Yijin Zhang

Superconducting Dome in a Gate-Tuned Band Insulator

What Do You Know? A Dome The superconducting dome—the appearance of a maximum in the transition temperature as a function of a tuning parameter—has been observed in compounds such as cuprates, pnictides, and heavy fermion materials and is thought of as a signature of unconventional superconductivity. Ye et al. (p. 1193) used a liquid gating technique combined with back gating to finely tune the carrier density in the band insulator MoS2, which allowed them to observe the formation of a dome. The unexpected finding awaits theoretical explanation but may suggest that the appearance of an optimal carrier density may be a more common occurrence than was previously thought. Liquid gating tunes the carrier density in molybdenum disulfide, revealing unconventional superconductivity. A dome-shaped superconducting region appears in the phase diagrams of many unconventional superconductors. In doped band insulators, however, reaching optimal superconductivity by the fine-tuning of carriers has seldom been seen. We report the observation of a superconducting dome in the temperature–carrier density phase diagram of MoS2, an archetypal band insulator. By quasi-continuous electrostatic carrier doping achieved through a combination of liquid and solid gating, we revealed a large enhancement in the transition temperature Tc occurring at optimal doping in the chemically inaccessible low–carrier density regime. This observation indicates that the superconducting dome may arise even in doped band insulators.

Electrically switchable chiral light-emitting transistor.

Controlling Chiral Light Emission Circularly polarized light plays important roles in a number of applications such as displays, communication, and sensing. Thus, the ability to produce compact and readily controllable polarized light sources is important, and dichalcogenide materials such as tungsten diselenide may provide a route to such sources. Zhang et al. (p. 725, published online 17 April; see the Perspective by Zaumseil) formed an electric-double-layer transistor structure with WSe2 and used a gated ionic liquid to control the carrier density. Electrical control of the output light was achieved with the polarization being switched by reversing the polarity of the applied field and injected charge. The valley degree of freedom in WSe2 is used to realize an electrically switchable, circularly polarized light source. [Also see Perspective by Zaumseil] Tungsten diselenide (WSe2) and related transition metal dichalcogenides exhibit interesting optoelectronic properties owing to their peculiar band structures originating from the valley degree of freedom. Although the optical generation and detection of valley polarization has been demonstrated, it has been difficult to realize active valley-dependent functions suitable for device applications. We report an electrically switchable, circularly polarized light source based on the material’s valley degree of freedom. Our WSe2-based ambipolar transistors emit circularly polarized electroluminescence from p-i-n junctions electrostatically formed in transistor channels. This phenomenon can be explained qualitatively by the electron-hole overlap controlled by the in-plane electric field. Our device demonstrates a route to exploit the valley degree of freedom and the possibility to develop a valley-optoelectronics technology.

Valley-dependent spin polarization in bulk MoS2 with broken inversion symmetry

The valley degree of freedom of electrons is attracting growing interest as a carrier of information in various materials, including graphene, diamond and monolayer transition-metal dichalcogenides. The monolayer transition-metal dichalcogenides are semiconducting and are unique due to the coupling between the spin and valley degrees of freedom originating from the relativistic spin-orbit interaction. Here, we report the direct observation of valley-dependent out-of-plane spin polarization in an archetypal transition-metal dichalcogenide--MoS2--using spin- and angle-resolved photoemission spectroscopy. The result is in fair agreement with a first-principles theoretical prediction. This was made possible by choosing a 3R polytype crystal, which has a non-centrosymmetric structure, rather than the conventional centrosymmetric 2H form. We also confirm robust valley polarization in the 3R form by means of circularly polarized photoluminescence spectroscopy. Non-centrosymmetric transition-metal dichalcogenide crystals may provide a firm basis for the development of magnetic and electric manipulation of spin/valley degrees of freedom.

Formation of a Stable p–n Junction in a Liquid-Gated MoS2 Ambipolar Transistor

Molybdenum disulfide (MoS2) has gained attention because of its high mobility and circular dichroism. As a crucial step to merge these advantages into a single device, we present a method that electronically controls and locates p-n junctions in liquid-gated ambipolar MoS2 transistors. A bias-independent p-n junction was formed, and it displayed rectifying I-V characteristics. This p-n diode could perform a crucial role in the development of optoelectronic valleytronic devices.

