Grain rotation and lattice deformation during photoinduced chemical reactions revealed by in situ X-ray nanodiffraction
An in situ X-ray nanodiffraction technique allows for the real-time study of the photoinduced chemical reaction to produce Ag from AgBr, and can spatially resolve structural changes at the submicrometre scale with a time resolution of 5 ms. In situ X-ray diffraction (XRD) and transmission electron m...
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Veröffentlicht in: | Nature materials 2015-07, Vol.14 (7), p.691-695 |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | An
in situ
X-ray nanodiffraction technique allows for the real-time study of the photoinduced chemical reaction to produce Ag from AgBr, and can spatially resolve structural changes at the submicrometre scale with a time resolution of 5 ms.
In situ
X-ray diffraction (XRD) and transmission electron microscopy (TEM) have been used to investigate many physical science phenomena, ranging from phase transitions, chemical reactions and crystal growth to grain boundary dynamics
1
,
2
,
3
,
4
,
5
,
6
. A major limitation of
in situ
XRD and TEM is a compromise that has to be made between spatial and temporal resolution
1
,
2
,
3
,
4
,
5
,
6
. Here, we report the development of
in situ
X-ray nanodiffraction to measure high-resolution diffraction patterns from single grains with up to 5 ms temporal resolution. We observed, for the first time, grain rotation and lattice deformation in chemical reactions induced by X-ray photons: Br
−
+
hv
→ Br + e
−
and e
−
+ Ag
+
→ Ag
0
. The grain rotation and lattice deformation associated with the chemical reactions were quantified to be as fast as 3.25 rad s
−1
and as large as 0.5 Å, respectively. The ability to measure high-resolution diffraction patterns from individual grains with a temporal resolution of several milliseconds is expected to find broad applications in materials science, physics, chemistry and nanoscience. |
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ISSN: | 1476-1122 1476-4660 |
DOI: | 10.1038/nmat4311 |