Gotowa bibliografia na temat „2H-MoTe2”

Atomically thin molybdenum ditelluride (MoTe2) has been intensively studied as an emerging material for electronics and optoelectronics due to its unique properties. While the small free energy difference between the 2H and 1T′ phases of MoTe2 always results in mixed-phase growth, precisely controlled phase transition of MoTe2 nanostructures is still a considerable challenge. Here, the centimeter-scale 1T′, 2H ultrathin MoTe2 films, and in-plane 1T′–2H homojunction have been synthesized by ambient pressure chemical vapor deposition based on the precursor design and space-confined strategies. The controllable growth of pure 1T′, 2H MoTe2, and 1T′–2H mixed-phase MoTe2 with phase separation and homogeneous mixture, respectively, has been achieved by adjusting growth temperature and growth time. The thickness of synthesized 1T′ and 2H ultrathin MoTe2 films can be effectively controlled by tuning the space-confined height. The corresponding growth mechanism was further illuminated based on systematically experimental characterizations and computational fluid dynamics simulations. The electrical transport properties of 1T′ and 2H MoTe2 films were investigated by conductive atomic force microscope and MoTe2-based thin-film field-effect transistors. Our experimental results provide a new route to realize the phase transition of two-dimensional materials, which makes these materials easily accessible as functional building blocks for next-generation electronic and optoelectronic devices.

Abstract We demonstrated a harmonic mode-locked Erbium-doped fiber laser based on a saturable absorber (SA) of 2H-MoTe2, which is a member of the transition metal dichalcogenides. The SA mode-locker was made by integrating the 2H-MoTe2 into a D-shaped fiber, and then was inserted into an erbium-doped fiber laser for mode-locking. The nonlinear modulation depth and saturation power of 2H-MoTe2-based SA were 10.9% and 19 MW cm−2, respectively. The fundamentally mode-locked pulse train had a pulse width of 577 fs and a repetition rate of 14.32 MHz. The highest order of harmonic mode locking was 55th, which had the repetition rate of 787.6 MHz, pulse width of 820 fs and average output power of 11.8 mW. To the best of our knowledge, this is the highest operating repetition frequency that has ever been demonstrated in a 2H-MoTe2-based fiber laser. The experimental results validate the feasibility of 2H-MoTe2 as a promising SA for generating ultrashort pulses with high repetition rates.

The 2H molybdenum telluride (MoTe2) photodetector structures were made with inserting 1T-MoTe2 interlayer contacts. The optical response properties such as photoconductivity (PC) spectroscopy, illumination intensity dependent photoresponsivity, frequency dependent photocurrent, and time-resolved photoresponse were carried out in this study. In PC spectra, a much higher photoresponsivity of 2H-MoTe2 were observed by inserting 1T-MoTe2 interlayer contact. The frequency dependent photocurrent and time-resolved photoresponse investigations explore the carrier kinetic decay process of MoTe2 with different electrode contact. The Schottky barrier heights (SBH) extracted by thermionic emission theory were also investigated by inserting 1T-MoTe2 interlayer contacts. The results show the potential applicability for photodetection devices based MoTe2 layered transition metal dichalcogenides semiconductors.

Two-dimensional (2D) molybdenum telluride (MoTe2) is attracting increasing attention for its potential applications in electronic, optoelectronic, photonic and catalytic fields, owing to the unique band structures of both stable 2H phase and 1T′ phase. However, the direct growth of high-quality atomically thin MoTe2 with the controllable proportion of 2H and 1T′ phase seems hard due to easy phase transformation since the potential barrier between the two phases is extremely small. Herein, we report a strategy of the phase-controllable chemical vapor deposition (CVD) synthesis for few-layer (<3 layer) MoTe2. Besides, a new understanding of the phase-controllable growth mechanism is presented based on a combination of experimental results and DFT calculations. The lattice distortion caused by Te vacancies or structural strain might make 1T′-MoTe2 more stable. The conditions for 2H to 1T′ phase conversion are determined to be the following: Te monovacancies exceeding 4% or Te divacancies exceeding 8%, or lattice strain beyond 6%. In contrast, sufficient Te supply and appropriate tellurization velocity are essential to obtaining the prevailing 2H-MoTe2. Our work provides a novel perspective on the preparation of 2D transition metal chalcogenides (TMDs) with the controllable proportion of 2H and 1T′ phase and paves the way to their subsequent potential application of these hybrid phases.

