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Chemical State Evolution in Ferroelectric Films during Tip-Induced Polarization and Electroresistive Switching

机译:尖端诱导极化和电阻切换过程中铁电薄膜中的化学态演化

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摘要

Domain formation and ferroelectric switching is fundamentally inseparable from polarization screening, which on free surfaces can be realized via band bending and ionic adsorption. In the latter case, polarization switching is intrinsically coupled to the surface electrochemical phenomena, and the electrochemical stage can control kinetics and induce long-range interactions. However, despite extensive evidence toward the critical role of surface electrochemistry, little is known about the nature of the associated processes. Here we combine SPM tip induce polarization switching and secondary ion mass spectrometry to explore the evolution of chemical state of ferroelectric during switching. Surprisingly, we find that even pristine surfaces contain ions (e.g., Cl-) that are not anticipated based on chemistry of the system and processing. In the ferroelectric switching regime, we find surprising changes in surface chemistry, including redistribution of base cations. At higher voltages in the electroforming regime significant surface deformation was observed and associated with a strong ion intermixing.
机译:磁畴形成和铁电转换从根本上与极化屏蔽是分不开的,极化屏蔽可以通过带弯曲和离子吸附在自由表面上实现。在后一种情况下,极化转换本质上与表面电化学现象相关,并且电化学阶段可以控制动力学并引发长程相互作用。然而,尽管有大量证据表明表面电化学起着关键作用,但对相关过程的性质知之甚少。在这里,我们结合了SPM尖端感应极化切换和二次离子质谱,以探讨切换期间铁电体化学状态的演变。令人惊讶地,我们发现,即使原始表面也包含基于系统化学和处理无法预料的离子(例如,Cl-)。在铁电转换机制中,我们发现了表面化学的令人惊讶的变化,包括碱阳离子的重新分布。在电铸态中较高的电压下,观察到明显的表面变形,并与强离子混合有关。

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