The functionality of computer memory elements is currently based on multi-stability, driven either by locally manipulating the density of electrons in transistors or by switching magnetic or ferroelectric order. Another possibility is switching between metallic and insulating phases by the motion of ions, but their speed is limited by slow nucleation and inhomogeneous percolative growth. Here we demonstrate fast resistance switching in a charge density wave system caused by pulsed current injection. As a charge pulse travels through the material, it converts a commensurately ordered polaronic Mott insulating state in 1T–TaS2 to a metastable electronic state with textured domain walls, accompanied with a conversion of polarons to band states, and concurrent rapid switching from an insulator to a metal. The large resistance change, high switching speed (30 ps) and ultralow energy per bit opens the way to new concepts in non-volatile memory devices manipulating all-electronic states.
Mesoscopic irregularly ordered and even amorphous self-assembled electronic structures were recently reported in two-dimensional metallic dichalcogenides (TMDs), created and manipulated with short light pulses or by charge injection. Apart from promising new all-electronic memory devices, such states are of great fundamental importance, since such aperiodic states cannot be described in terms of conventional charge-density-wave (CDW) physics. In this paper, we address the problem of metastable mesoscopic configurational charge ordering in TMDs with a sparsely filled charged lattice gas model in which electrons are subject only to screened Coulomb repulsion. The model correctly predicts commensurate CDW states corresponding to different TMDs at magic filling fractions = / / / / / f 1 3, 1 4, 1 9, 1 13, 1 16.mDoping away from f m results either in multiple neardegenerate configurational states, or an amorphous state at the correct density observed by scanning tunnelling microscopy. Quantum fluctuations between degenerate states predict a quantum charge liquid at low temperatures, revealing a new generalized viewpoint on both regular, irregular and amorphous charge ordering in transition metal dichalcogenides.
Ultrafast transient reflectivity across the unusual three-dimensional Peierls-like insulator-metal (IM) transition in CuIr2S4 was measured as a function of temperature. The low-temperature insulating-phase transient response is dominated by broken-symmetry-induced coherent lattice oscillations that abruptly vanish at the IM transition. The coherent mode spectra are consistent with Raman spectra reported in literature. The origin of the broken-symmetry-induced is also briefly discussed.
Controllable switching to and from metastable states of matter using electromagnetic fields could potentially revolutionize electronic logic and memory devices. Here, we investigate the effect of two-dimensional strain on switching between a photoinduced “hidden” state and a stable charge-ordered state in ultrathin 1T-TaS2 crystal films on different substrates, photoexcited by 35 fs laser pulses. The differential contraction of the sample and the substrate shows a very large and negative strain coefficient on the hidden state transition, implying that the stability of the hidden state could be markedly increased by tensile strain. Other transitions are not strongly affected by tensile strain.
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