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通过直写在聚合物-离子液体薄膜中形成银纳米丝的动力学

Silver Nanofilament Formation Dynamics in a Polymer-Ionic Liquid Thin Film by Direct-Write.

作者信息

Chao Zhongmou, Sezginel Kutay B, Xu Ke, Crouch Garrison M, Gray Abigale E, Wilmer Christopher E, Bohn Paul W, Go David B, Fullerton-Shirey Susan K

机构信息

Department of Chemical and Petroleum Engineering, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.

Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana 46556, United States.

出版信息

Adv Funct Mater. 2020 Feb 5;30(6). doi: 10.1002/adfm.201907950. Epub 2019 Nov 28.

Abstract

Silver nanofilament formation dynamics are reported for an ionic liquid (IL)-filled solid polymer electrolyte prepared by a direct-write process using a conductive atomic force microscope (C-AFM). Filaments are electrochemically formed at hundreds of locations on a 40 nm thick polymer electrolyte, polyethylene glycol diacrylate (PEGDA)/[BMIM]PF. Although the formation time generally decreases with increasing bias from 0.7 to 3.0 V, an unexpected non-monotonic maximum is observed 2.0 V. At voltages approaching this region of inverted kinetics, IL electric double layers (EDLs) becomes detectable; thus, the increased nanofilament formation time can be attributed to electric field screening which hinders silver electro-migration and deposition. Scanning electron microscopy confirms that nanofilaments formed in this inverted region have significantly more lateral and diffuse features. Time-dependent formation currents reveal two types of nanofilament growth dynamics: abrupt, where the resistance decreases sharply over as little as a few ms, and gradual where it decreases more slowly over hundreds of ms. Whether the resistance change is abrupt or gradual depends on the extent to which the EDL screens the electric field. Tuning the formation time and growth dynamics using an IL opens the range of accessible resistance states, which is useful for neuromorphic applications.

摘要

报道了使用导电原子力显微镜(C-AFM)通过直写工艺制备的填充离子液体(IL)的固体聚合物电解质的银纳米丝形成动力学。在40纳米厚的聚合物电解质聚乙二醇二丙烯酸酯(PEGDA)/[BMIM]PF上的数百个位置电化学形成细丝。尽管形成时间通常随着偏压从0.7伏增加到3.0伏而减少,但在2.0伏时观察到意外的非单调最大值。在接近这种反转动力学区域的电压下,IL双电层(EDL)变得可检测;因此,纳米丝形成时间增加可归因于电场屏蔽,这阻碍了银的电迁移和沉积。扫描电子显微镜证实,在这个反转区域形成的纳米丝具有明显更多的横向和扩散特征。随时间变化的形成电流揭示了两种类型的纳米丝生长动力学:突然型,电阻在短短几毫秒内急剧下降;渐变型,电阻在数百毫秒内下降得更慢。电阻变化是突然还是渐变取决于EDL对电场的屏蔽程度。使用IL调节形成时间和生长动力学可扩大可达到的电阻状态范围,这对神经形态应用很有用。

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