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Journal Articles

Crystal-like atomic arrangement and optical properties of 25La$$_{2}$$O$$_{3}$$-75MoO$$_{3}$$ binary glasses composed of isolated MoO$$_{4}$$$$^{2-}$$

Masuno, Atsunobu*; Munakata, Sae*; Okamoto, Yoshihiro; Yaji, Toyonari*; Kosugi, Yoshihisa*; Shimakawa, Yuichi*

Inorganic Chemistry, 63(12), p.5701 - 5708, 2024/03

https://doi.org/10.1021/acs.inorgchem.4c00176

Transparent and brown La$$_{2}$$O$$_{3}$$-MoO$$_{3}$$ binary glasses were prepared in bulk form using a levitation technique. The glass-forming range was limited, with the primary composition being approximately 25 mol% La$$_{2}$$O$$_{3}$$. This glass exhibited a clear crystallization at 546 $$^{circ}$$C, while determining its glass transition temperature was difficult. Notably, despite its amorphous nature, the glass possessed a density and packing density comparable to those of crystalline La$$_{2}$$Mo$$_{3}$$O$$_{12}$$. X-ray absorption fine structure and Raman scattering analyses revealed that the glass structure closely resembles La$$_{2}$$Mo$$_{3}$$O$$_{12}$$ due to the presence of isolated MoO$$_{4}$$$$^{2-}$$ units, whereas disordered atomic arrangement around La atoms was confirmed. The glass demonstrated transparency ranging from 378 to 5500 nm, and the refractive index at 1.0 $$mu$$m was estimated to be 2.0. The optical bandgap energy was 3.46 eV, which was slightly smaller than that of La$$_{2}$$Mo$$_{3}$$O$$_{12}$$. Additionally, the glass displayed a transparent region ranging from 6.5 to 8.0 $$mu$$m. This occurrence results from the decreased diversity of MoO$$_{n}$$ units and connectivity of Mo-O-Mo, which resulted in the reduced overlap of multiphonon absorption. This glass formation, with its departure from conventional glass-forming rules, resulted in distinctive glasses with crystal-like atomic arrangements.

Journal Articles

$$beta$$-MoO$$_{3}$$ whiskers in $$^{99}$$Mo/$$^{rm 99m}$$Tc radioisotope production and $$^{99}$$Mo/$$^{rm 99m}$$Tc extraction using hot atoms

Ngo, M. C.*; Fujita, Yoshitaka; Suzuki, Tatsuya*; Do, T. M. D.*; Seki, Misaki; Nakayama, Tadachika*; Niihara, Koichi*; Suematsu, Hisayuki*

Inorganic Chemistry, 62(32), p.13140 - 13147, 2023/08

https://doi.org/10.1021/acs.inorgchem.3c02125
 Times Cited Count：0 Percentile：0.01(Chemistry, Inorganic & Nuclear)

Technetium-99m ($$^{rm 99m}$$Tc) is one of the most important radioisotopes for diagnostic radio-imaging applications. $$^{rm 99m}$$Tc is a daughter product of the $$^{99}$$Mo isotope. There are two methods used to produce $$^{99}$$Mo/$$^{rm 99m}$$Tc: the nuclear fission (n,f) and the neutron capture (n,$$gamma$$) methods. Between them, the (n,f) method is the main route, used for approximately 90% of the world's production. However, the (n,f) method faces numerous problems, including the use of highly enriched uranium, the release of highly radioactive waste, and nonproliferation problems. Therefore, the (n,$$gamma$$) method is being developed as a future replacement for the (n,f) method. In this work, $$beta$$-MoO$$_{3}$$ whiskers prepared by the thermal evaporation method and $$alpha$$-MoO$$_{3}$$ particles were irradiated in a nuclear reactor to produce $$^{99}$$Mo/$$^{rm 99m}$$Tc via neutron capture. The irradiated targets were dispersed into water to extract the $$^{99}$$Mo/$$^{rm 99m}$$Tc. As a result, $$beta$$-MoO$$_{3}$$ whisker yielded higher $$^{99}$$Mo extraction rate than that from $$alpha$$-MoO$$_{3}$$. In addition, by comparing the dissolved $$^{98}$$Mo concentrations in water, we clarified a prominent hot-atom of $$beta$$-MoO$$_{3}$$ whiskers. This research is the first demonstration of $$beta$$-MoO$$_{3}$$ being used as an irradiation target in the neutron capture method. On the basis of the results, $$beta$$-MoO$$_{3}$$ is considered a promising irradiation target for producing $$^{99}$$Mo/$$^{rm 99m}$$Tc by neutron capture and using water for the radioisotope extraction process in the future.

