When using the Debye-Scherrer equation for calculating particle size (D=Kλ/(β cos θ)

Select a approiate peak that is not overlapp with others, then be sure

D and λ have the same unit  (e.g. nm )

FWHM is the full width at half maximum of the peak (not half of it) in rad.

then you can calculate.

I have attached my early papers.

Hi PRASANNA NITHIYA, use better a modified Williamson–Hall dependence, compare for instance:

Article Effect of Internal Interfaces on Hardness and Thermal Stabil...

Article Microstructure study on BN nanocomposites using XRD and HRTEM

D=Kλ/(β cos θ) use the formula to calculate the nanocrystallite size

Scherrer equation D=Kλ/(β cos θ)

D is the average thickness in vertical direction of the crystal face

K is Scherrer constant. (if β is FMHM,K=0.89.   if β is integral height to width of the diffraction peak, k=1 )

λ is the wavelength of X-ray

β is the half high width of the diffraction peak of the sample 

θ is diffraction angle(deg)

Scherrer formula is used to calculate the average size in vertical direction  of crystal.

D=Kλ/(β cos θ).

For cubic crystal structure, K =0.94, λ is wavelength of X-ray.

By using eq. D=0.9λ/(β cos θ) one can calculate the nanocrystallite size

Hi

Scherrer’s equation:

Particle Size = (0.9 x λ)/ (d cosθ)

λ = 1.54060 Å (in the case of CuKa1) so, 0.9 x λ = 1.38654

Θ = 2θ/2 (in the example = 20/2)

d = the full width at half maximum intensity of the peak (in Rad) – you can calculate it using Origin software.

To convert from angle to rad

Rad = (22 x angle) / (7 x 180) = angle x 0.01746

Example: if d = 0.5 angle (θ)

= (22 x 0.5)/ (7x 180) = 0.00873 rad

Have a very good day and best of luck

Thanks

Dear Fellows:

There are more than one peak for a given sample... then which peak should be selected to calculate particle size using scherrer's equation?

Dear Zia,

use the dominating peak for the phase that you want to calculate the particle size.

Hi,

Be aware that Sherrer's formula not really applicable for nano size and also not calculate larger size more than 0.1-0.2 micrometer.

Mustafa

I think this link can help

http://www.instanano.com/characterization/theoretical/xrd-size-calculation/

For nano size crystal  its difficult to study them with xrd   

try to use TEM or FESEM

Ahmed's answer explains the calculation quite well. I would like to add that this method of calculation, when applied to thin films, can sometimes yield the particle sizes which are of larger dimensions than the thickness of the films. This is not a discrepancy as the crystallites are assumed to be cylindrical plates in an extension to Scherrer's equation by Smilgies.  [D.-M. Smilgies, J. Appl. Cryst. 42, 1030 (2009)]

http://scripts.iucr.org/cgi-bin/paper?S0021889809040126

You can calculate FWHM using Origin software, but you should find the reference peak that reported in corresponding literature.

we have to used dominating peak for the phase that we want  to calculate the particale size

have good time

Please try this link

file:///C:/Users/hp/Downloads/CrystalSizeAnalysis.pdf

I confirm Prof Ahmed I. Osman to convert from angle to rad

But for calculating the crystallize size with high precision

crystallites size (Dv) can be calculated by analyzing the XRD data using the Scherrer's formula, Dv = kλ/βcos(θ), where β is the structural broadening, which is the difference in integral X-ray peak profile width between the sample and a standard (silicon) and is given by β = [(βabs)2-(βstd)2]1/2

"how to calculate nano crystallite size by Debye‐Scherrer equation using XRD ?" You do not and you cannot. Do edit your original question to avoid this misnomer.