The integration of two-dimensional (2D) van der Waals semiconductors into silicon electronics technology will require the production of large-scale, uniform, and highly crystalline films. We report a route for synthesizing wafer-scale single-crystalline 2H molybdenum ditelluride (MoTe2) semiconductors on an amorphous insulating substrate. In-plane 2D-epitaxy growth by tellurizing was triggered from a deliberately implanted single seed crystal. The resulting single-crystalline film completely covered a 2.5-centimeter wafer with excellent uniformity. The 2H MoTe2 2D single-crystalline film can use itself as a template for further rapid epitaxy in a vertical manner. Transistor arrays fabricated with the as-prepared 2H MoTe2 single crystals exhibited high electrical performance, with excellent uniformity and 100% device yield.

Among group VI transition metal dichalcogenides, MoTe2 is predicted to have the smallest energy offset between semiconducting 2H and semimetallic 1T′ states. This makes it an attractive phase change material for both electronic and optoelectronic applications. Here, we report fast, nondestructive, and full phase change in Al2O3-encapsulated 2H-MoTe2 thin films to 1T′-MoTe2 using rapid thermal annealing at 900 °C. Phase change was confirmed using Raman spectroscopy after a short annealing duration of 10 s in both vacuum and nitrogen ambient. No thickness dependence of the transition temperatures was observed for flake thickness ranging from 1.5 to 8 nm. These results represent a major step forward in understanding the structural phase transition properties of MoTe2 thin films using external heating and underline the importance of surface encapsulation for avoiding thin film degradation.

Abstract In this work, we explore the atomic vibration and local structure in 2H–MoTe2 by using high-pressure x-ray absorption fine structure spectroscopy up to ∼20 GPa. The discrepancy between the Mo–Te and Mo–Mo bond length in 2H–MoTe2 obtained from extended-XAFS and other techniques shows abnormal increase at 7.3 and 14.8 GPa, which is mainly due to the abrupt enhancement of vibration perpendicular to the bond direction. Ab initio calculations are performed to study the electronic structure of 2H–MoTe2 up to 20 GPa and confirm a semiconductor to semimetal transition around 8 GPa and a Lifshitz transition around 14 GPa. We attribute the anomalous enhancement of vibration perpendicular to the bond direction to electronic transitions. We find the electronic transition induced enhancement of local vibration for the first time. Our finding offers a novel insight into the local atomic vibration and provides a new platform for understanding the relationship between the electronic transition and atomic vibration.

Abstract The two-electron reduction of molecular oxygen represents an effective strategy to enable the green, mild and on-demand synthesis of hydrogen peroxide. Its practical viability, however, hinges on the development of advanced electrocatalysts, preferably composed of non-precious elements, to selectively expedite this reaction, particularly in acidic medium. Our study here introduces 2H-MoTe2 for the first time as the efficient non-precious-metal-based electrocatalyst for the electrochemical production of hydrogen peroxide in acids. We show that exfoliated 2H-MoTe2 nanoflakes have high activity (onset overpotential ∼140 mV and large mass activity of 27 A g−1 at 0.4 V versus reversible hydrogen electrode), great selectivity (H2O2 percentage up to 93%) and decent stability in 0.5 M H2SO4. Theoretical simulations evidence that the high activity and selectivity of 2H-MoTe2 arise from the proper binding energies of HOO* and O* at its zigzag edges that jointly favor the two-electron reduction instead of the four-electron reduction of molecular oxygen.

