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Physical Review A

Deterministic preparation of a dual-species two-ion crystal

Maximilian J. Zawierucha, Till Rehmert, Jonas Keller, T. E. Mehlstäubler, Piet O. Schmidt, Fabian Wolf

Published Jul 8, 2024• 3 citations
Publisher

Abstract

The demand for efficient preparation methods for dual-species ion crystals is rapidly expanding across quantum technology and fundamental physics applications with trapped ions. We present a deterministic and efficient technique to produce such crystals, utilizing the segmented structure of a linear Paul trap. By precisely tailoring the trapping potentials, we can split, move, and discard parts of an ion chain. This process is automated in a sequence that converts a larger ion sample into the desired configuration. A critical component of our approach is the accurate identification of crystal constituents. This is achieved by matching the measured positions of fluorescing ions against theoretical expectations for larger crystals, thus facilitating the detection of nonfluorescing ions and enabling accurate ion counting. We demonstrate that our method reliably produces two-ion crystals within minutes. These results represent a significant advance in the production of two-species ion crystals with applications ranging from quantum logic spectroscopy and optical clocks to quantum computing and simulations with trapped ions. Published by the American Physical Society 2024

DOI
10.1103/physreva.110.013107

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The demand for efficient preparation methods for dual-species ion crystals is rapidly expanding across quantum technology and fundamental physics applications with trapped ions. We present a deterministic and efficient technique to produce such crystals, utilizing the segmented structure of a linear Paul trap. By precisely tailoring the trapping potentials, we can split, move, and discard parts of an ion chain. This process is automated in a sequence that converts a larger ion sample into the desired configuration. A critical component of our approach is the accurate identification of crystal constituents. This is achieved by matching the measured positions of fluorescing ions against theoretical expectations for larger crystals, thus facilitating the detection of nonfluorescing ions and enabling accurate ion counting. We demonstrate that our method reliably produces two-ion crystals within minutes. These results represent a significant advance in the production of two-species ion crystals with applications ranging from quantum logic spectroscopy and optical clocks to quantum computing and simulations with trapped ions. Published by the American Physical Society 2024
The demand for efficient preparation methods for dual-species ion crystals is rapidly expanding across quantum technology and fundamental physics applications with trapped ions. We present a deterministic and efficient technique to produce such crystals, utilizing the segmented structure of a linear Paul trap. By precisely tailoring the trapping potentials, we can split, move, and discard parts of an ion chain. This process is automated in a sequence that converts a larger ion sample into the desired configuration. A critical component of our approach is the accurate identification of crystal constituents. This is achieved by matching the measured positions of fluorescing ions against theoretical expectations for larger crystals, thus facilitating the detection of nonfluorescing ions and enabling accurate ion counting. We demonstrate that our method reliably produces two-ion crystals within minutes. These results represent a significant advance in the production of two-species ion crystals with applications ranging from quantum logic spectroscopy and optical clocks to quantum computing and simulations with trapped ions.
The demand for efficient preparation methods for dual-species ion crystals is rapidly expanding across quantum technology and fundamental physics applications with trapped ions. We present a deterministic and efficient technique to produce such crystals, utilizing the segmented structure of a linear Paul trap. By precisely tailoring the trapping potentials, we can split, move, and discard parts of an ion chain. This process is automated in a sequence that converts a larger ion sample into the desired configuration. A critical component of our approach is the accurate identification of crystal constituents. This is achieved by matching the measured positions of fluorescing ions against theoretical expectations for larger crystals, thus facilitating the detection of non-fluorescing ions and enabling accurate ion counting. We demonstrate that our method reliably produces two-ion crystals within minutes. These results represent a significant advance in the production of two-species ion crystals with applications ranging from quantum logic spectroscopy and optical clocks to quantum computing and simulation with trapped ions.