Journal Articles

Unusually kinetically inert monocationic neptunyl complex with a fluorescein-modified 1,10-phenanthroline-2,9-dicarboxylate ligand; Specific separation and detection in gel electrophoresis

Yamagata, Kazuhito*; Ouchi, Kazuki; Marumo, Kazuki*; Tasaki-Handa, Yuiko*; Haraga, Tomoko; Saito, Shingo*

Inorganic Chemistry, 62(2), p.730 - 738, 2023/01

https://doi.org/10.1021/acs.inorgchem.2c02908
 Times Cited Count：2 Percentile：78.4(Chemistry, Inorganic & Nuclear)

The inert NpO$$_{2}$$$$^{+}$$ complex with a fluorescein-modified phenanthroline-2,9-dicarboxylic acid was found by kinetic selection using polyacrylamide gel electrophoresis (PAGE) from a small chemical library. The small spontaneous dissociation rate constant of 8$$times$$10$$^{-6}$$ s$$^{-1}$$ (the half-life of 23 hours) was determined. This is the singly-charged NpO$$_{2}$$$$^{+}$$ complex exhibiting unusual kinetic inertness in aqueous solution, one million times slower than widely accepted fast kinetics of neptunyl complexes. Selective fluorescence detection of NpO$$_{2}$$$$^{+}$$ was achieved in PAGE with a detection limit of 68 pmol dm$$^{-3}$$(17 fg). This system was successfully applied to simulated spent nuclear fuel and high-level radioactive waste samples.

Journal Articles

Lanthanide and actinide ion complexes containing organic ligands investigated by surface-enhanced infrared absorption spectroscopy

Hirata, Sakiko*; Kusaka, Ryoji; Meiji, Shogo*; Tamekuni, Seita*; Okudera, Kosuke*; Hamada, Shoken*; Sakamoto, Chihiro*; Honda, Takumi*; Matsushita, Kosuke*; Muramatsu, Satoru*; et al.

Inorganic Chemistry, 62(1), p.474 - 486, 2023/01

https://doi.org/10.1021/acs.inorgchem.2c03618
 Times Cited Count：0 Percentile：0.01(Chemistry, Inorganic & Nuclear)

Journal Articles

Composite with a glassy nonporous coordination polymer enhances gas adsorption selectivity

Zheng, X.*; Kato, Masaru*; Uemura, Yohei*; Matsumura, Daiju; Yagi, Ichizo*; Takahashi, Kiyonori*; Noro, Shinichiro*; Nakamura, Takayoshi*

Inorganic Chemistry, 62(3), p.1257 - 1263, 2023/01

https://doi.org/10.1021/acs.inorgchem.2c04068
 Times Cited Count：1 Percentile：58.61(Chemistry, Inorganic & Nuclear)

Journal Articles

Application of high-energy-resolution X-ray absorption spectroscopy at the U L$$_{3}$$-edge to assess the U(V) electronic structure in FeUO$$_{4}$$

Yomogida, Takumi; Akiyama, Daisuke*; Ouchi, Kazuki; Kumagai, Yuta; Higashi, Kotaro*; Kitatsuji, Yoshihiro; Kirishima, Akira*; Kawamura, Naomi*; Takahashi, Yoshio*

Inorganic Chemistry, 61(50), p.20206 - 20210, 2022/12

https://doi.org/10.1021/acs.inorgchem.2c03208
 Times Cited Count：2 Percentile：36.89(Chemistry, Inorganic & Nuclear)

FeUO$$_{4}$$ was studied to clarify the electronic structure of U(V) in a metal monouranate compound. We obtained the peak splitting of HERFD-XANES spectra utilizing high-energy-resolution fluorescence detection-X-ray absorption near edge structure (HERFD-XANES) spectroscopy at the U L$$_{3}$$-edge, which is a novel technique in the U(V) compounds. Theoretical calculations revealed that the peak splitting was caused by splitting the 6d orbital of U(V). Such distinctive electronic states are of major interest to researchers and engineers working in various fields, from fundamental physics to the nuclear industry and environmental sciences for actinide elements.

