Academic literature on the topic 'Transition Metal Di-chalcogenide'

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Journal articles on the topic "Transition Metal Di-chalcogenide"

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Yam, Vivian Wing-Wah. "Molecular design of luminescent metal-based materials." Pure and Applied Chemistry 73, no. 3 (2001): 543–48. http://dx.doi.org/10.1351/pac200173030543.

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A series of soluble di- and polynuclear transition-metal acetylides with rich luminescence behavior have been designed and successfully isolated. The photophysical and photochemical properties have been studied. Luminescent polynuclear metal complexes have also been obtained based on the metal chalcogenide building block. These high-nuclearity transition-metal chalcogenide complexes have been structurally characterized and shown to display rich luminescence behavior. Various approaches and strategies to design and synthesize luminescent polynuclear metal complexes that may find potential appli
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Bharucha, Shivani R., Mehul S. Dave, Sunil H. Chaki, and Tushar A. Limbani. "Thermal investigation of NbSe2 nanoparticles synthesized through a temperature-dependent sonochemical method." RSC Advances 14, no. 45 (2024): 33459–70. http://dx.doi.org/10.1039/d4ra05108d.

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Due to their unique size-dependent properties, transition metal di-chalcogenide nanoparticles are trending in research for their potential to revolutionize next-generation electronics, energy storage, and catalytic processes.
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Yang, Jun-Feng, Braham Parakash, Jens Hardell, and Qian-Feng Fang. "Tribological properties of transition metal di-chalcogenide based lubricant coatings." Frontiers of Materials Science 6, no. 2 (2012): 116–27. http://dx.doi.org/10.1007/s11706-012-0155-7.

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Sokolov, Maxim N., Alexander V. Anyushin, Rita Hernandez-Molina, Rosa Llusar, and Manuel G. Basallote. "Hydroxylated phosphines as ligands for chalcogenide clusters: self assembly, transformations and stabilization." Pure and Applied Chemistry 89, no. 3 (2017): 379–92. http://dx.doi.org/10.1515/pac-2017-0105.

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AbstractThis contribution is a documentation of recent advances in the chemistry of chalcogenide polynuclear transition metal complexes coordinated with mono- and di-phosphines functionalized with hydroxo groups. A survey of complexes containing tris(hydroxymethyl)phosphine (THP) is presented. The influence of the alkyl chain in bidentate phosphines, bearing the P–(CH2)x–OH arms, is also analyzed. Finally, isolation and structure elucidation of the complexes with HP(OH)2, P(OH)3, As(OH)3, PhP(OH)2, stabilized by coordination to Ni(0) and Pd(0) centers embedded into chalcogenide clusters, is di
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Chaudhary, Karan, Manoj Trivedi, Dhanraj T. Masram, and Nigam P. Rath. "Transition-metal complexes of group 12 with 1,1′-bis(phosphanyl)ferrocene ligands." Acta Crystallographica Section C Structural Chemistry 77, no. 5 (2021): 240–48. http://dx.doi.org/10.1107/s2053229621004162.

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The syntheses of four new cadmium and zinc complexes with 1,1′-bis(phosphanyl)ferrocene ligands and their phosphine chalcogenide derivatives are reported. The complexes were characterized by elemental analyses and IR, 1H NMR, 31P NMR and electronic absorption spectroscopy. The crystal structures of dichlorido[1-diphenylphosphinoyl-1′-(di-tert-butylphosphanyl)ferrocene-κ2 O,P]cadmium(II), [CdCl2{(C17H14OP)(C13H22P)Fe}] or CdCl2(κ2 P,O-dppOdtbpf) (1), bis[μ-(tert-butyl)(1′-diphenylphosphinoylferrocen-1-yl)phosphinato-κ3 O,O′:O′′]bis[chloridozinc(II)], [Zn2{(C9H13O2P)(C17H14OP)Fe}2Cl2] or [ZnOCl{
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Joe, Jemee, Hyunwoo Yang, Changdeuck Bae, and Hyunjung Shin. "Metal Chalcogenides on Silicon Photocathodes for Efficient Water Splitting: A Mini Overview." Catalysts 9, no. 2 (2019): 149. http://dx.doi.org/10.3390/catal9020149.

