Search results for "Chalcogenides"

showing 7 items of 27 documents

Structural and Spectroscopic Studies of the PCP-Bridged Heavy Chalcogen-Centered Monoanions [HC(PPh2E)(PPh2)]− (E = Se, Te) and [HC(PR2E)2]− (E = Se,…

2009

Selenium- and tellurium-containing bis(diphenylphosphinoyl)methane monoanions were prepared by oxidation of the anion [HC(PPh2)2]− with elemental chalcogens. The selenium-containing isopropyl derivative was synthesized by generating [H2C(PiPr2)2] via a reaction between [H2C(PCl2)2] and 4 equiv of iPrMgCl prior to insitu oxidation with selenium followed by deprotonation with LiNiPr2. The solid-state structures of the lithium salts of the monochalcogeno anions TMEDA·Li[HC(PPh2E)(PPh2)] (E = Se (Li7a), E = Te (Li7b)) and the dichalcogeno anions TMEDA·Li[HC(PR2Se)2] (R = Ph (Li8a), iPr (Li8c)) revealed five- and six-membered LiEPCP and LiSePCPSe rings, respectively. The homoleptic group 12 comp…

dichalcogenidesdikalkogenidit
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Experimental and Theoretical Investigations of the Contact Ion Pairs Formed by Reactions of the Anions [(EPR2)2N]− (R = iPr, tBu; E = S, Se) with the…

2009

Reactions of the sodium salts [(EPR2)2N]Na(TMEDA) (R = iPr, tBu; E = S, Se) with the iodide salts [(TePR2)2N]I (R = iPr, tBu) in toluene produce the mixed-chalcogen systems [(EPR2)2N][(TePR2)2N] (6b, E = Se, R = tBu; 6c, E = S, R = tBu; 7b, E = Se, R = iPr; 7c, E = S, R = iPr). Compounds 6b, 6c, 7b, and 7c have been characterized in solution by variable-temperature multinuclear (31P, 77Se, and 125Te) NMR spectroscopy and in the solid state by single-crystal X-ray crystallography. The structures are comprised of contact ion pairs linked by bonds between Te and S or Se atoms. For the tert-butyl derivatives 6b and 6c, the anionic half of the molecule is coordinated in a bidentate (E,E′) fashio…

dichalcogenidesdikalkogenidit
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Bond Stretching and Redox Behavior in Coinage Metal Complexes of the Dichalcogenide Dianions [(SPh2P)2CEEC(PPh2S)2]2− (E=S, Se): Diradical Character …

2011

The metathetical reactions of a) [Li(tmeda)]2[(S)C(PPh2S)2] (Li2⋅3 c) with CuCl2 and b) [Li(tmeda)]2[(SPh2P)2CSSC(PPh2S)2] (Li2⋅4 c) with two equivalents of CuCl both afford the binuclear CuI complex {Cu2[(SPh2P)2CSSC(PPh2S)2]} (5 c). The elongated (C)S[BOND]S(C) bond (ca. 2.54 and 2.72 Å) of the dianionic ligand observed in the solid-state structure of 5 c indicate the presence of diradical character as supported by theoretical analyses. The treatment of [Li(tmeda)]2[(SPh2P)2CSeSeC(PPh2S)2] (Li2⋅4 b) and Li2⋅4 c with AgOSO2CF3 produce the analogous AgI derivatives, {Ag2[(SPh2P)2CEEC(PPh2S)2]} (6 b, E=Se; 6 c, E=S), respectively. The diselenide complex 6 b exhibits notably weaker Ag[BOND]Se…

dichalcogenidesredox chemistrydikalkogenidithapetus-pelkistys-kemiaryhmän 11 metallitdiradikaaliluonneelectronic structurediradical characterelektronirakennecoinage metals
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CoS2/TiO2 Nanocomposites for Hydrogen Production under UV Irradiation

