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PART III: METALORGANIC CHEMICAL VAPOR DEPOSITION Description of the MOCVD equipment Analysis of the MOCVD growth process Growth modes in MOCVD.

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Presentation on theme: "PART III: METALORGANIC CHEMICAL VAPOR DEPOSITION Description of the MOCVD equipment Analysis of the MOCVD growth process Growth modes in MOCVD."— Presentation transcript:

1 PART III: METALORGANIC CHEMICAL VAPOR DEPOSITION Description of the MOCVD equipment Analysis of the MOCVD growth process Growth modes in MOCVD

2 Metalorgenic Chemical Vapor Deposition (MOCVD) [Metalorganic Vapor Phase Epitaxy (MOVPE), OMCVD, OMVPE] One of the premier techniques for epitaxial growth of thin layer structures (semiconductors, oxides, superconductors) Introduced around 25 years ago as the most versatile technique for growing semiconductor films. Wide application for devices such Lasers, LEDs, solar cells, photodetectors, HBTs, FETs. Principle of operation: transport of precursor molecules (group-III metalorganics + group-V hydrides or alkyls) by a carrier gas (H 2, N 2 ) onto a heated substrate; surface chemical reactions. Complex transport phenomena and reactions, complicated models to determine reactor designs,growth modes and rates. In-situ diagnostics less common than in MBE.

3 Description of the MOCVD equipment R. L. Moon and Y.-M. Houng, in Chemical vapor deposition - Principles and applications, edited by M. L. Hitchman and K. F. Jensen (Academic Press, London, 1993). G. B. Stringfellow, Organometallic vapor phase epitaxy: theory and practice (Academic Press, Boston, 1989).

4 MOCVD Facility, horizontal reactor Research system (left): AIX 200 1X2 wafer capacity Production system (right): AIX 2600 Up to 5X10 wafer capacity (AIX 3000) Gas handling Reactor Glove box

5 Schematics of a MOCVD system Carrier gas Material sources Gas handling system Reactor Exhaust system Safety system In-situ diagnostics NO electron beam probes! Reflectance Ellipsometry RAS

6 Gas handling system The function of gas handling system is mixing and metering of the gas that will enter the reactor. Timing and composition of the gas entering the reactor will determine the epilayer structure. Leak-tight of the gas panel is essential, because the oxygen contamination will degrade the growing films properties. Fast switch of valve system is very important for thin film and abrupt interface structure growth, Accurate control of flow rate, pressure and temperature can ensure stability and repeatability.

7 Carrier gas Inert carrier gas constitutes about 90 % of the gas phase stringent purity requirements. H 2 traditionally used, simple to purify by being passed through a palladium foil heated to 400 °C. Problem: H 2 is highly explosive in contact with O 2 high safety costs. Alternative precursor : N 2 : safer, recently with similar purity, more effective in cracking precursor molecules (heavier). High flux fast change of vapor phase composition. Regulation: mass flow controller P ~ mbar Mass flow controllers

8 Material sources Volatile precursor molecules transported by the carrier gas Growth of III-V semiconductors: Group III: generally metalorganic molecules (trimethyl- or triethyl- species) Group V: generally toxic hydrides (AsH 3 ; PH 3 flammable as well); alternative: alkyls (TBAs, TBP).

9 Hidrides and dopants Form: gases from high pressure cylinders Mixed into the carrier gas line Flow control: valve + mass flow controller (MFC)

10 Metalorganics Liquid (or finely divided solid – TMIn) contained in a stainess steel bubbler. Vapor pressure fixed by constant temperature in a thermal bath; T -20 o C ÷ 40 o C; T = ±1 o C. Controlled H 2 flow through the bubbler saturated stream; composition depends on H 2 flow rate adjustment through MFC P ressure controller (PC) to keep a fixed pressure in the bubbler and throttles the resulting mixture of H 2 and MO down to the reactor pressure. PC MFC Valve NC Valve NO H 2, N 2 To reactor Bubbler Thermal bath Bubblers

