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Controlled transport of electrons through tunnel junctions and their confinement by mesoscopic structures have opened up immense possibilities of single-electron device (SED) applications. The realization of a practical working SED has remained challenging largely owing to the poor understanding of the physics of operation of singe-electron tunneling devices, especially of those with multiple nanometer-sized islands. In this simulation study of one-dimensional (1D) multi-island chains, we propose physical mechanisms that lead to the coulomb blockade (CB) and coulomb staircase (CS) characteristics that are enhanced by the geometrical disorder in the chain. With increasing source-drain (V DS = V D − V S ) bias, a multi-island device has to overcome multiple discrete energy barriers (up-steps) for charge advancement before reaching the threshold voltage (V th ). Beyond V th , current flow is rate-limited by certain junctions with low transition rates, which leads to the CS structures in the current-voltage (IV) characteristic. Each step in the CS is characterized by a unique distribution of charges on the islands, each with an associated distribution of tunneling probabilities that depend on both the charge state and V DS . This study marks an important step in unraveling the microscopic details of SED operation and will inspire further experimental and theoretical studies. Two particularly interesting and important features of a singleelectron device (SED) are the coulomb blockade (CB) and coulomb staircase (CS) current-voltage (IV) characteristics that are manifestations of the charging effects of the islands due to their small size when they are at the nanometer scale. While many research groups 1-7 have fabricated SEDs, some demonstrating the CB and the CS features even at room temperature, 7 a few others have successfully explored the applications of a single-electron transistor (SET) device for nanometerscale displacement sensing, 8 thermometry, 9 and the SET as a fast and ultrasensitive electrometer.10,11 Single-electron behavior in materials such as single-wall carbon nanotubes has also been demonstrated. 12But to successfully design and fabricate a SED that can exhibit the CB and CS features, it is necessary to better understand the physics behind the charge transport leading to the CB and CS features in the device IV characteristics, which has remained poorly understood so far. A nearly linear variation of the device threshold voltage (V th ) with the number of islands along the chain (N), which is proportional to the chain length (L), has been observed in the experimental devices. 4,6,13 Middleton and Wingreen 14 carried out a theoretical investigation on an array of islands with uniform capacitances but with the potential levels randomly offset by quenched background charges showing the linear variation of device V th (N). The computational study by Elteto et al. 15 extended the work to a uniform system with the nearestneighbor inter-island coupling in order to explain the experimental device features o...
Controlled transport of electrons through tunnel junctions and their confinement by mesoscopic structures have opened up immense possibilities of single-electron device (SED) applications. The realization of a practical working SED has remained challenging largely owing to the poor understanding of the physics of operation of singe-electron tunneling devices, especially of those with multiple nanometer-sized islands. In this simulation study of one-dimensional (1D) multi-island chains, we propose physical mechanisms that lead to the coulomb blockade (CB) and coulomb staircase (CS) characteristics that are enhanced by the geometrical disorder in the chain. With increasing source-drain (V DS = V D − V S ) bias, a multi-island device has to overcome multiple discrete energy barriers (up-steps) for charge advancement before reaching the threshold voltage (V th ). Beyond V th , current flow is rate-limited by certain junctions with low transition rates, which leads to the CS structures in the current-voltage (IV) characteristic. Each step in the CS is characterized by a unique distribution of charges on the islands, each with an associated distribution of tunneling probabilities that depend on both the charge state and V DS . This study marks an important step in unraveling the microscopic details of SED operation and will inspire further experimental and theoretical studies. Two particularly interesting and important features of a singleelectron device (SED) are the coulomb blockade (CB) and coulomb staircase (CS) current-voltage (IV) characteristics that are manifestations of the charging effects of the islands due to their small size when they are at the nanometer scale. While many research groups 1-7 have fabricated SEDs, some demonstrating the CB and the CS features even at room temperature, 7 a few others have successfully explored the applications of a single-electron transistor (SET) device for nanometerscale displacement sensing, 8 thermometry, 9 and the SET as a fast and ultrasensitive electrometer.10,11 Single-electron behavior in materials such as single-wall carbon nanotubes has also been demonstrated. 12But to successfully design and fabricate a SED that can exhibit the CB and CS features, it is necessary to better understand the physics behind the charge transport leading to the CB and CS features in the device IV characteristics, which has remained poorly understood so far. A nearly linear variation of the device threshold voltage (V th ) with the number of islands along the chain (N), which is proportional to the chain length (L), has been observed in the experimental devices. 4,6,13 Middleton and Wingreen 14 carried out a theoretical investigation on an array of islands with uniform capacitances but with the potential levels randomly offset by quenched background charges showing the linear variation of device V th (N). The computational study by Elteto et al. 15 extended the work to a uniform system with the nearestneighbor inter-island coupling in order to explain the experimental device features o...