However, if you used the Scherrer equation (carefully) instead, you may be able to relatively compare samples. There are too many assumptions involved with the Scherrer approach that make it untenable like:

You may need the help of the W-H technique to separate (deconvolute) some of the above mentioned factors. Learn more here:

http://pd.chem.ucl.ac.uk/pdnn/peaks/sizedet.htm

"B = the full width at half maximum intensity of the peak (in Rad)"

This is the most common error while using many of the XRD "formulae". None of the "formulae" that I'm aware of, use the FWHM. Instead it is the "INTEGRATED BREADTH". They may be close but are not the same. You'd need the Bragg profile shape to convert FWHM to INTEGRATED BREADTH (Beta, β). If your diffractogram is digital then computing integrated breadth may be easier than figuring out FWHM :-)

E.g., for a Gaussian distribution, the integral breadth, β, is related to the FWHM peak width, H, by β = 0.5 H (π / loge2)1/2.

http://pd.chem.ucl.ac.uk/pdnn/peaks/gauss.htm

• BTW Radians is angle as well!
• Using β(hkl) would yield the size estimate along the direction.
• https://www.researchgate.net/post/Please_tell_me_how_to_calculate_Crystal_Size_using_XRD_Data?_sg=NjLSQp9e1eBz06p6HBPRbJy3ty-47Yc-bviJ6dsBdhl1XBfRsDf0ku2yvtTvdU4VmV09LcPaOOzf5YUJ77KJ8colw3gJgVIv

"use the dominating peak for the phase that you want to calculate the particle size."

Only if you assume that the diffracting domains are spherical and/or if you are interested in size only along that crystallographic direction.

Post your XRD data as Excel file so others might help you too :-) I also suggest you include additional relevant topics up top in your question to share with a larger audience of XRD experts on RG. Refer to this discussion noted below to see some other topics to include. You may include up to 15.

https://www.researchgate.net/post/How_do_I_figure_out_the_spatial_thickness_of_the_individual_layers_from_these_not_so_well_resolved_diffractograms

https://www.linkedin.com/groups/2683600/2683600-6359332934163451905

how to calculate the angle?

What are you talking about? This discussion is about XRD; the angle is the parameter which is being varied during the measurement.

1. Different diffraction angles will provide different FWHMs, when the crystal is not spherical. This is logical, as the number of lattice planes contributing to the diffraction determines the peak width. However, if you get different results from XRD software and from Origin, there must be a difference in data processing. Maybe Origin uses standard deviation instead of FWHM? You should check that.

2. Of course, FWHM has to be converted to radians. If you don't do that, you obtain a mismatch of dimensions in the formula.

3. λ must have the same dimension as the desired dimension of the crystal size. You can also fill in the wavelength in nanoinches and obtain the crystallite size in nanoinches as well.

Why u wanna use Scherrer Formula for powder XRD data instead modified WH-plot or WPPM ?

FIrst of all u have to substract the instrument broadening by using the SRM where u have to chose the same peak position as ur sample (exactly). And as rule of thumb u have to go to higher angle, but the peaks intensity decrease, broader and highly overlap. Yet u have to take into account the others contribution as mentioned by Dr. Ravi.

Unless u work with graphane kind of structure and thin film, Do not use Scherrer Formula manually, use software, use all the peaks and substract the instrument contribution (except those software that use FPA).

Look for advance method such as WPPM (size distribution), BGMN (isotropic or anisotropic mean size), Maud (mean and graphical size), GSAS (mean size), Topas (mean size), HSP (mean size), etc

Ravi, it depends on your definition of calculate.

I agree with Dr. Ahmed I. Osman.

Moreover, you can use one of the following web sites:

https://instanano.com/characterization/theoretical/xrd-size-calculation/

http://mahendrakoppolu.blogspot.com/2013/07/online-crystallite-size-calculator.html

Good luck!

First Calculate the FWHM from XRD plot and then put the value in D=0.9λ/(β cos θ) . β is the line broadening at half the maximum intensity (FWHM) . θ is the Bragg angle. λ is the X-ray wavelength;

Please see this video

How to calculate FWHM in Origin

https://youtu.be/WauGqgz3vy8

and use Debye‐Scherrer equation to calculate crystal size

Andrew R Garcia - "Ravi, it depends on your definition of calculate."

No matter the etymology of "calculate", the phrase "Debye‐Scherrer equation" is a misnomer, isn't it? Yet, it seems to perpetuate past all these admonishments. Is it deliberate or sub-conscious or something else? Do folks on RG even know the "Edit" option exists? Amazingly fundamental! :-)

Here's another one: "β is the line broadening at half the maximum intensity (FWHM)" - WRONG! It is "INTEGRATED BREADTH" not "FWHM"! Only for those who know not the difference are they the same. You are obviously not even reading the past comments Himadri! Do yourself a favor and read prior posts when convenient. Avoid embarassment. Learn to use the "Edit" option as well. The words on RG posts are not PERMANANT :-)

Amend your words on your posts and make me retract mine.