Journal Articles

Fully chelating N$$_{3}$$O$$_{2}$$-pentadentate planar ligands designed for the strongest and selective capture of uranium from seawater

Mizumachi, Takumi*; Sato, Minami*; Kaneko, Masashi; Takeyama, Tomoyuki*; Tsushima, Satoru*; Takao, Koichiro*

Inorganic Chemistry, 61(16), p.6175 - 6181, 2022/04

https://doi.org/10.1021/acs.inorgchem.2c00306
 Times Cited Count：2 Percentile：36.89(Chemistry, Inorganic & Nuclear)

Based on unique 5-fold equatorial coordination of UO$$_{2}$$$$^{2+}$$, water-compatible pentadentate planar ligands, H$$_{2}$$saldian and its derivatives, were designed as strong and selective capture of UO$$_{2}$$$$^{2+}$$ in seawater. In the simulated seawater condition (0.5 M NaCl + 2.3 mM HCO$$_{3}$$$$^{-}$$/CO$$_{3}$$$$^{2-}$$, pH 8), saldian$$^{2-}$$ shows the strongest complexation with UO$$_{2}$$$$^{2+}$$ to form UO$$_{2}$$(saldian) (log$$beta$$$$_{11}$$ = 28.05 $$pm$$ 0.07), which is more than 10 order of magnitude greater than amidoxime-based or -inspired ligand systems most commonly employed for U capture from seawater. Good selectivity for UO$$_{2}$$$$^{2+}$$ from other metal ions coexisting in seawater was also demonstrated.

Journal Articles

Coexistence of magnetoelectric and antiferroelectric-like orders in Mn$$_{3}$$Ta$$_{2}$$O$$_{8}$$

Kimura, Kenta*; Yagi, Naoki*; Hasegawa, Shunsuke*; Hagihara, Masato; Miyake, Atsushi*; Tokunaga, Masashi*; Cao, H.*; Masuda, Takatsugu*; Kimura, Tsuyoshi*

Inorganic Chemistry, 60(20), p.15078 - 15084, 2021/10

https://doi.org/10.1021/acs.inorgchem.1c02461
 Times Cited Count：1 Percentile：10.45(Chemistry, Inorganic & Nuclear)

Journal Articles

Density functional theory study on the $$^{193}$$Ir M$"o$ssbauer spectroscopic parameters of Vaska's complexes and their oxidative adducts

Kaneko, Masashi; Nakashima, Satoru*

Inorganic Chemistry, 60(17), p.12740 - 12752, 2021/09

https://doi.org/10.1021/acs.inorgchem.1c00239
 Times Cited Count：3 Percentile：32.49(Chemistry, Inorganic & Nuclear)

In the present study, density functional theory (DFT) calculation was applied to Vaska's complexes of formula ${it trans}$-[IrCl(CO)(PPh$$_{3}$$)$$_{2}$$], and their oxidative adducts with small molecules (YZ) including H$$_{2}$$, i.e., ${it trans}$-[IrCl(YZ)(CO))(PPh$$_{3}$$)$$_{2}$$], to successfully correlate the electronic states of the complexes with the corresponding $$^{193}$$Ir M$"o$ssbauer spectroscopic parameters. After confirming the reproducibility of the DFT methods for elucidating the equilibrium structures and $$^{193}$$Ir M$"o$ssbauer isomer shifts of the octahedral Ir complexes, the isomer shifts and quadrupole splitting values of Vaska's complexes and their oxidative adducts were calculated. A bond critical point analysis revealed that the tendency in the isomer shifts was correlated with the strength of the covalent interaction in the coordination bonds. In an electric field gradient (EFG) analysis of the oxidative adducts, the sign of the principal axis was found to be positive for the complex with YZ = Cl$$_{2}$$ and negative for the complex with YZ = H$$_{2}$$. This reversal of the sign of the EFG principal axis was caused by the difference in the electron density distribution for the coordination bonds between Ir and YZ, according to a density of states analysis.

Journal Articles

Study on phenanthroline carboxamide for lanthanide separation; Influence of amide substituents

Simonnet, M.; Kobayashi, Toru; Shimojo, Kojiro; Yokoyama, Keiichi; Yaita, Tsuyoshi

Inorganic Chemistry, 60(17), p.13409 - 13418, 2021/09

https://doi.org/10.1021/acs.inorgchem.1c01729
 Times Cited Count：15 Percentile：87.32(Chemistry, Inorganic & Nuclear)

Journal Articles

Programmable synthesis of silver wheels

Kwon, H.*; Pietrasiak, E.*; Ohara, Takashi; Nakao, Akiko*; Chae, B.*; Hwang, C.-C.*; Jung, D.*; Hwang, I.-C.*; Ko, Y. H.*; Kim, K.*; et al.

