ArticleScience advances2017
A molecular quantum spin network controlled by a single qubit.
Article in Science advances, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- High-Purity Quantum Emission from an AuACS nano · 2026Article
- In situ electron paramagnetic resonance spectroscopy using single nanodiamond sensors.Nature communications · 2023Article
- Quantum sensors for biomedical applications.Nature reviews. Physics · 2023Review
- Immunomagnetic microscopy of tumor tissues using quantum sensors in diamond.Proceedings of the National Academy of Sciences of the United States of America · 2022Article
- Entanglement of dark electron-nuclear spin defects in diamond.Nature communications · 2021Article
- Readout and control of an endofullerene electronic spin.Nature communications · 2020Article
- Kilohertz electron paramagnetic resonance spectroscopy of single nitrogen centers at zero magnetic field.Science advances · 2020Article
- Quantum diamond spectrometer for nanoscale NMR and ESR spectroscopy.Nature protocols · 2019Article
- Single-DNA electron spin resonance spectroscopy in aqueous solutions.Nature methods · 2018Article
- Nanoscale zero-field electron spin resonance spectroscopy.Nature communications · 2018Article
Corrections and comments
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Authors and funding
13 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Scalable quantum technologies require an unprecedented combination of precision and complexity for designing stable structures of well-controllable quantum systems on the nanoscale. It is a challenging task to find a suitable elementary building block, of which a quantum network can be comprised in a scalable way. We present the working principle of such a basic unit, engineered using molecular chemistry, whose collective 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 side groups separated by a few nanometers. We demonstrate the collective readout and coherent manipulation of very few (≤ 6) of these
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Registered trials
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