Long Spin Relaxation Times in CVD-Grown Nanodiamonds

TL;DR

This paper demonstrates significantly enhanced spin relaxation times in CVD-grown nanodiamonds, approaching bulk values, which improves their potential for biosensing applications.

Contribution

The authors introduce an advanced growth technique for nanodiamonds that achieves nearly ten-fold longer spin relaxation times compared to commercial counterparts.

Findings

Mean longitudinal coherence time of 800 μs achieved

Maximum coherence time exceeds 1.8 ms, near bulk values

Growth method scalable for sensing application volumes

Abstract

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.