Physical Chem Question - Xrays & Crystals

In summary, the homework statement is that X-rays of 1.54 angstroms are reflected off copper powder. @ 21.65º25.21º37.06º44.96º47.58ºThe cubic lattice and the length of an edge of the unit cell are found using the Bragg equation. The representative indices are found using the "assumption" that the lattice is in fact a face centered cubic. Neither of the plots are particularly linear.
  • #1
jbowers9
89
1
[Xray reflection
1. Homework Statement

X-rays of 1.54 angstroms are reflected off copper powder
@
21.65º
25.21º
37.06º
44.96º
47.58º

Find the cubic lattice and the length of an edge of the unit cell.

2. Homework Equations

nλ = 2d sin(Θ) ; the Bragg equation

3. The Attempt at a Solution

The cubic latice is face centered at d110? Because it has 5 planes of reflection?
I tried plotting sin(Θ) vs. n to get the slope and calculate a, but it doesn't seem right?
How do I find the length of an edge of the unit cell and what is the cubic lattice?
 
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  • #2
Why don't you use [tex]sin\theta_{hkl} = (0.5\lambda/a)(h^2+k^2+l^2)^{0.5}[/tex]

or
[tex]sin^2\theta_{hkl} = (0.5\lambda/a)^2(h^2+k^2+l^2)[/tex]


I believe that is another form of the Bragg condition.

Is that any help?
 
Last edited:
  • #3
h,k,l

Using this other Bragg equation, what would the representative indices be then for each reflected plane. I'm not sure of the geometry of the lattice in the first place.
 
  • #4
h,k,l

Is it {1,1,0},{1,2,0},{1,3,0},{1,4,0},{1,5,0}?
Or {1,1,0},{1,1,1},{1,1,2},{1,1,3},{1,1,4}?
This is using the "assumption" that the lattice is in fact a face centered cubic, 'cause the xray pics in the text show 5 planes of reflection for d110, and that's a face centered cubic.
Neither of the plots are particularly linear either.
 
  • #5
Your OP referred to a "cubic lattice", yes? h,k,l refers to the Miller indices.

The allowed values of h2+k2+l2 are:

hkl h2+k2+l2
100 1
110 2
111 3
200 4
210 5
211 6
220 8
300 9
221 9
310 10

These are multiples of [tex]((0.5\lambda/a)^2)[/tex]

For your plot, are you using [tex]sin^2\theta[/tex]? Are you also using [tex](0.5\lambda/a)^2[/tex]?
 
Last edited:
  • #6
Miller Indices

So then the Miller Indices would be {1,1,0},{2,2,0}, etc?
How, given only the five angle measurements, are you supposed to infer - discern - the lattice structure? I am ASSUMING that if I "guess" the structure or indices of the first angle measurement, the remainder are just increments along the appropriate axis?
 

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  • #7
You have a list of [tex]\theta[/tex]. Convert them to something like [tex]100sin^2\theta[/tex]. Examine the list again and look for the common difference (a multiple of [tex](0.5\lambda/a)^2[/tex].
 

1. How do X-rays interact with crystals?

When X-rays interact with crystals, they are diffracted according to the crystal's atomic structure. This is because the spacing between atoms in a crystal is on the same scale as the wavelength of X-rays, allowing for constructive and destructive interference of the X-rays. This results in a diffraction pattern that can be used to determine the crystal's atomic arrangement.

2. How are X-rays used in crystallography?

X-rays are used in crystallography to determine the atomic arrangement of crystals. By exposing a crystal to X-rays and analyzing the resulting diffraction pattern, scientists can create a detailed picture of the crystal's structure, including the positions of the atoms within the crystal.

3. What is the difference between X-ray crystallography and X-ray diffraction?

X-ray crystallography and X-ray diffraction are often used interchangeably, but there is a subtle difference between the two. X-ray crystallography refers to the overall process of using X-rays to determine the atomic arrangement of crystals, while X-ray diffraction specifically refers to the scattering of X-rays by a crystal to create a diffraction pattern.

4. Can X-ray crystallography be used for all types of crystals?

No, X-ray crystallography is not suitable for all types of crystals. Some crystals, such as those with large unit cells or disordered structures, may not produce a clear diffraction pattern. Additionally, some materials may be damaged by the high energy of X-rays, making it difficult to obtain accurate results.

5. How has X-ray crystallography contributed to scientific advancements?

X-ray crystallography has played a crucial role in many scientific advancements, particularly in the fields of chemistry, biology, and materials science. It has allowed scientists to determine the structures of molecules, proteins, and other complex compounds, leading to a better understanding of their properties and functions. X-ray crystallography has also helped in the development of new drugs and materials with specific properties, leading to advancements in various industries.

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