Also known as STIRAP · RAP · rapid adiabatic passage · stimulated Raman adiabatic passage · Landau-Zener
Adiabatic passage transfers population between quantum states by changing the Hamiltonian slowly, so that
the system follows an instantaneous eigenstate from the initial to the target state. Its great strength is
robustness. The result does not depend on the precise pulse area, timing or amplitude — only on the change being
slow enough and on the eigenstate connecting the right endpoints. Rapid adiabatic passage in two-level systems and
stimulated Raman adiabatic passage (STIRAP) in three-level systems are workhorses of atomic, molecular and
magnetic-resonance physics, and of quantum technologies.
The adiabatic theorem
If \(H(t)\) changes slowly compared with the energy gap separating an eigenstate from the rest of the spectrum, a system
prepared in that eigenstate remains in it [1, 2]. Adiabatic passage chooses
\(H(t)\) so that the relevant eigenstate is the initial state at the start and the target state at the end.
Rapid adiabatic passage (two levels)
Sweep the detuning of a drive through resonance,
\(H(t) = \tfrac{\hbar}{2}\big(\Delta(t)\,\sigma_z + \Omega(t)\,\sigma_x\big)\), from large negative to large positive
\(\Delta\). The instantaneous eigenstates rotate from \(|0\rangle\) to \(|1\rangle\), so a slow sweep inverts the
population. The Landau–Zener formula quantifies “slow” [3]. For a linear sweep \(\Delta = \alpha t\)
with constant coupling \(\Omega\), the probability of a diabatic transition (failure) is
exponentially small for slow sweeps. In NMR and MRI, frequency-swept adiabatic pulses invert spins uniformly over large
bandwidths, despite inhomogeneous radio-frequency fields [4]; see Spins — NMR, ESR & colour centres.
STIRAP (three levels)
To transfer population from \(|1\rangle\) to \(|3\rangle\) via a lossy intermediate state \(|2\rangle\), use a pump field
\(\Omega_P\) on \(1\leftrightarrow2\) and a Stokes field \(\Omega_S\) on \(2\leftrightarrow3\). On two-photon resonance the
Hamiltonian has a dark state
with no component on \(|2\rangle\). Applying the Stokes pulse before the pump — the “counterintuitive” order — rotates
\(\theta\) from \(0\) to \(\pi/2\), and the population moves from \(|1\rangle\) to \(|3\rangle\) without ever occupying the
lossy intermediate level [5]. The transfer is robust provided the pulses are adiabatic, typically
requiring a pulse area well above \(\pi\) (a common rule of thumb is \(\Omega_{\rm rms}T \gtrsim 10\)).
STIRAP is used for molecules, atoms, ions, solid-state spins and superconducting circuits — for example across the
three lowest levels of a transmon [6] — and has many extensions to multi-level systems
[7, 8, 9].
Adiabatic quantum computation
In adiabatic quantum computing, the ground state of a simple Hamiltonian is slowly deformed into the ground state of a
problem Hamiltonian that encodes the answer [10]. The run time is set by the minimum gap. Adapting the
speed locally to the gap, rather than sweeping at a constant rate, recovers the quadratic Grover speed-up for
unstructured search [11]. See Variational algorithms & QAOA as control.
Making it faster
The weakness of adiabatic passage is its duration, which competes with decoherence. Ways to speed it up:
Shortcuts to adiabaticity add counterdiabatic corrections or use invariants to
reach the adiabatic result in finite time;
dressed-state schemes harness non-adiabatic transitions with corrections that require no extra couplings,
while minimizing population in the intermediate level of STIRAP [12];
optimal control shapes the pulses for a given duration and error budget, often starting from an adiabatic
protocol. Robustness can be kept by optimizing over parameter ensembles; see Robust & ensemble optimal control.
Strengths and limitations
Strengths
Insensitive to pulse area, amplitude and exact timing; broadband.
STIRAP avoids populating lossy intermediate states.
Limitations
Slow: needs large pulse areas and long durations.
Sensitive to two-photon detuning (STIRAP) and to decoherence during the long passage.
Phases of the final state are less robust than populations, which matters for gates.
Key papers
U. Gaubatz, P. Rudecki, S. Schiemann and K. BergmannPopulation transfer between molecular vibrational levels by stimulated Raman scattering with partially overlapping laser fields. A new concept and experimental resultsThe Journal of Chemical Physics92, 5363-5376 (1990)doi
Introduces STIRAP — population transfer through a lossy intermediate level with partially overlapping, counterintuitively ordered pulses.
K. Bergmann, H. Theuer and B. W. ShoreCoherent population transfer among quantum states of atoms and moleculesRev. Mod. Phys.70, 1003-1025 (1998)doi
The classic review of coherent population transfer by adiabatic passage in atoms and molecules.
