J. Achard

Ultralong spin coherence time in isotopically engineered diamond

As quantum mechanics ventures into the world of applications and engineering, materials science faces the necessity to design matter to quantum grade purity. For such materials, quantum effects define their physical behaviour and open completely new (quantum) perspectives for applications. Carbon-based materials are particularly good examples, highlighted by the fascinating quantum properties of, for example, nanotubes or graphene. Here, we demonstrate the synthesis and application of ultrapure isotopically controlled single-crystal chemical vapour deposition (CVD) diamond with a remarkably low concentration of paramagnetic impurities. The content of nuclear spins associated with the (13)C isotope was depleted to 0.3% and the concentration of other paramagnetic defects was measured to be <10(13) cm(-3). Being placed in such a spin-free lattice, single electron spins show the longest room-temperature spin dephasing times ever observed in solid-state systems (T2=1.8 ms). This benchmark will potentially allow observation of coherent coupling between spins separated by a few tens of nanometres, making it a versatile material for room-temperature quantum information processing devices. We also show that single electron spins in the same isotopically engineered CVD diamond can be used to detect external magnetic fields with a sensitivity reaching 4 nT Hz(-1/2) and subnanometre spatial resolution.

CVD diamond films: from growth to applications

Abstract The present review provides an up-to-date report on the main potential of CVD diamond films for industrial applications as well as on recent basic research which seeks to understand diamond deposition microwave plasma reactors. This review includes firstly an overview of diamond film applications. Elements which explain variations in diamond film characteristics as a function of synthesis conditions are given. Also experimental results are reported which show variations in diamond characteristics (quality, microstructure, growth rate, growth mechanisms) as four plasma variables (pressure, power, percentage of methane, substrate temperature) are systematically changed. In the second part, we discuss the effects of these variables on local parameters such as electron temperature, gas temperature, carbon-containing species and H-atom densities. Finally, based on these results, relationships between key local parameters and diamond characteristics are established and discussed.

High quality MPACVD diamond single crystal growth: high microwave power density regime

The growth of monocrystalline diamond films of electronic quality and large thickness (>few hundreds of microns) is an important issue in particular for high-power electronics. In this paper, we will describe the different key parameters necessary to reach this objective. First, we will examine the deposition process and establish that only microwave assisted diamond deposition plasma reactors can achieve the optimal growth conditions for the efficient generation of the precursor species to diamond growth. Next, we will consider the influence of the monocrystalline diamond substrate orientation and quality on the growth of the epitaxial layer, especially when the deposited material thickness exceeds 100 µm. The need to use a specific pre-treatment procedure of the substrate before the growth and its impact will also be discussed. Finally we will look at the growth conditions themselves and assess the influence of the process parameters, such as the substrate temperature, the methane concentration, the microwave power density and the eventual presence of nitrogen in the gas phase, on both the morphology and quality of the films on the one hand and the growth rate on the other hand. For this, we will introduce the concept of supersaturation and comment on its evolution as a function of the process parameters.

Enhanced generation of single optically active spins in diamond by ion implantation

The nitrogen-vacancy (NV) centers in diamond are amongst the most promising candidates for quantum information applications. Up to now the creation of such defects was highly probabilistic, requiring many copies of the nanodevice. Here we show that by employing a two step implantation process which includes low dose N2+ molecular ion implantations followed by high dose C implantation can increase the generation efficiency of NV centers by over 50%. Moreover, we detected intrinsic N14 concentration as low as 0.07 ppb by converting the nitrogen impurities into NV and then counting the single centers by using a confocal microscope.

Engineered arrays of nitrogen-vacancy color centers in diamond based on implantation of CN− molecules through nanoapertures

We report a versatile method for engineering arrays of nitrogen-vacancy (NV) color centers in diamond at the nanoscale. The defects were produced in parallel by ion implantation through 80 nm diameter apertures patterned using electron beam lithography in a polymethyl methacrylate (PMMA) layer deposited on a diamond surface. The implantation was performed with CN− molecules that increased the NV defect-formation yield. This method could enable the realization of a solid-state coupled-spin array and could be used for positioning an optically active NV center on a photonic microstructure.

