Abstract

The switching mechanism of valence change resistive memory devices is widely accepted to be an ionic movement of oxygen vacancies resulting in a valence change of the metal cations. However, direct experimental proofs of valence changes in memristive devices are scarce. In this work, we have employed hard X-ray photoelectron emission microscopy (PEEM) to probe local valence changes in Pt/ZrOx/Ta memristive devices. The use of hard X-ray radiation increases the information depth, thus providing chemical information from buried layers. By extracting X-ray photoelectron spectra from different locations in the PEEM images, we show that zirconia in the active device area is reduced compared to a neighbouring region, confirming the valence change in the ZrOx film during electroforming. Furthermore, we succeeded in measuring the Ta 4f spectrum for two different resistance states on the same device. In both states, as well as outside the device region, the Ta electrode is composed of different suboxides without any metallic contribution, hinting to the formation of TaOx during the deposition of the Ta thin film. We observed a reduction of the Ta oxidation state in the low resistance state with respect to the high resistive state. This observation is contradictory to the established model, as the internal redistribution of oxygen between ZrOx and the Ta electrode during switching would lead to an oxidation of the Ta layer in the low resistance state. Instead, we have to conclude that the Ta electrode takes an active part in the switching process in our devices and that oxygen is released and reincorporated in the ZrOx/TaOx bilayer during switching. This is confirmed by the degradation of the high resistance state during endurance measurements under vacuum.

Highlights

  • The resistance of an oxide layer sandwiched between two metal electrodes can be modified by an external electrical stimulus between two or more resistance states

  • Thanks to its larger probing depth (>10 nm), hard X-ray photoemission spectroscopy (HAXPES) provides an excellent, nondestructive approach to probe chemical changes of interfaces buried inside layered heterostructures and thereby allows the investigation of ReRAM cells with conventional metallic electrodes.[16,17,18,19]

  • Whereas HAXPES analysis on large area cells has been successful in detecting valence changes in non-filamentary switching systems,[20] it failed to detect valence changes in filamentary systems such as HfO221 and TiO222 as a result of the insufficient amount of modified material in the cell

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Summary

Introduction

Redox-based memristive devices (ReRAM) are considered as one of the most promising emerging memory technologies, even allowing multibit operation, logic-in-memory, and neuromorphic computing applications.[1,2,3] In these devices, the resistance of an oxide layer sandwiched between two metal electrodes can be modified by an external electrical stimulus between two or more resistance states. This is likely caused by the fact that the 2 nm top electrode is too thin to prevent the reoxidation of the oxygen deficient filament within the ZrOx layer formed during the SET process.[13] In vacuum, both states are stable over 2 days, which is absolutely sufficient for the HAXPEEM measurements (cf Fig. S1 of the supplementary material).

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