Journal articles on the topic 'MnPX3'

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1

Jin, Yichen, Mouhui Yan, Yuriy Dedkov, and Elena Voloshina. "Realization of the electric-field driven “one-material”-based magnetic tunnel junction using van der Waals antiferromagnetic MnPX3 (X: S, Se)." Journal of Materials Chemistry C 10, no. 10 (2022): 3812–18. http://dx.doi.org/10.1039/d1tc05922j.

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Using electron or hole doping, the top layer of a van der Waals MnPX3 (X: S, Se) material can be converted to the half-metallic ferromagnetic state with the underlying layers remaining in the insulating antiferromagnetic state.
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2

Yang, Juntao, Yong Zhou, Qilin Guo, Yuriy Dedkov, and Elena Voloshina. "Electronic, magnetic and optical properties of MnPX3 (X = S, Se) monolayers with and without chalcogen defects: a first-principles study." RSC Advances 10, no. 2 (2020): 851–64. http://dx.doi.org/10.1039/c9ra09030d.

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3

Dai, Hongwei, Hui Cheng, Menghao Cai, Qinghua Hao, Yuntong Xing, Hongjing Chen, Xiaodie Chen, Xia Wang, and Jun-Bo Han. "Enhancement of the Coercive Field and Exchange Bias Effect in Fe3GeTe2/MnPX3 (X = S and Se) van der Waals Heterostructures." ACS Applied Materials & Interfaces 13, no. 20 (May 12, 2021): 24314–20. http://dx.doi.org/10.1021/acsami.1c05265.

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4

Togawa, Natsuko, Narinobu Juge, Takaaki Miyaji, Miki Hiasa, Hiroshi Omote, and Yoshinori Moriyama. "Wide expression of type I Na+-phosphate cotransporter 3 (NPT3/SLC17A2), a membrane potential-driven organic anion transporter." American Journal of Physiology-Cell Physiology 309, no. 2 (July 15, 2015): C71—C80. http://dx.doi.org/10.1152/ajpcell.00048.2015.

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Membrane potential (Δψ)-driven and Cl−-dependent organic anion transport is a primary function of the solute carrier family 17 (SLC17) transporter family. Although the transport substrates and physiological relevance of the major members are well understood, SLC17A2 protein known to be Na+-phosphate cotransporter 3 (NPT3) is far less well characterized. In the present study, we investigated the transport properties and expression patterns of mouse SLC17A2 protein (mNPT3). Proteoliposomes containing the purified mNPT3 protein took up radiolabeled p-aminohippuric acid (PAH) in a Δψ- and Cl−-dependent manner. The mNPT3-mediated PAH uptake was inhibited by 4,4′-diisothiocyanostilbene-2,2′-disulfonic acid (DIDs) and Evans blue, common inhibitors of SLC17 family members. The PAH uptake was also inhibited by various anionic compounds, such as hydrophilic nonsteroidal anti-inflammatory drugs (NSAIDs) and urate. Consistent with these observations, the proteoliposome took up radiolabeled urate in a Δψ- and Cl−-dependent manner. Immunohistochemistry with specific antibodies against mNPT3 combined with RT-PCR revealed that mNPT3 is present in various tissues, including the hepatic bile duct, luminal membranes of the renal urinary tubules, maternal side of syncytiotrophoblast in the placenta, apical membrane of follicle cells in the thyroid, bronchiole epithelial cells in the lungs, and astrocytes around blood vessels in the cerebrum. These results suggested that mNPT3 is a polyspecific organic anion transporter that is involved in circulation of urate throughout the body.
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5

Kang, Lili, Xiaohong Zheng, Peng Jiang, Zhenzhen Feng, and Gaofeng Zhao. "Tuning magnetism by electric field in MnPS3/Sc2CO2 van der Waals heterostructure." Applied Physics Letters 122, no. 8 (February 20, 2023): 082902. http://dx.doi.org/10.1063/5.0137508.

