Low-temperature photoluminescence in holmium-doped silicon

In this paper the photoluminescence (PL) of holmium-doped silicon is discussed. The silicon was first implanted with holmium ions at energies of 1–2 MeV and doses of 1×10¹³–3×10¹⁴ cm⁻², and then annealed at temperatures of 620–900 °C for 0.5–1 h. In order to increase the concentration of electrically and optically active centers, the silicon was implanted a second time with oxygen ions at energies of 0.14–0.29 MeV and doses of 1×10¹⁴–3×10¹⁵ cm⁻². Several photoluminescence lines, which are attributable to the transitions of electrons from the first excited state of the Ho³⁺ ion (⁵ I ₇) to the ground state (⁵ I ₈), were observed. The amplitudes of the most intense lines, which correspond to transitions at frequencies 5119 and 5103 cm⁻¹, decreased by more than an order of magnitude in the temperature range 4.2−78 K. The PL intensity of the holmium ions increased with increasing concentrations of the implanted rare-earth ions and oxygen. Fiz. Tekh. Poluprovodn. 33, 420–422 (April 1999)     

Zn-doping in OMVPE Grown lnP:Zn/lnGaAs/lnPp-i-n double heterojunctlons with lnGaAs:Zn contacting layers

We report on the control of zinc in organometallic vapor phase epitaxial (OMVPE) grown InP:Zn/InGaAs/InPp- i- n double heterojunctions with InGaAs:Zn contacting layers. As a function of diethylzinc (DEZn) flow, we measure net acceptor concentrations for the InP:Zn p-layer in the range 2 × 10¹⁷≤N _a−N _d≤ 9 × 10¹⁷ cm⁻³. A 435°C post-growth anneal for 300 sec increases the net acceptor concentrations by a factor of 3.6 − to 6 × 10¹⁷≤N _a−N _d≤ 3 × 10¹⁸ cm⁻³. When the annealed value ofN _a − N_din the InP:Zn layer is 6 × 10¹⁷ cm⁻³ , secondary ion mass spectrometry (SIMS) measurements show abrupt Zn-doping transitions at the heterojunction interfaces. In contrast, when the annealed value ofN _a − N_din the InP:Zn layer is near the saturation value of 3 × 10¹⁸ cm⁻³, SIMS measurements show significant movement of Zn into the nominally undoped InGaAs instrinsic layer. Increasedp-i-n diode capacitance is associated with the Zn movement.     

Nearly Perfect Electrical Activation Efficiencies from Silicon-Implanted Al<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>Ga<Subscript>1−<Emphasis Type="Italic">x</Emphasis></Subscript>N with High Aluminum Mole Fraction

Electrical activation studies of Al _x Ga_1−x N (x = 0.45 and 0.51) implanted with Si for n-type conductivity have been made as a function of ion dose and anneal temperature. Silicon ions were implanted at 200 keV with doses ranging from 1 × 10¹⁴ cm⁻² to 1 × 10¹⁵ cm⁻² at room temperature. The samples were subsequently annealed from 1150°C to 1350°C for 20 min in a nitrogen environment. Nearly 100% electrical activation efficiency was successfully obtained for the Si-implanted Al_0.45Ga_0.55N samples after annealing at 1350°C for doses of 1 × 10¹⁴ cm⁻² and 5 × 10¹⁴ cm⁻² and at 1200°C for a dose of 1 × 10¹⁵ cm⁻², and for the Al_0.51Ga_0.49N implanted with silicon doses of 1 × 10¹⁴ cm⁻² and 5 × 10¹⁴ cm⁻² after annealing at 1300°C. The highest room-temperature mobility obtained was 61 cm²/V s and 55 cm²/V s for the low-dose implanted Al_0.45Ga_0.55N and Al_0.51Ga_0.49N, respectively, after annealing at 1350°C for 20 min. These results show unprecedented activation efficiencies for Al _x Ga_1−x N with high Al mole fractions and provide suitable annealing conditions for Al _x Ga_1−x N-based device applications.     