This thesis presents experimental as well as theoretical studies of three dimensional topological in-sulators (TIs) and transition metal dichalcogenides (TMDs). Raman spectroscopic measurements of these systems have been carried out as a function of pressure. For structural characterization as a function of pressure, x-ray diffraction measurements using synchrotron source have been pur-sued. The Þeld effect transistor devices fabricated from MoS2 are used in experiments to probe Raman evidence of electrostrictive and piezoelectric effects in multilayer and monolayer, respec-tively. In-situ photoluminescence (PL) and Raman measurements are performed as a function of laser-irradiation time to show healing of defects in MoS2. We provide an overview of our work on these systems chapter-wise. In Chapter-1, the brief introduction of the systems studied in this thesis has been provided. For topological insulators, the 2 topological index has been discussed for three dimensional strong TIs as well as weak TIs. Then, the various properties of MoS2 and MoTe2 such as electronic, vibrational, structural and photoluminescence are discussed in details. Chapter-2 includes a short introduction to Raman spectroscopy and x-ray diffraction. The tech-nical details of the high pressure experiments which include the alignment of the diamond anvil cell, gasket preparation, loading the pressure medium are discussed. This is followed by the discussions on the sample preparation as well as the electron beam lithography techniques. In Chapter-3, we present Raman spectroscopic measurements on a band insulator Sb2Se3 under high pressure upto 24.6 GPa. Different experimental techniques are being pursued to capture the surface electronic properties due to Dirac electrons and hence, thereby characterizing 2 topology of the system. The topological characterization of 2 TIs is solely based on the isolated quantum system of electrons, but in real materials they are coupled to other low energy excitations of the system. Depending upon the strength of the coupling with the environment, it can induce an electronic topological transition. In fact, it has been proposed [Phys. Rev. B 89, 205103 (2014)] that the increment of temperature gives rise to an increase in electron-phonon coupling and thereby driving a trivial insulator to a topological insulator. Here, we address the inverse situation, i.e., can we trace the topological signature due to electronic topological transition (ETT) from the environment or nonelectronic baths of the system rather than from the electronic system itself, experimentally as well as theoretically ? High pressure Raman spectroscopic measurements show a ETT transition at ∼2.5 GPa marked by a large softening of the low frequency Raman mode by ∼ 16% together with an anomalous increase of its linewidth by ∼ 200% within a narrow pressure range of 0 to 2.5 GPa. Our calcula-tions based on model Hamiltonian determined by projecting the electron-phonon coupling term onto the identity representation of the double group corresponding to the phonons of different irreducible representations (thereby ensuring the symmetry invariant Hamiltonian) captures the phonon anomalies qualitatively. It is convincing that the linewidth of phonon carries the non-trivial topological signature but there are few subtle things need to be considered. It is obvious from the linewidth that there is a band inversion at Fermi level but, it is not obvious that it probes strong topological 2 invariant unless the band gap closing and opening occur at odd number of time reversal invariant momentum (TRIM) points in the Brillouin zone and hence, the observed maximum in linewidth of an optical phonon mode is necessary but not sufÞcient to probe the 2 invariant. To the best of our knowledge, this is the Þrst report where vibrational properties through the linewidth of a Raman mode can capture the electronic topological transition of 2-type. In Chapter-4, we present Raman spectroscopic measurements on three strong topological insu-lators as a function of pressure. This chapter consists of two parts: In Part(I), we discuss the following (A) Bi2Te3; (B) Bi2Se3; and (C) Bi1Sb1Te1.25Se1.75. The stoichiometric materials of A2B3 type (Bi2Te3 and Bi2Se3) belong to the family of strong 2 TIs at ambient conditions. Previous high pressure Raman and xÐray diffraction studies showed that there is an isoÐstructural transition at low pressure regime in the range of 3 to 5 GPa where the parallel component of bulk modulus shows a kink. Earlier, this low pressure transition had been assigned to be an ETT based on the changes observed in structural parameters without a detailed exploration of electronic structure or direct evidence for change in electronic topology around the transition pressure. Here, we address this particular low pressure transition regime to clarify whether it is associated with the ETT or not ? We revisit this low pressure transition in the present work using high pressure Raman experi-ments along with Þrst-principles calculations on Bi2Se3 taken as a prototype of the family of A2B3 type TIs. We do not Þnd any change in electronic topology of the both types (ETT of 2Ðtype and ETT of LifshitzÐtype) as a function of pressure (P ≤ 8 GPa) by examining the density of states