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Combining a two-dimensional (2D) antiferromagnetic (AFM) material, MnPS3 and a 2D ferroelectric material, Sc2CO2, we propose 2D van der Waals (vdW) heterostructure multiferroics to realize strong magnetoelectric coupling, which is important for designing high-performance magnetoelectric devices. By using first-principles simulations, it is found that the transition from an AFM state to a ferromagnetic (FM) state of a MnPS3 layer could be realized by reversing the polarization direction of a Sc2CO2 layer. We further reveal that such strong magnetoelectric effects originate from the large inter-layer charge transfer due to the competitive interaction between the difference of the interface work functions between MnPS3 and Sc2CO2 and the strong electronegativity of the O atom interface in the Sc2CO2 layer. Our results suggest a feasible scheme for constructing 2D vdW heterostructure multiferroics with very strong inter-layer magnetoelectric coupling effect.
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6

Han, Hui, Hong Lin, Wei Gan, Yucheng Liu, Ruichun Xiao, Lei Zhang, Yang Li, Changjin Zhang, and Hui Li. "Emergent mixed antiferromagnetic state in MnPS3(1-x)Se3x." Applied Physics Letters 122, no. 3 (January 16, 2023): 033101. http://dx.doi.org/10.1063/5.0135557.

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The discovery of magnetism in van der Waal (vdW) materials has aroused substantial interest in the exploration of magnetic interactions toward a two-dimensional (2D) limit. Here, we report the engineering of magnetic properties in MnPS3(1-x)Se3x compounds by substituting the non-magnetic chalcogenide S atoms with Se atoms. The anisotropic antiferromagnetic transition of MnPS3(1-x)Se3x compounds is gradually modulated by controlling the Se concentration, including the monotonic decrease in the Néel temperature and Curie–Weiss temperature with increasing Se concentration, and the Se concentration dependence of a spin-flop process. In addition, the magnetic phase diagram is established, in which an exotic mixed antiferromagnetic state appears due to the competition between the magnetic orderings in parent materials of MnPS3 and MnPSe3. Our findings validate the possibility of the manipulation of magnetic properties in magnetic vdW materials through the substitution of chalcogenide ions and pave the way toward the engineering of magnetic interactions and the designing of magnetic devices in two-dimensional magnetic vdW materials.
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7

Brotons-Alcázar, Isaac, Ramón Torres-Cavanillas, Marc Morant-Giner, Martin Cvikl, Samuel Mañas-Valero, Alicia Forment-Aliaga, and Eugenio Coronado. "Molecular stabilization of chemically exfoliated bare MnPS3 layers." Dalton Transactions 50, no. 44 (2021): 16281–89. http://dx.doi.org/10.1039/d1dt02536h.

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8

Frindt, R. F., D. Yang, and P. Westreich. "Exfoliated single molecular layers of Mn0.8PS3 and Cd0.8PS3." Journal of Materials Research 20, no. 5 (May 2005): 1107–12. http://dx.doi.org/10.1557/jmr.2005.0161.

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The layered compounds MnPS3 and CdPS3 were exfoliated to form single molecular layers of Mn0.8PS3 and Cd0.8PS3 in suspension in water by ion exchange. The x-ray diffraction patterns of the two single-layer suspensions showed profound differences in some of the Bragg peaks, and we demonstrated that the differences are not due to the quality or size of the single layers, but are caused by structure factor modulations of the Warren tail for two-dimensional systems. We also demonstrated that the Cd or Mn vacancies generated in the exfoliation process are not ordered at long range, in contrast to an earlier report of vacancy ordering on intercalated MnPS3.
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9

EL-MELIGI, A. A., A. M. AL-SAIE, H. AL-BUFLASA, and M. BOUOUDINA. "EFFECT OF PYRIDINE INTERCALATION ON SEMICONDUCTOR CRYSTALLINE MnPS3 MATERIALS PHASE TRANSFORMATION." International Journal of Nanoscience 09, no. 03 (June 2010): 215–23. http://dx.doi.org/10.1142/s0219581x10006612.

