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A chirped Gaussian wave packet adds a quadratic quantum phase to the zero-mean Gaussian wave packet already evaluated above. Here $\sigma >0$ and $\kappa$ is a real dimensionless parameter. Its probability density function $|{\psi }_{\sigma ,\kappa }(x){|}^2$ is unchanged for every $\kappa$, so $⟨x⟩=0$ and $(\Delta x{)}^2={\sigma }^2$. Nevertheless, applying the momentum operator givesThe sign of the quantum covariance follows directly, without assigning a classical trajectory to the wavefunction:Here $r$ is a normalized symmetrized quantum covariance, analogous to a correlation coefficient. Positive $\kappa$ gives positive $C_{xp}$, and reversing $\kappa$ reverses $C_{xp}$ while leaving both variances unchanged. In the negative-exponent Fourier transform convention used above, the momentum density isConsequently the quantum uncertainty product and the covariance matrix determinant tell different stories:Every member of this pure state family saturates the Robertson-Schrödinger uncertainty relation. Only $\kappa =0$ saturates the Heisenberg uncertainty relation for this fixed pair of position and momentum axes. Thus being a Gaussian wave packet alone does not imply a minimum $\Delta x\Delta p$.

For a concrete comparison, choose a reference length $L$, put $X=x/L$, $P=pL/\hslash$, and set $\sigma =L$. The choices $\kappa =0,+2,-2$ all have $(\Delta X{)}^2=1$, but give $(\Delta P{)}^2=1/4,5/4,5/4$ and $C_{XP}=0,+1,-1$, respectively. The two nonzero cases have $r=\pm 2/\sqrt{5}$ and product $\sqrt{5}/2$; all three covariance matrices have determinant $1/4$.

The phase space curves in the figure satisfy $z^T{\Sigma }^{-1}z=1$ in the dimensionless coordinates, where $z=(X,P{)}^T$. They display second moments, not observed simultaneous position and momentum pairs. Their common area is $\pi \sqrt{\det \Sigma }=\pi /2$, although their coordinate projections differ.

This distinction is useful for predicting focusing. Under free particle evolution with mass $m$, $x(t)=x(0)+tp(0)/m$, soA negative chirp initially narrows the position distribution; positive chirp initially broadens it. For $\kappa <0$, the minimum occurs at $t_{\ast }=-2m{\sigma }^2\kappa /[\hslash (1+{\kappa }^2)]>0$ and has variance ${\sigma }^2/(1+{\kappa }^2)$. At that time the quantum covariance vanishes, and the unchanged momentum spread gives $\Delta x(t_{\ast })\Delta p=\hslash /2$. The extra initial product was a usable position-momentum correlation, not extra measurement backaction.

A localized quantum particle is described by a wave packet: a coherent quantum superposition of momentum components, rather than a single delocalized plane wave. The Born rule assigns the position probability density $|\psi (x,t){|}^2$. A useful normalized initial Gaussian wave packet isIts mean position and momentum are $x_0$ and $p_0$, and its standard deviations satisfy ${\sigma }_x(0)={\sigma }_0$, ${\sigma }_p=\hslash /(2{\sigma }_0)$. This unchirped initial state saturates the Heisenberg uncertainty relation.

For a free particle, the momentum-space Schrödinger equation multiplies each amplitude by $e^{-i{p}^{2}t/(2m\hslash )}$. The inverse Fourier transform is a Gaussian integral, giving the free Gaussian wave packet evolutionOne way to obtain this expression explicitly is to write the initial momentum amplitude as proportional to $\exp [-{\sigma }_0^2(p-p_0{)}^2/{\hslash }^2-ip{x}_0/\hslash ]$, multiply by the free evolution phase and complete the square in $p$. Taking the modulus squared removes the position-dependent phase and leavesThe expectation value follows uniform classical motion while the density spreads. A narrower initial packet needs a wider momentum distribution and therefore spreads more rapidly. At long times its width grows linearly with $|t|$; its variance grows quadratically, unlike the linear variance growth of ordinary diffusion. The probability continuity equation preserves total probability despite the decreasing peak height. The mean momentum and the mean energy $(p_0^2+{\sigma }_p^2)/(2m)$ remain constant, since the momentum populations do not change.

The same result has a wave interpretation. For a free nonrelativistic particle $\omega (k)=\hslash k^2/(2m)$, so the group velocity is $d\omega /dk=\hslash k/m$, equal to $p_0/m$ at the packet center. The curvature $d^2\omega /d{k}^2=\hslash /m$ makes different momentum components travel with different group velocities, producing dispersion. The phase velocity is $\omega /k=\hslash k/(2m)$ for this energy convention and does not describe the motion of the envelope. The evolving quadratic spatial phase is essential to the spreading; a density snapshot alone does not specify the full quantum state.

A freely spreading Gaussian wave packet remains a pure Gaussian state but develops position-momentum correlations. Its symmetrized covariance is $C_{xp}=⟨\{x-⟨x⟩,p-⟨p⟩\}⟩/2=t{\sigma }_p^2/m$. ConsequentlyEquality in the Robertson-Schrödinger uncertainty relation survives at every time, whereas the simpler product ${\sigma }_x{\sigma }_p$ equals $\hslash /2$ only initially. A chirped Gaussian wave packet can already have $C_{xp}(0)\ne 0$. More generally, $x(t)=x(0)+p(0)t/m$ gives ${\sigma }_x(t{)}^2={\sigma }_x(0{)}^2+2t{C}_{xp}(0)/m+t^2{\sigma }_p(0{)}^2/m^2$. A sufficiently negative initial covariance permits initial contraction before subsequent spreading.

A potential energy changes this behavior. A quadratic potential preserves the Gaussian form because the evolution of position and momentum is linear. For a quantum harmonic oscillator, the Gaussian covariance in a harmonic potential isA coherent state has ${\sigma }_x^2=\hslash /(2m\omega )$, ${\sigma }_p^2=m\hslash \omega /2$ and zero centered covariance. Its width is constant, and its center follows $x_c(t)=x_0\cos \omega t+p_0\sin \omega t/(m\omega )$. In oscillator notation its coherent state label rotates as $\alpha (t)=\alpha (0)e^{-i\omega t}$, apart from the common ground-energy phase of the state vector. A squeezed coherent state generally has a width that breathes at $2\omega$. Thus being Gaussian does not imply either free spreading or constant width; the Hamiltonian operator and initial covariance determine the result.

For a general nonquadratic potential, different parts of the packet experience different nonlinear forces, and an initially Gaussian profile need not remain Gaussian. Ehrenfest theorem gives the exact relations $d⟨x⟩/dt=⟨p⟩/m$ and $d⟨p⟩/dt=-⟨V^{\prime }(x)⟩$. Replacing the last mean by $-V^{\prime }(⟨x⟩)$ is exact for a quadratic potential and approximate for a packet narrow compared with the scale on which the force varies. This connects packet motion to the correspondence principle without treating a quantum state as a definite classical path. Scattering can split a packet into reflected and transmitted components, while confinement can produce oscillations and interference between discrete energy eigenstates. Their relative phases evolve even when their populations remain constant. Localization, spreading and coherent motion all follow from the same linear unitary time evolution.