An official website of the United States government
Abstract The coherence times of solid-state spin qubits are often limited by the presence of a spin bath. Characterizing the spectrum of the local magnetic field fluctuations of the bath is key to understanding spin qubit decoherence. Here we use pulsed electron paramagnetic resonance (pEPR) based noise spectroscopy to measure the magnetic noise power spectra for ensembles of P1 (substitutional nitrogen) centers in diamond that typically form the bath for NV (nitrogen-vacancy) centers. The Carr-Purcell-Meiboom-Gill (CPMG) dynamical decoupling experiments on the P1 centers were performed on a low [N] CVD (chemical vapor deposition) sample and a high [N] HPHT (high-temperature, high-pressure) sample at 89 mT. We characterize the NV centers of the latter sample using the same 2.5 GHz pEPR spectrometer. All power spectra show two distinct features, a broad component that is observed to scale as approximately 1/ω^{0.7-1.0}, and a prominent peak at the 13C Larmor frequency. The behavior of the broad component is consistent with an inhomogeneous distribution of Lorentzian spectra due to clustering of P1 centers, which has recently been shown to be prevalent in HPHT diamond. We develop techniques utilizing harmonics of the CPMG filter function to improve characterization of high-frequency signals, which we demonstrate on the 13C nuclear Larmor frequency. At 190 mT this is 2.04 MHz, 5.7 times higher than the CPMG modulation frequency (<357 kHz, hardware-limited). Understanding the properties of the bath allow us to either exploit it as a quantum resource or optimize decoupling performance, while also informing sample fabrication technologies. The techniques are applicable to ac magnetometry for nanoscale nuclear magnetic resonance and chemical sensing.
more »
« less
P1 Center Electron Spin Clusters Are Prevalent in Type Ib Diamonds
Understanding the spatial distribution of the P1 centers is crucial for diamond-based sensors and quantum devices. P1 centers serve as polarization sources for dynamic nuclear polarization (DNP) quantum sensing and play a significant role in the relaxation of nitrogen vacancy (NV) centers. Additionally, the distribution of NV centers correlates with the distribution of P1 centers, as NV centers are formed through the conversion of P1 centers. We utilized DNP and pulsed electron paramagnetic resonance (EPR) techniques that revealed strong clustering of a significant population of P1 centers that exhibit exchange coupling and produce asymmetric line shapes. The 13C DNP frequency profile at a high magnetic field revealed a pattern that requires an asymmetric EPR line shape of the P1 clusters with electron–electron (e–e) coupling strengths exceeding the 13C nuclear Larmor frequency. EPR and DNP characterization at high magnetic fields was necessary to resolve energy contributions from different e–e couplings. We employed a two-frequency pump–probe pulsed electron double resonance technique to show cross-talk between the isolated and clustered P1 centers. This finding implies that the clustered P1 centers affect all of the P1 populations. Direct observation of clustered P1 centers and their asymmetric line shape offers a novel and crucial insight into understanding magnetic noise sources for quantum information applications of diamonds and for designing diamond-based polarizing agents with optimized DNP efficiency for 13C and other nuclear spins of analytes. We propose that room temperature 13C DNP at a high field, achievable through straightforward modifications to existing solution-state NMR systems, is a potent tool for evaluating and controlling diamond defects.
