Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

arXiv:1601.02409 · The Journal of Chemical Physics

Prospects for quantum computing with an array of ultracold polar paramagnetic molecules

Mallikarjun Karra, Ketan Sharma, Břetislav Friedrich, Sabre Kais, Dudley R. Herschbach

Published Mar 2, 2016• 81 citations
arXivHTMLPDF

Abstract

Arrays of trapped ultracold molecules represent a promising platform for implementing a universal quantum computer. DeMille [Phys. Rev. Lett. 88, 067901 (2002)] has detailed a prototype design based on Stark states of polar (1)Σ molecules as qubits. Herein, we consider an array of polar (2)Σ molecules which are, in addition, inherently paramagnetic and whose Hund's case (b) free-rotor pair-eigenstates are Bell states. We show that by subjecting the array to combinations of concurrent homogeneous and inhomogeneous electric and magnetic fields, the entanglement of the array's Stark and Zeeman states can be tuned and the qubit sites addressed. Two schemes for implementing an optically controlled CNOT gate are proposed and their feasibility discussed in the face of the broadening of spectral lines due to dipole-dipole coupling and the inhomogeneity of the electric and magnetic fields.

DOI
10.1063/1.4942928

Related papers

Quantum Computation with Trapped Polar Molecules

David P. DeMille

We propose a novel physical realization of a quantum computer. The qubits are electric dipole moments of ultracold diatomic molecules, oriented along or against an external electric field. Individual molecules are held in a 1D trap array, with an electric field gradient allowing spectroscopic addressing of each site. Bits are coupled via the electric dipole-dipole interaction. Using technologies similar to those already demonstrated, this design can plausibly lead to a quantum computer with greater, approximately > or = 10(4) qubits, which can perform approximately 10(5) CNOT gates in the anticipated decoherence time of approximately 5 s.

arXiv:quant-ph/0109083•Physical Review Letters•Jan 24, 2002•1,354 citations

Control, Readout, and Entanglement of Molecular Qubits

Lewis R. B. Picard

Ultracold polar molecules possess a manifold of long-lived molecular rotational states, which can be coherently controlled using microwave fields and entangled by the long-range dipole-dipole interactions between molecules. The ability to control these features at the individual molecule level provides a rich toolbox with which to engineer quantum simulations of exotic materials or build a molecular quantum computer. Until recently, this level of single molecule control has eluded researchers due to the challenges inherent in taming the complex internal structure of molecules. In this thesis, we demonstrate full control over the internal quantum states and coherent interactions of individual NaCs molecules in optical tweezers. This platform is based on coherent assembly of ultracold Na and Cs atoms trapped and cooled in separate arrays, before being magnetoassociated at a Feshbach resonance to form weakly-bound molecules. Using high-resolution spectroscopy of electronically excited molecular states, we identify an efficient two-photon pathway to the rovibrational ground state of NaCs that we use to prepare an array of ground state molecules in tweezers. We demonstrate a "magic ellipticity'' technique to eliminate differential light shifts between two molecular rotational states and achieve coherence times of up to 250(40) ms for a superposition of those states. We then show that we can rearrange molecules in an array to eliminate defects and perform single-shot readout of multiple rotational states using controlled molecule dissociation and imaging of constituent atoms at high magnetic field. Finally, we coherently control the dipole-dipole interactions between two molecules, producing a Bell state with a fidelity of 94(3) % and demonstrating a universal entangling iSWAP gate for qubits encoded in molecular hyperfine states.

•Jan 1, 2024•0 citations

Quantum engineering with ultracold polar molecules using trap-induced resonances

Sakthikumaran Ravichandran, Piotr Kulik, Krzysztof Jachymski

Polar molecules represent a promising platform for quantum simulation and computation protocols. Highly controllable arrays of optical tweezers are now accessible in experiments, allowing for unprecedented control of individual molecules. Motional dephasing is typically seen as an obstacle in quantum computing scenarios. Here, we instead consider using the trap structure as a resource for implementing efficient quantum gates. By numerically solving the two-body problem of dipoles trapped in separate tweezers, we identify trap-induced resonances that can serve as the mechanism for achieving state-dependent dynamics and can be further utilized for quantum sensing.

