ΔxΔp ≥ h/4π,where Δx is the uncertainty of a particle's position, Δp is the uncertainty of a particle's momentum, and h is the Planck constant. This inequality essentially states that if you attempt to accurately determine a particle's momentum, it won't be where you first found it. There's an alternate formulation of this principle,
ΔEΔt ≥ h, approximately,where ΔE is the uncertainty of an energy measurement and Δt is the uncertainty in a time measurement. The interpretation of this inequality, as perceived by no less than Niels Bohr, is that a short-lived state will not have a definite energy. Since the energy is proportional to the frequency, ν, by the equation, E = hν, the complementary interpretation is that only long-lived states will have a definite frequency. What this means in the real world is that transitions from excited states with a long lifetime have a very narrow linewidth. This second formulation of the uncertainty principle is important when you're building atomic clocks. Atomic clocks function by measuring the frequency of an atomic transition at microwave or optical frequencies. The most common such clocks use rubidium. There's a hyperfine transition in rubidium that occurs at 6,834,682,610.904324 Hz.[1]
The hyperfine splitting of the 5S1/2 energy level in Rubidium-87. (Drawing by author, rendered using Inkscape). |
The ion trap used in the Physikalisch-Technische Bundesanstalt experiments. The 467 nm laser radiation is a pretty blue color. (Physikalisch-Technische Bundesanstalt photograph). |