Chung-You Shih

Programmable XY-type couplings through parallel spin-dependent forces on the same trapped ion motional modes

Nikhil Kotibhaskar, Chung-You Shih, Sainath Motlakunta, Anthony Vogliano [1], Lewis Hahn [1], Yu-Ting Chen [1], Rajibul Islam [1]

Abstract

We propose and experimentally demonstrate an analog scheme for generating XY-type ($J_{ij}^x σ_x^i σ_x^j \;$ + $J_{ij}^y σ_y^i σ_y^j \;$) Hamiltonians on trapped ion spins with independent control over the $J_{ij}^x$ and $J_{ij}^y$ terms. The Ising-type interactions $σ_x^i σ_x^j \;$ and $σ_y^i σ_y^j \;$ are simultaneously generated by employing two spin-dependent forces operating in parallel on the same set of normal modes. We analytically calculate the region of validity of this scheme, and provide numerical and experimental validation with $^{171}\rm{Yb}^+\;$ ions. This scheme inherits the programmability and scalability of the Ising-type interactions with trapped ions that have been explored in numerous quantum simulation experiments. Our approach extends the capabilities of existing trapped ion quantum simulators to access a large class of spin Hamiltonians relevant for exploring exotic quantum phases such as superfluidity and spin liquids.

Fast and high-yield fabrication of axially symmetric ion-trap needle electrodes via two step electrochemical etching

Nikhil Kotibhaskar [1], Noah Greenberg [1], Sainath Motlakunta [1], Chung-You Shih [1], Rajibul Islam [1]

Abstract

Despite the progress in building sophisticated microfabricated ion traps, Paul traps employing needle electrodes retain their significance due to the simplicity of fabrication while producing high-quality systems suitable for quantum information processing, atomic clocks etc. For low noise operations such as minimizing `excess micromotion', needles should be geometrically straight and aligned precisely with respect to each other. Self-terminated electrochemical etching, previously employed for fabricating ion trap needle electrodes employs a sensitive and time-consuming technique resulting in a low success rate of usable electrodes. Here we demonstrate an etching technique for quick fabrication of straight and symmetric needles with a high success rate and a simple apparatus with reduced sensitivity to alignment imperfections. The novelty of our technique comes from using a two-step approach employing turbulent etching for fast shaping and slow etching/polishing for subsequent surface finish and tip cleaning. Using this technique, needle electrodes for an ion-trap can be fabricated within a day, significantly reducing the setup time for a new apparatus. The needles fabricated via this technique have been used in our ion-trap to achieve trapping lifetimes of several months.

Dynamic Hamiltonian engineering of 2D rectangular lattices in a one-dimensional ion chain

Fereshteh Rajabi [1], Sainath Motlakunta [1], Chung-You Shih [1], Nikhil Kotibhaskar [1], Qudsia Quraishi [3,4], Ashok Ajoy [2], Rajibul Islam [1]

Abstract

Controlling the interaction graph between spins or qubits in a quantum simulator allows user-controlled tailoring of native interactions to achieve a target Hamiltonian. The flexibility of engineering long-ranged phonon-mediated spin-spin interactions in a trapped ion quantum simulator offers such a possibility. Trapped ions, a leading candidate for simulating computationally hard quantum many-body dynamics, are most readily trapped in a linear 1D chain, limiting their utility for readily simulating higher dimensional spin models. In this work, we introduce a hybrid method of analog-digital simulation for simulating 2D spin models and dynamically changing interactions to achieve a new graph using a linear 1D chain. The method relies on time domain Hamiltonian engineering through a successive application of Stark shift gradient pulses, and wherein the pulse sequence can simply be obtained from a Fourier series decomposition of the target Hamiltonian over the space of lattice couplings. We focus on engineering 2D rectangular nearest-neighbor spin lattices, demonstrating that the required control parameters scale linearly with ion number. This hybrid approach offers compelling possibilities for the use of 1D chains in the study of Hamiltonian quenches, dynamical phase transitions, and quantum transport in 2D and 3D. We discuss a possible experimental implementation of this approach using real experimental parameters.