Inorganic Chemistry, 60(9), p.6403 - 6409, 2021/05

https://doi.org/10.1021/acs.inorgchem.1c00106
 Times Cited Count：0 Percentile：0.01(Chemistry, Inorganic & Nuclear)

Journal Articles

Observation of dihydrogen bonds in high-pressure phases of ammonia borane by X-ray and neutron diffraction measurements

Nakano, Satoshi*; Sano, Asami; Hattori, Takanori; Machida, Shinichi*; Komatsu, Kazuki*; Fujihisa, Hiroshi*; Yamawaki, Hiroshi*; Goto, Yoshito*; Kikegawa, Takumi*

Inorganic Chemistry, 60(5), p.3065 - 3073, 2021/03

https://doi.org/10.1021/acs.inorgchem.0c03345
 Times Cited Count：10 Percentile：74.02(Chemistry, Inorganic & Nuclear)

X-ray and neutron diffraction analyses of ammonia borane were conducted at ambient and high pressures. The H-H distance in dihydrogen bonds was shorter than twice the van der Waals radius (2.4 ${AA}$). The half of the dihydrogen bonds were broken on phase transition from AP to the first high pressure phase (HP1) at approximately 1.2 GPa as revealed by an increase in the H-H distances. On further pressure increase, all of the H-H distances became shorter than 2.4 ${AA}$ again, implying the pressure-induced reformation of the dihydrogen bonds. Furthermore, the HP1 transformed to the second one with the structure of $$P2_1$$ (Z = 2) at about 11 GPa. In this phase transition, the inclination of the molecule axis became larger and the number of types of dihydrogen bonds increased from 6 to 11. Just before the third transition at 18.9 GPa, the shortest dihydrogen bond decreased to 1.65 ${AA}$. The present study experimentally first confirmed the breakage and reformation of the dihydrogen bonds by the structural change under pressure.

Journal Articles

Effect of oxygen-donor charge on adjacent nitrogen-donor interactions in Eu$$^{3+}$$ complexes of mixed N,O-donor ligands demonstrated on a 10-fold [Eu(TPAMEN)]$$^{3+}$$ chelate complex

Schnaars, K.; Kaneko, Masashi; Fujisawa, Kiyoshi*

Inorganic Chemistry, 60(4), p.2477 - 2491, 2021/02

https://doi.org/10.1021/acs.inorgchem.0c03405
 Times Cited Count：6 Percentile：59.03(Chemistry, Inorganic & Nuclear)

To reduce high-level radiotoxic waste generated by nuclear power plants, highly selective separation agents for minor actinides are mandatory. The mixed N,O-donor ligand ${it N,N,N',N'}$-tetrakis[(6-carboxypyridin-2-yl)methyl]ethylenediamine (H$$_{4}$$TPAEN) has shown good performance as a masking agent in Am$$^{3+}$$/Eu$$^{3+}$$ separation studies. In this work, we examine whether a decrease in O-donor basicity can promote the M$$^{3+}$$-N$$_{am}$$ interactions. Therefore, we replace the deprotonated "charged" carboxylic acid groups of TPAEN$$^{4-}$$ by neutral amide groups and introduce ${it N,N,N',N'}$-tetrakis[(6-${it N",N"}$-diethylcarbamoylpyridin-2-yl)methyl]ethylenediamine (TPAMEN) as a new ligand. TPAMEN was crystallized with Eu(OTf)$$_{3}$$ and Eu(NO$$_{3}$$)$$_{3}$$ 6H$$_{2}$$O to form positively charged 1:1 [Eu(TPAMEN)]$$^{3+}$$ complexes in the solid state. Alterations in the M-O/N bond distances are compared to [Eu(TPAEN)]$$^{-}$$ and investigated by DFT calculations to expose the differences in charge/energy density distributions at europium(III) and the donor functionalities of the TPAEN$$^{4-}$$ and TPAMEN. On the basis of estimations of the bond orders, atomic charges spin populations, and density of states in the Eu and potential Am and Cm complexes, the specific contributions of the donor-metal interaction are analyzed. The prediction of complex formation energy differences for the [M(TPAEN)]$$^{-}$$ and [M(TPAMEN)]$$^{3+}$$ (M$$^{3+}$$ = Eu$$^{3+}$$, Am$$^{3+}$$) complexes provide an outlook on the potential performance of TPAMEN in Am$$^{3+}$$/Eu$$^{3+}$$ separation.

