Field Emission and Electric Discharge of Nanocrystalline Diamond Films

Nanocrystalline diamond (NCD) films were produced by microwave plasma-enhanced chemical vapor deposition (MPECVD) using gas mixtures of Ar, H₂, and CH₄. The structural properties, electron emission, and electric discharge behaviors of the NCD films varied with H₂ flow rates during MPECVD. The turn-on field for electron emission at a pressure of 2.66 × 10⁻⁴ Pa increased from 4.2 V μm⁻¹ for the NCD films that were deposited using a H₂ flow rate of 10 cm³ min⁻¹ to 7 V μm⁻¹ for films deposited at a H₂ flow rate of 20 cm³ min⁻¹. The NCD film with a low turn-on field also induced low breakdown voltages in N₂. The grain size and roughness of the NCD films may influence both the electron emission and the electric discharge behaviors of the NCD cathodes.     

Growth of CdTe Films on Amorphous Substrates Using CaF<Subscript>2</Subscript> Nanorods as a Buffer Layer

Continuous biaxially textured CdTe films were grown on biaxial CaF₂ buffer layers. The CaF₂ nanorods were grown by oblique angle vapor deposition and possessed a {111} 〈121〉 biaxial texture. The CdTe film was deposited by metal organic chemical vapor deposition (MOCVD). Film morphology and the CdTe/CaF₂ interface were studied by scanning electron microscopy and transmission electron microscopy. Characterization showed that small CdTe grains formed initially from the CaF₂ surfaces. These small grains then merged into large columnar grains during growth. Analysis revealed that the crystalline orientation of the CdTe film followed the biaxial texture of the CaF₂ nanorods.     

Growth and characterization of inTISb for IR-detectors

Epitaxial In_1-xTl_xSb films with compositions up to x = 0.1 have been demonstrated using the metalorganic chemical vapor deposition technique on InSb and GaAs substrates. A specially designed high-temperature source delivery system was used for the low vapor pressure cyclopentadienylthallium source. Tl-compositions in the deposited films were measured by Rutherford backscattering spectroscopy which confirmed the incorporation of up to 10% Tl. Room temperature infrared transmission spectra of InTISb exhibited considerable absorption beyond 7 μm. Photoconductive detectors were fabricated in InTISb films grown on semi-insulating GaAs. Spectral response measurements showed substantial photoresponse at 8.5 to 14 μm. In spite of the large lattice-mismatch (≈14%) between InTISb and GaAs, photoconductive detectors exhibited black-body detectivities (D^* _bb) of 5.0 × 10⁸ cm-Hz^1/2W⁻¹ at 40K.     

The properties of Si/Si1-xGex films grown on Si substrates by chemical vapor deposition

A growth parameter study was made to determine the proper of a SiGe superlattice-type configuration grown on Si substrates by chemical vapor deposition (CVD). The study included such variables as growth temperature, layer composition, layer thickness, total film thickness, doping concentrations, and film orientation. Si and SiGe layers were grown using SiH₄ as the Si source and GeH₄ as the Ge source. When intentional doping was desired, diluted diborane for p-type films and phosphine for n-type films were used. The study led to films grown at ∼1000°C with mobilities from ∼20 to 40 percent higher than that of epitaxial Si layers and ∼100 percent higher than that of epitaxial SiGe layers grown on (100) Si in the same deposition system for net carrier concentrations of ∼8x10¹⁵ cm^-3 to ∼2x10¹⁷ cm^-3. Enhanced mobilities were found in multilayer (100)-oriented Si/Si_1-xGe_x films for layer thicknesses ≥400A, for film thicknesses >2μm, and for layers with x = 0.15. No enhanced mobility was found for (111)-oriented films and for B-doped multilayered (100)-orlented films. Supported in part by NASA-Langley Research Center, Hampton, VA, Contract NAS1-16102 (R. Stermer & A. Fripp, Contr. Mon.)     

