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Jeroen Prooth

Publications and source records attributed to Jeroen Prooth.

2 recordsLinked to original sources

Irradiation-Induced Spin Bath Evolution and as-Grown Hydrogen Defects in CVD Diamond Revealed by NV-Based DEER Spectroscopy

The aim of this paper is to provide the reader with a review and current state of the art of the fabrication of high T2 coherence diamond, optimised by the use of double electron-electron resonance (DEER) spectroscopy. Using DEER, we study the formation, transformation, and annealing of paramagnetic defects in as-grown CVD diamond and after post-processing. Electron irradiation leads to the formation of an additional S = 1/2 resonance in the DEER spectrum, which we consider to be a composite X ensemble. By tracking the concentrations of X and P1 point defects during annealing from 650C to 1200C, we find that the X ensemble initially consists of a mixture of V- spins and interstitial spins, which disappear at about 650C. Vacancies migrate during annealing, forming clusters that persist to 1000C and disappear upon annealing at 1200C, contributing to the X ensemble signal. We have developed a model of the influence of the mixed spin bath on the coherence of NV centers, which includes independent couplings with P1 centers, V-, divacancies, and interstitials. Detailed DEER studies allowed us to reveal and resolve a weak signal from two additional S = 1/2 species associated with hydrogen: NVH- and consistent with a substitutional hydrogen defect, which overlaps the vacancy spectral line. Taken together, these results show that the NV-DEER method is a powerful tool for investigating paramagnetic defects in diamond with high precision and nanoscale resolution, essential for material optimisation. The achieved high T2 coherence time is consistent with the spin bath model, and the crystals reach the quality required for advanced quantum sensing applications.

quant-ph

Long Spin Relaxation Times in CVD-Grown Nanodiamonds

Currently, the primary applications of fluorescent nanodiamonds (FNDs) are in the area of biosensing, by using photoluminescence or spin properties of colour centres, mainly represented by the Nitrogen Vacancy (NV) point defect. The sensitivity of NV-FNDs to external fields is, however, limited by crystallographic defects, which influence their key quantum state characteristics - the spin longitudinal (\textit{T$_1$}) and spin transversal (\textit{T$_2$}) relaxation and coherence times, respectively. We report on utilising an advanced FND growth technique consisting of heterogeneous nucleation on pre-engineered sites to create FNDs averaging around 60 nm in size, with mean longitudinal coherence times of 800 $\mu$s and a maximum over 1.8 ms, close to bulk theoretical values. This is a major, nearly ten-fold improvement over commercially available nanodiamonds for the same size range of 50 to 150 nm. Heavy-N doped nanodiamond shells, important for sensing events in nm proximity to the diamond surface, are fabricated and discussed in terms of re-nucleation and twinning on \{111\} crystal facets. We also discuss scalability issues in order to enable the production of FND volumes matching the needs of sensing applications.

cond-mat.mes-hall