Journal Articles

Precious metal separations

Narita, Hirokazu*; Kasuya, Ryo*; Suzuki, Tomoya*; Motokawa, Ryuhei; Tanaka, Mikiya*

Encyclopedia of Inorganic and Bioinorganic Chemistry (Internet), 28 Pages, 2020/12

https://doi.org/10.1002/9781119951438.eibc2756

Journal Articles

Role of the hydroxo group in the coordination of citric acid to trivalent americium

Tamain, C.*; Bonato, L.*; Aupiais, J.*; Dumas, T.*; Guillaumont, D.*; Barkleit, A.*; Berthon, C.*; Solari, P. L.*; Ikeda, Atsushi; Guilbard, P.*; et al.

European Journal of Inorganic Chemistry, 2020(14), p.1331 - 1344, 2020/04

https://doi.org/10.1002/ejic.202000124
 Times Cited Count：3 Percentile：23.3(Chemistry, Inorganic & Nuclear)

The molecular characterization based on multi-technique approach has led to major highlights on revealing the coordination environment of americium (Am) surrounded by citric acid (H$$_{3}$$CitH). The structure of the different complexes at pH 1 and 3 are described. These characterizations are made possible by the comparison of the americium-citric acid system with the americium-tricarballylic acid (one analogue of the citric acid without the alpha-hydroxo group).

Journal Articles

Density Functional Theory (DFT)-based bonding analysis correlates ligand field strength with $$^{99}$$Ru M$"o$ssbauer parameters of ruthenium-nitrosyl complexes

Kaneko, Masashi; Kato, Akane*; Nakashima, Satoru*; Kitatsuji, Yoshihiro

Inorganic Chemistry, 58(20), p.14024 - 14033, 2019/10

https://doi.org/10.1021/acs.inorgchem.9b02024
 Times Cited Count：12 Percentile：63.71(Chemistry, Inorganic & Nuclear)

We applied density functional theory calculations to ruthenium-nitrosyl complexes, which are known to exist in high-level radioactive waste, to give a theoretical correlation between $$^{99}$$Ru M$"o$ssbauer spectroscopic parameters ($$delta$$ and $$Delta$$$$E_{rm Q}$$) and ligand field strength ($$Delta$$$$_{rm o}$$) for the first time. The structures of the series of complexes, [Ru(NO)L$$_{5}$$] (L = Br$$^{-}$$, Cl$$^{-}$$, NH$$_{3}$$, CN$$^{-}$$), were modeled based on the corresponding single-crystal X-ray coordinates. The comparisons of the geometries and total energies between the different spin states suggested that the singlet spin state of [Ru(II)(NO$$^{+}$$)L$$_{5}$$] complexes were the most stable. The calculated results of both the $$delta$$ and $$Delta$$$$E_{rm Q}$$ values reproduced the experimental results by reported previously and increased in the order of L = Br$$^{-}$$, Cl$$^{-}$$, NH$$_{3}$$, CN$$^{-}$$. Finally, we estimated the ligand field strength ($$Delta$$$$_{rm o}$$) based on molecular orbitals, assuming C$$_{rm 4v}$$ symmetry and showed the increase of $$Delta$$$$_{rm o}$$ values in that order, being consistent with well-known spectrochemical series of ligands. The increase attributes to the strengthening of the abilities of $$sigma$$-donor and $$pi$$-acceptor of the L-ligands to the Ru atom, resulting in the increase of the $$delta$$ values.

Journal Articles

Proton chelating ligands drive improved chemical separations for rhodium

Narita, Hirokazu*; Nicolson, R. M.*; Motokawa, Ryuhei; Ito, Fumiyuki*; Morisaku, Kazuko*; Goto, Midori*; Tanaka, Mikiya*; Heller, W. T.*; Shiwaku, Hideaki; Yaita, Tsuyoshi; et al.