Optical absorption enhancement of μc-SiGe:H films deposited via high pressure and high power

Hydrogenated microcrystalline silicon-germanium （μc-SiGe：H） films are fabricated by radio-frequency plasma-en- hanced chemical vapor deposition （RF-PECVD）. The optical absorption coefficient and the photosensitivity of the μc-SiGe：H films increase dramatically by increasing the plasma power and deposition pressure simultaneously. Addi- tionally, the microstructural properties of the μc-SiGe：H films are also studied. By combining Raman, Fourier trans- form infrared （FTIR） and X-ray fluoroscopy （XRF） measurements, it is shown that the Ge-bonding configuration and compactability of theμc-SiGe：H thin films play a crucial role in enhancing the optical absorption and optimizing the quality of the films via a significant reduction in the defect density.     

Improvement in dielectric properties of low temperature PECVD silicon dioxide by reaction with hydrazine

The dielectric properties of plasma-enhanced chemical vapor deposition (PECVD) SiO₂ deposited at 150°C were improved by reaction with anhydrous hydrazine vapor at 150–350°C. The permittivity and loss decreased ~32% and ~86%, respectively, after reaction with hydrazine at 150°C. The decrease in permittivity and loss correlated with a decrease in the dipole concentration (silanol + water). During exposure to humid conditions, water uptake in the SiO₂ films degraded the dielectric properties. A nitrogen anneal at 350°C did not improve the dielectric properties of the PECVD SiO₂. Although water was removed from the films, silanol remained. When the PECVD SiO₂ deposited at 150° was reacted with hydrazine vapor at 150°C, both silanol and water were removed from the films. The dielectric properties and resistance to water absorption improved.     

VHF-PFLWD法制备μc-SiGe薄膜的研究

分别以Si2 H6和GeH4及SiH4和GeH4两种组合气体为源气体,用甚高频等离子增强化学气相沉积(VHF-PECVD)制备μc-SiGe薄膜.用Raman散射光谱和原子力显微镜(AFM)对薄膜的结构进行研究.结果表明:与SiH4和GeH4制备的薄膜系列相比,Si2H6和GeH4制备的薄膜中Ge的融入速率相对较慢;用...     

Synthesis of low resistivity complex oxides on MgO using Pt as buffer layer

Highly crystalline SrRuO₃ (SRO) and La_0.5Sr_0.5CoO₃ (LSCO) thin films were deposited on (100) Pt/ MgO by pulsed laser deposition. The films were mainly (001) textured normal to the substrate surface with a high degree of in-plane orientation with respect to the substrate’s major axes. These films were characterized using x-ray diffraction, Rutherford backscattering, four-point probe resistivity measurement, and transmission electron microscopy. The room temperature resistivity for LSCO and SRO films on Pt/MgO was found to be ∼35 and ∼40 μΩ-cm, respectively. An ion beam minimum channeling yield of ∼43% and ∼33% was obtained for LSCO and SRO films, respectively. The interface between Pt and oxide was found to be smooth and free from any interfacial diffusion. This result showed that high-quality low resistivity oxide thin films can be deposited on Pt.     

Laser processing of TiSi2 and CoSi2 thin films on silicon (100) substrates

We have investigated the formation of TiSi₂ and CoSi₂ thin films on Si(100) substrates using laser (wave length 248 nm, pulse duration 40 ns and repetition rate 5 Hz) physical vapor deposition (LPVD). The films were deposited from solid targets of TiSi₂ and CoSi₂ in vacuum with the substrate temperature optimized at 600° C. The films were characterized using x-ray diffraction, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and four point probe ac resistivity. The films were found to be polycrystalline with a texture. The room temperature resistivity was found to be 16 μΩ-@#@ cm and 23 μΩ-cm for TiSi₂ and CoSi₂ films, respectively. We optimized the processing parameters so as to get particulate free surface. TEM results show that the silicide/silicon interface is quite smooth and there is no perceptible interdiffusion across the interface.     

