We demonstrate that ultracold polyatomic symmetric top molecules, such as methyl fluoride, loaded into an optical lattice and subject to DC electric and microwave field dressing, can display topological order via a self-consistent analog of a proximity effect in the internal state space of the molecule. The non-trivial topology arises from pairwise transitions between internal states induced by dipole-dipole interactions and made resonant by the field dressing. Topological order is explicitly demonstrated by matrix product state simulations on 1D chains. Additionally, we show that in the limit of pinned molecules our description maps onto a long-range and anisotropic XYZ spin model, where Majorana fermions are zero-energy edge excitations in the case of nearest-neighbor couplings.
We demonstrate that ultracold symmetric top molecules loaded into an optical lattice can realize highly tunable and unconventional models of quantum magnetism, such as an XYZ Heisenberg spin model. We show that anisotropic dipole–dipole interactions between molecules can lead to effective spin–spin interactions which exchange spin and orbital angular momentum. This exchange produces effective spin models which do not conserve magnetization and feature tunable degrees of spatial and spin–coupling anisotropy. In addition to deriving pure spin models when molecules are pinned in a deep optical lattice, we show that models of itinerant magnetism are possible when molecules can tunnel through the lattice. Additionally, we demonstrate rich tunability of effective model parameters using only a single microwave frequency, in contrast to proposals with diatomic molecules, which often require many microwave frequencies. Our results are germane not only for experiments with polyatomic symmetric top molecules, such as methyl fluoride (CH 3 F), but also diatomic molecules with an effective symmetric top structure, such as the hydroxyl radical OH.
We show how to use polar molecules in an optical lattice to engineer quantum spin models with arbitrary spin $S\ensuremath{\ge}1/2$ and with interactions featuring a direction-dependent spin anisotropy. This is achieved by encoding the effective spin degrees of freedom in microwave-dressed rotational states of the molecules and by coupling the spins through dipolar interactions. We demonstrate how one of the experimentally most accessible anisotropies stabilizes symmetry protected topological phases in spin ladders. Using the numerically exact density matrix renormalization group method, we find that these interacting phases---previously studied only in the nearest-neighbor case---survive in the presence of long-range dipolar interactions. We also show how to use our approach to realize the bilinear-biquadratic spin-1 and the Kitaev honeycomb models. Experimental detection schemes and imperfections are discussed.
Abstract I analyze the emergence of Majorana zero modes (MZM) in a one dimensional ultracold fermionic system confined by an optical lattice inside a high-Q cavity. This forms a quantum optical lattice due to the cavity backaction, with emergent long range interactions controlled by the light pumped into the system and thus long range pairing. I investigate the possibility of formation and emergence of edge modes using exact diagonalization with self-consistent order parameters and singular value decomposition of the Hamiltonian in the Majorana representation. I analyze the spectral properties of the system, the mass gap and amplitude of the MZM with a unified framework. The interplay of cavity induced interactions and effective p -wave short range interactions controls the emergence of the signatures of MZM. I find that under certain conditions MZM distinctively emerge leading to superradiant topological phases of matter. These MZM have potential applications for quantum information as they are topologically protected analogous to the behavior of the Kitaev chain. The techniques employed lead to a scheme based on the Majorana representation and exact diagonalization with self consistent conditions using Hartree–Fock–Bogoliubov theory in real space for finite systems that can be applied to other fermionic and analog systems termed Light-Matter-Majorana. A promising landscape for the exploration of short range and long range topological order with superradiance is found.
We establish a general theoretical framework for realizing topological edge states in dimerized arrays of chiral dipolar molecules and demonstrate that molecular handedness provides a natural and tunable route to SSH-like topology in an interacting one-dimensional setting. Starting from an effective spin-
21 model generated by Stark-dressed chiral molecules, we introduce bond dimerization and show that the chirality-induced Dzyaloshinskii--Moriya interaction amplifies the effective hopping amplitudes and enlarges the bulk topological gap relative to an achiral chain of equivalent dipole strength. Using self-consistent mean-field theory with periodic- and open-boundary calculations, we map out the trivial, critical, and topological regimes through bulk spectra, complex-plane winding, and boundary-localized probability densities. A central result is that the two in-gap boundary modes carry \emph{opposite molecular chirality}: the left edge state localizes on a left-handed molecule and the right edge state on a right-handed molecule, a stereochemical labeling with no analogue in conventional SSH implementations. The two-leg ladder extension supports a richer four-band bulk structure and a rung-split edge sector whose robustness is characterized by a continuous sweep of the interchain coupling. All results are expressed in dimensionless units of the reference hopping scale
t0, making the framework directly applicable to any dipolar molecular platform -- from bialkali polar molecules at MHz coupling scales to future arrays of ultracold chiral polyatomic species. These findings establish dimerized chiral molecular arrays as a controllable and chirality-addressable platform for quasi-one-dimensional topological quantum matter.
We establish a correspondence between the electric dipole matrix elements of a polyatomic symmetric top molecule in a state with nonzero projection of the total angular momentum on the symmetry axis of the molecule and the magnetic dipole matrix elements of a magnetic dipole associated with an elemental spin
F. It is shown that this correspondence makes it possible to perform quantum simulation of the single-particle spectrum and the dipole-dipole interactions of magnetic dipoles in a static external magnetic field
B with symmetric top molecules subject to a static external electric field
EDC. We further show that no such correspondence exists for
1Σ molecules in static fields, such as the alkali metal dimers. The effective spin angular momentum of the simulated magnetic dipole corresponds to the rotational angular momentum of the symmetric top molecule, and so quantum simulation of arbitrarily large integer spins is possible. Further, taking the molecule CH
3F as an example, we show that the characteristic dipole-dipole interaction energies of the simulated magnetic dipole are a factor of 620, 600, and 310 larger than for the highly magnetic atoms Chromium, Erbium, and Dysprosium, respectively. We present several applications of our correspondence for many-body physics, including long-range and anisotropic spin models with arbitrary integer spin
S using symmetric top molecules in optical lattices, quantum simulation of molecular magnets, and spontaneous demagnetization of Bose-Einstein condensates due to dipole-dipole interactions. Our results are expected to be relevant as cold symmetric top molecules reach quantum degeneracy through Stark deceleration and opto-electrical cooling.
Engineering synthetic dimensions, where the physics of additional spatial dimensions is simulated within the internal states of a quantum system, allows the realisation of phenomena not otherwise accessible in experiments. Ultracold ground-state polar molecules are an ideal platform to encode synthetic dimensions, offering access to large Hilbert spaces of long-lived internal states associated with the rotational and hyperfine degrees of freedom, that can be coupled together with microwave fields to simulate tunnelling. Here, to benchmark the advantages of ultracold molecules, we encode a 1D synthetic lattice in the rotational states of ultracold RbCs molecules and use it to investigate the well-known Su-Schrieffer-Heeger (SSH) model, a minimal model displaying topological properties. To probe the system, we perform spectroscopy using an auxiliary rotational state and study the time dynamics after deterministic state preparation. We demonstrate long coherence times, typically ~500 times the lattice tunnelling period, even for a synthetic lattice using 8 rotational states. Observations of dynamics at long times with full site-resolved readout of the synthetic dimension allow us to test the effects of chiral and non-chiral perturbations on the topologically protected edge states. Our work lays the foundation for further quantum simulations using the rich internal structure of molecules, including dipolar string phases in interacting samples of molecules, and adiabatic state preparation of many-body Hamiltonians.