Nikolay V. Vitanov, Andon A. Rangelov, Bruce W. Shore and Klaas BergmannStimulated Raman adiabatic passage in physics, chemistry, and beyondRev. Mod. Phys.89, 015006 (2017)doi
A comprehensive review of STIRAP and its extensions across physics, chemistry and quantum technology.
Michael Garwood and Lance DelaBarreThe Return of the Frequency Sweep: Designing Adiabatic Pulses for Contemporary NMRJournal of Magnetic Resonance153, 155-177 (2001)doi
Adiabatic, frequency-swept pulses in magnetic resonance — broadband and insensitive to field inhomogeneity.
Tameem Albash and Daniel A. LidarAdiabatic quantum computationRev. Mod. Phys.90, 015002 (2018)doi
Adiabatic quantum computation — the adiabatic theorem as a model of computation.
References
M. Born and V. FockBeweis des AdiabatensatzesZ. Physik51, 165-180 (1928)doi
Tosio KatoOn the Adiabatic Theorem of Quantum MechanicsJ. Phys. Soc. Jpn.5, 435-439 (1950)doi
Clarence ZenerNon-adiabatic crossing of energy levelsProceedings of the Royal Society of London. Series A, Containing Papers of a Mathematical and Physical Character137, 696-702 (1932)doi
Michael Garwood and Lance DelaBarreThe Return of the Frequency Sweep: Designing Adiabatic Pulses for Contemporary NMRJournal of Magnetic Resonance153, 155-177 (2001)doi
U. Gaubatz, P. Rudecki, S. Schiemann and K. BergmannPopulation transfer between molecular vibrational levels by stimulated Raman scattering with partially overlapping laser fields. A new concept and experimental resultsThe Journal of Chemical Physics92, 5363-5376 (1990)doi
K. S. Kumar, A. Vepsäläinen, S. Danilin and G. S. ParaoanuStimulated Raman adiabatic passage in a three-level superconducting circuitNat Commun7, 10628 (2016)doi
K. Bergmann, H. Theuer and B. W. ShoreCoherent population transfer among quantum states of atoms and moleculesRev. Mod. Phys.70, 1003-1025 (1998)doi
Nikolay V Vitanov, Thomas Halfmann, Bruce W Shore and Klaas BergmannLASER-INDUCED POPULATION TRANSFER BY ADIABATIC PASSAGE TECHNIQUESAnnu. Rev. Phys. Chem.52, 763-809 (2001)doi
Nikolay V. Vitanov, Andon A. Rangelov, Bruce W. Shore and Klaas BergmannStimulated Raman adiabatic passage in physics, chemistry, and beyondRev. Mod. Phys.89, 015006 (2017)doi
Tameem Albash and Daniel A. LidarAdiabatic quantum computationRev. Mod. Phys.90, 015002 (2018)doi
Jérémie Roland and Nicolas J. CerfQuantum search by local adiabatic evolutionPhys. Rev. A65, 042308 (2002)doi
Alexandre Baksic, Hugo Ribeiro and Aashish A. ClerkSpeeding up Adiabatic Quantum State Transfer by Using Dressed StatesPhys. Rev. Lett.116, 230503 (2016)doi
In molecules, electronic coherence typically decays within a few hundred femtoseconds, a timescale usually attributed to the environment. We show that it is set to a large extent by which coherences are excited: the molecule can host coherences that the bath barely sees, and optimal control can find and exploit them. Using gradient-based optimal control (GRAPE) with Redfield dynamics, we maximize the total vibronic coherence between the electronic ground and an optically bright electronic excited state in a three-state model with nonadiabatic features, in two regimes of low and high nonadiabatic mixing and for different system-bath coupling strengths. The Liouvillian spectrum reveals, in both regimes, a well-separated coherence mode with substantial ground-bright character that decays on a picosecond timescale. This mode is protected by mixing with the dark state, which brings the geometry of the optically accessible excited state close to that of the ground state and thus weakens its coupling to the bath. Without prior information, GRAPE finds this mode and keeps the photoexcited wave packet near the Franck-Condon region. At equal fluence, it increases the coherence at 800 fs by more than two orders of magnitude over a Gaussian pulse at the weakest coupling, and by many more at stronger coupling. The Liouvillian predicts the bath dependence of the long-lived coherence to within 1\%, and a Gaussian pulse tuned to the mode frequency comes within 10\% of the best pulse found. Beyond two-level and spin systems, our study puts forward the vibronic structure of molecules as a route to protected coherence subspaces, identifying a dark-state protection mechanism and a design criterion based on molecular parameters. These results lay the groundwork for our goal of using vibronic molecular systems as a resource for long-lived, controllable coherences in molecular quantum information science.
