Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1666853 | Thin Solid Films | 2013 | 5 Pages |
Sol–gel deposited Ag/TiO2/Pt tri-layers exhibit unipolar resistive switching (URS) with a negative turn-on voltage when fired in air. Variation in both the turn-on voltage and the on-state current at turn-off threshold is observed in successive current–voltage (I–V) measurements. Based on the same composition and processing flow, bipolar resistive switching (BRS) showing positive turn-on voltage by contrast is obtained by applying two alternative procedures: one procedure under oxygen ambience and another one in which indium–tin oxide is used as the bottom electrode. Conduction mechanisms induced by reduction/oxidation reactions explain how firing ambient and bottom electrode affect the switching mode, as well as the distinct turn-on voltage polarity. URS and BRS are related to the amount of ambient oxygen and the arrangement of internal oxygen vacancy, thus determining whether the direction-independent thermochemical heating or polarity-dependent electrochemical oxidation near the anode interface is responsible for the filament rupture. Additionally, the space-charge-limited transport is analyzed to examine how URS and BRS-activated samples significantly differ from each other. Importantly, the temperature-dependent I–V data helps to elucidate the dominant carrier behavior in the regime of low and high electric field.
► Resistive switching mode and polarity in TiO2 were discussed. ► Amounts of non-lattice oxygen were compared. ► Three sample sets of TiO2 were prepared and investigated.