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LED-pump-X-ray-multiprobe crystallography for sub-second timescales

The visualization of chemical processes that occur in the solid-state is key to the design of new functional materials. One of the challenges in these studies is to monitor the processes across a range of timescales in real-time. Here, we present a pump-multiprobe single-crystal X-ray diffraction (S...

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Detalles Bibliográficos
Autores principales: Hatcher, Lauren E., Warren, Mark R., Skelton, Jonathan M., Pallipurath, Anuradha R., Saunders, Lucy K., Allan, David R., Hathaway, Paul, Crevatin, Giulio, Omar, David, Williams, Ben H., Coulson, Ben A., Wilson, Chick C., Raithby, Paul R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814726/
https://www.ncbi.nlm.nih.gov/pubmed/36697958
http://dx.doi.org/10.1038/s42004-022-00716-1
Descripción
Sumario:The visualization of chemical processes that occur in the solid-state is key to the design of new functional materials. One of the challenges in these studies is to monitor the processes across a range of timescales in real-time. Here, we present a pump-multiprobe single-crystal X-ray diffraction (SCXRD) technique for studying photoexcited solid-state species with millisecond-to-minute lifetimes. We excite using pulsed LEDs and synchronise to a gated X-ray detector to collect 3D structures with sub-second time resolution while maximising photo-conversion and minimising beam damage. Our implementation provides complete control of the pump-multiprobe sequencing and can access a range of timescales using the same setup. Using LEDs allows variation of the intensity and pulse width and ensures uniform illumination of the crystal, spreading the energy load in time and space. We demonstrate our method by studying the variable-temperature kinetics of photo-activated linkage isomerism in [Pd(Bu(4)dien)(NO(2))][BPh(4)] single-crystals. We further show that our method extends to following indicative Bragg reflections with a continuous readout Timepix3 detector chip. Our approach is applicable to a range of physical and biological processes that occur on millisecond and slower timescales, which cannot be studied using existing techniques.