D. E. Ibbotson
Bell Labs
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Featured researches published by D. E. Ibbotson.
Journal of Applied Physics | 1989
J. A. Mucha; Daniel L. Flamm; D. E. Ibbotson
Plasma emission actinometry has been used to study the mechanism by which small additions of oxygen (∼0.5%) enhance the rate of diamond deposition in a dilute (4%) CH4/H2 discharge at high temperature (900–1300 K). Increasing amounts of CH4 in the feed depress [H], while increasing the O2 concentration, up to ∼5%, produces a fivefold increase in atomic hydrogen in the discharge zone. Invoking a mechanism where diamond growth competes with the formation of an amorphous/graphitic inhibiting layer, these results and earlier studies suggest that oxygen (1) increases [H] which selectively etches amorphous/graphitic carbon, (2) accelerates reaction of this layer with molecular hydrogen, and (3) may itself act as a selective etchant of nondiamond carbon. As a result, the number of active diamond growth sites is increased and enhanced growth rates are observed. We also have grown diamond by alternating a CH4/He discharge with a H2/O2/He discharge and results are consistent with this mechanism. Instantaneous growt...
Applied Physics Letters | 1984
D. E. Ibbotson; Daniel L. Flamm; J. A. Mucha; Vincent M. Donnelly
Silicon gasification by XeF2 is compared with F‐atom etching under conditions typical of those used in plasma etching. Temperatures ranged from −17 to 360 °C and XeF2 pressures were between 0.05 and 2 Torr. Silicon etching by XeF2 shows a sharply different etch rate/temperature dependence than the Si/F or Si/F2 reaction systems; there is no detectable reaction between XeF2 and SiO2 in contrast to the F‐atom/SiO2 system. These data indicate that physisorption can limit silicon etching by XeF2 and show that basic studies which use XeF2 as a model compound for the etching of silicon and SiO2 by F atoms should be interpreted with caution.
Journal of Applied Physics | 1988
C.‐P. Chang; Daniel L. Flamm; D. E. Ibbotson; J. A. Mucha
We have grown diamond crystals and polycrystalline diamond films from CH4/H2/O2 gas feeds in a simple, high‐power density, 2450‐MHz discharge tube reactor. Single‐crystal growth rates over 20 μm/h have been achieved. The material has been analyzed using Raman spectroscopy, Auger spectroscopy, and x‐ray diffraction. Control of nucleation is a major problem for growing sound films, and the high temperatures currently required for growth will limit applications. Oxygen additions were necessary to deposit diamonds over the range of feed composition we studied.
Journal of Vacuum Science & Technology B | 1983
Daniel L. Flamm; Vincent M. Donnelly; D. E. Ibbotson
A recent review of plasma etching is extended with discussions of similarity variables governing discharges, anisotropic oxide etching in fluorine and unsaturate‐rich plasmas, surface texture, the loading effect, and gas‐surface reactions.
Journal of Applied Physics | 1984
D. E. Ibbotson; J. A. Mucha; Daniel L. Flamm; Joel Malcolm Cook
Silicon is rapidly etched by the gas‐phase halogen fluorides ClF3, BrF3, BrF5, and IF5, in analogy to XeF2 etching silicon. Nearly complete selectivity over SiO2 is achieved in all cases. By contrast, ClF and Groups III and V fluorides such as NF3, BF3, PF3, and PF5 do not spontaneously etch either Si or SiO2 under the same experimental conditions. These relatively inexpensive interhalogens can be applied to pattern silicon and more generally to remove silicon or polysilicon layers without a plasma. Low‐temperature plasmaless gasification of substrates by these fluorine‐containing interhalogens is an economically attractive alternative to fluorine‐based plasma etching.
Journal of Vacuum Science & Technology B | 1989
Nur Selamoglu; J. A. Mucha; D. E. Ibbotson; Daniel L. Flamm
Isotopic labeling and step coverage studies of silicon oxide deposited from tetraethoxysilane (TEOS) have been carried out by introducing TEOS(16O) downstream from an 18O2 discharge. Rutherford backscattering (RBS) data on films deposited near 440 °C show that, on average, one Si–O bond in the original TEOS molecule is preserved in the process, while mass spectrometric results indicate only H216O and C18O16O as gaseous products of the cleavage of the remaining three Si–O bonds. Infrared analyses of films deposited at room temperature show large amounts of Si–OH in a gel‐like material, and the presence of a C■O species. The results suggest a mechanism dominated by diffusion and condensation of Si–OH species that form extensive chains and preserve an Si–16O bond from the original precursor. This is followed by cross‐linking to form the final silicate network; however, Si–O bond cleavage is apparently occurring at potential cross‐linking sites via a carbonate intermediate that promotes isotopic scrambling. S...