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The crystalline semiconductor material (MnPS3) has interlayer d-spacing gap of 6.4 Å. The main advantage of this gap is the ability to accommodate organic and inorganic compounds. Pyridine was intercalated in the MnPS3 interlayer gap under specific conditions. Four phases (d-spacing = 12.48 Å, 10.8 Å, 9.7 Å and 7.3 Å) were observed and the corresponding lattice expansions were determined, 5.8 Å, 4.4 Å, 3.3 Å and 1 Å, respectively. X-ray diffraction patterns of the samples after the experiment were stopped to reveal the presence of three phases together. The phase transformation occurred for the aforementioned phases. The crystallite size of certain phases is within nanorange. The magnetic properties of the materials are affected by the phase transformation. Complete intercalation was confirmed by the XRD and infrared (IR) measurements.
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10

Salame, Tomer M., Doriv Knop, Dana Levinson, Oded Yarden, and Yitzhak Hadar. "Redundancy among Manganese Peroxidases in Pleurotus ostreatus." Applied and Environmental Microbiology 79, no. 7 (February 1, 2013): 2405–15. http://dx.doi.org/10.1128/aem.03849-12.

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ABSTRACTManganese peroxidases (MnPs) are key players in the ligninolytic system of white rot fungi. InPleurotus ostreatus(the oyster mushroom) these enzymes are encoded by a gene family comprising nine members,mnp1to -9(mnpgenes). Mn2+amendment toP. ostreatuscultures results in enhanced degradation of recalcitrant compounds (such as the azo dye orange II) and lignin. In Mn2+-amended glucose-peptone medium,mnp3,mnp4, andmnp9were the most highly expressedmnpgenes. After 7 days of incubation, the time point at which the greatest capacity for orange II decolorization was observed,mnp3expression and the presence of MnP3 in the extracellular culture fluids were predominant. To determine the significance of MnP3 for ligninolytic functionality in Mn2+-sufficient cultures,mnp3was inactivated via the Δku80strain-basedP. ostreatusgene-targeting system. In Mn2+-sufficient medium, inactivation ofmnp3did not significantly affect expression of nontargeted MnPs or their genes, nor did it considerably diminish the fungal Mn2+-mediated orange II decolorization capacity, despite the significant reduction in total MnP activity. Similarly, inactivation of eithermnp4ormnp9did not affect orange II decolorization ability. These results indicate functional redundancy within theP. ostreatusMnP gene family, enabling compensation upon deficiency of one of its members.
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11

Yan, Sihan, Wei Wang, Cheng Wang, Limin Chen, Xiaoqian Ai, Qiyun Xie, and Guofeng Cheng. "Anharmonic phonon scattering study in MnPS3 crystal by Raman spectroscopy." Applied Physics Letters 121, no. 3 (July 18, 2022): 032203. http://dx.doi.org/10.1063/5.0096814.

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Phonons play a vital role in lattice dynamics, so a better understanding of anharmonic phonon scattering in van der Waals material MnPS3 is of great significance for its potential applications. Here, we employed Raman spectrum, in situ x-ray diffraction, and first-principles calculations for detailed research. The volume thermal expansion coefficient of MnPS3 was reported. Through the symmetric phonon scattering model, it is confirmed that cubic phonon processes play a major role in P2, P3, P4, and P5 peaks, while quartic phonon processes play an indispensable role in most peaks. The covalent bond was found to be more susceptible to anharmonic phonon scattering than ionic bonds, which is reflected in the wavenumber redshift. Moreover, asymmetric phonon scattering channels also play a meaningful role. Different cubic phonon scattering channels greatly influence the fitting results, and various quartic phonon scattering channels are diverse in highly nonlinear linewidth broadening.
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12

Okuda, K., S. Noguchi, K. Kurosawa, and S. Saito. "MAGNETISM OF Py-INTERCALATED MnPS3." Le Journal de Physique Colloques 49, no. C8 (December 1988): C8–1499—C8–1500. http://dx.doi.org/10.1051/jphyscol:19888690.

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13

Miyazaki, Takafumi, Kenji Ichimura, Susumu Matsuzaki, and Mizuka Sano. "Pyridine-intercalated MnPS3 single crystals." Journal of Physics and Chemistry of Solids 54, no. 9 (September 1993): 1023–26. http://dx.doi.org/10.1016/0022-3697(93)90008-f.

