Hi Manoj

Please visit http://www.iucr.org/resources/other-directories/software and select your own software for analysis

You cud post your analysis or your data (raw data, text, csv or anything), Include the chemical information.

Dear Manoj,

It would not be advisable to start using a software without being familiar with the basics of diffraction. It is quite easy to get spurious data if you don't know what you're doing.

Anyhow, the information you mentioned can be acquired manually from the pattern by using a graphing software such as Origin. Doing it manually will be foolproof and will help you grasp the process. Please take the time to study this document to get a hold of the basics:

https://www.google.co.in/url?sa=t&rct=j&q=&esrc=s&source=web&cd=5&cad=rja&uact=8&ved=0ahUKEwj7ybqVnu3UAhUHto8KHc6DB6AQFghYMAQ&url=https%3A%2F%2Fwww.researchgate.net%2Ffile.PostFileLoader.html%3Fid%3D58d22df3dc332d06c7245969%26assetKey%3DAS%253A474618730422273%25401490169331513&usg=AFQjCNFCDW2PA_giyRKJ_ZAeH5uqKhHHLQ

'Elements of X-Ray Diffraction' by BD Cullity is the Bible for this field, you could go through it for more details.

If you must use a software, I think HighScore by PANalytical is quite popular for this purpose.

I support the thesis by Aashranth B. above.  It's best to understand the (very simple) basics behind XRD - Bragg's Law and do some hand calculations (as I had to do from the raw film from a Debye-Scherrer camera) to get a feeling for 2 theta positions, the form of the diffractogram and its meaning, peak broadening (Scherrer; Williamson-Hall); calculation of lattice parameters; Miller's indices etc. how mixtures behave.  Read textbooks such as Klug and Alexander and talk to experienced colleagues who can mentor you.  Then start to explore software when you have a good grasp and understanding.  The danger with blind use of software is to generate the wrong interpretation to an infinite number of decimal places.

You can visit the JCPDS database for the identification of the XRD peaks and as far as the peak shifts are concerned they are due to stresses in your sample arising due to doping or thermal/mechanical effects but mainly it has to be due to doping.

JADE software.