RYDBERG PHYSICS

Rydberg Calculator

Quantum defect theory for alkali Rydberg states — effective quantum number, binding energy, orbital radius, radiative lifetime, and van der Waals blockade radius.

n*Quantum defect
C₆van der Waals coeff.
R_bBlockade radius
5 speciesRb · Cs · Li · Na · K
Rydberg State Selector
Select a state above to see Rydberg properties.
Effective quantum number
n* = n − δ₀ − δ₂/(n−δ₀)²
Binding energy
— cm⁻¹
Orbital radius ⟨r⟩
— nm
≈ n*² a₀ (mean radius, l=0)
Radiative lifetime
τ ≈ τ₀ × n*³

Quantum defect formula

In alkali atoms the core electrons shift the effective principal quantum number from n to n* = n − δ(n,l,j). The Rydberg–Ritz formula:

δ(n, l, j) = δ₀ + δ₂ / (n − δ₀)²

gives the binding energy E_b = R_y / n*² (in eV) with R_y = 13.6057 eV. Orbital radius scales as ⟨r⟩ ≈ n*² a₀ (mean value for s-wave; accurate to ~10%). Radiative lifetime: τ ∝ n*³ for low-l states, ∝ n*⁵ for high-l circular states.


Rydberg Blockade Calculator

Van der Waals blockade radius Rb for two atoms both driven to the Rydberg state. C₆ values are approximations scaled from published data — use ARC for precision calculations.

Blockade Parameters
Logarithmic scale: 0.01 – 100 MHz
💡 Typical experiment: Tweezer arrays use atom spacings of 3–10 μm with Rydberg Rabi frequencies of 0.1–10 MHz. For a 2-qubit gate you need r < Rb.
|C₆| approx
GHz · μm⁶
Blockade radius Rb
μm
Interaction at r
MHz

Van der Waals blockade

Two atoms in |n,l,j⟩ interact via U(r) = −C₆/r⁶ (van der Waals regime, r ≫ rLeRoy). When |U(r)| ≫ ℏΩ, double excitation |rr⟩ is energetically forbidden — the Rydberg blockade. The blockade radius is defined by |U(Rb)| = ℏΩ:

R_b = (|C₆| / ℏΩ)^(1/6)

C₆ scales as n*¹¹ — doubling n roughly multiplies Rb by 2¹¹/⁶ ≈ 3.6. S states have weaker (smaller C₆) blockade than P or D states due to Förster resonance structure. For Rydberg gates, P₃/₂ and D₅/₂ states are often preferred precisely because of their larger C₆.


Blockade radius Rb vs. principal quantum number n — Rb nS₁/₂
Shaded region: Rb for Ω/2π = 0.1 – 10 MHz. Dashed line: current Ω. Dot: selected n.

Quantum defects reference — selected species

Values from published literature (Li et al. 2003 for Rb; Goy et al. 1982 / Weber & Sansonetti 1987 for Cs; Lorenzen & Niemax 1983 for Li, Na, K). n* = n − δ₀ − δ₂/(n−δ₀)².

Species Series δ₀ δ₂ n*(n=50)

C₆ scaling and Förster resonances

For like-state pairs |nℓj, nℓj⟩, C₆ arises from second-order dipole-dipole coupling to nearly degenerate pair states |n'l', n''l''⟩. C₆ diverges near a Förster resonance (exact degeneracy between initial and intermediate pair states), shifting to a C₃/r³ interaction. For P₃/₂ states in Cs at n ≈ 43 a near-perfect Förster resonance gives anomalously large and controllable interactions — exploited in early blockade experiments by the Browaeys group (Gaëtan et al. 2009).

Blackbody radiation limit

At room temperature (T = 300 K, k_BT/h = 6.25 THz), Rydberg states with ℏω_n,n' < k_BT are strongly mixed by blackbody photons. Effective lifetime drops below the spontaneous emission limit for n > 30–40 at 300 K. Cryogenic environments (4 K, 77 K) extend T₁ by orders of magnitude. For n = 50 Rb at 300 K: τ_eff ~ 50 μs (vs ~100 μs spontaneous-only).

Rydberg gate fidelity estimate

A Rydberg CZ gate requires: (1) Ω t_gate = π (π-pulse to |r⟩), (2) blockade U ≫ ℏΩ, (3) gate time t_gate ≪ τ_Rydberg. Key fidelity-limiting errors:

$$\varepsilon_{\rm se} \approx \frac{\pi}{\Omega\,\tau_{\rm Ryd}} \quad \text{[spontaneous emission error]}$$ $$\varepsilon_{\rm blk} \approx \left(\frac{\hbar\Omega}{U(r)}\right)^2 = \left(\frac{r}{R_b}\right)^{12} \quad \text{[imperfect blockade error]}$$ Typical: $n=70$, $\Omega = 2\pi\times1$ MHz, $\tau \approx 400\,\mu$s $\Rightarrow \varepsilon_{\rm se} \sim 10^{-3}$
$r = 5\,\mu$m, $R_b = 10\,\mu$m $\Rightarrow \varepsilon_{\rm blk} \sim 10^{-4}$

Two-photon excitation

Direct UV single-photon excitation (e.g., 318 nm for Cs, ~297 nm for Rb) is possible but common experiments use two-photon excitation via an intermediate state (e.g., Rb: 780 nm (D2) + 480 nm → nS/nD; Cs: 852 nm + 509 nm → nP). The effective Rabi frequency is Ω_eff = Ω₁Ω₂ / (2Δ) where Δ is the single-photon detuning. Large Δ reduces photon scattering from the intermediate state.


References & Tools