In the endeavour to scale up the number of qubits in an ion-based quantum computer several groups have started to develop miniaturized ion traps for extended spatial control and manipulation of the ions. Shuttling and separation of ion strings have been the foremost issues in linear-trap arrangements and some prototypes of junctions have been demonstrated for the extension of ion motion to two dimensions (2D). While junctions require complex trap structures, small extensions to the 1D motion can be accomplished in simple linear trap arrangements. Here, control of the extended field in a planar, linear chip trap is used to shuttle ions in 2D. With this approach, the order of ions in a string is deterministically reversed. Optimized potentials are theoretically derived and simulations show that the reordering can be carried out adiabatically. The control over individual ion positions in a linear trap presents a new tool for ion-trap quantum computing. The method is also expected to work with mixed crystals of different ion species and as such could have applications for sympathetic cooling of an ion string.
The outstanding degree of control over trapped ions in Paul traps gives rise to the development of novel quantum manipulation techniques. Optical transitions can be used for precise manipulation of internal and external states. This way, non-classical states can be created which are a key component of quantum algorithms based on quantum logic operations. This powerful optical toolbox enabled the trapped ion system to assume leadership in the field of quantum computation. This thesis addresses two major challenges in the field of micro ion trap quantum optics. The temperature dependence of the heating rate from the ion trap surface is analysed in a novel cryogenic micro ion trap. Furthermore segmented traps allow state manipulations by time dependent electrical potentials, generated by the control voltages. These electrical fields provide a fast and reliable control handle to the ions external degrees of freedom. Quantum computation in Paul trap arrays is based on a combination of ion crystal transport, splitting and merging operations, while laser driven quantum state manipulations are mainly carried out on small ion crystals. Within this thesis a basic building block was realised by performing transport operations with a single ground-state cooled ion. As a highlight of experimental achievements, shuttling in the non-adiabatic regime, on the timescale of the motional period was demonstrated with low residual energy transfer. For his endeavour a specialised low noise arbitrary function generator was designed and manufactured during this thesis. Arbitrary voltage ramps at a sampling rate of up to 2.5 MS/s on up to 12 channels allow the study of a novel excitation method by directly manipulating the ion using electrical forces. Accurate numerical simulations in combination with the fast high resolution voltage supply allow deterministic quantum manipulations via momentum kicks. I report the first experimental demonstration of displaced number states with trapped ions.
Qubits based on ions trapped in linear radio-frequency traps form a successful platform for quantum computing, due to their high fidelity of operations, all-to-all connectivity, and degree of local control. In principle, there is no fundamental limit to the number of ion-based qubits that can be confined in a single 1D register. However, in practice, there are two main issues associated with long trapped-ion crystals, that stem from the “softening” of their modes of motion, upon scaling up: high heating rates of the ions’ motion and a dense motional spectrum; both impede the performance of high-fidelity qubit operations. Here, we propose a holistic, scalable architecture for quantum computing with large ion crystals that overcomes these issues. Our method relies on dynamically operated optical potentials that instantaneously segment the ion crystal into cells of a manageable size. We show that these cells behave as nearly independent quantum registers, allowing for parallel entangling gates on all cells. The ability to reconfigure the optical potentials guarantees connectivity across the full ion crystal and also enables efficient midcircuit measurements. We study the implementation of large-scale parallel multiqubit entangling gates that operate simultaneously on all cells and present a protocol to compensate for crosstalk errors, enabling full-scale usage of an extensively large register. We illustrate that this architecture is advantageous both for fault-tolerant digital quantum computation and for analog quantum simulations. Published by the American Physical Society 2024
Trapped-ion systems are a leading platform for quantum information processing, but they are currently limited to 1D and 2D arrays, which imposes restrictions on both their scalability and their range of applications. Here, we propose a path to overcome this limitation by demonstrating that Penning traps can be used to realize remarkably clean bilayer crystals, wherein hundreds of ions self-organize into two well-defined layers. These bilayer crystals are made possible by the inclusion of an anharmonic trapping potential, which is readily implementable with current technology. We study the normal modes of this system and discover salient differences compared to the modes of single-plane crystals. The bilayer geometry and the unique properties of the normal modes open new opportunities—in particular, in quantum sensing and quantum simulation—that are not straightforward in single-plane crystals. Furthermore, we illustrate that it may be possible to extend the ideas presented here to realize multilayer crystals with more than two layers. Our work increases the dimensionality of trapped-ion systems by efficiently utilizing all three spatial dimensions, and it lays the foundation for a new generation of quantum information processing experiments with multilayer 3D crystals of trapped ions. Published by the American Physical Society 2024