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14

Joy, P. A., and S. Vasudevan. "Magnetism and spin dynamics in MnPS3 and pyridine intercalated MnPS3: An electron paramagnetic resonance study." Journal of Chemical Physics 99, no. 6 (September 15, 1993): 4411–22. http://dx.doi.org/10.1063/1.466094.

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15

Yang, D., and R. F. Frindt. "Structure of polymer intercalated MnPS3 and CdPS3." Journal of Materials Research 15, no. 11 (November 2000): 2408–13. http://dx.doi.org/10.1557/jmr.2000.0346.

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Layered MnPS3 and CdPS3 powders were used to prepare M1−xK2xPS3/poly(ethylene glycol) (PEG) and M1−xK2xPS3/poly(vinyl pyrrolidone) (PVP) (M = Cd, Mn) intercalation nanocomposites. The structure of these compounds was studied by x-ray diffraction. The host layers in Cd0.8K0.4PS3 (PEG)2.0 and Mn0.8K0.4PS3(PEG)2.0 nanocomposites were 3-dimensional crystals with a monoclinic unit cell. The in-plane spacings were slightly expanded from original monoclinic MPS3 (0.2% for CdPS3 and 0.5% for MnPS3), while the inter-layer spacing was expanded by 8.87 Å for Cd0.8K0.4PS3(PEG)2.0 and 8.86 Å for Mn0.8K0.4PS3(PEG)2.0. The Cd0.8K0.4PS3(PVP)1.1 and Mn0.8K0.4PS3(PVP)1.1 nanocomposites, on the other hand, had an expanded interlayer spacing of about 30 Å and the diffraction patterns contained only (00l) and (hk0) peaks, and no mixed (hkl) peaks were observed. The (hk0) peaks were 2-dimensional, with strongly asymmetric line shapes, and there was excellent agreement with pattern calculations for single molecular layers. This demonstrated that the host layers in Cd0.8K0.4PS3(PVP)1.1 and Mn0.8K0.4PS3(PVP)1.1 nanocomposites were tubostratically stacked layered systems.
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16

Wildes, A. R., M. J. Harris, and K. W. Godfrey. "Two-dimensional critical fluctuations in MnPS3." Journal of Magnetism and Magnetic Materials 177-181 (January 1998): 143–44. http://dx.doi.org/10.1016/s0304-8853(97)00666-5.

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17

Okuda, Kiichi, Ko Kurosawa, Shozo Saito, Makoto Honda, Zhihong Yu, and Muneyuki Date. "Magnetic Properties of Layered Compound MnPS3." Journal of the Physical Society of Japan 55, no. 12 (December 15, 1986): 4456–63. http://dx.doi.org/10.1143/jpsj.55.4456.

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18

Koo, Hyun-Joo, Reinhard Kremer, and Myung-Hwan Whangbo. "Unusual Spin Exchanges Mediated by the Molecular Anion P2S64−: Theoretical Analyses of the Magnetic Ground States, Magnetic Anisotropy and Spin Exchanges of MPS3 (M = Mn, Fe, Co, Ni)." Molecules 26, no. 5 (March 5, 2021): 1410. http://dx.doi.org/10.3390/molecules26051410.

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We examined the magnetic ground states, the preferred spin orientations and the spin exchanges of four layered phases MPS3 (M = Mn, Fe, Co, Ni) by first principles density functional theory plus onsite repulsion (DFT + U) calculations. The magnetic ground states predicted for MPS3 by DFT + U calculations using their optimized crystal structures are in agreement with experiment for M = Mn, Co and Ni, but not for FePS3. DFT + U calculations including spin-orbit coupling correctly predict the observed spin orientations for FePS3, CoPS3 and NiPS3, but not for MnPS3. Further analyses suggest that the ||z spin direction observed for the Mn2+ ions of MnPS3 is caused by the magnetic dipole–dipole interaction in its magnetic ground state. Noting that the spin exchanges are determined by the ligand p-orbital tails of magnetic orbitals, we formulated qualitative rules governing spin exchanges as the guidelines for discussing and estimating the spin exchanges of magnetic solids. Use of these rules allowed us to recognize several unusual exchanges of MPS3, which are mediated by the symmetry-adapted group orbitals of P2S64− and exhibit unusual features unknown from other types of spin exchanges.
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19

Vergöhl, M., and J. Schoenes. "POLAR KERR EFFECT OF MnPt3 AND CrPt3." Journal of the Magnetics Society of Japan 20, S_1_MORIS_96 (1996): S1_141–144. http://dx.doi.org/10.3379/jmsjmag.20.s1_141.

