Schrodinger’s Equation
The Schrödinger equation is the fundamental governing equation of non-relativistic quantum mechanics, describing how the quantum state of a physical system evolves over time.
1. Core Formulations
Time-Dependent Schrödinger Equation
The TDSE describes the dynamic evolution of a wave function $\psi(\mathbf{r}, t)$ in a state space:
Where $\hat{H}$ is the Hamiltonian operator, representing the total energy of the system. For a single particle of mass $m$ moving in a potential $V(\mathbf{r}, t)$, the explicit coordinate-space Hamiltonian is:
Time-Independent Schrödinger Equation
When the potential $V(\mathbf{r})$ is stationary (independent of time), we can look for separable solutions of the form $\Psi(\mathbf{r}, t) = \psi(\mathbf{r})\phi(t)$. This separation of variables reduces the problem to an eigenvalue problem of the form:
Where $E$ represents the definite energy eigenvalues of the stationary states. The temporal component simply evolves as a phase factor: $\phi(t) = e^{-iEt/\hbar}$.
2. Properties of Solutions
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Linearity & Superposition: If $\psi_1$ and $\psi_2$ are solutions to the TDSE, then any linear combination $c_1\psi_1 + c_2\psi_2$ is also a solution.
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Normalization: The total probability of finding the particle somewhere in space must equal $1$: $$\int_{-\infty}^{\infty} |\psi(x,t)|^2 dx = 1$$
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Orthogonality: Stationary states belonging to distinct energy eigenvalues are orthogonal: $$\int_{-\infty}^{\infty} \psi_m^*(x) \psi_n(x) dx = \delta_{mn}$$
3. Particular Solutions (1D Systems)
The Free Particle
For a particle experiencing zero potential everywhere, the hamiltonian simplifies to:
Since $[\hat{H}, \hat{p}] = 0$, we can choose the eigenstate of the hamiltonian to be those of the impulse operator, which acts as:
$$-\frac{\hbar^2}{2m} \frac{d^2\psi}{dx^2} = E \psi$$
- General Solution: $$\psi(x) = A e^{ikx} + B e^{-ikx}$$
Where the wavenumber $k$ is defined by:
$$k^2 = \frac{2mE}{\hbar^2}$$
- Physical Meaning: Represents a superposition of forward- and backward-propagating plane waves with continuous energy spectra ($E \ge 0$). Note that these idealized states cannot be normalized across infinite space without forming wave packets.
Infinite Potential Well
Finite Potential Step
Finite Potential Barrier
A particle confined to a 1D box of length $L$, where: $$V(x) = \begin{cases} 0 & 0 < x < L \\ \infty & \text{otherwise} \end{cases}$$
Applying boundary conditions ($\psi(0) = \psi(L) = 0$) yields quantized energy levels and strictly bounded wave functions:
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Normalized Eigenfunctions: $$\psi_n(x) = \sqrt{\frac{2}{L}} \sin\left(\frac{n\pi x}{L}\right), \quad n = 1, 2, 3, \dots$$
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Energy Quantization: $$E_n = \frac{n^2 \pi^2 \hbar^2}{2mL^2}$$
Case C: Quantum Harmonic Oscillator
A particle subject to a parabolic restoring potential, modeling smooth localized fluctuations: $$V(x) = \frac{1}{2}m\omega^2 x^2$$
Solving this requires transforming the TISE into Hermite’s differential equation.
- Energy Quantization: $$E_n = \hbar\omega\left(n + \frac{1}{2}\right), \quad n = 0, 1, 2, \dots$$
Note: The ground state ($n=0$) possesses a non-zero minimum energy $E_0 = \frac{1}{2}\hbar\omega$, known as the zero-point energy, a direct consequence of the uncertainty principle.
- Eigenfunctions: $$\psi_n(x) = \left( \frac{m\omega}{\pi \hbar} \right)^{1/4} \frac{1}{\sqrt{2^n n!}} H_n(\xi) e^{-\xi^2 / 2}$$
Where $\xi = \sqrt{\frac{m\omega}{\hbar}} x$ and $H_n(\xi)$ are the physicist’s Hermite polynomials.