首页> 外文期刊>ACS applied materials & interfaces >Aluminum Electrode Modulated Bipolar Resistive Switching of Al/ Fuel-Assisted NiO_x/ITO Memory Devices Modeled with a Dual-Oxygen-Reservoir Structure
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Aluminum Electrode Modulated Bipolar Resistive Switching of Al/ Fuel-Assisted NiO_x/ITO Memory Devices Modeled with a Dual-Oxygen-Reservoir Structure

机译:铝电极调制双氧储层结构的Al /燃料辅助NiO_x / ITO存储器件的双极电阻开关

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Bipolar resistive switching in Al/fuel-assisted NiO., (40 nm)/ITO devices is demonstrated in this work. XPS analysis reveals the simultaneous presence of metallic Ni, Ni2O3, and NiO components in the fuel-assisted NiO_x. The concentration, as well as spreading of the metallic Ni and accompanying oxygen vacancies, are related to the Al/NiO_x interfacial reaction, which is enhanced by the increasing thickness of the Al top electrode. Correspondingly, the preswitching-on voltage decreases while the preswitching-off voltage increases with increasing thickness (from 15 to 60 nm) of Al. However, in regular switching operation, set and reset voltages are considerably lowered for devices with an increased thickness of the Al top electrode. The bipolar resistive switching behaviors of Al/fuel-assisted NiO_x/ITO devices are therefore discussed based on the formation of conductive paths and their correlation with the Al-electrode modulated composition in the fuel-assisted NiO_x. The Al/NiO_x interfacial reaction region pairs with ITO to form a dual-oxygen-reservoir structure. Mechanisms of construction/destruction of conducting paths originating from the electrochemical redox reactions at the interface between NiO_x, and the dual oxygen reservoirs will also be explicated.
机译:在这项工作中展示了Al /燃料辅助NiO。(40 nm)/ ITO器件中的双极电阻切换。 XPS分析表明,在燃料辅助的NiO_x中同时存在金属Ni,Ni2O3和NiO组分。金属Ni的浓度以及扩散以及随之而来的氧空位与Al / NiO_x界面反应有关,Al / NiO_x界面反应由于Al顶部电极厚度的增加而增强。相应地,随着Al的厚度增加(从15nm到60nm),预接通电压降低而预断开电压升高。但是,在常规开关操作中,对于Al顶部电极厚度增加的器件,设置和复位电压会大大降低。因此,基于导电路径的形成及其与燃料辅助的NiO_x中的Al电极调制成分的相关性,讨论了Al /燃料辅助的NiO_x / ITO器件的双极电阻切换行为。 Al / NiO_x界面反应区与ITO配对以形成双氧储​​层结构。还将阐述在NiO_x与双氧储库之间的界面上源自电化学氧化还原反应的传导路径的构建/破坏机理。

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