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beginner · Physics · The Schrödinger Equation (Intro)

Phase Evolution e^{-iEt/ħ}

When a quantum system is in a stationary state — an energy eigenstate of its Hamiltonian — the time-dependent Schrödinger equation tells us exactly how the wave function evolves. If ψn(x)\psi_n(x) is a spatial eigenfunction with energy eigenvalue EnE_n, the full time-dependent solution is

Ψn(x,t)=ψn(x)eiEnt/.\Psi_n(x, t) = \psi_n(x)\, e^{-iE_n t/\hbar}.

The exponential eiEnt/e^{-iE_n t/\hbar} is the phase factor, and it deserves close attention.

The phase factor is a unit complex number

Because EnE_n, tt, and \hbar are all real, the exponent iEnt/-iE_n t/\hbar is purely imaginary. A complex exponential of the form eiθe^{i\theta} (with θR\theta \in \mathbb{R}) lies on the unit circle in the complex plane: its real part is cosθ\cos\theta and its imaginary part is sinθ\sin\theta, so

eiθ=cos2θ+sin2θ=1.\left|e^{i\theta}\right| = \sqrt{\cos^2\theta + \sin^2\theta} = 1.

Setting θ=Ent/\theta = -E_n t/\hbar confirms that eiEnt/=1|e^{-iE_n t/\hbar}| = 1 for every energy, every time, and every value of \hbar.

Why the magnitude of the wave function does not change

Because the phase factor has unit magnitude, multiplying ψn(x)\psi_n(x) by it leaves the spatial probability density unchanged:

Ψn(x,t)2=ψn(x)2eiEnt/2=ψn(x)2.|\Psi_n(x,t)|^2 = \left|\psi_n(x)\right|^2 \left|e^{-iE_n t/\hbar}\right|^2 = |\psi_n(x)|^2.

This is precisely what earns these solutions the name stationary states: the probability distribution Ψn(x,t)2|\Psi_n(x,t)|^2 is independent of time. The phase rotates continuously at angular frequency ωn=En/\omega_n = E_n/\hbar, but nothing measurable oscillates — at least not until two stationary states are superposed.

The phase rotates at angular frequency E/ħ

Writing the phase factor in polar form makes the rotation explicit:

eiEnt/=cos ⁣(Ent)isin ⁣(Ent).e^{-iE_n t/\hbar} = \cos\!\left(\frac{E_n t}{\hbar}\right) - i\sin\!\left(\frac{E_n t}{\hbar}\right).

The argument decreases linearly in time, so the phase vector sweeps clockwise around the unit circle at a rate ωn=En/\omega_n = E_n/\hbar radians per second. A higher energy eigenstate rotates faster. In natural units where 6.582×1016eVs\hbar \approx 6.582 \times 10^{-16}\,\text{eV}\cdot\text{s}, a state with E=1eVE = 1\,\text{eV} completes a full 2π2\pi rotation in a period

T=2πE=2π×6.582×1016eVs1eV4.13×1015s,T = \frac{2\pi\hbar}{E} = \frac{2\pi \times 6.582 \times 10^{-16}\,\text{eV}\cdot\text{s}}{1\,\text{eV}} \approx 4.13 \times 10^{-15}\,\text{s},

which is on the scale of a few femtoseconds — an astonishingly fast oscillation that is physically meaningful when two states of different energy interfere.

Try it

This exercise focuses on the key insight above. Your code should return a number.

Run your code to see the quantum state.

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