Why is XRD baseline different for different samples? i have done XRD for NiZnFe2O4 and for CoZnFe2O4 nanoparticles, for first one the baseline starts from 1500 and for second one from 1200. please explain why it is not started from Zero. tahnks
Ok, firstly you need to remember that the intensity values are arbitrary units and will differ from equipment to equipment and sample to sample.
In simple words, there could be many reasons for the difference in intensity values;
1) Different materials (you can not get exactly same intensities for different materials, due to difference in structural features,
2) Difference in particle size and morphology distributions of your samples,
3) sample preparation (you can have different values for exactly the same sample if not prepared properly,
4) background noise possibly due to contamination/ moisture and so on,
Having said all this, you no need to worry about this difference in your two different materials XRD, because you can not compare them with each other and it doesn't mean anything anyways,
The relative intensity of 1 sample helps you to see the peaks intensities of that sample relative to each other.
For more details and to understand what it means in terms of mathematics/ chemistry, please read the Brag's Law and other basic XRD concepts, its easy!!
Ok, firstly you need to remember that the intensity values are arbitrary units and will differ from equipment to equipment and sample to sample.
In simple words, there could be many reasons for the difference in intensity values;
1) Different materials (you can not get exactly same intensities for different materials, due to difference in structural features,
2) Difference in particle size and morphology distributions of your samples,
3) sample preparation (you can have different values for exactly the same sample if not prepared properly,
4) background noise possibly due to contamination/ moisture and so on,
Having said all this, you no need to worry about this difference in your two different materials XRD, because you can not compare them with each other and it doesn't mean anything anyways,
The relative intensity of 1 sample helps you to see the peaks intensities of that sample relative to each other.
For more details and to understand what it means in terms of mathematics/ chemistry, please read the Brag's Law and other basic XRD concepts, its easy!!
Good answers from M Rehan. I would just add the obvious - that since the difference between your samples is Ni versus Co, the differences in "baseline" (by which I am assuming you mean background) would be primarily due to differences in scattering power, absorption, and fluorescence of these elements for the radiation (Cu k-alpha ?) selected.
Depending on your set up and what kind of diffractometer you have, there can be different fluorescence backgrounds, or perhaps differences in the bremstrahlung.
Is it a theta - two theta Bragg-Brentano diffractometer? I newer design which makes use of an energy dispersive detector along with a sample that turns in an angle? There are too many different types of x-ray diffractometers to enumerate here.
Thanks Edward for your endorsement, I listed the few possible reasons for basic understanding, but I also believe the main reason to be the background effect due to both samples being different material.
Again, what kind of diffractometer do you have? Do you have a copper anode? With a copper anode the wavelength of the copper K alpha line is 1.54 Angstroms and the wavelength of the copper K beta line is 1.38 Angstroms. If you have an old fashioned instrument you would have a Ni filter, The K absorption edge of Ni is at a wave length of 1.49 Angstroms, slightly lower in energy than the copper K alpha but higher in energy than the copper K beta. The filter then serves to remove almost all of the copper K beta, greatly simplifying the interpretation of your data. However, Ni atoms in the sample are not excited to higher K states by the Characteristic K emission of copper. However; cobalt atoms are excited to higher K states by the copper K alpha line. More modern instruments would probably have some means of instrumentally monochromatizing the output from your tube.
But if, as I suspect, you are using a filter in concert with a copper anode, probably the only solution would be to switch (carefully, because they can take less power input) to a cobalt anode and then change from a nickel to an iron filter.