Journal of Applied Physics | 1983
D. E. Ibbotson; Daniel L. Flamm; Vincent M. Donnelly
We report results that show (100)GaAs can be crystallographically etched by a bromine or chlorine plasma. Specifically, {110}, {100}, and {111}A crystal facets develop under masked portions when the substrate is etched under ‘‘isotropic’’ or chemical plasma etching conditions (0.15–0.30 Torr, 0.1–14 MHz, ≲0.5 W cm−2). The etch rate of GaAs(100) is ∼20 to ∼70 μ/min in a pure Br2 discharge under these conditions. Absolute Br and Br2 concentrations were measured as a function of applied frequency by absorption spectroscopy. Relative optical emission from Br, Br+, and Br+2 was also recorded. The relationship between Br emission at 700.5 nm and Br concentration is quantitatively accounted for by an increase in the population of electrons above 13.5 eV with discharge frequency. The etch rate of GaAs(100) is directly proportional to Br concentration, and increases by a factor of 2.0 between 0.1 and 14 MHz.
Journal of Vacuum Science & Technology B | 1988
C. C. Chang; Daniel L. Flamm; D. E. Ibbotson; J. A. Mucha
The properties of low‐hydrogen, fluorinated plasma‐enhanced chemical vapor deposition (PECVD) silicon nitride films grown using NF3/SiH4/N2 feed mixtures in 200 kHz and 14 MHz discharges were compared. High‐energy ion bombardment at 200 kHz is expected to enhance surface diffusion and chemical reconstruction. Compared to fluorinated silicon nitride deposited at 14 MHz under otherwise comparable conditions, the 200 kHz films had a lower Si–H bond concentration (≲1×1021 cm−3), lower total hydrogen content (5–8×1021 cm−3), better resistance to oxidation, lower compressive stress (−0.7 to −1.5 Gdyne/cm), and higher density (3.1 g/cm3). The dielectric constant of better low‐frequency Class I films was constant to 500 MHz, while that of high‐frequency films fell up to 15% between 100 Hz and 10 MHz. The absorption edges of low‐frequency PECVD fluorinated silicon nitride films were between 5.0 and 6.1 eV, which compare with 4.4 to 5.6 eV for the high‐excitation frequency fluorinated material and 3 to 4 eV for con...
Journal of Applied Physics | 1990
Elmer A. Ogryzlo; D. E. Ibbotson; Daniel L. Flamm; J. A. Mucha
Absolute rates for the intrinsic reaction between Cl atoms and surfaces of P‐doped polycrystalline silicon, P‐doped Si(100) and As, Sb‐doped Si(111) substrates were measured for the first time as a function of dopant concentration (Ne) and substrate temperature in a downstream reaction system. This study clearly shows that when there is no ion bombardment, increasing Ne increases the Si‐Cl reaction rate even when silicon is lightly doped (∼1015 cm−3), in contrast to in‐discharge studies. Moreover, results showed that crystal orientation influences the Cl‐Si reaction more than Ne, for Ne<1020 cm−3. The data are fitted to a modified Arrhenius expression, R=νNγenClT1/2e−E/kT, with R the etch rate and nCl the gas phase Cl concentration. The calculated values of the activation energy E are 4.1–4.7 kcal/mole for all doping levels and crystallographic orientations. Therefore, the doping effect is manifested solely in the preexponential (νNγe) of the Arrhenius expression, and the data qualitatively agree with a c...
Journal of Vacuum Science & Technology B | 1990
J. M. Cook; D. E. Ibbotson; Daniel L. Flamm
We have shown that a discharge can be sustained at low pressure (≲10−3 Torr) in a single‐wafer reactor using experimental quarter‐wave helical resonator structures operated at radio frequencies. These discharge sources have been used to etch submicron‐wide polysilicon gates with chlorine and chlorine/oxygen mixtures. Selectivities for undoped polysilicon over oxide and hard baked trilevel photoresist were 70:1 and 2.8:1, respectively, in a 75 W discharge operated at 0.1 mTorr with a Cl2/1% O2 feed gas mixture. Anisotropic profiles of 0.25 μm lines were obtained across 100 mm wafers with negligible linewidth loss. These preliminary experiments show that rf resonator discharges may offer an alternative to low‐pressure microwave discharges such as those based on electron cyclotron resonance.