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In the photoelectrochemical (PEC) water splitting (WS) reactions, a photon is absorbed by a semiconductor, generating electron-hole pairs which are transferred across the semiconductor/electrolyte interface to reduce or oxidize water into oxygen or hydrogen. Catalytic junctions are commonly combined with semiconductor absorbers, providing electrochemically active sites for charge transfer across the interface and increasing the surface band bending to improve the PEC performance. In this review, we focus on transition metal (di)chalcogenide [TM(D)C] catalysts in conjunction with silicon photoe
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Devi, Anjna, Neha Dhiman, Narender Kumar, et al. "Ferromagnetism in Defected TMD (MoX2, X = S, Se) Monolayer and Its Sustainability under O2, O3, and H2O Gas Exposure: DFT Study." Nanomaterials 13, no. 10 (2023): 1642. http://dx.doi.org/10.3390/nano13101642.

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Spin-polarized density-functional theory (DFT) has been employed to study the effects of atmospheric gases on the electronic and magnetic properties of a defective transition-metal dichalcogenide (TMD) monolayer, MoX2 with X = S or Se. This study focuses on three single vacancies: (i) molybdenum “VMo”; (ii) chalcogenide “VX”; and (iii) di-chalcogenide “VX2”. Five different samples of sizes ranging from 4 × 4 to 8 × 8 primitive cells (PCs) were considered in order to assess the effect of vacancy–vacancy interaction. The results showed that all defected samples were paramagnetic semiconductors,
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KIRITO, CHO, Naomi Sawamoto, Hideaki Machida, et al. "Conformal deposition of WS2 layered film by low-temperature metal-organic chemical vapor deposition." Japanese Journal of Applied Physics, April 7, 2023. http://dx.doi.org/10.35848/1347-4065/accb62.

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Abstract WS2 metal-organic (MO) chemical vapor deposition was demonstrated on Si and Al2O3 substrates. Novel MO W precursor of n-BuNC-W(CO)5 and (t-C4H9)2S2. as S precursor were synthesized for the purpose. The obtained films were layered 1T structure as a typical transition metal di-chalcogenide with almost the stoichiometric compositions. The film was significantly stable for 60 days shelf time in the air atmosphere. The layered structure can cover conformally on the 3-simensional fin structure with the layers parallel to the fin surface everywhere.
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"(Invited) Advanced CMOS Device Technologies Discussed Also with Transition-Metal Di-Chalcogenide (TMDC) Channel." ECS Meeting Abstracts, 2015. http://dx.doi.org/10.1149/ma2015-02/29/1098.

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Kharadi, Mubashir Ahmad, Tarun Agarwal, Ibrahim Mahariq, and Jhuma Saha. "Type-II band-alignment in vertical transition metal-di-chalcogenide heterostructures for near infrared and visible light detection." Physica Scripta, February 18, 2025. https://doi.org/10.1088/1402-4896/adb79b.

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Abstract In this work, group-6 and group-7 (ReSe2) transition metal-di-chalcogenide (TMD) heterostructures are studied systematically using density functional theory (DFT). Different combinations of ReSe2and group-6 TMDs are explored to identify the heterostructures with “type-II band-alignment”. ReSe2 monolayer is chosen as group-7 TMD because of its dynamic stability. Materials like MoS2, MoSe2, MoTe2, WS2 and WSe2 are chosen as group-6 TMDs. The heterostructures are evaluated in terms of metrics like; type of band-alignment, band-offsets, optical absorption and potential difference across t
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Dissertations / Theses on the topic "Transition Metal Di-chalcogenide"

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Pal, Srishti. "Spectroscopic and Diffraction Signatures of Quantum Spin Liquids, Skyrmion Lattices and Transition Metal Dichalcogenides at Low Temperatures and High Pressures." Thesis, 2022. https://etd.iisc.ac.in/handle/2005/5727.

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This thesis presents experimental as well as theoretical studies on several contemporary systems like quantum spin liquids (QSLs), skyrmion lattices, and transition metal dichalcogenides (TMDs) under extreme conditions like low temperature (down to 4K) and ultra high pressures (up to 26 GPa). Temperature-dependent Raman studies are carried out to investigate Raman signatures of Kitaev quantum spin liquid (QSL) state of Cu2IrO3 and Ag3LiIr2O6 and orbital ordering in Heisenberg quantum magnet Ca10Cr7O28. High-pressure studies are performed on Kitaev QSL candidates -RuCl3, Cu2IrO3, kagomé
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Conference papers on the topic "Transition Metal Di-chalcogenide"

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Wakabayashi, Hitoshi. "Two-Dimensional Transition-Metal Di-Chalcogenide Devices for Chiplets." In 2024 IEEE International Meeting for Future of Electron Devices, Kansai (IMFEDK). IEEE, 2024. https://doi.org/10.1109/imfedk64776.2024.10814223.

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