I notice that most XRD users here on RG are still "groping in the dark" (still using a conventional point counter) without having the advantage of seeing and visualizing the XRD phenomena. Still practicing it as a "dark" art which it was never meant to be. The Braggs clearly visualized it a century ago.

Are you folks not even reading what Maykel has posted? Come on fellows be considerate. Don't be lulled by the comfort of reading only your own words. Let's wake up and face modernity and reality.

HOW CAN I CALCULATE THE BRAG ANGLE?

Particle Size = (0.9 x λ)/ (d cosθ)

λ = 1.54060 Å (in the case of CuKa1) so, 0.9 x λ = 1.38654

Θ = 2θ/2 (in the example = 20/2)

d = the full width at half maximum intensity of the peak (in Rad) – you can calculate it using Origin software.

To convert from angle to rad

Rad = (22 x angle) / (7 x 180) = angle x 0.01746

Example: if d = 0.5 angle (θ)

= (22 x 0.5)/ (7x 180) = 0.00873 rad

I wonder how many more times the Scherrer formula will be posted here.

Scherrer’s equation: Particle Size Dxrd = (0.9 x λ)/ (d cosθ)

λ = 1.54060 Å (in the case of CuKalpha) ==> 0.9 x λ = 1.38654

note that Θ = 2θ/2

d = the full width at half maximum intensity of the peak (in Rad).

To convert from angle to rad; Rad = (22 x angle) / (7 x 180) = angle x 0.01746

Thanks a lot

I asked that if any possible to find the size metal complexes by using scherrer's equation. In case what are the range of size in metal complexes compare with nanocrystalline form

I agree with Dr. Ahmed ,Osman and Slimani. It is easy to find by following those.

In XRD pattern, You should select most relevant and high intense peak for the calculation. Then, You can use above methods to calculate. It will be easy.

to converts angstrom to nanometers divide to 10 .........1 λ /10

FWHM divide to 57.3 to convert to radias ........2 FWHM/ 57.3

then application Scherrer’s equation

why do you keep answering this post? it is overly simplistic and outdated approach.

I wouldn't say that, Maykel! The complex conversions from angstroms to nanometers and from degrees to radians maybe completely new concepts for some readers ;-).

Yes, I agree with Claus Moseke. It is a confusing point for some researchers!

Particle Size Dxrd = (0.95 x λ)/ (d cosθ)

λ = 1.54060 Å (in the case of CuKalpha) ==> 0.95 x λ = 1.46357

Θ = 2θ/2

d = the full width at half maximum intensity of the peak (in Rad).

This is getting absurd!

Hello,

See CH2 in the attachment thesis.

Scherrer introduced the equation taking into account the integral breadths (β) and never mentioned FWHM values. So, in order to "estimate" the crystallite size (not particle size!) you first must eliminate the instrumental contributions (veryyy important) to β_sample using the instrumental function,

 β_sample =  β_experiment -  β_instrumental.

where β_instrumental is a function that are unique for a certain XRD diffracto-meter. So you should measure line position and line shape crystallographic standards for the powder diffraction in order to obtain the parameters that describe your function and so your diffractometer.

Finally, you can use Scherrer as follows:

L_hkl = k * lambda /  β_sample * cos (theta).

FOLLOWING LINK ABSOLUTELY WILL BE HELPFUL REGARDING THE QUESTION:

http://prism.mit.edu/xray/oldsite/CrystalSizeAnalysis.pdf

https://www.youtube.com/watch?v=mO86asczIDc

https://file.scirp.org/pdf/WJNSE20120300002_83393552.pdf

Agree with Farhad Saba.

Scherrer’s equation:

Particle Size = (0.9 x λ)/ (d cosθ)

Oh c'mon... @#$%

This is like facebook, when someone presents a stupid riddle asking for some number. People will keep on typing in the numbers for days and weeks, and if only to prove that they can c&p.

