Spherical harmonics and wavefunctions

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Spherical harmonics and orbital wave functions share identical angular components, leading to confusion about their representation. While they appear the same, orbital wave functions also include a significant radial part derived from solving the Schrödinger equation for specific potentials. This radial component influences the overall shape and size of the orbital but does not alter the angular part. For example, 2p and 3p orbitals have the same angular representation despite differing radial functions. Ultimately, the distinction lies in the inclusion of the radial component in orbital wave functions, which affects their probability density surfaces.
Chemist20
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What's the difference in the representation of spherical harmonics and the orbitals themselves? they look exactly the same to me... unlike the radial part of the wavefunction though.
 
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The angular part of an orbital wave function for hydrogen (or any other spherically symmetric potential) is a spherical harmonic:

\Psi_{nlm}(r,\theta,\phi) = R_{nl}(r)Y_{lm}(\theta,\phi)
 
jtbell said:
The angular part of an orbital wave function for hydrogen (or any other spherically symmetric potential) is a spherical harmonic:

\Psi_{nlm}(r,\theta,\phi) = R_{nl}(r)Y_{lm}(\theta,\phi)

yes but for a 2p for example, what's the difference in representation between the orbital itself and the spherical harmonic? they look the same to me.
 
Chemist20 said:
yes but for a 2p for example, what's the difference in representation between the orbital itself and the spherical harmonic? they look the same to me.
The angular parts look the same, because they are identical (see jtbell's comment). Unlike spherical harmonics, orbital wave functions, however, do not consist only of an angular part. They also have a radial part. And this radial part is non-trival and comes from solving the Schroedinger equation for some potential (e.g., in hydrogen the nuclear attraction of the proton, in higher spherical atoms from nuclear attraction and the mean field of the other electrons (Fock potential)). But this has no influence on the angular part. E.g., 2p and 3p orbitals have the same angular part, not only in a single atom, but across all atoms (in the nonrelativistic case etc.).
 
cgk said:
The angular parts look the same, because they are identical (see jtbell's comment). Unlike spherical harmonics, orbital wave functions, however, do not consist only of an angular part. They also have a radial part. And this radial part is non-trival and comes from solving the Schroedinger equation for some potential (e.g., in hydrogen the nuclear attraction of the proton, in higher spherical atoms from nuclear attraction and the mean field of the other electrons (Fock potential)). But this has no influence on the angular part. E.g., 2p and 3p orbitals have the same angular part, not only in a single atom, but across all atoms (in the nonrelativistic case etc.).

yes, but when drawing the 2p orbital and the 2p spherical harmonic what's the difference? THEY ARE THE SAME!
 
If they are the same, then by the property of sharing the same identity they are not different.
 
Chemist20 said:
yes, but when drawing the 2p orbital and the 2p spherical harmonic what's the difference? THEY ARE THE SAME!
Note that multiplying the radial wave function by constant factor changes the size, not the shape, of the "drawing" of the orbital, which is really just a drawing of the surface of maximum probability density. By looking at how more general changes in the radial wave function affects this surface, you can see why spherical harmonics look so much like these surfaces.
 

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