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Correlations between electronic order and structural distortions and their ultrafast dynamics in the single-layer manganite Pr0.5Ca1.5MnO4

机译:单层锰矿石中的电子订单与结构扭曲与结构扭曲的相关性PR0.5ca1.5mno4

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摘要

Time-resolved x-ray diffraction experiments on the half-doped single-layered manganite Pr0.5Ca1.5MnO4 are used to monitor the ultrafast photoinduced dynamics of the structural distortion associated with the charge and orbital ordering (CO/OO). As in the nonlayered three-dimensional counterpart, the ordered phase melts in less than 100 fs after 800-nm photoexcitation and subsequently partially recovers due to thermal equilibration of electronic and vibrational systems. Photoexciting Pr0.5Ca1.5MnO4 below the transition temperature of a second structural phase transition that occurs around 146 K (deep inside the CO/OO phase) releases this structural transition, but progresses on a much slower timescale. This additional reduction of crystal symmetry, which we ascribe to a further tilt of the oxygen octahedra, can thus be considered to be only weakly coupled to CO/OO. Furthermore, static hard-x-ray and resonant soft-x-ray diffraction at the Mn L-2,L-3 edges experiments identify correlations between structural distortions and electronic order in thermal equilibrium.
机译:在掺杂半单层水锰矿Pr0.5Ca1.5MnO4时间分辨X射线衍射实验被用来监测超快光敏反应与充电和轨道有序(CO / OO)相关的结构畸变的动态。如在非层状三维对方,有序相熔体在小于100fs的后800nm的光激发,并随后部分地恢复由于电子和振动系统的热平衡。光激发Pr0.5Ca1.5MnO4低于周围发生146 K(深的CO / OO相内)的第二结构相转变的转变温度释放此结构转变,但在低得多的时间刻度进行。此晶体对称性,这是我们归于氧八面体的进一步的倾斜的额外减少,因此可以被认为是只有弱耦合到CO / OO。此外,静态的硬X射线和软谐振-X射线衍射在Mn的L-2,L-3的边缘识别实验结构扭曲和热平衡电子顺序之间的相关性。

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