Temperature-Dependent Studies of Si-Implanted Al<Subscript>0.33</Subscript>Ga<Subscript>0.67</Subscript>N with Different Annealing Temperatures and Times

Electrical activation studies were carried out on Si-implanted Al_0.33Ga_0.67N as a function of ion dose, annealing temperature, and annealing time. The samples were implanted at room temperature with Si ions at 200 keV in doses ranging from 1 × 10¹⁴ cm⁻² to 1 × 10¹⁵ cm⁻², and subsequently proximity-cap annealed from 1150°C to 1350°C for 20 min to 60 min in a nitrogen environment. One hundred percent electrical activation efficiency was obtained for Al_0.33Ga_0.67N samples implanted with a dose of 1 × 10¹⁵ cm⁻² after annealing at either 1200°C for 40 min or at 1300°C for 20 min. The samples implanted with doses of 1 × 10¹⁴ cm⁻² and 5 × 10¹⁴ cm⁻² exhibited significant activations of 74% and 90% after annealing for 20 min at 1300°C and 1350°C, respectively. The mobility increased as the annealing temperature increased from 1150°C to 1350°C, showing peak mobilities of 80 cm²/V s, 64 cm²/V s, and 61 cm²/V s for doses of 1 × 10¹⁴ cm⁻², 5 × 10¹⁴ cm⁻², and 1 × 10¹⁵ cm⁻², respectively. Temperature-dependent Hall-effect measurements showed that most of the implanted layers were degenerately doped. Cathodoluminescence measurements for all samples exhibited a sharp neutral donor-bound exciton peak at 4.08 eV, indicating excellent recovery of damage caused by ion implantation.     

Metalorganic vapor phase epitaxial growth,characterization and annealing experiments on InP doping superlattices

InP doping superlattices (DSLs) were grown by atmospheric pressure metalorganic vapor phase epitaxy (MOVPE) and their stability was examined by annealing at high temperatures. Diethylzinc (DEZ) and H₂S were used asp- andn-type doping sources, respectively. Photoluminescence (PL) measurements performed on as grown layers show a shift of the main emission peak with increasing excitation power in very good agreement with theoretical models. A comparison of the PL results between these structures and the annealed samples show that even at very high temperatures (up to 850° C) the tunability of the effective bandgap of the annealed superlattices is possible, although less pronounced than for the as grown layers. This is due to diffusion of the dopants, into adjacent layers and partial compensation of each other. Secondary ion mass spectrometry (SIMS) done on the as grown and annealed samples shows that only the Zn atoms diffuse. Diffusion coefficients obtained from the SIMS profiles give values in the range 1 × 10⁻¹⁴ <D < 9 × 10⁻¹⁴ cm²/s, still smaller than other published values estimated on layers, which did not suffer any treatment. This shows the high quality and stability of our layers even at high temperatures.     

Electrical Activation Studies of Silicon-Implanted Al<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>Ga<Subscript>1−<Emphasis Type="Italic">x</Emphasis></Subscript>N with Aluminum Mole Fraction of 11% to 51%

Electrical activation studies of Si-implanted Al _x Ga_1−x N with an Al mole fraction of 11% to 51% have been carried out as a function of ion dose and annealing temperature. The Al _x Ga_1−x N samples were implanted at room temperature with Si ions at 200 keV in doses ranging from 1 × 10¹⁴ cm⁻² to 1 × 10¹⁵ cm⁻², and subsequently annealed from 1100°C to 1350°C for 20 min in a nitrogen environment. The maximum electrical activation efficiencies for the Al _x Ga_1−x N samples with an Al mole fraction less than 40% were obtained for samples implanted with the highest Si dose of 1 × 10¹⁵ cm⁻². On the other hand, for the Al _x Ga_1−x N samples with an Al mole fraction more than 40%, nearly perfect activation efficiencies of 99% and 100% were obtained for the samples implanted with the lowest Si dose of 1 × 10¹⁴ cm⁻². The mobility of the Si-implanted Al _x Ga_1−x N samples increased with increasing annealing temperature in spite of the increased number of ionized donors and thus increased impurity scattering, indicating that a greater amount of lattice damage is being repaired with each successive increase in annealing temperature. These results provide suitable annealing conditions for Si-implanted Al _x Ga_1−x N-based devices with an Al mole fraction from 11% to 51%.     