As well as C & P, previous answers remain unread or not understood....

See the attachment paper.

Use the attachment

Paramasivam Balasubramanian , Nice job making an excel

Alireza Bargahi

Thank you guys, nice discussion.

Article Impact of surface modification on adsorptive removal of BTX ...

Article Investigation of green functionalization of multiwall carbon...

Follow these articles.

https://instanano.com/characterization/theoretical/xrd-size-calculation/

It is Scherrer’s equation, not Debye-Scherrerr:

Scherrer’s equation:

Particle Size = (0.9 x λ)/ (d cosθ)

λ = 1.54060 Å (in the case of CuKa1) so, 0.9 x λ = 1.38654

Θ = 2θ/2 (in the example = 20/2)

d = the full width at half maximum intensity of the peak (in Rad) – you can calculate it using Origin software.

To convert from angle to rad

Rad = (22 x angle) / (7 x 180) = angle x 0.01746

Example: if d = 0.5 angle (θ)

= (22 x 0.5)/ (7x 180) = 0.00873 rad

Dear Dr Fatameh Mostaghni

I had a look at your paper. Can you explain equation (1) in that paper in more details? Also, can this equation be used to calculate size of soft and spherical objects like biological cells, drug delivery vesicles, etc. ?

If you have access to Origin software, then this tutorial video can give you a quick snap of what to do, and its easy. This way of analysis makes it more applicable.

https://www.youtube.com/watch?v=m8L-B4A75Ec

The Debye-Scherer formula in very simple way one may calculate:

Please see the attached file

I just don't understand it, why STILL people post an answer to a question which has been answered YEARS ago. And - for the hundredth time: It is called SCHERRER formula, not Debye-Scherrer. How difficult can this be?

See this video

How to Calculate FWHM in XRD

https://youtu.be/WauGqgz3vy8

then you can use this value for further calculation

To calculate strains in a material using XRD I will suggest you to have a look at the following link which is a discription of Williamson-Hall Plot

Determination of Size and Strain

And to calculate crystallite size you can use Scherrer Equation and Modified Scherrer Equation for nano-crystallte sizes. Go through the following paper by Ahmad Monshi et al.

http://file.scirp.org/pdf/WJNSE20120300002_83393552.pdf

Hope this will help you. All the best.

you can see the following manuscripts..

Scherrer equation: τ = K*𝜆/(β *cos(θ))

Where

𝜆 (wavelength): 0,154 [nm] (but depends on your equipment)

β (FWHM: line broadening at half the maximum intensity): ..... [rad] --> remember divide it into 2 because the angle recorded is 2θ

θ (angle): ...... [deegres]

K (shape factor): 0,9 [- ]

τ (particle size): ...... [nm]

Judit Nuñez Welcome to the fun!

It is not possible to calculate the particle size of an amorphous compound by

Debye‐Scherrer eqN because XRD can only determine crystalline compounds or substances. Hence no data will be available if an amorphous compound will be analysed under XRD spectra

Agreed to the answer of Mr. Ravi Ananth

Crystal size of crystalline materials can be calculated using Debye-Scherer equation if it is homogeneous then take (k=0.94) and if it heterogeneous (k=0.89). Thi can be indicated from SEM images for the investigated material. then beta(FWHM= β) converts from deg into radian scale and applying Scherer equation:

use all the peaks that you take from patterns and compare it with SEM or TEM in 100 nm range

This is a new and improved method of Sherer's equation, I suggest studying it.

DOI:10.4236 / wjnse.2012.23020

Modified Scherrer equation to estimate more accurately nano-crystallite size using XRD

Scherrer equation

T = Kλ/(β cos θ)

Where

2 θ = 7.210

So θ=3.6050

And

cos(3.605)=0.998

D=(0.9*0.154)/(0.00285 x cos(3.605))=48.729 nm

D=(0.9*0.154)/(0.00285*0.998)

D = 48.729 nm

DOI 10.1007/s10853-016-0017-2

Siddique Shah You quote D = 48.279 nm. Do you know what the diameter of a hydrogen atom is? You should reconsider the number of decimal points you are stating.

