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Dive into the research topics where E. Gheeraert is active.

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Featured researches published by E. Gheeraert.


Journal of Applied Physics | 1995

Characterization of heavily B‐doped polycrystalline diamond films using Raman spectroscopy and electron spin resonance

P. Gonon; E. Gheeraert; A. Deneuville; F. Fontaine; L. Abello; G. Lucazeau

Heavily B‐doped polycrystalline diamond films ([B]≳1019 cm−3) are studied by Raman spectroscopy and electron spin resonance. The formation of an impurity band is accompanied by a Fano‐type interference for the one‐phonon scattering. Bands at 1200 and 500 cm−1 are observed in Raman spectroscopy for concentrations above 1020 cm−3. They are related to maxima in the phonon density of states, and are ascribed to disordered regions or crystalline regions of very small size. The concentration of defects associated with the paramagnetic signal observed around g=2.0030 increases drastically above 1021 B cm−3. The Mott insulator‐metal transition is accompanied by the presence of a new paramagnetic signal (g=2.0007 for 2×1020 B cm−3, g=1.9990 for 1021 B cm−3) ascribed to free holes in the impurity band.


Physical Review Letters | 2004

Dependence of the superconducting transition temperature on the doping level in single crystalline diamond films.

E. Bustarret; Jozef Kacmarcik; C. Marcenat; E. Gheeraert; C. Cytermann; J. Marcus; Thierry Klein

Homoepitaxial diamond layers doped with boron in the 10(20)-10(21) cm(-3) range are shown to be type II superconductors with sharp transitions (approximately 0.2 K) at temperatures increasing from 0 to 2.1 K with boron contents. The critical concentration for the onset of superconductivity in those 001-oriented single-crystalline films is about 5-7 10(20) cm(-3). The H-T phase diagram has been obtained from transport and ac-susceptibility measurements down to 300 mK.


Diamond and Related Materials | 1993

Effect of boron incorporation on the “quality” of MPCVD diamond films

E. Gheeraert; P. Gonon; A. Deneuville; L. Abello; G. Lucazeau

We report the morphology and Raman signals of MPCVD (microwave-plasma-assisted chemical vapour deposition) boron-doped diamond films deposited on Si with a B:C ratio in the gas phase ranging from 20 to 10000 ppm. The crystal shape remains cubooctahedral in the whole range of doping, while the growth rate is reduced as B:C increases. Up to B:C = 400 ppm the full width at half-maximum (FWHM) and a very weak 1500 cm−1 component decrease as the B:C ratio increases. From B:C = 1000 ppm, an asymmetric deformation is observed in the Raman spectra and at the same time the FWHM and the 1500 cm−1 component increase with increasing B:C. For the highest B:C ratio of 10000 ppm additional bands appear around 550 and 1220 cm−1.


Journal of Applied Physics | 1995

Electrical conduction and deep levels in polycrystalline diamond films

P. Gonon; A. Deneuville; F. Fontaine; E. Gheeraert

We have studied the dark conductivity (field, temperature, and frequency dependence), and the photoconductivity in undoped polycrystalline diamond films. Detailed analysis reveals that either of two alternative models can be invoked to explain all the observed features of the dark conductivity. The first model is a Hill‐type hopping conduction involving the presence of discrete acceptor states located at 0.91 eV above the valence band with a density around 1017 cm−3. The second model involves the presence of a band‐tail of acceptor states extending about 1 eV above the valence band. In this case, variable range hopping conduction dominates at low fields with a density of states at the Fermi level around 5×1015 cm−3 eV−1, while space charge limited currents dominate at high fields. The states controlling the dark conductivity give rise to photoconduction with a threshold around 0.85 eV and a peak at 1.1 eV. The shape of the photoconductivity spectrum suggests that lattice relaxation (with a Franck‐Condon s...


Applied Physics Letters | 2014

Zr/oxidized diamond interface for high power Schottky diodes

Aboulaye Traore; P. Muret; Alexandre Fiori; David Eon; E. Gheeraert; Julien Pernot

High forward current density of 103 A/cm2 (at 6 V) and a breakdown field larger than 7.7 MV/cm for diamond diodes with a pseudo-vertical architecture, are demonstrated. The power figure of merit is above 244 MW/cm2 and the relative standard deviation of the reverse current density over 83 diodes is 10% with a mean value of 10−9 A/cm2. These results are obtained with zirconium as Schottky contacts on the oxygenated (100) oriented surface of a stack comprising an optimized lightly boron doped diamond layer on a heavily boron doped one, epitaxially grown on a Ib substrate. The origin of such performances are discussed.


Physica Status Solidi (a) | 1999

Electronic states of boron and phosphorus in diamond

E. Gheeraert; Satoshi Koizumi; T. Teraji; Hisao Kanda; Milos Nesladek

The electronic states of boron and phosphorus in diamond have been studied by infrared absorption and photo-thermal ionisation spectroscopies. High quality boron doped synthetic diamond (p-type conductive) and phosphorus-doped CVD diamond film (n-type conductive) were used for this study. In the case of boron-doped diamond, the four main excited states of the bound hole follow a Rydberg series, suggesting that boron has a hydrogen-like behaviour, with a weak splitting of the excited states. The consistent values of the optical ionisation energy (E0 = 382 meV), of an “average” effective mass (m* = 0.74m0) and of the Bohr radius of the ground state (a* = 4.1 A) deduced from the Rydberg series support this suggestion. The comparison with the effective mass approximation, applied for acceptor states in diamond, suggests that the top of the valence band of diamond is different from that of silicon and germanium. In the case of phosphorus-doped diamond, two excited states of the bound electron have been observed for the first time, at 523 and 562 meV from the ground level. The good agreement with the effective mass approximation suggests that phosphorus is a shallow donor, and allows us to propose a first value of the optical ionisation energy of phosphorus in diamond of about 600 meV, consistent with Hall effect measurements.