Effect of annealing temperature on 1.5 μm photoluminescence from Er-lmplanted 6H-SiC

The effect of post-implantation anneal on erbium-doped 6H-SiC has been investigated. 6H-SiC has been implanted with 330 keV Er⁺ at a dose of 1 × 1013 /cm2. Er depth profiles were obtained by secondary ion mass spectrometry (SIMS). The as-implanted Er-profile had a peak concentration of∼1.3 × 10¹⁸/cm³ at a depth of 770Å. The samples were annealed in Ar at temperatures from 1200 to 1900°C. The photoluminescence intensity integrated over the 1.5 to 1.6 μm region is essentially independent of annealing temperature from 1400 to 1900°C. Reduced, but still significant PL intensity, was measured from the sample annealed at 1200°C. The approximate diffusivity of Er in 6H SiC was calculated from the SIMS profiles, yielding values from 4.5 × 10⁻¹⁶ cm²/s at 1200°C to 5.5 × 10⁻¹⁵ cm²/s at 1900°C.     

High-Dose Phosphorus-Implanted 4H-SiC: Microwave and Conventional Post-Implantation Annealing at Temperatures ≥1700°C

Semi-insulating 4H-SiC ⟨0001⟩ wafers have been phosphorus ion implanted at 500°C to obtain phosphorus box depth profiles with dopant concentration from 5 × 10¹⁹ cm⁻³ to 8 × 10²⁰ cm⁻³. These samples have been annealed by microwave and conventional inductively heated systems in the temperature range 1700°C to 2050°C. Resistivity, Hall electron density, and Hall mobility of the phosphorus-implanted and annealed 4H-SiC layers have been measured in the temperature range from room temperature to 450°C. The high-resolution x-ray diffraction and rocking curve of both virgin and processed 4H-SiC samples have been analyzed to obtain the sample crystal quality up to about 3 μm depth from the wafer surface. For both increasing implanted phosphorus concentration and increasing post-implantation annealing temperature the implanted material resistivity decreases to an asymptotic value of about 1.5 × 10⁻³ Ω cm. Increasing the implanted phosphorus concentration and post-implantation annealing temperature beyond 4 × 10²⁰ cm⁻³ and 2000°C, respectively, does not bring any apparent benefit with respect to the minimum obtainable resistivity. Sheet resistance and sheet electron density increase with increasing measurement temperature. Electron density saturates at 1.5 × 10²⁰ cm⁻³ for implanted phosphorus plateau values ≥4 × 10²⁰ cm⁻³, irrespective of the post-implantation annealing method. Implantation produces an increase of the lattice parameter in the bulk 4H-SiC underneath the phosphorus-implanted layer. Microwave and conventional annealing produce a further increase of the lattice parameter in such a depth region and an equivalent recovered lattice in the phosphorus-implanted layers.     

Activation of silicon ion-implanted gallium nitride by furnace annealing

Ion implantation into III–V nitride materials is animportant technology for high-power and high-temperature digital and monolithic microwave integrated circuits. We report the results of the electrical, optical, and surface morphology of Si ion-implanted GaN films using furnace annealing. We demonstrate high sheet-carrier densities for relatively low-dose (n_atoms=5×10¹⁴ cm⁻²) Si implants into AlN/GaN/sapphire heteroepitaxial films. The samples that were annealed at 1150°C in N₂ for 5 min exhibited a smooth surface morphology and a sheet electron concentration n_s ∼9.0×10¹³ cm⁻², corresponding to an estimated 19% electrical activation and a 38% Si donor activation in GaN films grown on sapphire substrates. Variable-temperature Hall-effect measurem entsindicate a Si donor ionization energy ∼15 meV.     