2019

Transition metal chalcogenides have intensively focused on photocatalytic hydrogen production for a decade due to their stronger edge and the quantum confinement effect. This work mainly focuses on synthesis and hydrogen production efficiencies of cobalt disulfide (CoS2)-embedded TiO2 nanocomposites. Materials are synthesized by using a hydrothermal approach and the hydrogen production efficiencies of pristine CoS2, TiO2 nanoparticles and CoS2/TiO2 nanocomposites are compared under UV irradiation. A higher amount of hydrogen production (2.55 mmol g&minus

hydrothermalMaterials scienceHydrogenNanoparticlechemistry.chemical_element02 engineering and technology010402 general chemistry01 natural scienceswater splittingArticleTransition metalGeneral Materials Sciencetitaniatransition metal chalcogenidesHydrogen productionNanocompositeVDP::Teknologi: 500::Materialteknologi: 520::Funksjonelle materialer: 522021001 nanoscience & nanotechnology0104 chemical sciencesVDP::Teknologi: 500Chemical engineeringchemistryhydrogenPhotocatalysisWater splitting0210 nano-technologyCobaltMaterials
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Long-Term Stability of TiS2–Alkylamine Hybrid Materials

2022

Layered TiS2 intercalated with linear alkylamines has recently attracted significant interest as a model compound for flexible n-type thermoelectric applications, showing remarkably high power factors at room temperature. The thermal and, particularly, environmental stability of such materials is, however, a still an open challenge. In this paper, we show that amine-intercalated TiS2 prepared by a simple mechanochemical process is prone to chemical decomposition through sulfur exsolution, and that the presence of molecular oxygen is likely to mediate the decomposition reaction. Through computational analysis of the possible reaction pathways, we propose that Ti-N adducts are formed as a con…

intercalationSettore CHIM/03 - Chimica Generale E Inorganicachalcogenides; thermoelectrics; X-ray diffraction; Raman; intercalationchalcogenidesGeneral Materials ScienceRamanthermoelectricsX-ray diffractionMaterials
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Strongly Coupled Coherent Phonons in Single-Layer MoS 2

2019

We present a transient absorption setup combining broadband detection over the visible-UV range with high temporal resolution ($\sim$20fs) which is ideally suited to trigger and detect vibrational coherences in different classes of materials. We generate and detect coherent phonons (CPs) in single layer (1L) MoS$_2$, as a representative semiconducting 1L-transition metal dichalcogenide (TMD), where the confined dynamical interaction between excitons and phonons is unexplored. The coherent oscillatory motion of the out-of-plane $A'_{1}$ phonons, triggered by the ultrashort laser pulses, dynamically modulates the excitonic resonances on a timescale of few tens fs. We observe an enhancement by…

ramanspectroscopyPhononExcitonGeneral Physics and AstronomyFOS: Physical sciences02 engineering and technologyApplied Physics (physics.app-ph)thz phonons010402 general chemistry01 natural sciencesMolecular physicssymbols.namesakephotoinduced bandgap renormalizationtransient absorption spectroscopyUltrafast laser spectroscopyMesoscale and Nanoscale Physics (cond-mat.mes-hall)General Materials Sciencepulsesexciton−phonon interactionPhysicsab initio calculationCondensed Matter - Materials ScienceCondensed Matter - Mesoscale and Nanoscale Physicstransition metal dichalcogenidesgrapheneGeneral Engineeringmonolayer mos2ResonanceMaterials Science (cond-mat.mtrl-sci)excitationmonodynamicsPhysics - Applied Physics021001 nanoscience & nanotechnology0104 chemical sciencesAmplitudeOrders of magnitude (time)coherent phononsexciton-phonon interactionsymbols0210 nano-technologyRaman spectroscopyExcitationACS Nano
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Density-Functional Tight-Binding Simulations of Curvature-Controlled Layer Decoupling and Band-Gap Tuning in Bilayer MoS2

2014

Monolayer transition-metal dichalcogenides (TMDCs) display valley-selective circular dichroism due to the presence of time-reversal symmetry and the absence of inversion symmetry, making them promising candidates for valleytronics. In contrast, in bilayer TMDCs both symmetries are present and these desirable valley-selective properties are lost. Here, by using density-functional tight-binding electronic structure simulations and revised periodic boundary conditions, we show that bending of bilayer MoS2 sheets breaks band degeneracies and localizes states on separate layers due to bendinginduced strain gradients across the sheets. We propose a strategy for employing bending deformations in b…

transition-metal dichalcogenidesaugmented-wave method
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