We are exploring a second order alternative formulation of Schrödinger's wave equation as the basic model of quantum mechanics, which for a Hydrogen atom takes the form
- $h^2\ddot\psi +H^2\psi =0$, (1)
We introduce the eigenfunctions $\psi_j$ and corresponding real eigenvalues $E_j$ of the Hamiltonian $H$ satisfying
- $H\psi_j = E_j\psi$ for $j=1,2,3...$ with $E_1\leq E_2\leq E_3,...$
- $\exp(i\frac{E_j}{h}t)\psi_j(x)$ for $j=1,2,3,...$
We seek guidance comparing with the equation for a vibrating thin 2d elastic plate with plane stress-free ground configuration, which may take the form
- $\ddot\phi +\Delta^2\phi =0$, (2)
- $OE= \frac{1}{2}\int (H\psi )^2 + h^2\dot\psi^2)dx$, (3)
- $AE= \frac{1}{2}\int (\psi H\psi+h^2\dot\psi H^{-1}\dot\psi )dx$ (4)
- $Q=\frac{1}{2}\int (\psi^2+h^2(H^{-1}\dot\psi )^2dx$ (5)
It is here natural to view $OE$ as total oscillator energy, $AE$ as total atomic energy, and it may also be natural to view $Q$ as total charge, viewing thus charge as a form of energy. We are thus led to define
- $\frac{1}{2}(H\psi )^2 + h^2\dot\psi^2) = $ local oscillator energy
- $\frac{1}{2}(\psi H\psi +h^2\dot\psi H^{-1}\dot\psi ) =$ local atomic energy
- $\frac{1}{2}(\psi^2+h^2(H^{-1}\dot\psi )^2) =$ local charge.
Note that
- $\int \psi H\psi dx =\frac{h^2}{2m}\int\nabla\psi\vert^2dx +\int V(x)\psi^2(x)dx$, (6)
potential energy under Laplacian space regularization.
This is radically different from the standard interpretation with $\vert\psi\vert^2$ as a probability distribution of particle position with $\psi$ complex-valued.
Let us thus compare the two interpretations of (i) $\psi^2$ as charge distribution and (ii) $\vert\psi\vert^2$ as probability distribution of particle position:
1. A function value $\vert\psi\vert^2(x,t)$ is a non-negative number and as such cannot represent a 3d position coordinate, while $\psi^2 (x,t)$ may naturally directly represent a scalar quantity like charge (or mass).
2. The scalar function $\psi^2(x,t)$ generates a 3d charge distribution through the dependence on $x$ and thus has a 3d quality, which gets expressed in radiation from oscillating charges.
3. The only way to connect the scalar $\vert\psi\vert^2$ to 3d space is to interpret
it as a probability distribution in space, but a probability is not a direct physical quantity.
The conclusion is that connecting the scalar $\vert\psi\vert^2$ to 3d particle position, as in standard quantum mechanics, is both irrational and unneccessary.
We will next extend to radiation summarizing previous posts on the radiating atom.
Then we will extend to atoms/ions with more than one electron. With the wave function $\psi (x,t)$
connecting to charge distribution $\psi^2(x,t)$, we will not be misl(led) to introduce a multi-dimensional wave function $\psi (x1,x2,...,xN,t)$ depending on $N$ 3d space coordinates $x1,x2,...xN$ as in the standard formulation (which makes the Schrödinger equation uncomputable for several electrons) because such a function does not connect to a physical many-electron charge distribution, only to a probability distribution of many-particle positions without direct physical interpretation. Instead we will be led to a system of one-electron Schrödinger equations with direct physical meaning.


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