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20

Grasso, V., F. Neri, S. Santangelo, L. Silipigni, and M. Piacentini. "Electronic conduction in the layered semiconductor MnPS3." Journal of Physics: Condensed Matter 1, no. 21 (May 29, 1989): 3337–47. http://dx.doi.org/10.1088/0953-8984/1/21/004.

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21

El-Meligi, A. A. "Investigation of MnPS3 intercalates with pyridinium ion." Materials Chemistry and Physics 84, no. 2-3 (April 2004): 331–40. http://dx.doi.org/10.1016/j.matchemphys.2003.11.019.

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22

Kato, T., H. Kikuzawa, S. Iwata, S. Tsunashima, and S. Uchiyama. "Magneto-optical effect in MnPt3 alloy films." Journal of Magnetism and Magnetic Materials 140-144 (February 1995): 713–14. http://dx.doi.org/10.1016/0304-8853(94)01572-4.

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23

Chen, Xingguo, Jingui Qin, Makoto Inokuchi, Minoru Kinoshita, and Kyuya Yakushi. "Magnetic intercalate of pararosaniline into layered MnPS3." Synthetic Metals 137, no. 1-3 (April 2003): 1339–40. http://dx.doi.org/10.1016/s0379-6779(02)01083-4.

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24

Wildes, A. R., S. J. Kennedy, and T. J. Hicks. "True two-dimensional magnetic ordering in MnPS3." Journal of Physics: Condensed Matter 6, no. 24 (June 13, 1994): L335—L341. http://dx.doi.org/10.1088/0953-8984/6/24/002.

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25

Grasso, V., F. Neri, P. Perillo, and L. Silipigni. "Temperature dependence of the MnPS3 crystal fluorescence." Il Nuovo Cimento D 15, no. 1 (January 1993): 9–16. http://dx.doi.org/10.1007/bf02455846.

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26

Hangyo, M., S. Nakashima, A. Mitsuishi, K. Kurosawa, and S. Saito. "Raman spectra of MnPS3 intercalated with pyridine." Solid State Communications 65, no. 5 (February 1988): 419–23. http://dx.doi.org/10.1016/0038-1098(88)90729-6.

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27

Cohen, Roni, Oded Yarden, and Yitzhak Hadar. "Lignocellulose Affects Mn2+ Regulation of Peroxidase Transcript Levels in Solid-State Cultures of Pleurotus ostreatus." Applied and Environmental Microbiology 68, no. 6 (June 2002): 3156–58. http://dx.doi.org/10.1128/aem.68.6.3156-3158.2002.

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ABSTRACT The effect of Mn2+ amendment on peroxidase gene expression was studied during Pleurotus ostreatus growth on cotton stalks. Four peroxidase-encoding genes were expressed differentially and in a manner different from that observed in defined media. Mn2+ affects mnp3 expression even 2 h after its addition to the cultures, suggesting a direct effect of the metal ion on expression.
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28

Holesova, Zuzana, Michaela Jakubkova, Ivana Zavadiakova, Igor Zeman, Lubomir Tomaska, and Jozef Nosek. "Gentisate and 3-oxoadipate pathways in the yeast Candida parapsilosis: identification and functional analysis of the genes coding for 3-hydroxybenzoate 6-hydroxylase and 4-hydroxybenzoate 1-hydroxylase." Microbiology 157, no. 7 (July 1, 2011): 2152–63. http://dx.doi.org/10.1099/mic.0.048215-0.