Abbas Jassim Lafta If you've read the previous answers you'll know that there's no such animal as the 'Debye-Scherer equation' or even the Debye-Scherrer equation. It's solely the Scherrer equation with all its foibles.

Dear Researchers,

The formula is not "Debye-Scherrer formula". Its simply "Scherrer formula"

Please refer the below linked nature article.

https://www.nature.com/articles/nnano.2011.145

I agree with Jayadheepan that there is NO such Debye-Scherrer formula and misleading so should be avoided.

Additionally while using Scherrer’s equation: Particle Size = (K x λ)/ (FWHM cosθ), few points to be considered:

(i) A care must be taken in converting degree into radians and also writing the final answer with errors, as without errors, the number may be misleading. Also if possible, this should be crosschecked with microscopic (TEM) measurements.

(ii) Usually K is considered constant and taken 0.9 (which is true for spherical particles), and for different shaped like cube and rod a smaller K value should be used.

The standard reference by J. I. Langford and A. J. C. Wilson "Scherrer after sixty years: A survey and some new results in the determination of crystallite size" J. Appl. Cryst. (1978). 11, 102-113, should be used for better analysis.

Best

You can solve this automatically by Using Jade Software

By Jade You can calculate 2 theta, Intensity Peak ,HKL, Lattice parameters, Stress constant, and peak etc

Hi, You may find this interesting:

"The equation is Dhkl = Kλ/(Bhklcosθ), where Dhkl is the crystallite size in the direction perpendicular to the lattice planes, hkl are the Miller indices of the planes being analysed, K is a numerical factor frequently referred to as the crystallite-shape factor5, λ is the wavelength of the X-rays ..." Source: Holzwarth, U., & Gibson, N. (2011). The Scherrer equation versus the'Debye-Scherrer equation'. Nature Nanotechnology, 6(9), 534. Webpage: https://www.nature.com/articles/nnano.2011.145

Hi, I find W-H plot more accurate method to calculate crystallite size. In Scherrer equation, we use the most intense xrd peak. In W-H plot, we use average 4-5 peaks.

I have made a tutorial video on W-H plot for XRD analysis to calculate crystallite size, strain and find the FWHM of each peaks using Gaussian Peak fitting method.

Link is here: https://youtu.be/BrZOpfvKUo0

hi, you can use the following manuscript...

Debye was Scherrer's PhD mentor. He obtained his PhD in 1916, while he published his landmark equation in 1918. Debye-Scherrer equation does not exist.

@ Ravi Ananth

Preferred orientation factor or in order way to say is texture development, which is not expected commonly unless a special treatments applied.

Instrumental factor, should be the same form to batch to batch.

I agree, d = the full width at half maximum intensity is not integrated/integral Breadth, which is required for calculation.

PRASANNA NITHIYA SUDHAN

see the attached document for guidance.

regards

Santanu

Agree with @Ravi

I'am agree with Jeyadheepan Karu it's Scherrer formula

you need to be attention th the value of λ = 1.54060 Å, if you want to get the crystallite size directly in " nm " you must put λ = 0.154060 nm.

Guys have u ever read the recent publications on this ?

Are u really wanna calculate it manually just with a single information ?

Read the size-strain round robin article from IUCR website below as well as find all the related information, instead discussing this obsolete method.

https://scripts.iucr.org/cgi-bin/paper?ks0213

Serch for whole powder pattern modeling as well as an advance recent method.

I have calculated the crystalline size by MDI Jade 6.5 this version calculate the Size, lattices, hkl,angles values and many more

I have added a photo of demo material with its crystalline size

https://www.researchgate.net/profile/Alexei_Kuznetsov/answers

Dimitrios A. Giannakoudakis thank you for your fact.

Please see also. The Scherrer equation versus the 'Debye-Scherrer equation' Uwe Holzwarth & Neil Gibson.

Is there any English paper that we can cite the Scherrer formula?

@dogankaya There are thousands of papers. You can find them easily via Google Scholar

I think Scherrer’s equation is using to calculate crystallite size, not particle size. The crystallite size and particle size is not same. So, Scherrer’s equation is not valid for both. If I want to calculate the particle size, which formula is better?@ Imane Mayouf @ Ahmed I. Osman