Search for: All records

Precision measurements of molecules offer an unparalleled paradigm to probe physics beyond the standard model. The rich internal structure within these molecules makes them exquisite sensors for detecting fundamental symmetry violations, local position invariance, and dark matter. While trapping and control of diatomic and a few very simple polyatomic molecules have been experimentally demonstrated, leveraging the complex rovibrational structure of more general polyatomics demands the development of robust and efficient quantum control algorithms. In this study, we present reinforcement-learning quantum-logic spectroscopy (RL-QLS), a general, reinforcement-learning-designed quantum-logic approach to prepare molecular ions in single, pure quantum states. The reinforcement-learning agent optimizes the pulse sequence, each followed by a projective measurement, and probabilistically manipulates the collapse of the quantum system to a single state. The performance of the RL-QLS control algorithm is numerically demonstrated for the polyatomic molecule ${\mathrm{H}}_3{\mathrm{O}}^{+}$with 130 thermally populated eigenstates and degenerate transitions within inversion doublets, as well as for ${\mathrm{CaH}}^{+}$under the disturbance of environmental thermal radiation. We expect that the developed theoretical framework can be readily implemented for quantum control of polyatomic molecular ions with densely populated structures, thereby facilitating experimental tests of fundamental theories. 

Abstract The maximum amount of entanglement achievable under passive transformations by continuous-variable states is called the entanglement potential. Recent work has demonstrated that the entanglement potential is upper-bounded by a simple function of the squeezing of formation, and that certain classes of two-mode Gaussian states can indeed saturate this bound, though saturability in the general case remains an open problem. In this study, we introduce a larger class of states that we prove saturates the bound, and we conjecture that all two-mode Gaussian states can be passively transformed into this class, meaning that for all two-mode Gaussian states, entanglement potential is equivalent to squeezing of formation. We provide an explicit algorithm for the passive transformations and perform extensive numerical testing of our claim, which seeks to unite the resource theories of two characteristic quantum properties of continuous-variable systems. 

Abstract The collective mode spectrum of a symmetry-breaking state, such as a superconductor, provides crucial insight into the nature of the order parameter. In this work, we study two collective modes which are unique to unconventional superconductors that spontaneously break time reversal symmetry. We show that these modes are coherent and underdamped for a wide variety of time-reversal symmetry breaking superconducting states. By further demonstrating that these modes can be detected using a number of existing experimental techniques, we propose that our work can be leveraged as a form of “collective mode spectroscopy” that drastically expands the number of experimental probes capable of detecting time-reversal symmetry breaking in unconventional superconductors. 

Abstract The exploration of 1D magnetism, frequently portrayed as spin chains, constitutes an actively pursued research field that illuminates fundamental principles in many‐body problems and applications in magnonics and spintronics. The inherent reduction in dimensionality often leads to robust spin fluctuations, impacting magnetic ordering and resulting in novel magnetic phenomena. Here, structural, magnetic, and optical properties of highly anisotropic 2D van der Waals antiferromagnets that uniquely host spin chains are explored. First‐principle calculations reveal that the weakest interaction is interchain, leading to essentially 1D magnetic behavior in each layer. With the additional degree of freedom arising from its anisotropic structure, the structure is engineered by alloying, varying the 1D spin chain lengths using electron beam irradiation, or twisting for localized patterning, and spin textures are calculated, predicting robust stability of the antiferromagnetic ordering. Comparing with other spin chain magnets, these materials are anticipated to bring fresh perspectives on harvesting low‐dimensional magnetism.