950 publications from this institution
Memristive devices based on layered materials have the potential to enable low power electronics with ultra-fast operations toward the development of next generation memory and computing technologies. Memristor performance and switching behavior crucially depend on the switching matrix and on the type of electrodes used. In this work, we investigate the effect of different electrodes in 1D MoO2–MoS2 core shell nanowire memristors by highlighting their role in achieving distinct switching behavior. Analog and digital resistive switching are realized with carbon based passive (multi-layer graphene and multiwall carbon nanotube) and 3D active metal (silver and nickel) electrodes, respectively. Temperature dependent electrical transport studies of the conducting filament down to cryogenic temperatures reveal its semiconducting and metallic nature for passive and active top electrodes, respectively. These investigations shed light on the physics of the filament formation and provide a knob to design and develop the memristors with specific switching characteristics for desired end uses.
Abstract Selective anion transport is essential for energy conversion, water purification, and electrochemical systems, yet achieving precise ion selectivity in membranes remains a challenge. Here, we present an amino-functionalized graphene oxide (am-GO) membrane that enables tunable anion transport through nanochannels. Using a combined experimental and computational approach, we consider the three stages of ionic transport—absorption, diffusion, and desorption—to reveal that Cl− selectively diffuses through nanochannels, while NO3 −, SO4 2−, and PO4 3− are excluded. In ionic mixtures, the chemical transistor effect emerges, where Cl− pulls water from NO3 − hydration shell, enhancing its mobility, while SO4 2− and PO4 3− remain excluded due to size constraints. This mechanism enables precisely regulated Cl− and NO3 − transport, with ultrahigh rejection rates of 99.99% for SO4 2− and PO4 3−, even in complex ionic environments. The am-GO exhibits stability and anion-hopping mechanisms, making it a versatile platform for anion exchange membranes in electrolysis, energy storage, and environmental applications.