Superconductivity Series in Transition Metal Dichalcogenides by Ionic Gating

Functionalities of two-dimensional (2D) crystals based on semiconducting transition metal dichalcogenides (TMDs) have now stemmed from simple field effect transistors (FETs) to a variety of electronic and opto-valleytronic devices, and even to superconductivity. Among them, superconductivity is the least studied property in TMDs due to methodological difficulty accessing it in different TMD species. Here, we report the systematic study of superconductivity in MoSe2, MoTe2 and WS2 by ionic gating in different regimes. Electrostatic gating using ionic liquid was able to induce superconductivity in MoSe2 but not in MoTe2 because of inefficient electron accumulation limited by electronic band alignment. Alternative gating using KClO4/polyethylene glycol enabled a crossover from surface doping to bulk doping, which induced superconductivities in MoTe2 and WS2 electrochemically. These new varieties greatly enriched the TMD superconductor families and unveiled critical methodology to expand the capability of ionic gating to other materials.

Fabrication of stretchable MoS2 thin-film transistors using elastic ion-gel gate dielectrics

We fabricated stretchable molybdenum disulfide thin-film transistors (MoS2 TFTs) on poly(dimethylsiloxane) substrates using ion gels as elastic gate dielectrics. The TFTs exhibited an electron mobility of 1.40 cm2/(V·s) and an on/off current ratio of 104 with a notably low threshold voltage (∼1 V). Furthermore, our MoS2 TFTs operated at a mechanical strain of 5% without significant degradation of their electrical properties. These results demonstrate the potential for using MoS2 films for stretchable electronics.

Controlling charge-density-wave states in nano-thick crystals of 1T-TaS2

Two-dimensional crystals, especially graphene and transition metal dichalcogenides (TMDs), are attracting growing interests because they provide an ideal platform for novel and unconventional electronic band structures derived by thinning. The thinning may also affect collective phenomena of electrons in interacting electron systems and can lead to exotic states beyond the simple band picture. Here, we report the systematic control of charge-density-wave (CDW) transitions by changing thickness, cooling rate and gate voltage in nano-thick crystals of 1T-type tantalum disulfide (1T-TaS2). Particularly the clear cooling rate dependence, which has never been observed in bulk crystals, revealed the nearly-commensurate CDW state in nano-thick crystals is a super-cooled state. The present results demonstrate that, in the two-dimensional crystals with nanometer thickness, the first-order phase transitions are susceptible to various perturbations, suggestive of potential functions of electronic phase control.

Memristive phase switching in two-dimensional 1T-TaS2 crystals

Electrical switching to multiple novel metastable states in a correlated two-dimensional crystal. Scaling down materials to an atomic-layer level produces rich physical and chemical properties as exemplified in various two-dimensional (2D) crystals including graphene, transition metal dichalcogenides, and black phosphorus. This is caused by the dramatic modification of electronic band structures. In such reduced dimensions, the electron correlation effects are also expected to be significantly changed from bulk systems. However, there are few attempts to realize novel phenomena in correlated 2D crystals. We report memristive phase switching in nano-thick crystals of 1T-type tantalum disulfide (1T-TaS2), a first-order phase transition system. The ordering kinetics of the phase transition were found to become extremely slow as the thickness is reduced, resulting in an emergence of metastable states. Furthermore, we realized unprecedented memristive switching to multistep nonvolatile states by applying an in-plane electric field. The reduction of thickness is essential to achieve such nonvolatile electrical switching behavior. The thinning-induced slow kinetics possibly make the various metastable states robust and consequently realize the nonvolatile memory operation. The present result indicates that a 2D crystal with correlated electrons is a novel nano-system to explore and functionalize multiple metastable states that are inaccessible in its bulk form.

Gate-Optimized Thermoelectric Power Factor in Ultrathin WSe2 Single Crystals

We report an electric field tuning of the thermopower in ultrathin WSe2 single crystals over a wide range of carrier concentration by using electric double-layer (EDL) technique. We succeeded in the optimization of power factor not only in the hole but also in the electron side, which has never been chemically accessed. The maximized values of power factor are one-order larger than that obtained by changing chemical composition, reflecting the clean nature of electrostatic doping.

High circular polarization in electroluminescence from MoSe2

The coupling between the valley degree of freedom and the optical helicity is one of the unique phenomena in transition metal dichalcogenides. The significant valley polarization evaluated from circularly polarized photoluminescence (PL) has been reported in many transition metal dichalcogenides, except in MoSe2. This compound is an anomalous material showing ultra-fast relaxation of the valley polarized states, which causes negligible polarization in the PL. Meanwhile, circularly polarized electroluminescence (EL) has been recently reported in a WSe2 light-emitting transistor, providing another method for using the valley degree of freedom. Here, we report the EL properties of MoSe2, demonstrating electrical switching of the optical helicity. Importantly, we observed high circular polarization reaching 66%. The results imply that the dominant mechanism of circularly polarized EL is robust against intervalley scattering, in marked contrast to the PL.