physics.atom-phCross-listedarXiv:2603.28270•Physica Scripta•Mar 31, 2026•0 citations

Controlling the dynamics of ultracold polar molecules in optical tweezers

Marta Sroczyńska, Anna Dawid, Michał Tomza +3 more

Abstract Ultracold molecules trapped in optical tweezers show great promise for the implementation of quantum technologies and precision measurements. We study a prototypical scenario where two interacting polar molecules placed in separate traps are controlled using an external electric field. This, for instance, enables a quantum computing scheme in which the rotational structure is used to encode the qubit states. We estimate the typical operation timescales needed for state engineering to be in the range of few microseconds. We further underline the important role of the spatial structure of the two-body states, with the potential for significant gate speedup employing trap-induced resonances.

arXiv:2110.05541•New Journal of Physics•Dec 15, 2021•13 citations

Scalable platform for qudit-based quantum computing using polar molecules

Soleh Kh. Muminov, Evgeniy O. Kiktenko, Anastasiia S. Nikolaeva +4 more

We propose a scalable qudit-based quantum processor using rotational states of polar molecules. Previously, molecular internal states were used to enlarge Hilbert space, whereas our approach uses optical tweezer arrays to achieve scalable architectures with exponential state-space growth without increasing qudit dimensionality d . Entangling gates are implemented by adiabatically bringing traps together to activate dipole-dipole interactions. We develop encoding schemes mapping single qubits into qudits with 2 ≤ d ≤ 5 and pairs of qubits into d = 4 , 5 qudits, enabling universal set of quantum gates. Additional levels in d = 3 and d = 5 qudits simplify multiqubit gate decompositions. We analyze experimental parameters for SrF and NaCs molecules. This approach provides a promising route to scalable quantum information processing with multilevel systems using existing experimental platforms.

arXiv:2508.10850•Physical Review Research•Mar 2, 2026•0 citations

Analysis of experimental feasibility of polar-molecule-based phase gates

Elena Kuznetsova, Robin Côté, K. Kirby +1 more

We analyze a recently proposed physical implementation of a quantum computer based on polar molecules with ``switchable'' dipoles, i.e., dipole moments that can be switched ``on'' and ``off''. Conditional dipole-dipole interaction is an efficient tool for realizing two-qubit quantum gates necessary to construct universal gates. A set of general requirements for a molecular system is presented, which would provide an optimal combination of quantum gate times, coherence times, number of operations, high gate accuracy, and experimental feasibility. We proceed with an analysis of a two-qubit phase gate realization based on switchable dipole-dipole interactions between polar molecules in an optical lattice architecture. We consider one of the schemes proposed in our previous work [Phys. Rev. A 74, 050301(R) (2006)], using specific molecules, such as CO and NF. We suggest suitable electronic states and transitions, and investigate requirements for the laser pulses driving them. Finally, we analyze possible sources of decoherence and list practical difficulties of the scheme.

