ArticleJournal of the American Chemical Society2024
Nitrogen Substitutions Aggregation and Clustering in Diamonds as Revealed by High-Field Electron Paramagnetic Resonance.
Article in Journal of the American Chemical Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 23 citations in OpenAlex.
- Clustering and Heterogeneous P1 Distributions in Diamond Govern DNP Mechanisms at 6.9 and 13.8 T.The journal of physical chemistry letters · 2025Article
- Temperature-Dependent Dynamic Nuclear Polarization of Diamond.The journal of physical chemistry. C, Nanomaterials and interfaces · 2025Article
- Electronic Spin Relaxation and Clustering in High Pressure High Temperature Synthesized Microcrystalline Diamond Particles with Reduced Nitrogen Content.The journal of physical chemistry. C, Nanomaterials and interfaces · 2025Article
- Dynamic Nuclear Polarization with P1 Centers in Diamond.The journal of physical chemistry letters · 2024Article
- High-field pulsed EPR spectroscopy under magic angle spinning.Science advances · 2024Article
- Dynamic Nuclear Polarization Using Electron Spin Cluster.The journal of physical chemistry letters · 2024Article
- High-frequency high-power DNP/EPR spectrometer operating at 7 T magnetic field.Journal of magnetic resonance (San Diego, Calif. : 1997) · 2024Article
- Magnetic Resonance Study of Bulky CVD Diamond Disc.Materials (Basel, Switzerland) · 2024Article
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Authors and funding
5 authors at 1 institution in 1 country.
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Abstract
Diamonds have been shown to be an excellent platform for quantum computing and quantum sensing applications. These applications are enabled by the presence of defects in the lattice, which are also known as color centers. The most common nitrogen-based defect in synthetic diamonds is the paramagnetic nitrogen substitution (P1) center. While the majority of quantum applications rely on nitrogen-vacancy (NV) centers, the properties of the latter are heavily influenced by the presence and the spatial distribution of the P1 centers. Hence, understanding the spatial distribution and mutual interactions of P1 centers is crucial for the successful development of diamond-based quantum devices. Unlike NV centers, P1 centers do not have a spin-dependent optical signature, and their spin-related properties, therefore, have to be detected and characterized using magnetic resonance methods. We show that using high-field (6.9 and 13.8 T) pulsed electron paramagnetic resonance (EPR) and dynamic nuclear polarization (DNP) experiments, we can distinguish and quantify three distinct populations of P1 centers: isolated P1 centers, weakly interacting ones, and exchange-coupled ones that are clustered together. While such clustering was suggested before, these clusters were never detected directly and unambiguously. Moreover, by using electron-electron double resonance (ELDOR) pump-probe experiments, we demonstrate that the latter clustered population does not exist in isolation but coexists with the more weakly interacting P1 centers throughout the diamond lattice. Its presence thus strongly affects the quantum properties of the diamond. We also show that the existence of this population can explain recent hyperpolarization results in type Ib high-pressure, high-temperature (HPHT) diamonds. We propose a combination of high-field pulsed EPR, ELDOR, and DNP as a tool for probing the aggregation state and interactions among different populations of nitrogen substitution centers.
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