Introduction to Quantum States & Wavefunctions
In quantum mechanics, physical systems are described by a complex-valued mathematical entity called a wavefunction, typically denoted by the Greek letter .
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Time-dependent wave equation governing non-relativistic state evolution.
Statistical interpretation of wavefunction norm squared |Ψ|².
Energy operator derived from kinetic and potential operators.
Total probability across all space sums to 1.
The Schrödinger Equation
The time-development of a non-relativistic quantum state is governed by the time-dependent Schrödinger Equation:
Where:
- is the reduced Planck constant ().
- is the mass of the particle.
- is the potential energy function.
- is the Hamiltonian operator.
Step-by-Step State Evolution Workflow
Define the boundary conditions and potential energy barrier (e.g., Infinite Square Well or Harmonic Oscillator).
Separate spatial variables to find stationary energy eigenfunctions and eigenvalues .
Superpose energy eigenstates with phase factors .
Interactive Code Implementation
import numpy as np
def wave_packet(x, x0, sigma, k0):
return (1.0 / (np.pi**0.25 * np.sqrt(sigma))) * np.exp(-0.5 * ((x - x0)/sigma)**2 + 1j * k0 * x)Probability Density & Normalization
According to Max Born's statistical interpretation, the square of the magnitude of the wavefunction represents a probability density:
This leads to the normalization condition, asserting that the particle must exist somewhere in space:
Due to the hermiticity of the Hamiltonian operator , the norm remains constant in time.