NMR of a single nuclear spin detected by a scanning tunnelling microscope

We detect a single spin nuclear magnetic resonance (NMR) by monitoring the intensity modulations of a selected hyperfine line in the electron spin resonance (ESR) spectrum. We analyse the power spectrum of the corresponding hyperfine intensity and obtain the nuclear magnetic resonance (NMR) spectrum. Our process also demonstrates ionization of a molecule with the bias voltage of a Scanning Tunnelling Microscope (STM), allowing detection of NMR even in molecules that are non-radical in their neutral state. We have observed this phenomenon in four types of molecules: toluene, triphenylphosphine, TEMPO and adenosine triphosphate (ATP) showing NMR of <sup>1</sup>H, <sup>13</sup>C, <sup>31</sup>P and <sup>14</sup>N nuclei. The spectra are detailed and show signatures of the chemical environment, i.e. chemical shifts. A theoretical model to account for these data is outlined.

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Publication Details

Journal
Journal of Magnetic Resonance
Published
2025-03-12
DOI
https://doi.org/10.1016/j.jmr.2025.107863
Primary Topic
Atomic and Subatomic Physics Research
Type
article
Field-Weighted Citation Impact
0.00

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article

NMR of a single nuclear spin detected by a scanning tunnelling microscope

B. Horovitz, Alexander Shnirman, Zion Hazan, Yishay Manassen et al.
Journal of Magnetic Resonance
Atomic and Subatomic Physics Research
article

NMR of a single nuclear spin detected by a scanning tunnelling microscope

B. Horovitz, Alexander Shnirman, Zion Hazan, Yishay Manassen, Michael Averbukh, Yahel Tzuriel, Pino Boscolo
article en

Abstract

We detect a single spin nuclear magnetic resonance (NMR) by monitoring the intensity modulations of a selected hyperfine line in the electron spin resonance (ESR) spectrum. We analyse the power spectrum of the corresponding hyperfine intensity and obtain the nuclear magnetic resonance (NMR) spectrum. Our process also demonstrates ionization of a molecule with the bias voltage of a Scanning Tunnelling Microscope (STM), allowing detection of NMR even in molecules that are non-radical in their neutral state. We have observed this phenomenon in four types of molecules: toluene, triphenylphosphine, TEMPO and adenosine triphosphate (ATP) showing NMR of <sup>1</sup>H, <sup>13</sup>C, <sup>31</sup>P and <sup>14</sup>N nuclei. The spectra are detailed and show signatures of the chemical environment, i.e. chemical shifts. A theoretical model to account for these data is outlined.

Journal of Magnetic ResonanceVol. 374
Karlsruhe Institute of Technology (DE), Ben-Gurion University of the Negev (IL), Tecnologie Avanzate (Italy) (IT)
Deutsche Forschungsgemeinschaft, Israel Science Foundation, HORIZON EUROPE European Innovation Council
Affordable and clean energy
Openalex Percentile: Top 97%
Atomic and Subatomic Physics Research
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