Sin‐Hyung Lee, Hea-Lim Park, C. Keum, Min‐Hoi Kim, S. Lee
{"title":"Dependence of resistive switching on ion-migration process in organic electrochemical metallization memory (Conference Presentation)","authors":"Sin‐Hyung Lee, Hea-Lim Park, C. Keum, Min‐Hoi Kim, S. Lee","doi":"10.1117/12.2320946","DOIUrl":null,"url":null,"abstract":"Organic-based electrochemical metallization memory (ECM) has been paid much attention for non-volatile memory devices owing to high integration and mechanical flexibility. In such ECM systems, the formation of conductive filaments (CFs) is typically composed of two activation steps: i) the electrochemical redox reactions at an interface between an electrode and an electrolyte and ii) the migration of the cations of metal across the electrolyte. Accordingly, the overall electrical performance of the ECM device is primarily governed by the kinetics of the two steps. However, in the ECM devices using organic electrolytes, a rather compete picture of the resistive switching during the ion-migration process has not been described so far since filamentary paths are barely observable.\n\n In this work, we investigated how the resistive switching depends on the ion-migration properties including the drift velocity and the migration path in the organic ECM device. Two types of polymer electrolytes, having different molecular weights, were used for the control of the ion drift velocity. The topography of ion-migration paths was modified by the deposition rate of metal for the top electrode. The formation and the retention of the CFs depend critically on the ion mobility of the polymer electrolyte and the topography of the ion-migration paths as well. These results will provide a useful guideline for constructing high- performance ECM storage systems based on organic materials.\n\nThis work was supported by the Brain Korea 21 Plus Project in 2018.","PeriodicalId":366222,"journal":{"name":"Organic and Hybrid Sensors and Bioelectronics XI","volume":"60 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic and Hybrid Sensors and Bioelectronics XI","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1117/12.2320946","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Organic-based electrochemical metallization memory (ECM) has been paid much attention for non-volatile memory devices owing to high integration and mechanical flexibility. In such ECM systems, the formation of conductive filaments (CFs) is typically composed of two activation steps: i) the electrochemical redox reactions at an interface between an electrode and an electrolyte and ii) the migration of the cations of metal across the electrolyte. Accordingly, the overall electrical performance of the ECM device is primarily governed by the kinetics of the two steps. However, in the ECM devices using organic electrolytes, a rather compete picture of the resistive switching during the ion-migration process has not been described so far since filamentary paths are barely observable.
In this work, we investigated how the resistive switching depends on the ion-migration properties including the drift velocity and the migration path in the organic ECM device. Two types of polymer electrolytes, having different molecular weights, were used for the control of the ion drift velocity. The topography of ion-migration paths was modified by the deposition rate of metal for the top electrode. The formation and the retention of the CFs depend critically on the ion mobility of the polymer electrolyte and the topography of the ion-migration paths as well. These results will provide a useful guideline for constructing high- performance ECM storage systems based on organic materials.
This work was supported by the Brain Korea 21 Plus Project in 2018.
有机基电化学金属化存储器(ECM)因其集成度高、机械柔韧性好等优点,在非易失性存储器件中受到广泛关注。在这样的ECM系统中,导电细丝(CFs)的形成通常由两个激活步骤组成:i)电极和电解质界面上的电化学氧化还原反应和ii)金属阳离子在电解质上的迁移。因此,ECM装置的整体电性能主要由这两个步骤的动力学决定。然而,在使用有机电解质的ECM器件中,由于纤维路径几乎无法观察到,因此到目前为止还没有描述离子迁移过程中电阻开关的相当竞争的画面。在这项工作中,我们研究了有机ECM器件中的电阻开关如何依赖于离子迁移特性,包括漂移速度和迁移路径。采用两种分子量不同的聚合物电解质来控制离子漂移速度。离子迁移路径的形貌受顶部电极金属沉积速率的影响。CFs的形成和保留主要取决于聚合物电解质的离子迁移率和离子迁移路径的形貌。这些结果将为构建基于有机材料的高性能ECM存储系统提供有益的指导。这项工作在2018年得到了Brain Korea 21 +项目的支持。