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Physical chemistry of the TiN/Hf0.5Zr0.5O2 interface

退火(玻璃) X射线光电子能谱 铁电性 肖特基势垒 空位缺陷 兴奋剂 电极 材料科学 化学 纳米技术 光电子学 物理化学 冶金 结晶学 化学工程 复合材料 电介质 二极管 工程类
作者
Wassim Hamouda,A. Pancotti,C. Lubin,Ludovic Tortech,Claudia Richter,Thomas Mikolajick,Uwe Schroeder,N. Barrett
出处
期刊:Journal of Applied Physics [American Institute of Physics]
卷期号:127 (6) 被引量:162
标识
DOI:10.1063/1.5128502
摘要

Ferroelectric hafnia-based thin films are promising candidates for emerging high-density embedded nonvolatile memory technologies, thanks to their compatibility with silicon technology and the possibility of 3D integration. The electrode–ferroelectric interface and the crystallization annealing temperature may play an important role in such memory cells. The top interface in a TiN/Hf0.5Zr0.5O2/TiN metal–ferroelectric–metal stack annealed at different temperatures was investigated with X-ray photoelectron spectroscopy. The uniformity and continuity of the 2 nm TiN top electrode was verified by photoemission electron microscopy and conductive atomic force microscopy. Partial oxidation of the electrode at the interface is identified. Hf is reduced near the top interface due to oxygen scavenging by the top electrode. The oxygen vacancy (VO) profile showed a maximum at the top interface (0.71%) and a sharp decrease into the film, giving rise to an internal field. Annealing at higher temperatures did not affect the VO concentration at the top interface but causes the generation of additional VO in the film, leading to a decrease of the Schottky Barrier Height for electrons. The interface chemistry and n-type film doping are believed to be at the origin of several phenomena, including wake-up, imprint, and fatigue. Our results give insights into the physical chemistry of the top interface with the accumulation of defective charges acting as electronic traps, causing a local imprint effect. This may explain the wake-up behavior as well and also can be a possible reason of the weaker endurance observed in these systems when increasing the annealing temperature.
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