Although the kinetics of CF formation/ dissolution is still unclear, it is widely accepted that the CF formation/dissolution is strongly related to the electromigration and electrochemical reaction of anion (i.e., oxygen vacancy) [13][14][15][16] or cation (i.e., Cu 2+ , Ag + or Ni 2+ ). [17][18][19][20][21][22] Generally, RS behavior can be classifi ed as two modes: nonvolatile memory switching (MS) and volatile threshold switching (TS). In the MS mode, both LRS and HRS can be maintained after removing the external voltage, while the LRS in the TS mode will be back to the HRS once the applied voltage is smaller than a critical value. [23][24][25] To avoid confusion with MS, the LRS and HRS in TS are renamed as "TS ON-state" and "TS OFFstate" in this article. The MS device can be used for the non-volatile data storage [1][2][3][4][5] while TS device can be as a selector in series with memory cell to suppress crosstalk effect in the crossbar array. [26][27][28][29][30] Recently, some groups reported that TS and MS can coexist and mutually transform in a single device at suitable external excitation. [23][24][25][26][27][28] Several models have been proposed to explain this phenomenon, including CF thermal instability, [ 23 ] strong electron correlation effect, [ 24 ] quantum-wire model, [ 25 ] interface barrier modulation, [ 26 ] and space charge effect. [ 27 ] However, the underlying mechanism of the phenomenon is still unclear, especially lacking of direct evidences to uncover when and how the two RS modes happen and what is the internal relationship between them.Here, we demonstrate that the TS and MS modes can be modulated in the Ag/SiO 2 /Pt structure by controlling the compliance current ( I CC ) in electroforming. We systematically investigate the morphologies, chemical components, and dynamic growth of the CF using scanning electron microscope (SEM), high-resolution transmission electron microscopy (HRTEM) and electron energy loss spectroscopy (EELS) analysis. The results confi rm that the TS and MS modes correspond to the CF consisting of isolated and continuous Ag nanocrystals, respectively. In addition, by Kelvin probe force microscopy (KPFM) studies, the voltage potential distribution of CF in the ON-and OFF-state further indicate that the TS mode is Volatile threshold switching (TS) and non-volatile memory switching (MS) are two typical resistive switching (RS) phenomena in oxides, which could form the basis for memory, analog circuits, and neuromorphic applications. Interestingly, TS and MS can be coexistent and converted in a single device under the suitable external excitation. However, the origin of the transition from TS to MS is still unclear due to the lack of direct experimental evidence. Here, conversion between TS and MS induced by conductive fi lament (CF) morphology in Ag/SiO 2 /Pt device is directly observed using scanning electron microscopy and high-resolution transmission electron microscopy. The MS mechanism is related to the formation and dissolution of CF consisting of continuous Ag...
Metal nanowires (NWs) networks with high conductance have shown potential applications in modern electronic components, especially the transparent electrodes over the past decade. In metal NW networks, the electrical connectivity of nanoscale NW junction can be modulated for various applications. In this work, silver nanowire (Ag NW) networks were selected to achieve the desired functions. The Ag NWs were first synthesized by a classic polyol process, and spin-coated on glass to fabricate transparent electrodes. The as-fabricated electrode showed a sheet resistance of 7.158 Ω □ with an optical transmittance of 79.19% at 550 nm, indicating a comparable figure of merit (FOM, or Φ) (13.55 × 10 Ω). Then, two different post-treatments were designed to tune the Ag NWs for not only transparent electrode but also for threshold resistive switching (RS) application. On the one hand, the Ag NW film was mechanically pressed to significantly improve the conductance by reducing the junction resistance. On the other hand, an Ag@AgO core-shell structure was deliberately designed by partial oxidation of Ag NWs through simple ultraviolet (UV)-ozone treatment. The Ag core can act as metallic interconnect and the insulating AgO shell acts as a switching medium to provide a conductive pathway for Ag filament migration. By fabricating Ag/Ag@AgO/Ag planar structure, a volatile threshold switching characteristic was observed and an on/off ratio of ∼100 was achieved. This work showed that through different post-treatments, Ag NW network can be engineered for diverse functions, transforming from transparent electrodes to RS devices.
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