Inorganic Chemistry, 58(13), p.8720 - 8734, 2019/07

https://doi.org/10.1021/acs.inorgchem.9b01136
 Times Cited Count：14 Percentile：69.69(Chemistry, Inorganic & Nuclear)

Journal Articles

Ion hydration and association in an aqueous calcium chloride solution in the GPa range

Yamaguchi, Toshio*; Nishino, Masaaki*; Yoshida, Koji*; Takumi, Masaharu*; Nagata, Kiyofumi*; Hattori, Takanori

European Journal of Inorganic Chemistry, 2019(8), p.1170 - 1177, 2019/02

https://doi.org/10.1002/ejic.201900016
 Times Cited Count：16 Percentile：74.57(Chemistry, Inorganic & Nuclear)

Neutron diffraction measurements of an aqueous 2 mol dm$$^{-3}$$ CaCl$$_2$$ solutions in D$$_{2}$$O have been made at 1 GPa, 298 K as well as 0.1 MPa, 298 K. The experimental structure factors are subjected to Empirical Potential Structure Refinement (EPSR) modeling to reveal the ion hydration and association and solvent water at the atomic level. About seven water molecules surround Ca$$^{2+}$$ at the Ca-O and Ca-D distances of 2.44 ${AA}$ and 3.70 ${AA}$, respectively, at both pressures, suggesting no significant pressure effect on the cation hydration. On the other hand, the Cl$$^{-}$$ ion shows a drastic change in water oxygen coordination from 7 at 0.1 MPa to 14 at 1 GPa, accompanied by shortening of Cl-O distance from 3.18 ${AA}$ to 3.15 ${AA}$. However, the number of water hydrogen atoms around Cl$$^{-}$$ does not change significantly as 6.0 $$sim$$ 6.7 with shortening Cl-D distance from 2.22 to 2.18 ${AA}$ on compression. The pressure effect on the solvent water structure is also drastic as an increase in water oxygen atoms of 4.7 at the O-O distance of 2.79 ${AA}$ at 0.1 MPa to 10.3 at 2.85 ${AA}$ at 1 GPa. The number of water hydrogen atoms, however, does not change as 1.2 at the O-D distance of 1.74 ${AA}$ for both pressures, demonstrating the presence of the O$$cdots$$D hydrogen bonds which are significantly bent at 1 GPa at 298 K. This change of hydrogen bonds in water with pressure probably causes the drastic increase in water oxygen atoms around Cl$$^{-}$$.

Journal Articles

Theoretical elucidation of Am(III)/Cm(III) separation mechanism with diamide-type ligands using relativistic density functional theory calculation

Kaneko, Masashi; Suzuki, Hideya; Matsumura, Tatsuro

Inorganic Chemistry, 57(23), p.14513 - 14523, 2018/12

https://doi.org/10.1021/acs.inorgchem.8b01624
 Times Cited Count：20 Percentile：78.15(Chemistry, Inorganic & Nuclear)

We elucidated the separation mechanism between Am(III) and Cm(III) ions by using two different types of diamide ligands, diglycolamide (DGA) and alkylated diamide amine (ADAAM), by means of the density functional theory technique and electron density analysis. The molecular geometries and formation reactions of the metal-ligand complexes were modeled by using [M(DGA)$$_{3}$$]$$^{3+}$$ and [M(ADAAM)(NO$$_{3}$$)$$_{3}$$(H$$_{2}$$O)]. We successfully reproduced Cm(III) selectivity over Am(III) with DGA and Am(III) selectivity over Cm(III) with ADAAM. Furthermore, we analyzed the bonding properties between the metal ion and the diamide-type ligands by using model complexes, [M(DGA)$$_{3}$$]$$^{3+}$$ and [M(ADAAM)(NO$$_{3}$$)$$_{3}$$(H$$_{2}$$O)], and revealed the differences in terms of the bond dissociation energy and the metal 5f-orbital participation in the covalency between the Am(III) and the Cm(III) complexes. It was suggested that the differences were key factors to understand the Am(III)/Cm(III) selectivity.

Journal Articles

Synthesis, direct formation under high pressure, structure, and electronic properties of LiNbO$$_{3}$$-type oxide PbZnO$$_{3}$$

Mori, Daisuke*; Tanaka, Kie*; Saito, Hiroyuki; Kikegawa, Takumi*; Inaguma, Yoshiyuki*

Inorganic Chemistry, 54(23), p.11405 - 11410, 2015/12

https://doi.org/10.1021/acs.inorgchem.5b02049
 Times Cited Count：28 Percentile：81.65(Chemistry, Inorganic & Nuclear)

112 (Records 1-20 displayed on this page)