When I do a phi scan about the substrate peak, the phi scan peaks seems to be split or shows multiple peaks at the same value of Phi. And also omega scan about the substrate peak give multiple peaks. Why is this happening can anyone have any idea?
Hi Pramod, Can you forward me the results so that I can have a look.
This is an effect that can be observed by insufficiant grain statistics. What is your crystallite size?
I have taken PHI scans of many substrates but never came across this type of issue. Generally, sharp peaks are observed.
Please check, whether this doublet is from the K-Alpha 1 and 2 both ???
Use of monochromator solves this type of doublets in routine XRD measurements.
Thanks
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