Ultrafast dynamics and scattering of protic ionic liquids induced by XFEL pulses

被引:5
作者
Patra, Kajwal Kumar [1 ]
Dawod, Ibrahim Eliah [1 ,2 ]
Martin, Andrew, V [3 ]
Greaves, Tamar L. [3 ]
Persson, Daniel [1 ]
Caleman, Carl [1 ,4 ]
Timneanu, Nicusor [1 ]
机构
[1] Uppsala Univ, Dept Phys & Astron, Box 516, SE-75120 Uppsala, Sweden
[2] European XFEL, Holzkoppel 4, DE-22869 Schenefeld, Germany
[3] RMIT Univ, Sch Sci, 124 La Trobe St, Melbourne, Vic 3000, Australia
[4] DESY, Ctr Free Electron Laser Sci, Notkestr 85, DE-22607 Hamburg, Germany
基金
澳大利亚研究理事会; 瑞典研究理事会;
关键词
radiation damage; molecular dynamics; non-local thermodynamic equilibrium; protic ionic liquids; X-ray free-electron lasers; PROTEIN-STRUCTURE DETERMINATION; FREE-ELECTRON LASER; X-RAY-SCATTERING; RADIATION-DAMAGE; MOLECULAR-DYNAMICS; BOND-BREAKING; SIMULATION; CODE; CRYSTALLOGRAPHY; NANOCRYSTALS;
D O I
10.1107/S1600577521007657
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
X-rays are routinely used for structural studies through scattering, and femtosecond X-ray lasers can probe ultrafast dynamics. We aim to capture the femtosecond dynamics of liquid samples using simulations and deconstruct the interplay of ionization and atomic motion within the X-ray laser pulse. This deconstruction is resolution dependent, as ionization influences the low momentum transfers through changes in scattering form factors, while atomic motion has a greater effect at high momentum transfers through loss of coherence. Our methodology uses a combination of classical molecular dynamics and plasma simulation on a protic ionic liquid to quantify the contributions to the scattering signal and how these evolve with time during the X-ray laser pulse. Our method is relevant for studies of organic liquids, biomolecules in solution or any low-Z materials at liquid densities that quickly turn into a plasma while probed with X-rays.
引用
收藏
页码:1296 / 1308
页数:13
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