more »
« less
- PAR ID:
- 10520556
- Publisher / Repository:
- American Chemical Society
- Date Published:
- Journal Name:
- Journal of the American Chemical Society
- Volume:
- 146
- Issue:
- 8
- ISSN:
- 0002-7863
- Page Range / eLocation ID:
- 5088 to 5099
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
We describe a 395 GHz pulsed electron paramagnetic resonance (EPR) setup, and initial results of relaxation measure-ments and cw EPR at these frequencies in samples used for liquid- and solid-state nuclear magnetic resonance enhanced by dynamic nuclear polarization (DNP). Depending on the amount of spin –orbit coupling, the spin lattice relaxation becomes significantly faster at higher fields and frequencies, which has consequences for some DNP applications at high fields and frequencies. We will dis-cuss the requirements for (sub)millimeter-wave sources and com-ponents for DNP and pulsed EPR at even higher frequencies and fields, as even higher magnetic fields will become available in the near future.more » « less
-
Color-center–hosting semiconductors are emerging as promising source materials for low-field dynamic nuclear polarization (DNP) at or near room temperature, but hyperfine broadening, susceptibility to magnetic field heterogeneity, and nuclear spin relaxation induced by other paramagnetic defects set practical constraints difficult to circumvent. Here, we explore an alternate route to color-center–assisted DNP using nitrogen-vacancy (NV) centers in diamond coupled to substitutional nitrogen impurities, the so-called P1 centers. Working near the level anticrossing condition—where the P1 Zeeman splitting matches one of the NV spin transitions—we demonstrate efficient microwave-free 13 C DNP through the use of consecutive magnetic field sweeps and continuous optical excitation. The amplitude and sign of the polarization can be controlled by adjusting the low-to-high and high-to-low magnetic field sweep rates in each cycle so that one is much faster than the other. By comparing the 13 C DNP response for different crystal orientations, we show that the process is robust to magnetic field/NV misalignment, a feature that makes the present technique suitable to diamond powders and settings where the field is heterogeneous. Applications to shallow NVs could capitalize on the greater physical proximity between surface paramagnetic defects and outer nuclei to efficiently polarize target samples in contact with the diamond crystal.more » « less
-
Dynamic Nuclear Polarization (DNP) utilizing Electron Spin Clusters to achieve resonance matching with the nucleus and to generate an Asymmetric Polarization Elevation (ESCAPE-DNP, or ESC-DNP for short) by monochromatic microwave irradiation at a select frequency is debuted as a promising mechanism to achieve NMR signal enhancements with a wide design scope requiring low microwave power at high magnetic field. In this paper, we present the design for a trityl-based tetra-radical (TetraTrityl) to achieve DNP for 1H NMR at 7 Tesla, supported by experimental data and quantum mechanical simulations. A slow relaxing (T1e ≈ 1 ms) four electron spin cluster is found to require at least two electron pairs with e-e distances of 8 Å or below to yield any meaningful 1H ESC-DNP NMR enhancement, while squeezing the rest of the e-e distances to 12 Å or below gives rise to near maximum 1H ESC-DNP-NMR enhancements. For the more common case of a fast-relaxing spin cluster (T1e ≈ 1 μs), efficient ESC-DNP is found to require an asymmetric ESC that contains a cluster of strongly coupled narrow-line radicals coexisting with a weakly coupled narrow-line radical acting as a sensitizer to extract polarization from the cluster. This study highlights the untapped potential of utilizing strong coupling of narrow-line radical clusters to achieve microwave power-efficient DNP that extends design options beyond what is available today and offers great tunability at high magnetic field.more » « less
-
Dynamic nuclear polarization (DNP) is a method of enhancing NMR signals via the transfer of polarization from electron spins to nuclear spins using microwave (MW) irradiation. In most cases, monochromatic continuous-wave (MCW) MW irradiation is used. Recently, several groups have shown that frequency modulation of the MW irradiation can result in an additional increase in DNP enhancement above that obtained with MCW. The effect of frequency modulation on the solid effect (SE) and the cross effect (CE) has previously been studied using the stable organic radical 4-hydroxy TEMPO (TEMPOL) at temperatures under 20 K. Here, in addition to the SE and CE, we discuss the effect of frequency modulation on the Overhauser effect (OE) and the truncated CE (tCE) in the room-temperature 13C-DNP of diamond powders. We recently showed that diamond powders can exhibit multiple DNP mechanisms simultaneously due to the heterogeneity of P1 (substitutional nitrogen) environments within diamond crystallites. We explore how the two parameters that define the frequency modulation: (i) the Modulation frequency, fm (how fast the microwave frequency is varied) and (ii) the Modulation amplitude, Δω (the magnitude of the change in microwave frequency) influence the enhancement obtained via each mechanism. Frequency modulation during DNP not only allows us to improve DNP enhancement, but also gives us a way to control which DNP mechanism is most active. By choosing the appropriate modulation parameters, we can selectively enhance some mechanisms while simultaneously suppressing others.more » « less
- Free Publicly Accessible Full Text
-
Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1021/jacs.3c06705
