Using friction force microscopy, we compared the nanoscale frictional characteristics of atomically thin sheets of graphene, molybdenum disulfide (MoS2), niobium diselenide, and hexagonal boron nitride exfoliated onto a weakly adherent substrate (silicon oxide) to those of their bulk counterparts. Measurements down to single atomic sheets revealed that friction monotonically increased as the number of layers decreased for all four materials. Suspended graphene membranes showed the same trend, but binding the graphene strongly to a mica surface suppressed the trend. Tip-sample adhesion forces were indistinguishable for all thicknesses and substrate arrangements. Both graphene and MoS2 exhibited atomic lattice stick-slip friction, with the thinnest sheets possessing a sliding-length-dependent increase in static friction. These observations, coupled with finite element modeling, suggest that the trend arises from the thinner sheets' increased susceptibility to out-of-plane elastic deformation. The generality of the results indicates that this may be a universal characteristic of nanoscale friction for atomically thin materials weakly bound to substrates.
Two-dimensional transition metal dichalcogenides with strong spin-orbit interactions and valley-dependentBerry curvature effects have attracted tremendous recent interests 1-7 . Although novel single-particle and excitonic phenomena related to spin-valley coupling have been extensively studied 1,3-6 , effects of spin-momentum locking on collective quantum phenomena remain unexplored. Here we report an observation of superconducting monolayer NbSe2 with an inplane upper critical field over six times of the Pauli paramagnetic limit by magnetotransport measurements. The effect can be understood in terms of the competing Zeeman effect and large intrinsic spin-orbit interactions in non-centrosymmetric NbSe2 monolayers, where the electronic spin is locked to the out-of-plane direction. Our results provide a strong evidence of unconventional Ising pairing protected by spin-momentum locking and open up a new avenue for studies of noncentrosymmetric superconductivity with unique spin and valley degrees of freedom in the exact two-dimensional limit.Monolayer transition metal dichalcogenide (TMD) of the hexagonal structure consists of a layer of transition metal atoms sandwiched between two layers of chalcogen atoms in the trigonal prismatic structure 8 (Fig. 1a). It possesses out-of-plane mirror symmetry and in-plane inversion asymmetry. The presence of the transition metal also gives rise to large spin-orbit interactions (SOIs). The mirror symmetry restricts the crystal field ( ⃗) to the plane. The SOIs split the spin states at finite momentum ⃗⃗ in the absence of inversion symmetry. They manifest as an effective magnetic field along the direction of ⃗⃗ × ⃗ , which is out-of-plane for the restricted two-dimensional (2D) motion of electrons in the plane. The electronic spin is thus oriented in the out-of-plane direction and in opposite directions for electrons of opposite momenta 1-3 (Fig. 1a). Such spinmomentum locking is destroyed in the bulk where inversion symmetry and spin degeneracy are restored 1,2,7 (Fig. 1b). Novel valley-and spin-dependent phenomena including optical orientation of the valley polarization 3,4 and the valley Hall effect 5 arisen from spin-momentum locking have been recently demonstrated in group-VI TMD
Two-dimensional materials possess very different properties from their bulk counterparts. While changes in single-particle electronic properties have been investigated extensively, modifications in the many-body collective phenomena in the exact two-dimensional limit remain relatively unexplored. Here, we report a combined optical and electrical transport study on the many-body collective-order phase diagram of NbSe2 down to a thickness of one monolayer. Both the charge density wave and the superconducting phase have been observed down to the monolayer limit. The superconducting transition temperature decreases on lowering the layer thickness, but the newly observed charge-density-wave transition temperature increases from 33 K in the bulk to 145 K in the monolayer. Such highly unusual enhancement of charge density waves in atomically thin samples can be understood to be a result of significantly enhanced electron-phonon interactions in two-dimensional NbSe2 (ref. 4) and is supported by the large blueshift of the collective amplitude vibration observed in our experiment. Our results open up a new window for search and control of collective phases of two-dimensional matter, as well as expanding the functionalities of these materials for electronic applications.
Femtosecond time-resolved photoemission is used to investigate the time evolution of electronic structure in the Mott insulator 1T-TaS2. A collapse of the electronic gap is observed within 100 femtoseconds after optical excitation. The photoemission spectra and the spectral function calculated by dynamical mean field theory show that this insulator-metal transition is driven solely by hot electrons. A coherently excited lattice displacement results in a periodic shift of the spectra lasting for 20 ps without perturbing the insulating phase. This capability to disentangle electronic and phononic excitations opens new directions to study electron correlation in solids.
We realized ambipolar Field-Effect Transistors by coupling exfoliated thin flakes of tungsten disulphide (WS 2 ) with an ionic liquid-dielectric. The devices show ideal electrical characteristics, including very steep sub-threshold slopes for both electrons and holes and extremely low OFFstate currents. Thanks to these ideal characteristics, we determine with high precision the size of the band-gap of WS 2 directly from the gate-voltage dependence of the source-drain current. Our results demonstrate how a careful use of ionic liquid dielectrics offers a powerful strategy to study quantitatively the electronic properties of nano-scale materials.
We report a long-wavelength helimagnetic superstructure in bulk samples of the ferrimagnetic insulator Cu2OSeO3. The magnetic phase diagram associated with the helimagnetic modulation inferred from small-angle neutron scattering and magnetization measurements includes a skyrmion lattice phase and is strongly reminiscent of MnSi, FeGe, and Fe(1-x)Co(x)Si, i.e., binary isostructural siblings of Cu2OSeO3 that order helimagnetically. The temperature dependence of the specific heat of Cu2OSeO3 is characteristic of nearly critical spin fluctuations at the helimagnetic transition. This provides putative evidence for effective spin currents as the origin of enhancements of the magnetodielectric response instead of atomic displacements considered so far.
Interfacial interactions allow the electronic properties of graphene to be modified, as recently demonstrated by the appearance of satellite Dirac cones in graphene on hexagonal boron nitride substrates. Ongoing research strives to explore interfacial interactions with other materials to engineer targeted electronic properties. Here we show that with a tungsten disulfide (WS2) substrate, the strength of the spin–orbit interaction (SOI) in graphene is very strongly enhanced. The induced SOI leads to a pronounced low-temperature weak anti-localization effect and to a spin-relaxation time two to three orders of magnitude smaller than in graphene on conventional substrates. To interpret our findings we have performed first-principle electronic structure calculations, which confirm that carriers in graphene on WS2 experience a strong SOI and allow us to extract a spin-dependent low-energy effective Hamiltonian. Our analysis shows that the use of WS2 substrates opens a possible new route to access topological states of matter in graphene-based systems.
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