Electrophysical properties of solid solutions of silver in PbTe

The thermopower coefficient α₀ and the electrical conductivity σ of Pb_{1 − x} Ag _x Te solid solutions, where x = (0–0.007), are measured at T = 300 K. The hole concentration p is calculated. All samples are of the p type. With increasing silver content, α₀ decreases, while p and σ increase. For undoped crystals, α₀ = 251.0 μV/K, p = 1.1 × 10¹⁸ cm⁻³, and σ = 165 Ω⁻¹ cm⁻¹. At the silver-solubility limit for x = 0.007, α₀ = 193.8 μV/K, p = 2.3 × 10¹⁸ cm⁻³, and σ = 216 Ω⁻¹ cm⁻¹. The hole concentration in all samples is much lower than the concentration of introduced silver atoms. The hole gas in Pb_{1 − x} Ag _x Te solid solutions is weakly degenerate in the entire silver-concentration range.     

Hot-implantation of nitrogen donors into p- type α-SiC and characterization of n+-p junction

N⁺ implantation into p-type a-SiC (6H-SiC, 4H-SiC) epilayers at elevated temperatures was investigated and compared with implantation at room temperature (RT). When the implant dose exceeded 4 × 10₁₅ cm₋₂, a complete amorphous layer was formed in RT implantation and severe damage remained even after post implantation annealing at 1500°C. By employing hot implantation at 500~800°C, the formation of a complete amorphous layer was suppressed and the residual damage after annealing was significantly reduced. For implant doses higher than 10¹⁵ cm⁻², the sheet resistance of implanted layers was much reduced by hot implantation. The lowest sheet resistance of 542Ω/ was obtained by implantation at 500 ~ 800°C with a 4 × 10¹⁵ cm⁻² dose. Characterization of n⁺-p junctions fabricated by N⁺ implantation into p-type epilayers was carried out in detail. The net doping concentration in the region close to the junction showed a linearly graded profile. The forward current was clearly divided into two components of diffusion and recombination. A high breakdown voltage of 615 ∼ 810V, that is almost an ideal value, was obtained, even if the implant dose exceeded 10¹⁵ cm⁻². By employing hot implantation at 800°C, the reverse leakage current was significantly reduced.     

A technique to reduce the contact resistance to 4H-silicon carbide using germanium implantation

The effects of implanted Ge on the resistance of nickel-metal contacts to n-type and p-type 4H-SiC are reported. The Ge was implanted with an energy of 346 keV and a dose of 1.7×10¹⁶ cm⁻², and the wafer was annealed up to 1700°C for 30 min. Contact resistance measurements using the transfer length method (TLM) were performed on etched mesas of n-type and p-type 4H-SiC, with and without the Ge. For the annealed-Ni metal contacts, the Ge lowered the specific contact resistivity from 5.3×10⁻⁴ Ωcm² to 6.0×10⁻⁵ Ωcm² for n-type SiC and from 1.2×10⁻³ Ωcm² to 8.3×10⁻⁵ Ωcm² for p-type SiC. For the as-deposited (unannealed) Ni, the Ge produced ohmic contacts, whereas the contacts without Ge were rectifying. These results suggest that the addition of Ge can be an important process step to reduce the contact resistance for SiC-device applications.     