Control of molecular angular momentum orientation enables state-resolved studies of molecular interactions and provides a basis for quantum information processing. Here we propose all-optical Autler-Townes state-selective adiabatic passage (ASAP) to prepare molecules in a single $|J,M\rangle$ sublevel. An Autler-Townes branch created by a strong coupling field is selectively populated and adiabatically mapped onto the target vibrational state. We resolve detuning-dependent rovibrational Autler-Townes splitting in $^{13}$CO$_2$, establishing the spectroscopic basis for the selective excitation of the target dressed branch. The density-matrix model calibrated by these spectra predicts transfer approaching 90\%. The scheme can exploit millisecond vibrational radiative lifetimes within the electronic ground state and extend to polar and nonpolar molecules with infrared-active vibrational modes.
The stimulated Raman shortcut-to-adiabatic passage (STIRSAP) technique has been demonstrated to accelerate adiabatic population transfer processes. Traditionally applied to three-level atomic systems, this method enables rapid and efficient population transfer in a short interaction time. In this work, we extend this approach to a four-level N -type system driven by three laser fields. Under the three-photon phase matching condition, the first-order Doppler effect can be completely eliminated, making this configuration more suitable for applications in frequency metrology and quantum information processing. By adiabatically eliminating the intermediate state, the four-level system is effectively reduced to a two-level model, enabling the application of counterdiabatic driving without requiring additional couplings. This approach allows for fast and efficient population transfer between metastable states. We analyze the influence of laser intensity peaks and detuning, and we show that the transfer time is significantly shorter than that achieved with the STIRAP technique. Moreover, we also show 1 that an optimal coupling strength between the ground and metastable states further minimizes the operation time.
We investigate collective chirped stimulated Raman adiabatic passage (STIRAP) in a pair of identical three-level atoms using a symmetric six-state model. Numerical simulations reveal a pronounced oscillatory dependence of the population transfer to the doubly excited Rydberg state on the peak Rabi frequency, indicating dynamics beyond the conventional single-dark-state description of STIRAP. To identify the underlying mechanism, we develop a dressed-manifold description based on gauge-invariant projections onto nearly degenerate instantaneous dressed manifolds. The analysis demonstrates that the wavefunction remains predominantly confined to a two-dimensional dark manifold while becoming transiently coupled to a neighboring bright manifold during the pulse-overlap interval. We further show that in the dressed-manifold representation, the Rydberg-Rydberg interaction modifies the collective resonance structure while preserving the dark-bright manifold dynamics responsible for the oscillatory transfer; an appropriately chosen frequency chirp compensates the interaction-induced detuning and restores efficient population transfer. This dressed-manifold picture provides a consistent interpretation of oscillatory collective transfer and establishes a framework for controlling adiabatic dynamics in interacting multilevel systems by linearly chirped STIRAP, opening a route toward manifold-based control of Rydberg-mediated quantum gates, correlated-state preparation, and other coherent operations in interacting atomic systems.
Nitrogen-vacancy (NV) centers have emerged as a highly sensitive platform for spatially resolved temperature measurements. When the $\lvert0\rangle\to\lvert+1\rangle$ and $\lvert0\rangle\to\lvert-1\rangle$ transitions are nearly degenerate and the Rabi frequency is comparable to the transition splitting, the spin dynamics encountered during pulsed protocols for temperature measurement can significantly alter the intended accumulation of temperature-dependent phase. We investigate these triplet ($\lvert0\rangle$, $\lvert\pm1\rangle$) spin dynamics and their effect on pulsed thermometry protocols under these conditions. We find that the conventional thermal-echo timing produces negligible temperature-sensitive signal amplitudes at the common-mode detuning. However, we find that the nominal spin-echo timing produces resolvable oscillations at the common-mode detuning, leading to a strong temperature-sensitive carrier signal. This departure from the expected protocol behavior is qualitatively captured by an ensemble model of the triplet dynamics, which supports significant dark-state leakage as a plausible mechanism for the temperature-sensitive response. This mixing-enabled thermal echo uses a four-phase quadrature readout that resolves the signed oscillation frequency and is validated using independent sweeps of the microwave carrier frequency and fluid temperature. We further assess the ability of a four-refocusing-pulse (LDD4B) low-field dynamical-decoupling sequence to extend the NV coherence and find that while the echo retains a sensitivity to common-mode detuning, the effective phase-accumulation interval corresponds to approximately half the total evolution time. These findings could support the use of pulsed NV thermometry in biological or mobile applications where applying magnetic bias fields is impractical and microwave power may be limited.