Nuclear Instruments & Methods in Physics Research Section A-accelerators Spectrometers Detectors and Associated Equipment | 1999

Review of the development of diamond radiation sensors

Wolfgang Adam; C. Bauer; E. Berdermann; P. Bergonzo; F. Bogani; E. Borchi; A. Brambilla; M. Bruzzi; C. Colledani; J. Conway; Wladyslaw Dabrowski; P. Delpierre; A. Deneuville; W. Dulinski; B. Van Eijk; A. Fallou; F. Fizzotti; F. Foulon; M. Friedl; K. K. Gan; E. Gheeraert; E. Grigoriev; G. Hallewell; R. Hall-Wilton; S. Han; F. Hartjes; J. Hrubec; D. Husson; H. Kagan; D Kania

Abstract Diamond radiation sensors produced by chemical vapour deposition are studied for the application as tracking detectors in high luminosity experiments. Sensors with a charge collection distance up to 250 μm have been manufactured. Their radiation hardness has been studied with pions, proton and neutrons up to fluences of 1.9×10 15 π cm −2 , 5×10 15 p cm −2 and 1.35×10 15 n cm −2 , respectively. Diamond micro-strip detectors with 50 μm pitch have been exposed in a high-energy test beam in order to investigate their charge collection properties. The measured spatial resolution using a centre-of-gravity position finding algorithm corresponds to the digital resolution for this strip pitch. First results from a strip tracker with a 2×4 cm 2 surface area are reported as well as the performance of a diamond tracker read out by radiation-hard electronics with 25 ns shaping time. Diamond pixel sensors have been prepared to match the geometries of the recently available read-out chip prototypes for ATLAS and CMS. Beam test results are shown from a diamond detector bump-bonded to an ATLAS prototype read-out. They demonstrate a 98% bump-bonding efficiency and a digital resolution in both dimensions.


Diamond and Related Materials | 1992

Defects and stress analysis of the Raman spectrum of diamond films

E. Gheeraert; A. Deneuville; A.M. Bonnot; L. Abello

Abstract Diamond films were deposited on silicon substrates at 750 °C, by the hot-filament technique, from a reactive CH 4 (0.1–2%) H 2 mixtures. Two wide Gaussian lines around 1330 and 1500 cm−1 with coupled variations in the whole preparation range appeared in the global Raman spectra. They were attributed to intermediate carbon defects in the diamond crystallites, which might control the confinement length of diamond phonons. Their contributions to the diamond line shift and width for all the samples is calculated and compared with the experimental results. The remaining shift is attributed to the stress (up to 1.2 GPa), while the origin of the remaining widening (large distribution of stress or Raman inactive additional defects) is discussed.


Diamond and Related Materials | 2001

Hydrogen-acceptor interactions in diamond

J. Chevallier; A. Lusson; D. Ballutaud; B. Theys; François Jomard; A. Deneuville; M. Bernard; E. Gheeraert; E. Bustarret

Abstract Hydrogen-acceptor interactions are investigated in boron-doped diamond through deuterium diffusion experiments followed by SIMS measurements and through infrared absorption spectroscopy. From deuterium diffusion, we show that BD interactions can be properly demonstrated in low compensation B-doped homoepitaxial layers. However, the presence of defects in such layers strongly affects this interaction. The degree of passivation of boron acceptors by deuterium depends on the diffusion temperature. At 550°C or below, the B and D concentrations exactly match giving rise to a complete disappearance of the absorption bands related to the electronic transitions of neutral boron acceptors. Under thermal annealing above 500°C, (B,D) pairs dissociate and neutral boron acceptors recover. At deuterium diffusion temperatures of 700°C, the B passivation is absent.


Carbon | 1999

A large range of boron doping with low compensation ratio for homoepitaxial diamond films

J.P. Lagrange; A. Deneuville; E. Gheeraert

Abstract A large range ([B] from 5×1016 to 8×1020 cm−3) of boron concentration has been obtained for homoepitaxial diamond films. From the variation of the conductivity versus temperature between 300 and 1000 K, a simpler method is used to derive the activation energy(ies) Ea and the compensation ratio than from the variation of the hole concentration and mobility with temperature. For [B]

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A. Deneuville

Centre national de la recherche scientifique

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E. Bustarret

Centre national de la recherche scientifique

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Julien Pernot

Centre national de la recherche scientifique

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David Eon

Centre national de la recherche scientifique

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Satoshi Koizumi

National Institute for Materials Science

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P. Gonon

Centre national de la recherche scientifique

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Alexandre Fiori

National Institute for Materials Science

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A. Fallou

Ohio State University

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E. Borchi

University of Florence

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