Polycrystalline silicon thin film transistors fabricated in various solid phase crystallized films deposited on glass substrates

In this work, we have characterized various types of polysilicon films, crystallized upon thermal annealing from films deposited by low pressure chemical vapor deposition in the amorphous phase and a mixed phase using silane or in the amorphous phase using disilane. Polysilicon thin film transistors (TFTs) were fabricated, at low processing temperatures, in these three types of films on high strain point Corning Code 1734 and 1735 glass substrates. Double layer films, with the bottom layer deposited in a mixed phase and the top in the amorphous phase, allowed TFT fabrication at a drastically reduced thermal budget; optimum values of thicknesses and deposition rates of the layers are reported for reducing the crystallization time and improving film quality. Optimum deposition conditions for TFT fabrication were also obtained for films deposited using disilane. The grain size distribution for all types of films was shown to be wider for a larger grain size. Fabricated TFTs exhibited field effect electron mobility values in the range of 20 to 50 cm²/V·s, subthreshold swings of about 0.5–1.5 V/dec and threshold voltage values of 2–4 V.     

Effects of oxygen doping on properties of microcrystalline silicon film grown using rapid thermal chemical vapor deposition

An oxygen doped microcrystalline silicon (μc-Si) deposition process is developed by mixing small amounts of nitrous oxide (N₂O) with silane (SiH₄) in a rapid thermal chemical vapor deposition (RTCVD) reactor. The effects of oxygen doping on the properties of RTCVD μc-Si films are studied. Experimental results show that the RTCVD process provides high deposition rates for μc-Si and polycrystalline silicon (polySi) films at elevated deposition temperatures and pressures. The surface roughness of the RTCVD μc-Si films can be significantly reduced compared to that of conventional LPCVD polySi films. Steep side walls can be realized due to the small grain size of the μc-Si films. The sheet resistance of BF₂ doped μc-Si films is slightly higher than that of BF₂ doped polySi films, whereas sheet resistances of P and As doped μc-Si films are much higher than those of the corresponding P and As doped polySi films. Measurements of the catastrophic breakdown strength of metal-oxide-semiconductor (MOS) capacitors indicate that the quality of gate electrodes fabricated using μc-Si is improved relative to that of MOS capacitors fabricated using polySi gate electrodes.     

Characteristics of thin film transistors fabricated in polysilicon films deposited by plasma enhanced chemical vapor deposition

Thin-film transistors (TFTs) fabricated in polysilicon films deposited by plasma enhanced chemical vapor deposition (PECVD) were characterized. The transistors were fabricated using a low temperature process (i.e., <- 700° C). The characteristics of the devices were found to improve as the deposition temperature of the polysilicon film increased. The best characteristics (μ _FE of 15 cm²/V _s andV _TH of 2.2V) were measured in the devices fabricated in the film deposited at 700° C. The devices fabricated in the PECVD polysilicon films were compared to those fabricated in polysilicon films deposited by thermal CVD in the same reactor in order to decouple the effect of the plasma. A coplanar electrode structure TFT with adequate characteristics (μ _FE of 8 cm²/V _s) was also demonstrated in the PECVD polysilicon films.     

Preparation of (Pb0.88La0.12)TiO3 thin films for dynamic random access memory by low pressure-metalorganic chemical vapor deposition

La-modified lead titanate (PLT) thin films were prepared by hot-wall type low pressure-metalorganic chemical vapor deposition method. Pb(dpm)₂, La(dpm)₃, and titanium tetraisopropoxide were used as source materials. The films were deposited at 500°C under the low pressure of 1000 mTorr and then annealed at 650°C for 10 min in oxygen ambient. Sputter-deposited platinum electrodes and 180 nm thick PLT thin films were employed to form MIM capacitors with the best combination of high charge storage density (26.7 μC/cm² at 3V) and low leakage current density (1.5 × 10^-7 A/cm² at 3V). The measured dielectric constant and dielectric loss were 1000∼1200 and 0.06∼0.07 at zero bias and 100 kHz, respectively.     