Nuclear magnetic resonance spectra of 119Sn and 125Te in SnTe and SnTe:Mn

A study is reported of the nuclear magnetic resonance spectra of ¹¹⁹Sn and ¹²⁵Te in SnTe with hole concentrations p ₇₇=1.42×10²⁰−2.3×10²¹ cm⁻³ and in SnTe:Mn (N _Mn=0.5 and 5 at. %, p ₇₇=8×10²⁰ cm⁻³) at T=4.2–300 K. Considerable broadening of NMR lines due to hyperfine magnetic interactions between nuclear and electron spins was observed in SnTe with p ₇₇>2ײ⁰ cm⁻³. Asymmetric broadening of the resonance lines was observed in the rhombohedral phase of SnTe and SnTe:Mn. The temperature dependence of the NMR line width of ¹²⁵Te in SnTe:Mn is in agreement with the magnetic phase diagram for N _Mn=5 at. %. The superparamagnetic phase of SnTe:Mn is formed at T=20±2 K and the ferromagnetic phase is formed at T=4.2 K. Fiz. Tekh. Poluprovodn. 31, 1187–1191 (October 1997)     

Exfoliation and blistering of Cd<Subscript>0.96</Subscript>Zn<Subscript>0.04</Subscript>Te substrates by ion implantation

As part of a series of wafer bonding experiments, the exfoliation/blistering of ion-implanted Cd_0.96Zn_0.04Te substrates was investigated as a function of postimplantation annealing conditions. (211) Cd_0.96Zn_0.04Te samples were implanted either with hydrogen (5×10¹⁶ cm⁻²; 40–200 keV) or co-implanted with boron (1×10¹⁵ cm⁻²; 147 keV) and hydrogen (1–5×10¹⁶ cm⁻²; 40 keV) at intended implant temperatures of 253 K or 77 K. Silicon reference samples were simultaneously co-implanted. The change in the implant profile after annealing at low temperatures (<300°C) was monitored using high-resolution x-ray diffraction, atomic force microscopy (AFM), and optical microscopy. The samples implanted at the higher temperature did not show any evidence of blistering after annealing, although there was evidence of sample heating above 253 K during the implant. The samples implanted at 77 K blistered at temperatures ranging from 150°C to 300°C, depending on the hydrogen implant dose and the presence of the boron co-implant. The production of blisters under different implant and annealing conditions is consistent with nucleation of subsurface defects at lower temperature, followed by blistering/exfoliation at higher temperature. The surface roughness remained comparable to that of the as-implanted sample after the lower temperature anneal sequence, so this defect nucleation step is consistent with a wafer bond annealing step prior to exfoliation. Higher temperature anneals lead to exfoliation of all samples implanted at 77 K, although the blistering temperature (150–300°C) was a strong function of the implant conditions. The exfoliated layer thickness was 330 nm, in good agreement with the projected range. The “optimum” conditions based on our experimental data showed that implanting CdZnTe with H⁺ at 77 K and a dose of 5×10¹⁶/cm² is compatible with developing high interfacial energy at the bonded interface during a low-temperature (150°C) anneal followed by layer exfoliation at higher (300°C) temperature.     

Surface roughening in ion implanted 4H-silicon carbide

Silicon carbide (SiC) devices have the potential to yield new components with functional capabilities that far exceed components based on silicon devices. Selective doping of SiC by ion implantation is an important fabrication technology that must be completely understood if SiC devices are to achieve their potential. One major problem with ion implantation into SiC is the surface roughening that results from annealing SiC at the high temperatures which are needed to activate implanted acceptor ions, boron or aluminum. This paper examines the causes and possible solutions to surface roughening of implanted and annealed 4H-SiC. Samples consisting of n-type epilayers (5 × 10¹⁵ cm⁻³, 4 μm thick) on 4H-SiC substrates were implanted with B or Al to a total dose of 4 × 10¹⁴ cm⁻² or 2 × 10¹⁵ cm⁻², respectively. Roughness measurements were made using atomic force microscopy. From the variation of root mean square (rms) roughness with annealing temperature, apparent activation energies for roughening following implantation with Al and B were 1.1 and 2.2 eV, respectively, when annealed in argon. Time-dependent activation and surface morphology analyses show a sublinear dependence of implant activation on time; activation percentages after a 5 min anneal following boron implantation are about a factor of two less than after a 40 min anneal. The rms surface roughness remained relatively constant with time for anneals in argon at 1750°C. Roughness values at this temperature were approximately 8.0 nm. Annealing experiments performed in different ambients demonstrated the benefits of using silane to maintain good surface morphology. Roughnesses were 1.0 nm (rms) when boron or aluminum implants were annealed in silane at 1700°C, but were about 8 and 11 nm for B and Al, respectively, when annealed in argon at the same temperature.     

