control the diffusion of metal cations and their reduction/oxidation processes in the switching operation to form/annihilate a metal atomic bridge, which is a conductive path between two electrodes in the on-state. In contrast to conventional semiconductor devices, atomic switches can provide a highly conductive channel even if their size is of nanometer order. In addition to their small size and low on-resistance, their nonvolatility has enabled the development of new types of programmable devices, which may achieve all the required functions on a single chip. Three-terminal atomic switches have also been developed, in which the formation and annihilation of a metal atomic bridge between a source electrode and a drain electrode are controlled by a third (gate) electrode. Three-terminal atomic switches are expected to enhance the development of new types of logic circuits, such as nonvolatile logic. The recent development of atomic switches that use a metal oxide as the ionic conductive material has enabled the integration of atomic switches with complementary metal-oxide-semiconductor (CMOS) devices, which will facilitate the commercialization of atomic switches. The novel characteristics of atomic switches, such as their learning and photosensing abilities, are also introduced in the latter part of this review. [ABSTRACT FROM AUTHOR]
- Published
- 2011
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5. Structural studies of copper sulfide films: effect of ambient atmosphere.
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Kundu, Manisha, Hasegawa, Tsuyoshi, Terabe, Kazuya, Yamamoto, Kazuhiro, and Aono, Masakazu
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COPPER sulfide , *STOICHIOMETRY , *CHEMICAL reactions , *PHYSICAL & theoretical chemistry , *HYDROXIDES - Abstract
We examined the structural properties of copper sulfide films as a function of the sulfurization time of 70-nm-thick Cu films. Copper sulfide films with various phases such as mixed metallic Cu-chalcocite, chalcocite, roxbyite, and covellite phases were formed with increasing sulfurization time. To evaluate the structural stability of various films, all the films were exposed to the ambient atmosphere for the same amount of time. Although the phase structure and stoichiometry of the films were maintained at a greater depth, the near-surface region of the films was oxidized and covered with overlayers of oxide, hydroxide, and/or sulfate species due to the exposure and reaction with the ambient atmosphere. The oxygen uptake and its reactivity with the copper sulfide film surfaces were enhanced with increasing sulfur content of the films. In addition, the type of divalent state of copper formed on the film surfaces depended on the phase structure, composition, and stoichiometry of the films. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
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6. NANOSCALE SURFACE ENGINEERING OF LITHIUM NIOBATE SINGLE CRYSTALS.
- Author
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DONGFENG XUE, SIXIN WU, TERABE, KAZUYA, and KITAMURA, KENJI
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SURFACES (Technology) , *SCANNING probe microscopy , *CHEMICAL bonds , *LITHIUM niobate , *NANOPARTICLES , *CRYSTALS , *PHOTOCHEMISTRY - Abstract
Surface engineering at the nanoscale level of lithium niobate crystals is performed by scanning probe microscopy and is theoretically analyzed by the structural property and the chemical bonding structure. The present work shows that -Z surface of lithium niobate crystals may be well fabricated by precisely artificial patterns, which has potential applications in future nanodevices. [ABSTRACT FROM AUTHOR]
- Published
- 2006
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7. The electric double layer effect and its strong suppression at Li+ solid electrolyte/hydrogenated diamond interfaces.
- Author
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Tsuchiya, Takashi, Takayanagi, Makoto, Mitsuishi, Kazutaka, Imura, Masataka, Ueda, Shigenori, Koide, Yasuo, Higuchi, Tohru, and Terabe, Kazuya
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ELECTRIC double layer , *SOLID electrolytes , *HYDROGENATION , *NANOELECTRONICS , *MEMRISTORS , *ELECTRIC conductivity - Abstract
The electric double layer (EDL) effect at solid electrolyte/electrode interfaces has been a key topic in many energy and nanoelectronics applications (e.g., all-solid-state Li+ batteries and memristors). However, its characterization remains difficult in comparison with liquid electrolytes. Herein, we use a novel method to show that the EDL effect, and its suppression at solid electrolyte/electronic material interfaces, can be characterized on the basis of the electric conduction characteristics of hydrogenated diamond(H-diamond)-based EDL transistors (EDLTs). Whereas H-diamond-based EDLT with a Li-Si-Zr-O Li+ solid electrolyte showed EDL-induced hole density modulation over a range of up to three orders of magnitude, EDLT with a Li-La-Ti-O (LLTO) Li+ solid electrolyte showed negligible enhancement, which indicates strong suppression of the EDL effect. Such suppression is attributed to charge neutralization in the LLTO, which is due to variation in the valence state of the Ti ions present. The method described is useful for quantitatively evaluating the EDL effect in various solid electrolytes. The effect of the electric double layer with solid electrolytes remains hard to characterize. In this study, the authors show how to evaluate the electric double layer effect with various lithium solid electrolytes using a hydrogenated diamond-based transistor. [ABSTRACT FROM AUTHOR]
- Published
- 2021
- Full Text
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8. Room temperature redox reaction by oxide ion migration at carbon/Gd-doped CeO2 heterointerface probed by an in situ hard x-ray photoemission and soft x-ray absorption spectroscopies.