at Fermi level and the smallest electronic band gap as well as the 2 index and the surface Dirac conical electronic structure. The pressure derivatives of Raman modes show a clear change at 2.4 GPa, without the appearance of any new mode. Hence, the lowest pressure transition should be better termed as an isostructural transition, and not an ETT. Many authors assign this low pressure transition regime as an ETT for all the 3D-topological insulators just by observing the structural distortions and consequent changes in the phonon spectrum. The signature of ETT will reßect in the anomalies for the phonons, but the reverse is not true, i.e. it is not correct to assign an ETT prior to the detailed exploration of electronic band structure. In Part(II), we present Raman spectroscopic measurements on a weak topological insulator Bi1Se1 as a function of pressure. The essential thing in order to understand TIs is the concept of band inversion. What it means that band orderings of valence and conduction bands are changed in such a way that it cannot be connected adiabatically to the atomic limit of the system. When the bands are inverted, the phonons signatures will be useful in order to capture a transition to a band-inverted phase. If a weak topological insulator (WTI) can undergo a transition to a trivial insulator or to a strong topological insulator (STI) by inverting band structures at even or odd number of TRIMs respectively, the corresponding signatures will be reßected in the phonon spectrum. However, it is worthy to remind that WTIs have been identiÞed as strong/robust against the changes in the topology of the even number of Dirac cones at its surface as long as time reversal, translational invariance and (1) gauge symmetries are preserved on average. In our work, we have shown that with the application of hydrostatic pressure (as a tunable parameter) upto ∼ 7 GPa, there is no change in topological signature of Bi1Se1 by probing optical phonons using Raman spectroscopic measurements. Chapter-5 : It is not only the monolayer TMDs possessing tunable and electrical properties, they (TMDs) also exist in different bulk forms (polytypes) having different structure like 2H, 1T, 3R with different electrical and optical properties. Essentially the electrical and physical properties are not only limited to the dimension reduction or sample thickness, but also different crystal structures (polytypes) can also induce different electrical properties and high pressure technique is a powerful way to switch between different thermodynamically stable structural polytypes with-out introducing impurities unlike chemical doping. Recent high pressure Raman studies [Phys. Rev. Lett. 113, 036802 (2014) and J. Phys. Chem. C 118, 3230 (2014)] on 2H-MoS2 (P63/mmc) reveal that there is a onset of lateral shift of the adjacent S−Mo−S layers around ∼ 20 GPa lead-ing to a mixed phase of 2Hc (2H) and 2Ha structures with the 2Hc -phase being the dominant one [J. Phys. Chem. C 118, 3230 (2014)] and thereby changes the pressure coefÞcients of the Raman modes. Motivated by the results of high pressure research on MoS2, we investigated the high pressure induced different phase transitions in MoTe2 and MoSSe using Raman, XRD and Þrst-principles studies. In Part(A), we discuss the high pressure Raman spectroscopic studies of MoTe2 upto ∼ 29 GPa. We have observed a pressure induced semiconductor to semi-metal transition at ∼ 6 GPa and a Lifshitz transition at ∼ 18 GPa in 2H-MoTe2 by combining Raman measurements and Þrst-principles calculations. The frequencies of the Þrst order A1g and E12g Raman modes carry the signatures of semiconductor to semimetal and the Lifshitz transitions. The occurrence of a max-imum in the integrated area ratio of the A1g and E12g modes is mainly due to non-monotonous change in Raman tensor of E12g mode with pressure. DFT calculations of pressure effects on Ra-man active modes show that pressure inßuences the electron-phonon coupling of the A1g mode most strongly. In Part(B), we present high pressure Raman (upto ∼ 26 GPa) and XRD studies (upto ∼ 20 GPa) of MoSSe. All the three Mo-based TMDs (MoS2, MoSe2 and MoTe2) undergo semimetal transition and only for MoS2, iso-structural transition precedes the metallization phase. The rea-son possibly could be attributed to the d-electron propagation which favors the Mo-atoms on top of each other in metallic 2Ha-phase than semiconducting 2Hc (2H)-phase where Mo-atoms sit on top of S-atoms. However, in case of MoTe2 and MoSe2 the larger radius of chalcogen atoms increases the interlayer distance and thereby hinders the d-electron propagation mechanism, and hence favors the 2Hc -structural polytypes. The question we will address is that if we substitute one S-atom with the Se-atom, i.e. for MoSSe compound, what happens to pressure-induced phase transitions. We have shown that the substitution of S by Se reduces its crystal symmetry to P63mc (# 186) and an isostructural transition to a 2Ha-phase with the same space group takes place around 10.8 GPa, similar to the case of MoS2. We suggest that layer sliding transition completes around 18 GPa as reßected in our Raman data where few modes undergo a slope change in pressure-dependent frequency (ω) plot. We also observe a low pressure (P) transition around ∼ 2 GPa where Raman modes show a change in dω/dP, which is also reßected in c/a ratio variations obtained by synchrotron based x-ray diffraction experiments as a function of pressure. This low pressure transition at ∼ 2 GPa has not been reported so far for any of three MoX2 (X = S, Se and Te) compounds discussed before. Chapter–6 : Piezoelectric and electrostrictive materials are of signiÞcant interest in electrome-chanical devices to harvest energy as well as in a wide range of applications of sensors and ac-tuators. Here, we report in-situ Raman spectroscopic studies on multilayer MoS2 device to show that the observed changes in frequencies ( ω) of the A1g and E12g optical modes varies quadrati-cally as a function of applied electric Þeld ( ω ∝ E2DS ) due to the electrostrictive effects and to the best of our knowledge, this is the Þrst evidence of the observed electrostriction in multilayer MoS2. The observed ω are ∼ 1.6 cm−1 and 1.4 cm−1 for the A1g and E12g modes, respectively for the applied maximum electric Þeld of 45 kV/cm. The electrostrictive coefÞcient is ∼ 3.6 × 10−14 m2/V2, corresponding to ∼ 0.7 % in-plane uniaxial tensile strain. This value is ∼ 428 times higher than the most commonly used electrostrictive material PMN (PbMg1/3Nb2/3O3). We also carried out similar experiments on monolayer MoS2 device and the observed frequency of the A1g mode varies linearly ( ω ∝ EDS ) due to piezoelectric effect. The A1g mode hardens by ∼ 1.2 cm−1 with the applied electric Þled of 7.2 kV/cm. In Chapter–7, we present PL and Raman spectroscopic studies of monolayer MoS2 as a function of laser irradiation time. The two-dimensional monolayer MoS2 has enhanced Coulomb interactions than its bulk-counterpart. The change in the carrier concentration in the channel will lead to the renormalized binding energy for the relatively loosely bound trions and this fact will facilitate to modulate the PL spectrum of monolayer MoS2 as a function of channel doping. By depleting the excess electrons from the monolayer MoS2, we can not only destabilize the trion formation but also enhance radiative recombinations and hence, an increase in PL efÞciency. While extracting or adding electrons change the optical properties, it also renormalize phonons. To the best of our knowledge, there is no quantitative reported data on Raman study and the dynamics of enhanced trion as well as B-exciton PL emission as a function of laser irradiation time. Here, we show that exposing the monolayer MoS2 in air to a modest laser intensity for a brief period of time enhances simultaneously the PL intensity associated with both the trions and excitons, together with ∼ 3 to 5 times increase in the Raman intensity of Þrst and second order modes. The simultaneous increase of PL from trions and excitons cannot be understood based only on known-scenario of depletion of electron concentration in MoS2 by adsorption of O2 and H2O molecules. This is explained by laser induced healing of defect states resulting in reduction of non-radiative Auger processes. This laser healing is corroborated by an observed increase in intensity of both the Þrst order and second order 2LA(M) Raman modes by a factor of ∼ 3 to 5. The A1g mode hardens by ∼ 1.4 cm−1 whereas the E12g mode softens by ∼ 1 cm−1. The second order 2LA(M) Raman mode at ∼ 440 cm−1 shows an increase in wavenumber by ∼ 8 cm−1 with laser exposure. These changes are a combined effect of the change in electron concentrations and oxygen-induced lattice displacements. In Chapter–8, we have summarized our Þndings and highlighted few possibilities which can be pursued in future in order to have a better understanding of these systems.

The discovery and control of new phases of matter are a central endeavor in materials research. Phase transition in two-dimensional (2D) materials has been achieved through laser irradiation, strain engineering, electrostatic doping, and controlled chemical vapor deposition growth, and laser irradiation is considered as a fast and clean technique for triggering phase transition. By using first-principles calculations, we predict that the monolayer MoTe2 exhibits a photo-induced phase transition (PIPT) from the semiconducting 2H phase to the topological 1T′ phase. The purely electronic excitations by photon soften multiple lattice vibrational modes and lead to structural symmetry breaking within sub-picosecond timescales, which is shorter than the timescale of a thermally driven phase transition, enabling a controllable phase transition by means of photons. This finding provides deep insight into the underlying physics of the phase transition in 2D transition-metal ditellurides and show an ultrafast phase-transition mechanism for manipulation of the topological properties of 2D systems. More importantly, our finding opens a new avenue to discover the new families of PIPT materials that are very limited at present but are essential to design the next generation of devices operated at ultrafast speed.

We explore non-equilibrium states in a two-dimensional transition-metal dichalcogenide under periodical phonon driving. A time-frequency analysis reveals strong coupling between electrons and a long-lived coherent phonon, leading to phonon-combination modes in the early time region.