Capacitance-Voltage characteristics of metal-insulator-semiconductor diodes with S passivation and Si interface control layers on GaAs and InP

GaAs and InP surfaces have been prepared by gas-phase and liquid-phase polysulfide passivation techniques followed by the deposition of Si interface control layers (ICLs) by e-beam evaporation. For GaAs surfaces, the performance of an ICL consisting of 1.5 nm Si on top of 0.5 nm of Ge has also been evaluated. Metal-insulator-semiconductor diodes with aluminum top electrodes were fabricated on these surfaces using silicon nitride deposited by a remote plasma-enhanced chemical vapor technique or silicon dioxide deposited by a conventional direct plasma-enhanced chemical vapor deposition technique. The quality of the interfaces was analyzed by capacitance-voltage (C-V) measurements and the interface state densities D_it were deduced from the C-V data using the high-low method. Values as low as 1.5 × 10¹² eV⁻¹cm⁻² were obtained for polysulfide-passivated GaAs surfaces with a Ge-Si or Si ICL, the lowest ever demonstrated using the high-low method for an ex-situ technique not involving GaAs epitaxy. For InP, the Si ICL does not reduce D_it below that of 2 × 10¹² eV⁻¹ cm ⁻² that was obtained for the polysulfide passivated surface. The Si ICL produces an interface that degrades more slowly on exposure to air for both GaAs and InP.     

Low-temperature metal-organic chemical vapor deposition (LTMOCVD) of device-quality copper films for microelectronic applications

Copper films for potential use in multilevel metallization in ULSIC’s were produced by low temperature (250–350° C) metal-organic chemical vapor deposition (LTMOCVD) in atmospheres of pure H₂ or mixture Ar/H₂ from the β-diketonate precursor bis(1,1,1,5,5,5-hexafluoroacetylacetonato) copper(ll), Cu(hfa)₂. The films were analyzed by x-ray diffraction (XRD), Rutherford backscattering (RBS), Auger electron spectroscopy (AES), scanning electron microscopy (SEM), and energy-dispersive x-ray spectroscopy (EDXS). The results of these studies showed that the films were uniform, continuous, adherent and highly pure—oxygen and carbon contents were below the detection limits of AES. Four point resistivity measurements showed that the copper films had very low resistivity, as low as 1.9 μΩcm for the films deposited in pure hydrogen atmosphere. Our preliminary results seem to indicate that LTMOCVD is a very attractive technique for copper multilevel metallizations.     

The CVD growth of Cu films using H2 as carrier gas

Copper chemical vapor deposition from Cu(hexafluoroacetylacetonate)trimethylvinylsilane (Cu(hfac)TMVS) was studied using a low pressure chemical vapor deposition system of a cold wall vertical reactor. The Cu films deposited using H₂ as a carrier gas revealed no impurities in the films within the detection limits of Auger electron spectroscopy and x-ray photoelectron spectroscopy. Using hydrogen as a carrier gas, the hydrogen not only acts as a reducing agent, but also reacts with the residual fragment of precursor. As a result, using H₂ as a carrier gas for Cu(hfac)TMVS resulted in Cu films of lower resistivity, denser microstructure and faster deposition rate than using Ar or N₂ as the carrier gas. Moreover, we found that N₂ plasma treatment on the substrate surface prior to Cu deposition increased the deposition rate of Cu films.     

a-Si:C:H and a-Si:N:H Thin Films Obtained by PECVD for Applications in Silicon Solar Cells

Hydrogenated amorphous silicon-carbon (a-Si:C:H) and hydrogenated silicon-nitrogen (a-Si:N:H) antireflective films were deposited by plasma-enhanced chemical vapor deposition (PECVD) at 13.56 MHz in SiH₄ + CH₄ and SiH₄ + NH₃ gaseous mixtures of various compositions. The silicon and glass samples were investigated by optical spectroscopy, Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). A correlation between film properties and process parameters was found. The refractive index decreased and the energy gap increased with an increase of carbon and nitrogen in the films. For some process parameters, it was possible to obtain smooth, hydrogen rich, and homogeneous films of low reflectivity. The silicon solar cells with antireflective coatings revealed an increase in efficiency.     

