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because i got only binge energy ,data,fit data only

i want to.know from where you take data of p1 p2 and bakg

please tell.me how you gave different colours of this peaks

In my data x axis is not in equal interval but in this matrix method this takes equispaced values so how can we resolve this or any other way to plot 2D contour plot

Thank you so much 😊🙏🏼

Sir layer content ma jo data ha wo udr kch b data already ni ha iski kia reason ha or wo kaise ay ga?

very useful thx

OH MY GOD, YOU JUST SAVED MY LIFE! Literally, I was going to crawl under the bed and stay there, because I was at the end of my rope not being able to figure out how to create a table to go into my book for formatting for publication, and I didn't want to pay someone to do something I should be able to do myself!! I have been trying every thing I could imagine, going to Reddit and Quora and NOTHING was working!!! Finally, as I was about to give up today, I found your video and BAM!!!!! These tables look amazing in the editor - finally! THANK YOU!!!!!!!!!

Hello , can u please make a video on Graphene monolayer +MnO2 monolayer (hexagonal) 2D structure ?? I will be sincerely consider your help

I am not able stack the graph even after clicking

Thank you

If I want to creat a XRD spectrum of Bi2O2Se using VESTA, should I use the structure before or after these adjustments.

Could you please make a video on how to make Mn02 2D structure??

How to measure the distance between those two layers?

Sir, please explain what is the meaning of negative and positive slopes in the W-H plot. and how we can correlate the strain of a material with electrochemical data.

Thank you

Could yo show to me, how to make a vacancy structure in graphene for example. And could you please give me some idea to add some atom to the structure?

sir. stacked y-axis is didn't work for me. what i do

Hello sir how to calculate crystalline and amorphous percentage here ?

Thanks brother

where can i get these slides sir ?

Please explain how to make composites oxides in vesta, thanks

thank you for this one.

USEFUL

Hi sir, can you tell me one thing here.. in this your plotted values didn't coincide with the straight line right? then is this correct? please clarify

I need free originlab software

Hi; I don't have this line in my origin; what can I do?

Dear Bro. It is really great video. Will this approach work for hexagonal crystal structures as well for example AlN like systems

I think you are missing out the point that while simulating heterostructures, we need to ensure that both phase must have the similar lattice constants to avoid lattice mismatch. Therefore, we must multiply each one of them by a factor to attain the same. Please have a look at the following tutorial th-cam.com/video/GcRWRLTSj-w/w-d-xo.htmlsi=mUfo1vEnEyAmvJ8w. Thanks!!

i am an inorganic chemistry student in Morocco. I found that your courses are very usefull, i hope your channel will be very known. Thank you so much.

Background is so annoying 😔

Hello, i am pressing command + shift on the "cannot be opened" window and nothing is happening. Would you be able to help me with this?

Rietveld is possible in organic field...yes or no???....sir

Wonderfull

👍👍👍👍👍

Thanks

Very helpful. Thank you!

Thank you for your video. Can you help me how to draw chain structure in blender with ball and stick model?

Salvatore Squares

*Typically, the I(L2)/I(L1) value is expected to be around 0.5 for most X-ray sources, like Cu Kα radiation. However, if you're seeing a refined result around 0.01 (as shown in this tutorial), it could be due to a few reasons: Refinement Process: The refinement might have overfit the data or introduced too many free parameters, leading to an unrealistic value. In such cases, constraining the I(L2)/I(L1) value to 0.5 often helps to achieve a more reasonable result.z Instrument Parameters: A mismatch in the instrument model or profile settings could affect the intensity ratios. Double-checking the calibration and profile function can help refine this correctly. Data Quality: A low signal-to-noise ratio or peak overlap can also cause this deviation. Ensuring high-quality data collection can often resolve this issue. I'd recommend fixing the I(L2)/I(L1) value to 0.5 during refinement and observing how it affects the fit.*

Thanks Buen video

Thank you so much, this is really helpful

Hello, could you please explain again why the refined result of the I(L2)/I(L1) parameter in the instrument settings is around 0.01 (I learned from other tutorials that this value should be around 0.5)?

Thanks Dr.Gandhi for your wonderful explanations. I would like to know, how I can plot the exported data from vesta simulated XRD and plot it in Origin ? I tried but failed, can you upload a video on this ? Thanks in advance

Hi sir Please explain how to get the PRM file , where it available?

Hello! Thank you. I did not know about this software. I have used Origin software to deconvoluted but is difficult do it. I have some question. What are the most important parameters to be taken care of in order to deconvolute? How important is it to maintain the same curve width in each of the components that adjust the envelope? Could you suggest any bibliography that could help me with deconvolution of Raman spectroscopy?

no high fedility option in my word only 220 and below ppi how i can solve my problem

how to find the angle between two planes in vesta?

Which software sir can you send the software download link

From the video i convert 3D ti 2D structure but Sir how to save 2D cif file ?