Perfect preferential orientation of nitrogen-vacancy defects in a synthetic diamond sample

We show that the orientation of nitrogen-vacancy (NV) defects in diamond can be efficiently controlled through chemical vapor deposition growth on a (111)-oriented diamond substrate. More precisely, we demonstrate that spontaneously generated NV defects are oriented with a ∼97% probability along the [111] axis, corresponding to the most appealing orientation among the four possible crystallographic axes. Such a nearly perfect preferential orientation is explained by analyzing the diamond growth mechanism on a (111)-oriented substrate and could be extended to other types of defects. This work is a significant step towards the design of optimized diamond samples for quantum information and sensing applications.

Magnetic imaging with an ensemble of nitrogen-vacancy centers in diamond

The nitrogen-vacancy (NV) color center in diamond is an atom-like system in the solid-state which specific spin properties can be efficiently used as a sensitive magnetic sensor. An external magnetic field induces Zeeman shifts of the NV center levels which can be measured using optically detected magnetic resonance (ODMR). In this work, we quantitatively map the vectorial structure of the magnetic field produced by a sample close to the surface of a CVD diamond hosting a thin layer of NV centers. The magnetic field reconstruction is based on a maximum-likelihood technique which exploits the response of the four intrinsic orientations of the NV center inside the diamond lattice. The sensitivity associated to a 1 μm2 area of the doped layer, equivalent to a sensor consisting of approximately 104 NV centers, is of the order of 2 μT/√Hz. The spatial resolution of the imaging device is 480 nm, limited by the numerical aperture of the optical microscope which is used to collect the photoluminescence of the NV layer. The effectiveness of the method is illustrated by the accurate reconstruction of the magnetic field created by a DC current inside a copper wire deposited on the diamond sample.Graphical abstract

Photonic nano-structures on (111)-oriented diamond

We demonstrate the fabrication of single-crystalline diamond nanopillars on a (111)-oriented chemical vapor deposited diamond substrate. This crystal orientation offers optimal coupling of nitrogen-vacancy (NV) center emission to the nanopillar mode and is thus advantageous over previous approaches. We characterize single native NV centers in these nanopillars and find one of the highest reported saturated fluorescence count rates in single crystalline diamond in excess of 106 counts per second. We show that our nano-fabrication procedure conserves the preferential alignment as well as the spin coherence of the NVs in our structures. Our results will enable a new generation of highly sensitive probes for NV magnetometry and pave the way toward photonic crystals with optimal orientation of the NV centers emission dipole.

Electro-optical response of a single-crystal diamond ultraviolet photoconductor in transverse configuration

Diamond has been identified as a very promising material for X and ultraviolet sensing. In this Letter, a photoconductive device based on a freestanding homoepitaxial chemically vapor deposition (CVD) single-crystal diamond 500μm thick has been tested. Photoconductive measurements in coplanar and transverse configurations have been performed to characterize the device sensitivity in the 140–250 nm spectral range. Very high sensitivity values were achieved in both configurations. The sensitivity in the transverse configuration is at least 300 times higher than in the coplanar configuration.

Growth of thick heavily boron-doped diamond single crystals: Effect of microwave power density

The fabrication of diamond-based vertical power devices which are the most suited for high current applications requires the use of thick heavily boron-doped (B-doped) diamond single crystals. Although the growth of thin B-doped diamond films is well controlled over a large concentration range, little is known about the growth conditions leading to heavily doped thick single crystals. In this paper, it was found that the microwave power densities (MWPD) coupled to the plasma used to synthesize B-doped diamond by chemical vapor deposition is one of the key parameters allowing tuning doping efficiencies over two orders of magnitude. At high MWPD (above 100 W cm−3) the boron doping efficiency (DE) is extremely low while further increasing the boron concentration in the gas phase is no use as this leads to plasma instability. On the other hand, when low MWPD are used (<50 W cm−3), DE can be strongly increased but twinning and defects formation hampers the surface morphology. The use of intermediate MWPD densi...