ZnO Thin Film, Device, and Circuit Fabrication using Low-Temperature PECVD Processes

We report undoped ZnO films deposited at low temperature (200°C) using plasma-enhanced chemical vapor deposition (PECVD). ZnO thin-film transistors (TFTs) fabricated using ZnO and Al₂O₃ deposited in situ by PECVD with moderate gate leakage show a field-effect mobility of 10 cm²/V s, threshold voltage of 7.5 V, subthreshold slope <1 V/dec, and current on/off ratios >10⁴. Inverter circuits fabricated using these ZnO TFTs show peak gain magnitude (dV _out/dV _in) ~5. These devices appear to be strongly limited by interface states and reducing the gate leakage results in TFTs with lower mobility. For example, ZnO TFTs fabricated with low-leakage Al₂O₃ have mobility near 0.05 cm²/V s, and five-stage ring-oscillator integrated circuits fabricated using these TFTs have a 1.2 kHz oscillation frequency at 60 V, likely limited by interface states.     

Properties of low-k SiCOH films prepared by plasma-enhanced chemical vapor deposition using trimethylsilane

The properties of low-k SiCOH film deposited by plasma-enhanced chemical vapor deposition using trimethylsilane are reported here. The deposition process was performed at different temperatures from 200 to 400 °C. The influence of deposition temperature on the films were characterized using Fourier transform infrared spectroscopy (FTIR) to understand its impact on the studied properties. The films were annealed at ∼450 °C in an inert ambient after deposition in all the cases. The deposition rate decreases with increase in deposition temperature. The refractive index of the films increases as a function of deposition temperature. From FTIR spectra, OH-related bonds were not detected in films even when deposited at 200 °C. The Si-CH₃ bonds were detected in all the films and decreased monotonically from 200 to 400 °C. All deposition conditions studied resulted in films with dielectric constant less than 3, the lowest being ∼2.7 when deposited at 200 °C. All films exhibited good thermal stability.     

Effects of nitrogen doping on the growth and properties of plasma-enhanced chemical-vapor-deposited diamond-like-carbon films

Nitrogen-doped diamond-like carbon (DLC) or amorphous hydrogenated carbon (a-C:H) films were grown by plasma enhanced chemical vapor deposition using methane and nitrogen gases as precursors. The effects of nitrogen trifluoride (NF₃) on these nitrogen-doped DLC films were also investigated. The deposition rate decreases sharply with the addition of nitrogen in the absence of NFF₃ due to dilution, while it increases in the presence of NFF₃ due, presumably, to the reduction of activated hydrogen species by the fluorine radical (F϶. X-ray photoelectron spectra reveal a nitrogen concentration in the range of 9.3 to 13.8% in these DLC films with a C Is electron binding energy of 287-288 eV, indicating the diamond-like structure. Infrared spectra of DLC films indicate the presence of amino groups (N-H) and nitrile and/or isonitrile (C= N) groups giving strong evidence of sp carbon. Diamond like carbon films deposited in CHF₄ +NF₄ (with and without NFF₃) have a lower refractive index, a lower bulk resistivity, and a lower optical bandgap than films deposited using CHF₄ due to a lower hydrogen content in the films. Moreover, the bulk resistivity of these films decreases by over four orders of magnitude and the optical bandgap decreases from 2.65 eV to about 0.75 eV following annealing at a temperature of 500°C.