Why is separation constant l(l+1) instead of +-l^2?

In summary, while separating variables in the Schrodinger Equation for the hydrogen atom, we take the separation constant to be l(l+1) instead of just l^2 or -l^2. This is not just to make the angular equation in the form of the Associated Legendre Equation, but it is also because these are the eigenvalues of the angular operator. These eigenvalues are not chosen, but rather determined by the differential equation and boundary conditions. Additionally, Ballentine's textbook provides a more direct and rigorous approach to deriving the quantum angular momentum spectrum using operators on an abstract Hilbert space.
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Rupul Chandna
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While separating variables in the Schrodinger Equation for hydrogen atom, why are we taking separation constant to be l(l+1) instead of just l^2 or -l^2, is it just to make the angular equation in the form of Associated Legendre Equation or is there a deeper meaning to it?
 
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Because those are the eigenvalues to the angular operator. You do not ”choose” the eigenvalues, they are what they are based on the differential equation and boundary conditions. In the case of the angular part of the Laplace operator, the eigenfunctions have those eigenvalues.
 
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Rupul Chandna said:
While separating variables in the Schrodinger Equation for hydrogen atom, why are we taking separation constant to be l(l+1) instead of just l^2 or -l^2, is it just to make the angular equation in the form of Associated Legendre Equation or is there a deeper meaning to it?
Take a look at Ballentine section 7.1, where he derives the quantum angular momentum spectrum very directly using operators on an abstract Hilbert space, without all the extra baggage of differential equations.

He starts of using a symbol ##\beta## as the eigenvalue of ##{\mathbf J}^2##, but after further analysis using ##J_z## and ##J_\pm## to determine ##J_z##'s range of eigenvalues he derives a constraint on ##\beta## such that ##\beta = j(j+1)##, where ##|j|## bounds the possible eigenvalues of ##J_z##.

When you see an author simply choosing the value ##j(j+1)## (or ##\ell(\ell+1)## in your text), it just means that author is lazily skipping over the necessary extra analysis, as given in Ballentine's textbook.
 
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1. Why is the separation constant l(l+1) instead of +-l^2?

The separation constant l(l+1) is used in the context of solving differential equations in quantum mechanics. It arises from the fact that the solutions to these equations involve spherical harmonics, which are functions of the form Ylm(θ,φ). The separation constant l(l+1) is related to the degree l of the spherical harmonic, and represents the eigenvalue of the angular momentum operator in quantum mechanics.

2. What does the separation constant l(l+1) represent?

The separation constant l(l+1) represents the eigenvalue of the angular momentum operator in quantum mechanics. It is related to the degree l of the spherical harmonic, and is used to solve differential equations in quantum mechanics involving spherical harmonics.

3. How is the separation constant l(l+1) derived?

The separation constant l(l+1) is derived from the eigenvalues of the angular momentum operator, which are given by l(l+1)ħ, where ħ is the reduced Planck's constant. This is determined by solving the differential equations involving spherical harmonics, and is a fundamental result in quantum mechanics.

4. Is the separation constant l(l+1) always positive?

The separation constant l(l+1) can take on both positive and negative values, depending on the context in which it is used. In quantum mechanics, it is typically used as an eigenvalue of the angular momentum operator, and therefore can take on positive or negative values depending on the specific problem being solved.

5. Can the separation constant l(l+1) be generalized to higher dimensions?

Yes, the separation constant l(l+1) can be generalized to higher dimensions in the context of solving differential equations involving spherical harmonics. In higher dimensions, it is referred to as l(l+n), where n represents the number of dimensions. This generalization is necessary for solving problems in higher dimensions, such as those involving multi-electron atoms.

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