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The pathogenic yeast Candida parapsilosis degrades various hydroxy derivatives of benzenes and benzoates by the gentisate and 3-oxoadipate pathways. We identified the genes MNX1, MNX2, MNX3, GDX1, HDX1 and FPH1 that code for enzymes involved in these pathways in the complete genome sequence of C. parapsilosis. Next, we demonstrated that MNX1, MNX2, MNX3 and GDX1 are inducible and transcriptionally controlled by hydroxyaromatic substrates present in cultivation media. Our results indicate that MNX1 and MNX2 code for flavoprotein monooxygenases catalysing the first steps in the 3-oxoadipate and gentisate pathways, respectively (i.e. 4-hydroxybenzoate 1-hydroxylase and 3-hydroxybenzoate 6-hydroxylase). Moreover, we found that the two pathways differ by their intracellular localization. The enzymes of the 3-oxoadipate pathway, Mnx1p and Mnx3p, localize predominantly in the cytosol. In contrast, intracellular localization of the components of the gentisate pathway, Mnx2p and Gdx1p, depends on the substrate in the cultivation medium. In cells growing on glucose these proteins localize in the cytosol, whereas in media containing hydroxyaromatic compounds they associate with mitochondria. Finally, we showed that the overexpression of MNX1 or MNX2 increases the tolerance of C. parapsilosis cells to the antifungal drug terbinafine.
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29

Coradin, Thibaud, Aurélie Coupé, and Jacques Livage. "Intercalation of biomolecules in the MnPS3 layered phase." Journal of Materials Chemistry 13, no. 4 (February 18, 2003): 705–7. http://dx.doi.org/10.1039/b210514d.

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30

Kumar, Rajat, Ramesh Naidu, Muthu P. Austeria, and Srinivasan Sampath. "Layered, 2D MnPS3: UV Photodetectors and Humidity Sensors." ECS Meeting Abstracts MA2020-01, no. 10 (May 1, 2020): 822. http://dx.doi.org/10.1149/ma2020-0110822mtgabs.

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31

Sabiryanov, R. F., and S. S. Jaswal. "Magneto-optical properties of MnPt3: LDA+U calculations." Journal of Applied Physics 83, no. 11 (June 1998): 6745–46. http://dx.doi.org/10.1063/1.367582.

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32

Nautiyal, T., and S. Auluck. "The electronic structure and magnetism of MoPd3and MnPd3." Journal of Physics: Condensed Matter 1, no. 12 (March 27, 1989): 2211–15. http://dx.doi.org/10.1088/0953-8984/1/12/005.

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33

Yang, Chuluo, Jingui Qin, Kyuya Yakushi, Yasuhiro Nakazawa, and Kenji Ichimura. "BEDT-TTF being inserted into a layered MnPS3." Synthetic Metals 102, no. 1-3 (June 1999): 1482. http://dx.doi.org/10.1016/s0379-6779(98)00675-4.

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34

Ismail, N., Y. M. Temerk, A. A. El-Meligi, M. A. Badr, and M. Madian. "Synthesis and characterization of MnPS3 for hydrogen sorption." Journal of Solid State Chemistry 183, no. 5 (May 2010): 984–87. http://dx.doi.org/10.1016/j.jssc.2010.02.021.

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35

Long, Gen, Hugo Henck, Marco Gibertini, Dumitru Dumcenco, Zhe Wang, Takashi Taniguchi, Kenji Watanabe, Enrico Giannini, and Alberto F. Morpurgo. "Persistence of Magnetism in Atomically Thin MnPS3 Crystals." Nano Letters 20, no. 4 (March 6, 2020): 2452–59. http://dx.doi.org/10.1021/acs.nanolett.9b05165.

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36

Kato, T., Y. Fujiwara, S. Iwata, and S. Tsunashima. "Magnetic circular dichroism spectra of MnPt3/Co multilayers." Journal of Magnetism and Magnetic Materials 240, no. 1-3 (February 2002): 517–19. http://dx.doi.org/10.1016/s0304-8853(01)00896-4.

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37

Miyazaki, T., S. Matsuzaki, K. Ichimura, and M. Sano. "Mixed-valence TTF intercalated in lamellar MnPS3 crystals." Solid State Communications 85, no. 11 (March 1993): 949–51. http://dx.doi.org/10.1016/0038-1098(93)90710-5.

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38

Goossens, D. J. "Dipolar anisotropy in quasi-2D honeycomb antiferromagnet MnPS3." European Physical Journal B 78, no. 3 (November 12, 2010): 305–9. http://dx.doi.org/10.1140/epjb/e2010-10569-x.