Physical Review A•Jul 9, 2008•50 citations
Arrays of trapped ultracold molecules represent a promising platform for implementing a universal quantum computer. DeMille [Phys. Rev. Lett. 88, 067901 (2002)] has detailed a prototype design based on Stark states of polar (1)Σ molecules as qubits. Herein, we consider an array of polar (2)Σ molecules which are, in addition, inherently paramagnetic and whose Hund's case (b) free-rotor pair-eigenstates are Bell states. We show that by subjecting the array to combinations of concurrent homogeneous and inhomogeneous electric and magnetic fields, the entanglement of the array's Stark and Zeeman states can be tuned and the qubit sites addressed. Two schemes for implementing an optically controlled CNOT gate are proposed and their feasibility discussed in the face of the broadening of spectral lines due to dipole-dipole coupling and the inhomogeneity of the electric and magnetic fields.
We propose a novel physical realization of a quantum computer. The qubits are electric dipole moments of ultracold diatomic molecules, oriented along or against an external electric field. Individual molecules are held in a 1D trap array, with an electric field gradient allowing spectroscopic addressing of each site. Bits are coupled via the electric dipole-dipole interaction. Using technologies similar to those already demonstrated, this design can plausibly lead to a quantum computer with greater, approximately > or = 10(4) qubits, which can perform approximately 10(5) CNOT gates in the anticipated decoherence time of approximately 5 s.
Ultracold polar molecules possess a manifold of long-lived molecular rotational states, which can be coherently controlled using microwave fields and entangled by the long-range dipole-dipole interactions between molecules. The ability to control these features at the individual molecule level provides a rich toolbox with which to engineer quantum simulations of exotic materials or build a molecular quantum computer. Until recently, this level of single molecule control has eluded researchers due to the challenges inherent in taming the complex internal structure of molecules. In this thesis, we demonstrate full control over the internal quantum states and coherent interactions of individual NaCs molecules in optical tweezers. This platform is based on coherent assembly of ultracold Na and Cs atoms trapped and cooled in separate arrays, before being magnetoassociated at a Feshbach resonance to form weakly-bound molecules. Using high-resolution spectroscopy of electronically excited molecular states, we identify an efficient two-photon pathway to the rovibrational ground state of NaCs that we use to prepare an array of ground state molecules in tweezers. We demonstrate a "magic ellipticity'' technique to eliminate differential light shifts between two molecular rotational states and achieve coherence times of up to 250(40) ms for a superposition of those states. We then show that we can rearrange molecules in an array to eliminate defects and perform single-shot readout of multiple rotational states using controlled molecule dissociation and imaging of constituent atoms at high magnetic field. Finally, we coherently control the dipole-dipole interactions between two molecules, producing a Bell state with a fidelity of 94(3) % and demonstrating a universal entangling iSWAP gate for qubits encoded in molecular hyperfine states.
Polar molecules represent a promising platform for quantum simulation and computation protocols. Highly controllable arrays of optical tweezers are now accessible in experiments, allowing for unprecedented control of individual molecules. Motional dephasing is typically seen as an obstacle in quantum computing scenarios. Here, we instead consider using the trap structure as a resource for implementing efficient quantum gates. By numerically solving the two-body problem of dipoles trapped in separate tweezers, we identify trap-induced resonances that can serve as the mechanism for achieving state-dependent dynamics and can be further utilized for quantum sensing.
Abstract Ultracold molecules trapped in optical tweezers show great promise for the implementation of quantum technologies and precision measurements. We study a prototypical scenario where two interacting polar molecules placed in separate traps are controlled using an external electric field. This, for instance, enables a quantum computing scheme in which the rotational structure is used to encode the qubit states. We estimate the typical operation timescales needed for state engineering to be in the range of few microseconds. We further underline the important role of the spatial structure of the two-body states, with the potential for significant gate speedup employing trap-induced resonances.
We propose a scalable qudit-based quantum processor using rotational states of polar molecules. Previously, molecular internal states were used to enlarge Hilbert space, whereas our approach uses optical tweezer arrays to achieve scalable architectures with exponential state-space growth without increasing qudit dimensionality d . Entangling gates are implemented by adiabatically bringing traps together to activate dipole-dipole interactions. We develop encoding schemes mapping single qubits into qudits with 2 ≤ d ≤ 5 and pairs of qubits into d = 4 , 5 qudits, enabling universal set of quantum gates. Additional levels in d = 3 and d = 5 qudits simplify multiqubit gate decompositions. We analyze experimental parameters for SrF and NaCs molecules. This approach provides a promising route to scalable quantum information processing with multilevel systems using existing experimental platforms.
We analyze a recently proposed physical implementation of a quantum computer based on polar molecules with ``switchable'' dipoles, i.e., dipole moments that can be switched ``on'' and ``off''. Conditional dipole-dipole interaction is an efficient tool for realizing two-qubit quantum gates necessary to construct universal gates. A set of general requirements for a molecular system is presented, which would provide an optimal combination of quantum gate times, coherence times, number of operations, high gate accuracy, and experimental feasibility. We proceed with an analysis of a two-qubit phase gate realization based on switchable dipole-dipole interactions between polar molecules in an optical lattice architecture. We consider one of the schemes proposed in our previous work [Phys. Rev. A 74, 050301(R) (2006)], using specific molecules, such as CO and NF. We suggest suitable electronic states and transitions, and investigate requirements for the laser pulses driving them. Finally, we analyze possible sources of decoherence and list practical difficulties of the scheme.