Low-pressure diamond: from the unbelievable to technical products

The idea to grow diamond from the gas phase was born in the 1950s but it took about 30 years until first diamond layers directly grown from the gas phase on substrates were shown in Japan by Matsumoto and co-workers. During the first years of research the function of atomic hydrogen, various growth methods and process parameters were investigated. Research was primarily focused on applications for wear-resistant tools. For this topic the interactions of substrates like hardmetals and ceramics, with diamond deposition gas atmosphere, were investigated. Beside its superior hardness, diamond exhibits the highest heat conductivity, high transparency, high chemical inertness and suitable semiconducting properties. The various requirements for the areas of application of diamond required a division of diamond research into corresponding sub-areas. The hot-filament method is used mainly for wear applications, because it is highly suited to coat complex geometries, but the diamond contains some impurities. Another method is the microwave plasma system which allows the growth of pure diamond used for optical windows and applications requiring high thermal conductivity. Other research areas investigated include doped diamond for microelectronic or electrochemical applications (e.g. waste water treatment); ballas (polycrystalline, spherical diamond), NCD (nanocrystalline diamond) and UNCD (ultra-nanocrystalline diamond) for wear applications.It should be noted that CVD (chemical vapour deposition) diamond synthesis has reached the stage of industrial production and several companies are selling different diamond products. This work is intended to convey to the reader that CVD diamond is an industrially manufactured product that can be used in many ways. With correspondingly low costs for this diamond, new innovative applications appear possible.

Electron spectroscopy with a diamond detector

An electronic grade single crystal chemical vapour deposition diamond was investigated as a prototype high temperature spectroscopic electron (β− particle) detector for future space science instruments. The diamond detector was coupled to a custom-built charge-sensitive preamplifier of low noise. A 63Ni radioisotope source (endpoint energy 66 keV) was used to provide a spectrum of β− particles incident on the detector. The operating temperature of the detector/preamplifier assembly was controlled to allow its performance to be investigated between + 100°C and − 20°C, in 20°C steps. Monte Carlo modelling was used to: a) calculate the β− particle spectrum incident on the detector; b) calculate the fraction of β− particle energy deposited into the detector; and c) predict the β− particle spectrum accumulated by the instrument. Comparison between the model and experimental data suggested that there was a 4.5 µm thick recombination region at the front of the detector. The spectrometer was demonstrated to be fully operable at temperatures, T, -20°C ≤ T ≤ 80°C; the results suggested that some form of polarisation phenomenon occurred in the detector at > 80°C. This article presents the first report of a calibrated low energy (⪅ 50 keV) spectroscopic β− particle diamond detector.

Glutamate biosensors based on diamond and graphene platforms

l-Glutamate is one of the most important neurotransmitters in the mammalian central nervous system, playing a vital role in many physiological processes and implicated in several neurological disorders, for which monitoring of dynamic levels of extracellular glutamate in the living brain tissues may contribute to medical understanding and treatments. Electrochemical sensing of glutamate has been developed recently mainly using platinum, carbon fibre and carbon nanotube electrodes. In the present work, we explore the fabrication and properties of electrochemical glutamate sensors fabricated on doped chemical vapour deposition diamond electrodes and graphene nanoplatelet structures. The sensors incorporate platinum nanoparticles to catalyse the electrooxidation of hydrogen peroxide, glutamate oxidase to oxidise glutamate, and a layer of poly-phenylenediamine to impart selectivity. The performance of the devices was compared to a similar sensor fabricated on glassy carbon. Both the diamond and the graphene sensor showed very competitive performance compared to the majority of existing electrochemical sensors. The graphene based sensor showed the best performance of the three investigated in terms of sensitivity, linear dynamic range and long term stability, whereas it was found that the diamond device showed the best limit of detection.