论文标题

NDNIO $ _3 $中的磁性顺序驱动的超快相过渡

Magnetic Order Driven Ultrafast Phase Transition in NdNiO$_3$

论文作者

Stoica, V., Puggioni, D., Zhang, J., Singla, R., Dakovski, G. L., Coslovich, G., Seaberg, M. H., Kareev, M., Middey, S., Kissin, P., Averitt, R. D., Chakhalian, J., Wen, H., Rondinelli, J. M., Freeland, J. W.

论文摘要

Ultrashort X射线脉冲可用于解散磁性和结构动力学,因此在这里用于研究NDNIO $ _3 $(NNO)的光激发,这是一种模型镍(表现出结构性和磁动力学),该结构和磁动力学共同诱导IMT。在光诱导的绝缘体到金属过渡(IMT)的过程中,我们观察到超快($ <$ <$ <$ 180 fs)的磁性淬灭,然后是通过X射线吸收和THZ传输(〜450 FS)探测的绝缘阶段的时间延迟崩溃(〜450 FS),与最慢的光音元素转换相关联。 NI位点的同时订购式响应,在超快磁反应中共存的ND位点的位移响应。至关重要的是,我们通过其连贯的耦合与ND磁顺序观察光语音子,这表明磁性和结构性自由度均有助于驱动IMT。密度函数理论(DFT)计算揭示了一个一致的情况,其中光学驱动的现场电荷转移(ICT)驱动了抗磁性顺序的崩溃,进而破坏了导致IMT的电荷订购相位的稳定。这些实验为控制量子材料中的电子相变的结构和磁性相互作用提供了新的方式,以控制量子材料中的电子相变。

Ultrashort x-ray pulses can be used to disentangle magnetic and structural dynamics and are accordingly utilized here to study the photoexcitation of NdNiO$_3$ (NNO), a model nickelate exhibiting structural and magnetic dynamics that conspire to induce an IMT. During the course of the photoinduced insulator to metal transition (IMT) with above gap excitation, we observe an ultrafast ($<$ 180 fs) quenching of magnetic order followed by a time delayed collapse of the insulating phase probed by X-ray absorption and THz transmission (~ 450 fs) that correlates with the slowest optical phonon mode involved in the structural transition. A simultaneous order-disorder response at the Ni site and displacive response at the Nd site coexist in the ultrafast magnetic response. Crucially, we observe the optical phonon through its coherent coupling with Nd magnetic order, demonstrating that the magnetic and structural degrees of freedom both contribute in driving the IMT. Density functional theory (DFT) calculations reveal a consistent scenario where optically driven inter-site charge transfer (ICT) drives a collapse of antiferromagnetic order that in turn destabilizes the charge-ordered phase resulting in an IMT. These experiments provide new modalities for control of electronic phase transitions in quantum materials based on ultrafast interplay between structural and magnetic orders created by femtosecond photoexcitation.

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