Probing the non-equilibrium transient state in magnetite by a jitter-free two-color X-ray pump and X-ray probe experiment

被引:7
|
作者
Pontius, N. [1 ]
Beye, M. [1 ]
Trabant, C. [1 ,6 ]
Mitzner, R. [1 ]
Sorgenfrei, F. [1 ]
Kachel, T. [1 ]
Woestmann, M. [2 ]
Roling, S. [2 ]
Zacharias, H. [2 ]
Ivanov, R. [3 ]
Treusch, R. [3 ]
Buchholz, M. [4 ]
Metcalf, P. [5 ]
Schuessler-Langeheine, C. [1 ]
Foehlisch, A. [1 ,7 ]
机构
[1] Helmholtz Zentrum Berlin Mat & Energie, Inst Methoden & Instrumentierung Forsch Synchron, Albert Einstein Str 15, D-12489 Berlin, Germany
[2] WWU Munster, Phys Inst, Wilhelm Klemm Str 10, D-48149 Munster, Germany
[3] DESY, Notkestr 85, D-22607 Hamburg, Germany
[4] Univ Cologne, Phys Inst 2, Zulpicher Str 77, D-50937 Cologne, Germany
[5] Purdue Univ, Sch Mat Engn, W Lafayette, IN 47907 USA
[6] Free Univ Berlin, Fachbereich Phys, Arnimallee 14, D-14195 Berlin, Germany
[7] Univ Potsdam, Inst Phys & Astron, Karl Liebknecht Str 24-25, D-14476 Potsdam, Germany
来源
STRUCTURAL DYNAMICS-US | 2018年 / 5卷 / 05期
关键词
FREE-ELECTRON LASER; TRANSITION; OPERATION;
D O I
10.1063/1.5042847
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We present a general experimental concept for jitter-free pump and probe experiments at free electron lasers. By generating pump and probe pulse from one and the same X-ray pulse using an optical split-and-delay unit, we obtain a temporal resolution that is limited only by the X-ray pulse lengths. In a two-color X-ray pump and X-ray probe experiment with sub 70 fs temporal resolution, we selectively probe the response of orbital and charge degree of freedom in the prototypical functional oxide magnetite after photoexcitation. We find electronic order to be quenched on a time scale of (30 +/- 30) fs and hence most likely faster than what is to be expected for any lattice dynamics. Our experimental result hints to the formation of a short lived transient state with decoupled electronic and lattice degree of freedom in magnetite. The excitation and relaxation mechanism for X-ray pumping is discussed within a simple model leading to the conclusion that within the first 10 fs the original photoexcitation decays into low-energy electronic excitations comparable to what is achieved by optical pump pulse excitation. Our findings show on which time scales dynamical decoupling of degrees of freedom in functional oxides can be expected and how to probe this selectively with soft X-ray pulses. Results can be expected to provide crucial information for theories for ultrafast behavior of materials and help to develop concepts for novel switching devices. (C) 2018 Author(s).
引用
收藏
页数:8
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