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Olga Krafcsik

Publications and source records attributed to Olga Krafcsik.

3 recordsLinked to original sources

Solution-phase fluorination of nanodiamond: near-surface NV$^-$ activation and spin relaxation

Nanodiamonds hosting luminescent point defects, known as fluorescent nanodiamonds (FND), are a leading platform for quantum technology. The nitrogen-vacancy (NV) centre is the most intensively studied of these; its negatively charged state (NV$^-$) can serve as a qubit at room temperature, and its stability is governed by surface functional groups. We present two solution-phase fluorination routes for stabilising NV$^-$: direct C-F bond formation by decarboxylation with xenon difluoride via a radical mechanism, and the Balz-Schiemann reaction, which replaces surface amino groups with fluorine. The two routes were compared by infrared, X-ray photoelectron, energy-dispersive X-ray, Raman and photoluminescence spectroscopy. Both gave a high NV$^-$ fraction, up to $\sim$90% on average and approaching 100% in fluorine-rich regions, which to our knowledge is among the highest reported for surface-terminated nanodiamonds of this size and, in particular, for fluorine termination. Frequency-domain relaxometry shows that the fluorinated particles retain a long spin-lattice relaxation time, $733\pm56$ and $712\pm20$ $\mu$s for the XeF$_2$ and Balz-Schiemann routes, several times the values reported for commercial HPHT nanodiamonds, although shorter than the $1173\pm123$ $\mu$s of the as-received material. Charge-state stability and spin lifetime therefore do not improve together: fluorination activates near-surface NV$^-$ centres, which are the most exposed to surface noise but also the ones that dominate relaxometric sensing.

quant-ph

Thiolation and PEGylation of silicon carbide nanoparticle

In this study, we implement thiol termination on the surface of few-nanometer-sized silicon carbide (SiC) nanoparticles (NPs) to enable further applications, such as fluorescent biomarkers. Various spectroscopic techniques are employed to monitor the effectiveness of the surface treatment. A thiol-Michael addition reaction is performed by conjugating 4-arm PEGmaleimide molecules to the thiol groups of SiC NPs, further demonstrating the reactivity of thiol-terminated SiC NPs, which also acts as a protection layer against oxidation. These fluorescent thiolated SiC NPs, both with and without conjugated molecules, are directly applicable as bioinert probes. Since SiC NPs can potentially host room-temperature fluorescent defect quantum bits, our results are an important step to realize a bioinert, ultrasmall quantum sensor bioagents, which may open new avenues in biotechnology.

cond-mat.mtrl-sci

Materials and Spin Characteristics of Nanodiamonds Partially Covered with Amino Groups and Embedded with Nitrogen-Vacancy Color Centers

Fluorescent nanodiamonds (FNDs) with optically read qubits hold great potential for detecting electric and magnetic fields, temperature, and other nanoscale physicochemical quantities relevant to chemistry and biology. Proper surface functionalization is essential for their application as probes, but surface modifications can impact qubit sensor properties. We systematically study nitrogen-vacancy (NV) color centers in FNDs as a function of size and surface termination. FNDs were produced from high-pressure, high-temperature diamonds, with NV centers introduced via electron irradiation and annealing. The initial oxygen-covered FNDs were homogenized with hydroxyl (-OH) groups as reference samples, while the noninvasive Hofmann degradation introduced amino (-NH2) groups for potential direct biomolecule attachment. Amino groups may not cover the nanodiamonds homogeneously, but we label them as -NH2 terminated throughout. We monitored charge state stability and the zero-field splitting parameters of the embedded NV centers. First, we resolve the size dependence of the NV(-) zero-field splitting parameters across the 10-140 nm range and show that the symmetry-breaking E parameter decreases monotonically from about 8 to about 5 MHz with increasing size while the axial D parameter is shifted only in the smallest (<= 30 nm) particles, thereby disentangling the static-strain and fluctuating electric-field contributions to the spin levels. Second, while NV charge state stabilization was observed in both -OH- and -NH2-terminated FNDs above a certain size, we demonstrate that a remarkably high and laser-power-independent NV(-) content (f_NV(-) of about 0.8) is achieved by wet-chemical Hofmann amino termination only in 140 nm particles, an effect we link through electron spin resonance to the degradation of surface paramagnetic defects rather than to the introduction of new ones.

quant-ph