Femtosecond time-delay X-ray holography

被引:202
|
作者
Chapman, Henry N.
Hau-Riege, Stefan P.
Bogan, Michael J.
Bajt, Sasa
Barty, Anton
Boutet, Sebastien
Marchesini, Stefano
Frank, Matthias
Woods, Bruce W.
Benner, W. Henry
London, Richard A.
Rohner, Urs
Szoeke, Abraham
Spiller, Eberhard
Moeller, Thomas
Bostedt, Christoph
Shapiro, David A.
Kuhlmann, Marion
Treusch, Rolf
Ploenjes, Elke
Burmeister, Florian
Bergh, Magnus
Caleman, Carl
Huldt, Goesta
Seibert, M. Marvin
Hajdu, Janos
机构
[1] Lawrence Livermore Natl Lab, Livermore, CA 94550 USA
[2] Univ Calif Davis, Ctr Biophoton Sci & Technol, Sacramento, CA 95817 USA
[3] Stanford Univ, Stanford Linear Accelerator Ctr, Stanford Synchrotron Radiat Lab, Stanford, CA 94305 USA
[4] Uppsala Univ, Dept Cell & Mol Biol, Lab Mol Biophys, SE-75124 Uppsala, Sweden
[5] Tech Univ Berlin, Inst Opt & Atomare Phys, D-10623 Berlin, Germany
[6] DESY, D-22607 Hamburg, Germany
基金
加拿大自然科学与工程研究理事会; 美国国家科学基金会;
关键词
D O I
10.1038/nature06049
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Extremely intense and ultrafast X-ray pulses from free-electron lasers offer unique opportunities to study fundamental aspects of complex transient phenomena in materials. Ultrafast time-resolved methods usually require highly synchronized pulses to initiate a transition and then probe it after a precisely defined time delay. In the X-ray regime, these methods are challenging because they require complex optical systems and diagnostics. Here we propose and apply a simple holographic measurement scheme, inspired by Newton's 'dusty mirror' experiment(1), to monitor the X-ray-induced explosion of microscopic objects. The sample is placed near an X-ray mirror; after the pulse traverses the sample, triggering the reaction, it is reflected back onto the sample by the mirror to probe this reaction. The delay is encoded in the resulting diffraction pattern to an accuracy of one femtosecond, and the structural change is holographically recorded with high resolution. We apply the technique to monitor the dynamics of polystyrene spheres in intense free-electron-laser pulses, and observe an explosion occurring well after the initial pulse. Our results support the notion that X-ray flash imaging(2,3) can be used to achieve high resolution, beyond radiation damage limits for biological samples(4). With upcoming ultrafast X-ray sources we will be able to explore the three-dimensional dynamics of materials at the time-scale of atomic motion.
引用
收藏
页码:676 / 679
页数:4
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