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Akhil Ayyadevara

Publications and source records attributed to Akhil Ayyadevara.

3 recordsLinked to original sources

Endcap-Type Paul Trap for Precision Spectroscopy and Studies of Controlled Interactions

We present the design and fabrication of an endcap-type Paul trap. The trap is designed for studies with Ca$^{+}$ and Yb$^{+}$. The design, fabrication process, and characterization are presented in detail with a focus on trapping a single compensated ion at the rf node. A custom-built imaging system of $NA = 0.14$ and magnification $\approx 22 \times$ performs close to diffraction-limit and resolves multi-ion clusters. Controlled ion loading and characterization of the trap are performed using $^{40}$Ca$^{+}$. The experimentally determined quadrupole coefficient of the trap is $\approx 0.3$, which is very close to the design value. The relative frequency shift along the spectroscopy beam due to excess micromotion (EMM) is at the level of $3.5\times 10^{-18}$ for $^{40}$Ca$^{+}$. Applications of this trap encompass single-ion-based optical frequency standards, tests of fundamental physics, the study of mesoscopic Coulomb clusters, and the controlled interaction of a single ion with co-trapped atoms.

physics.atom-ph

Symmetry-controlled thermal activation in pyramidal Coulomb clusters: Testing Kramers-Langer theory

Laser-cooled ions confined in electromagnetic traps provide a unique, tunable mesoscopic system where the interplay of the trapping potential, nonlinear Coulomb interactions, and laser-ion scattering generates rich, collective dynamics. In this work, we engineer thermally activated switching between two oppositely oriented, square-pyramidal configurations of five laser-cooled ions in a Paul trap. For identical ions ($^{40}\mathrm{Ca}^{+}$), the inversions proceed via a \textit{Berry pseudo-rotation} mechanism with a low activation barrier, enabled by the permutation symmetry, in contrast to the \textit{umbrella inversion} observed in ammonia. The experimentally measured inversion rates, spanning two orders of magnitude, are accurately captured by the multidimensional Kramers-Langer theory, enabling thermometry of the Doppler-cooled ion cluster at $1.8 \pm 0.1$ mK. By substituting the apex ion with a heavier isotope ($^{44}\mathrm{Ca}^{+}$), we break the permutation symmetry and observe a suppression of thermally activated inversions. Numerical analysis reveals that this symmetry breaking closes the low-barrier channel, forcing the system to invert through a high-barrier \textit{turnstile rotation}. Thus, we demonstrate a structural analogue of molecular kinetic isotope effects, establishing trapped ions as a versatile platform to explore symmetry-controlled collective dynamics.

physics.atom-ph

Observing the dynamics of octupolar structural transitions in trapped-ion clusters

Interacting many-particle systems can self-organize into a rich variety of crystalline structures. While symmetry provides a powerful framework for predicting whether transitions between crystal states are continuous or discontinuous, collective lattice dynamics offer complementary insights into the microscopic mechanisms that drive these transitions. Trapped laser-cooled ions present a pristine and highly controllable few-body system for studying this interplay of symmetry and dynamics. Here, we use real-time fluorescence imaging while deforming the trap potential to observe a variety of structural transitions in three-dimensional (3D), unit-cell-like ion clusters. We identify a set of transitions signaled by parity-odd octupole order parameters, and probe their distinct dynamical signatures. Our observations reveal the softening of a collective Higgs-like mode indicating spontaneous symmetry-breaking, hysteresis resulting from a catastrophe where a metastable state vanishes abruptly, and stochastic switching between metastable states of differing symmetries. We also uncover a remarkable coincidence of symmetry-breaking and discontinuous transitions, analogous to a thermodynamic triple point. Our results establish 3D trapped-ion clusters as a versatile platform to engineer complex potential energy landscapes, opening new avenues for studies of reaction kinetics, geometric frustration, and related phenomena in mesoscopic platforms.

physics.atom-ph