Influence of Surface Treatment and Annealing Temperature on the Formation of Low-Resistance Au/Ni Ohmic Contacts to <Emphasis Type="Italic">p</Emphasis>-GaN

We have studied the influence of surface treatment and annealing temperature on the specific contact resistance of Au/Ni ohmic contacts to p-GaN with hole concentrations in the range of 10¹⁶ cm⁻³ to 10¹⁸ cm⁻³. The sample with a hole concentration of 1 × 10¹⁸ cm⁻³, treated with the surface treatment HCl:H₂O = 3:1 solution and annealed at 500°C in a 90% N₂ and 10% O₂ atmosphere, yielded the lowest specific contact resistance of ~4 × 10⁻⁵ Ω cm² and ~2 × 10⁻⁷ Ω cm² at room temperature and at 150°C, respectively. To investigate the roles of interdiffusion between layer interfaces and the formation of NiO and nickel gallides, we examined the metallization stacks before and after annealing using high-resolution x-ray diffraction. We conclude that the nickel-gallide formation and the deterioration of the NiO layer are together responsible for the large deviation in contact resistances observed for samples annealed at various temperatures.     

Passivation of infrared photodiodes with alcoholic sulfide solution

The effect of passivation with the solution of sodium sulfide (Na₂S) in isopropyl alcohol on the room-temperature performance of the GaInAsSb/GaAlAsSb and InAs/InAsSbP photodiodes is investigated. After such a treatment the dark current density of the GaInAsSb/GaAlAsSb photodiodes at a reverse bias of 0.1 V is reduced from 5.5 × 10⁻² to 2.1 × 10⁻³ A/cm² and a zero-bias resistance-area product (R ₀ A) is improved from 1.0 to 25.6 Ω cm². For the InAs/InAsSbP photodiodes, the dark current density at U = −0.1 V is decreased from 1.34 to 8.1 × 10⁻¹ A/cm², while the R ₀ A value increases from 4.4 × 10⁻² to 7.3 × 10⁻² Ω cm². The method offers long-term stability of the photodiode performance.     

Characterization of Hg0.7Cd0.3Te n- on p-type structures obtained by reactive ion etching induced p- to n conversion

This paper presents transport measurements on both vacancy doped and gold doped Hg_0.7Cd_0.3Te p-type epilayers grown by liquid phase epitaxy (LPE), with N_A=2×10¹⁶ cm⁻³, in which a thin 2 μm surface layer has been converted to n-type by a short reactive ion etching (RIE) process. Hall and resistivity measurements were performed on the n-on-p structures in van der Pauw configuration for the temperature range from 30 K to 400 K and magnetic field range up to 12 T. The experimental Hall coefficient and resistivity data has been analyzed using the quantitative mobility spectrum analysis procedure to extract the transport properties of each individual carrier contributing to the total conduction process. In both samples three distinct carrier species have been identified. For 77 K, the individual carrier species exhibited the following properties for the vacancy and Au-doped samples, respectively, holes associated with the unconverted p-type epilayer with p ≈ 2 × 10¹⁶ cm⁻³, μ ≈ 350 cm²V⁻¹s⁻¹, and p ≈ 6 × 10¹⁵ cm⁻³, μ ≈ 400 cm²V⁻¹s⁻¹; bulk electrons associated with the RIE converted region with n ≈ 3 × 10¹⁵cm⁻³, μ ≈ 4 × 10⁴ cm²V⁻¹s⁻¹, and n ≈ 1.5 × 10¹⁵ cm⁻³, μ ≈ 6 × 10⁴ cm²V⁻¹s⁻¹; and surface electrons (2D concentration) n ≈ 9 × 10¹² cm⁻² and n ≈ 1 × 10¹³ cm⁻², with mobility in the range 1.5 × 10³ cm²V⁻¹s⁻¹ to 1.5 × 10⁴ cm²V⁻¹s⁻¹ in both samples. The high mobility of bulk electrons in the RIE converted n-layer indicates that a diffusion process rather than damage induced conversion is responsible for the p-to-n conversion deep in the bulk. On the other hand, these results indicate that the surface electron mobility is affected by RIE induced damage in a very thin layer at the HgCdTe surface.     