- Author
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Tsuchiya, Takashi, Miyoshi, Shogo, Yamashita, Yoshiyuki, Yoshikawa, Hideki, Terabe, Kazuya, Kobayashi, Keisuke, and Yamaguchi, Shu
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PHOTOELECTRON spectroscopy , *X-ray computed microtomography , *IONS , *OXIDATION-reduction reaction , *TRANSISTORS , *ATOMS , *PHOTOSYNTHETIC oxygen evolution - Abstract
In situ hard x-ray photoemission spectroscopy (HX-PES) and soft x-ray absorption spectroscopy (SX-XAS) have been employed to investigate a local redox reaction at the carbon/Gd-doped CeO2 (GDC) thin film heterointerface under applied dc bias. In HX-PES, Ce3d and O1s core levels show a parallel chemical shift as large as 3.2 eV, corresponding to the redox window where ionic conductivity is predominant. The window width is equal to the energy gap between donor and acceptor levels of the GDC electrolyte. The Ce M-edge SX-XAS spectra also show a considerable increase of Ce3+ satellite peak intensity, corresponding to electrochemical reduction by oxide ion migration. In addition to the reversible redox reaction, two distinct phenomena by the electrochemical transport of oxide ions are observed as an irreversible reduction of the entire oxide film by O2 evolution from the GDC film to the gas phase, as well as a vigorous precipitation of oxygen gas at the bottom electrode to lift off the GDC film. These in situ spectroscopic observations describe well the electrochemical polarization behavior of a metal/GDC/metal capacitor-like two-electrode cell at room temperature. [ABSTRACT FROM AUTHOR]
- Published
- 2013
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9. Effects of Oxygen Partial Pressure and Substrate Temperature on the Structure and Morphology of Sc and Y Co-Doped ZrO 2 Solid Electrolyte Thin Films Prepared via Pulsed Laser Deposition.
- Author
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Rabo, Jennet R., Takayanagi, Makoto, Tsuchiya, Takashi, Nakajima, Hideki, Terabe, Kazuya, and Cervera, Rinlee Butch M.
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PULSED laser deposition , *PARTIAL pressure , *THIN films , *SOLID electrolytes , *LASER deposition , *PHOTOELECTRON spectroscopy - Abstract
Scandium (Sc) and yttrium (Y) co-doped ZrO2 (ScYSZ) thin films were prepared on a SiO2-Si substrate via pulsed laser deposition (PLD) method. In order to obtain good quality thin films with the desired microstructure, various oxygen partial pressures ( P O 2 ) from 0.01 Pa to 10 Pa and substrate temperatures (Ts) from 25 °C to 800 °C were investigated. X-ray diffraction (XRD) patterns results showed that amorphous ScYSZ thin films were formed at room substrate temperature while cubic polycrystalline thin films were obtained at higher substrate temperatures (Ts = 200 °C, 400 °C, 600 °C, 800 °C). Raman spectra revealed a distinct Raman shift at around 600 cm−1 supporting a cubic phase. However, a transition from cubic to tetragonal phase can be observed with increasing oxygen partial pressure. Photoemission spectroscopy (PES) spectra suggested supporting analysis that more oxygen vacancies in the lattice can be observed for samples deposited at lower oxygen partial pressures resulting in a cubic structure with higher dopant cation binding energies as compared to the tetragonal structure observed at higher oxygen partial pressure. On the other hand, dense morphologies can be obtained at lower P O 2 (0.01 Pa and 0.1 Pa) while more porous morphologies can be obtained at higher P O 2 (1.0 Pa and 10 Pa). [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
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10. Diffusivity of Cu Ions in Solid Electrolyte and Its Effect on the Performance of Nanometer-Scale Switch.
- Author
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Banno, Naoki, Sakamoto, Toshitsugu, Iguchi, Noriyuki, Sunamura, Hiroshi, Terabe, Kazuya, Hasegawa, Tsuyoshi, and Aono, Masakazu
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COPPER ions , *ELECTROLYTES , *ELECTROCHEMICAL apparatus , *PROGRAMMABLE logic devices , *SWITCHING circuits , *DIFFUSION , *ION migration & velocity , *COPPER - Abstract
A novel solid-electrolyte nonvolatile switch that we previously developed for programmable large-scale-integration circuits turns on or off when a conducting Cu budge is formed or dissolved in the solid electrolyte. Cu+ ion migration and an electrochemical reaction are involved in the switching process. For logic applications, we need to adjust its turn-on voltage (VON), which was too small to maintain the conductance state during logic operations. In this paper, we clarified that VON is mainly affected by the rate of Cu+ ion migration in the solid electrolyte. Considering the relationship between the migration rate and VON, we replaced the former electrolyte, Cu2-αS, with Ta2O5, which enabled us to appropriately adjust VON with a smaller Cu+ ion diffusion coefficient. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
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