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Lukas Schlipf

Publications and source records attributed to Lukas Schlipf.

3 recordsLinked to original sources

Quantum-classical processing and benchmarking at the pulse-level

Towards the practical use of quantum computers in the NISQ era, as well as the realization of fault-tolerant quantum computers that utilize quantum error correction codes, pressing needs have emerged for the control hardware and software platforms. In particular, a clear demand has arisen for platforms that allow classical processing to be integrated with quantum processing. While recent works discuss the requirements for such quantum-classical processing integration that is formulated at the gate-level, pulse-level discussions are lacking and are critically important. Moreover, defining concrete performance benchmarks for the control system at the pulse-level is key to the necessary quantum-classical integration. In this work, we categorize the requirements for quantum-classical processing at the pulse-level, demonstrate these requirements with a variety of use cases, including recently published works, and propose well-defined performance benchmarks for quantum control systems. We utilize a comprehensive pulse-level language that allows embedding universal classical processing in the quantum program and hence allows for a general formulation of benchmarks. We expect the metrics defined in this work to form a solid basis to continue to push the boundaries of quantum computing via control systems, bridging the gap between low-level and application-level implementations with relevant metrics.

quant-ph

Molecular quantum spin network controlled by a single qubit

Scalable quantum technologies will require an unprecedented combination of precision and complexity for designing stable structures of well-controllable quantum systems. It is a challenging task to find a suitable elementary building block, of which a quantum network can be comprised in a scalable way. Here we present the working principle of such a basic unit, engineered using molecular chemistry, whose control and readout are executed using a nitrogen vacancy (NV) center in diamond. The basic unit we investigate is a synthetic polyproline with electron spins localized on attached molecular sidegroups separated by a few nanometers. We demonstrate the readout and coherent manipulation of very few ($\leq 6 $) of these $S=1/2$ electronic spin systems and access their direct dipolar coupling tensor. Our results show, that it is feasible to use spin-labeled peptides as a resource for a molecular-qubit based network, while at the same time providing simple optical readout of single quantum states through NV-magnetometry. This work lays the foundation for building arbitrary quantum networks using well-established chemistry methods, which has many applications ranging from mapping distances in single molecules to quantum information processing.

cond-mat.mes-hall

Tracking Temperature Dependent Relaxation Times of Individual Ferritin Nanomagnets with a Wide-band Quantum Spectrometer

We demonstrate the tracking of the spin dynamics of ensemble and individual magnetic ferritin proteins from cryogenic up to room temperature using the nitrogen-vacancy color center in diamond as magnetic sensor. We employ different detection protocols to probe the influence of the ferritin nanomagnets on the longitudinal and transverse relaxation of the nitrogen-vacancy center, which enables magnetic sensing over a wide frequency range from Hz to GHz. The temperature dependence of the observed spectral features can be well understood by the thermally induced magnetization reversals of the ferritin and enables the determination of the anisotropy barrier of single ferritin molecules.

cond-mat.mes-hall