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39

Toyoshima, Wataru, Toshihiro Masubuchi, Tadataka Watanabe, Kouichi Takase, Kazuyuki Matsubayashi, Yoshiya Uwatoko, and Yoshiki Takano. "Pressure dependence of the magnetic properties of MnPS3." Journal of Physics: Conference Series 150, no. 4 (March 1, 2009): 042215. http://dx.doi.org/10.1088/1742-6596/150/4/042215.

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40

Rønnow, H. M., A. R. Wildes, and S. T. Bramwell. "Magnetic correlations in the 2D honeycomb antiferromagnet MnPS3." Physica B: Condensed Matter 276-278 (March 2000): 676–77. http://dx.doi.org/10.1016/s0921-4526(99)01520-3.

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41

Hasegawa, Akira. "Spin-Polarised Energy Bands for MnPt3, FePd3and PtFe3." Journal of the Physical Society of Japan 54, no. 4 (April 15, 1985): 1477–85. http://dx.doi.org/10.1143/jpsj.54.1477.

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42

Mohamad Latiff, Naziah, Nur Farhanah Rosli, Carmen C. Mayorga-Martinez, Katerina Szokolava, Zdenek Sofer, Adrian C. Fisher, and Martin Pumera. "MnPS3 shows anticancer behaviour towards lung cancer cells." FlatChem 18 (November 2019): 100134. http://dx.doi.org/10.1016/j.flatc.2019.100134.

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43

Hong, Soon Cheol. "Magnetism of the MnPt3 (001) Surface: First-Principles Study." Journal of the Korean Physical Society 53, no. 3 (September 12, 2008): 1525–28. http://dx.doi.org/10.3938/jkps.53.1525.

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44

Kato, T., S. Iwata, S. Tsunashima, and S. Uchiyama. "Magnetic and Magneto-Optical Properties of MnPt3 Alloy Films." Journal of the Magnetics Society of Japan 19, no. 2 (1995): 205–8. http://dx.doi.org/10.3379/jmsjmag.19.205.

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Fukae, F., T. Kato, S. Iwata, and S. Tsunashima. "Magnetic and Magneto-Optical Properties of MnPt3/CoPt3 Superlattices." Journal of the Magnetics Society of Japan 22, no. 4_2 (1998): 317–20. http://dx.doi.org/10.3379/jmsjmag.22.317.

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Shugurov, S. M., A. Yu Timoshkin, and S. I. Lopatin. "THERMODYNAMIC STUDY OF GASEOUS MANGANESE PHOSPHATES MnPO3 and MnPO2." Phosphorus, Sulfur, and Silicon and the Related Elements 179, no. 10 (October 1, 2004): 2091–98. http://dx.doi.org/10.1080/10426500490474950.

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Wierman, K. W., J. N. Hilfiker, R. F. Sabiryanov, S. S. Jaswal, R. D. Kirby, and J. A. Woollam. "Optical and magneto-optical properties of MnPt3 films (abstract)." Journal of Applied Physics 81, no. 8 (April 15, 1997): 5674. http://dx.doi.org/10.1063/1.364692.

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Kokuryu, M., T. Kato, S. Iwata, and S. Tsunashima. "Magnetic and magneto-optical properties of MnPt3/Co multilayer." Journal of Applied Physics 81, no. 8 (April 15, 1997): 4779–81. http://dx.doi.org/10.1063/1.365461.

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Köseoğlu, Y., F. Yildiz, J. V. Yakhmi, J. Qin, X. Chen, and B. Aktaş. "EPR studies on BEDT-TTF intercalated MnPS3 molecular magnet." Journal of Magnetism and Magnetic Materials 258-259 (March 2003): 416–18. http://dx.doi.org/10.1016/s0304-8853(02)01077-6.

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Joy, Pattayil Alias, and Sukumaran Vasudevan. "The intercalation reaction of pyridine with manganese thiophosphate, MnPS3." Journal of the American Chemical Society 114, no. 20 (September 1992): 7792–801. http://dx.doi.org/10.1021/ja00046a027.

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