Density measurement of Sn-40Pb,Sn-57Bi,and Sn-9Zn by indirect Archimedean method

By the indirect Archimedean method, the density and the density-temperature relationship of the Sn-40Pb eutectic alloy and two Pb-free solders, Sn-57Bi and Sn-9Zn eutectic alloys, were measured from room temperature to about 250°C. The results showed that the density-temperature dependence for each alloy in both solid and melting states can be fitted linearly as ρ_S(Sn-40Pb)=8.51−8.94×10⁻⁴(T−25°C), ρ_L(Sn-40Pb)=8.15−13.8×10⁻⁴(T−T_m); ρ_S(Sn-57Bi)=8.54−5.86 × 10⁻⁴(T−25°C), ρ_L(Sn-57Bi)=8.51−10.9×10⁻⁴(T−T_m); and ρ_s(Sn-9Zn)=7.22−7.78×10⁻⁴(T−25°C), ρ_L(Sn-9Zn)=6.89−5.88×10 ⁻⁴(T−T_m), where the density unit was g/cm³. At the melting point, density of the melt of these solders is 8.15 g/cm³, 8.51 g/cm³, and 6.89 g/cm³, respectively. The density decreased 2.6% for Sn-40Pb eutectic alloy during melting, and 2.7% for Sn-9Zn eutectic alloy, but increased 0.5% for Sn-57Bi eutectic alloy. The excess molar volume for these alloys after mixing at their melting point is 0.03 cm³/mol for Sn-40Pb, 0.09 cm³/mol for Sn-57Bi, and 0.21 cm³/mol for Sn-9Zn.     

Boron implantation and epitaxial regrowth studies of 6H SiC

Implantation of B has been performed into an epitaxially grown layer of 6H SiC, at two different B concentrations, 2×10¹⁶ cm⁻³ and 2×10¹⁸ cm⁻³. Subsequently, an epitaxial layer was regrown on the B implanted layer. The samples were investigated by transmission electron microscopy (TEM) and secondary ion mass spectrometry (SIMS). In the highly B-doped layers plate-like defects were found, associated with large strain fields, and an increased B concentration. These defects were stable at the originally implanted region during regrowth and at anneal temperatures up to 1700°C. In the samples implanted with the lower B concentration, no crystal defects could be detected by TEM. No threading dislocations or other defects were observed in the regrown epitaxial layer, which shows the possibility to grow a layer with high crystalline quality on B implanted 6H SiC. By SIMS, it was found that B piles up at the interface to the regrown layer, which could be explained by enhanced diffusion from an increased concentration of point defects created by implantation damage in the region. B is also spread out into the original crystal and in the regrown layer at a concentration of below 2×10¹⁶ cm⁻³, with a diffusion constant estimated to 1.3×10⁻¹² cm²s⁻¹. This diffusion is most probably not driven by implantation damage, but by intrinsic defects in the grown crystal. Our investigation shows that the combination of implantation and subsequent regrowth techniques could be used in SiC for building advanced device structures, with the crystal quality in the regrown layer not being deteriorated by crystal defects in the implanted region. A device process using B implantation and subsequent regrowth could on the other hand be limited by the diffusion of B.