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Abstract Emerging non-volatile memristor-based devices with resistive switching (RS) materials are being widely researched as promising contenders for the next generation of data storage and neuromorphic technologies. Titanium nitride (TiN_x) is a common industry-friendly electrode system for RS; however, the precise TiN_xproperties required for optimum RS performance is still lacking. Herein, using ion-assisted DC magnetron sputtering, we demonstrate the key importance not only of engineering the TiN_xbottom electrodes to be dense, smooth, and conductive, but also understoichiometric in N. With these properties, RS in HfO₂-based memristive devices is shown to be optimised for TiN_0.96. These devices have switching voltages ≤ ±1 V with promising device-to-device uniformity, endurance, memory window of ~40, and multiple non-volatile intermediate conductance levels. This study highlights the importance of precise tuning of TiN_xbottom electrodes to achieve robust performance of oxide resistive switching materials. 

Tuning spin and charge degrees of freedom of complex oxide materials can enable significant advancements in future spintronics. In this study, by three dimensional strain engineering, we demonstrate room temperature ferroelectricity and magnetoelectricity in a vertically aligned nanocomposite thin film structure, composed of vertical nanopillars of SmFeO3 (SFO) embedded within the NiFeO4 (NFO) matrix. A three-dimensional tensile strain is induced in the SFO as a result of the unique film architecture. The tensile strain in SFO produces strong room temperature ferroelectric response instead of the normally very weak ferroelectricity of unstrained SFO, which is an improper ferroelectric. The induced ferroelectricity in SFO enables self-biased magnetoelectric coupling to be achieved between the two phases (magnetoelectric coupling coefficient ∼4 × 10−11 sm−1 at room temperature). The magnetoelectric coupling is facilitated by strain transfer across the vertical interfaces of the two phases. We additionally observe an exchange bias of ∼200 Oe (at 2 K) surviving up to the room temperature, indicating strongly coupled interfaces of SFO and NFO. These findings represent a step forward in future magnetoelectric RAM devices. 

Resistive switching devices are promising candidates for the next generation of nonvolatile memory and neuromorphic computing applications. Despite the advantages in retention and on/off ratio, filamentary-based memristors still suffer from challenges, particularly endurance (flash being a benchmark system showing 10⁴to 10⁶ cycles) and uniformity. Here, we use WO₃as a complementary metal-oxide semiconductor–compatible switching oxide and demonstrate a proof-of-concept materials design approach to enhance endurance and device-to-device uniformity in WO₃-based memristive devices while preserving other performance metrics. These devices show stable resistive switching behavior with >10⁶ cycles, >10⁵-second retention, >10 on/off ratio, and good device-to-device uniformity, without using current compliance. All these metrics are achieved using a one-step pulsed laser deposition process to create self-assembled nanocomposite thin films that have regular guided filaments of ≈100-nanometer pitch, preformed between WO₃grains and interspersed smaller Ce₂O₃grains. 

The integration of nanocomposite thin films with combined multifunctionalities on flexible substrates is desired for flexible device design and applications. For example, combined plasmonic and magnetic properties could lead to unique optical switchable magnetic devices and sensors. In this work, a multiphase TiN-Au-Ni nanocomposite system with core–shell-like Au-Ni nanopillars embedded in a TiN matrix has been demonstrated on flexible mica substrates. The three-phase nanocomposite film has been compared with its single metal nanocomposite counterparts, i.e., TiN-Au and TiN-Ni. Magnetic measurement results suggest that both TiN-Au-Ni/mica and TiN-Ni/mica present room-temperature ferromagnetic property. Tunable plasmonic property has been achieved by varying the metallic component of the nanocomposite films. The cyclic bending test was performed to verify the property reliability of the flexible nanocomposite thin films upon bending. This work opens a new path for integrating complex nitride-based nanocomposite designs on mica towards multifunctional flexible nanodevice applications. 

The unique redox properties and high oxygen capacity of nanostructured CeO₂demonstrate a wide range of applications, such as electrolytes for solid oxide fuel cells, gas sensors, and catalysis for automotive exhaust gas. Most CeO₂nanomaterials are prepared by chemical synthesis or hard templating methods. An effective way to obtain highly textured, small‐radius dimensions with high specific surface area remains challenging. Here, highly textured CeO₂nanostructures with various shapes ranging from nanowires to nanoporous thin films are successfully synthesized. Vertically aligned nanocomposites (VANs) of Sr₃Al₂O₆(SAO) and CeO₂are synthesized first while varying concentration ratio between them. Once the SAO is dissolved in water, the remaining CeO₂forms distinct nanostructures. The thermal stability of the nanostructured CeO₂is evaluated byin situheating XRD and thermal annealing tests. This method provides an alternative approach to preparing nanostructured CeO₂without toxic chemical solutions or complex micro/nanofabrication techniques. These results present a novel approach to prepare nanostructured CeO₂for future sensing and energy device applications.