11 Metalorganic compounds Optimal thermal decomposition temperature between 300 and 500°C availability of transported reactant at the substrate surface. The vapor pressure of the MO source is an important consideration in MOCVD, since it determines the concentration of source material in the reactor and the deposition rate. Too low a vapor pressure makes it difficult to transport the source into the deposition zone and to achieve reasonable growth rates. Too high a vapor pressure may raise safety concerns if the compound is toxic. Vapor pressures of Metalorganic compounds are calculated in terms of the expression Log(p)=B-A/T

12 Vapor pressure of most common MO compounds CompoundP at 298 K (torr) AB Melt point ( o C) (Al(CH 3 ) 3 ) 2 TMAl Al(C 2 H 5 ) 3 TEAl Ga(CH 3 ) 3 TMGa Ga(C 2 H 5 ) 3 TEGa In(CH3) 3 TMIn In(C 2 H 5 ) 3 TEIn Zn(C 2 H 5 ) 2 DEZn Mg(C 5 H 5 ) 2 Cp2Mg Log(p)=B-A/T

13 Flow rate of MO sources Ideal gas equation MO flux Q MO P MO (T bub ) = equilibrium vapor pressure of the metalorganic component T bub = bubbler temperature Q B = carrier gas flux at standard atmosphere P standard = standard atmosphere P B = regulated bubbler pressure (Rolf Engelhardt, Ph.D. Thesis, TU Berlin, 2000,

14 Partial pressure of MO sources P MO-reactor = partial pressure of the metalorganic components in the reactor P MO (T bub ) = equilibrium vapor pressure of the metalorganic component Q B = carrier gas flux P standard = standard atmosphere P B = regulated bubbler pressure Q tot = total gas flux (Rolf Engelhardt, Ph.D. Thesis, TU Berlin, 2000,

15 MOCVD reactors Different orientations and geometries. Most common: Horizontal reactors: gases inserted laterally with respect to sample standing horizontally on a slowly- rotating (~60RPM) susceptor plate. Vertical reactors: gases enter from top, sample mounted horizontally on a fast-rotating (~ RPM) susceptor plate.

16 Horizontal reactors Primary vendors: AIXTRON (Germany). The substrate rests on a graphite susceptor heated by RF induction or by IR lamps. Quartz liner tube, generally rectangular Gas flow is horizontal, parallel to the sample. Rotation ~ 60RPM for uniformity by H 2 flux below the sample holder.

17 Horizontal reactors Advantages Common reactor high experience. Uniform epitaxial growth provided the gas velocity is large enough, and attention is paid to hydrodynamic flow. Small height above the wafer the effect of natural convection is minimized. Quite large gas velocity very rapid changes in the gas phase composition. Disadvantages Uniformity can either be achieved by very high gas flow, ( inefficient deposition), or by implementing rotation, which is tricky in this type of design. Throughput: difficult to scale this design up to accommodate large volume production.

18 Planetary reactors Primary vendors: AIXTRON. Derived from horizontal reactor. Material: stainless steel Very widespread now for production, and can achieve very good wafer uniformities. Uniformity: rotation of the main disk + individual satellites. Up to 5X10 wafer capacity (AIX 3000, see photo)

19 Vertical reactors Primary vendors: Veeco (former Emcore (USA)). Gas flow generally normal to the wafer. Temperature gradients buoyancy induced convection high residence time of the gases degradation of heterostructure compositional abruptness. Solution: rotation of susceptor at high angular velocities (centrifugal pumping action to suppress convection and obtain more efficient use of precursors. Simulated streamlines in a vertical spinning cylinder reactor for MOCVD of GaAs from TMGa, AsH 3, H 2. Gases enter at 600K through the top plane and react at the flat top surface of the spinning inside cylinder. The rotation rate is 1000rpm and the deposition surface temperature is 900K (http://www.cs.sandia.gov/CRF/MPSalsa/ )http://www.cs.sandia.gov/CRF/MPSalsa/

20 Vertical reactors Features All stainless construction MBE vacuum technology Safety (no glass) Electrical resistance heating Gate valve, and antechamber for minimizing O 2 /H 2 O contamination. Advantages High precursor utilization efficiency Scaling to very large wafers/ multiple wafers. Multiple wafer capacity: Up to 3 x 8", 5 x 6", 12 x 4", and 20 x 3" Disadvantages: Very high speed rotation, up to 1200 rpm. Possible memory effects.

21 Reflectance anisotropy spectroscopy (Reflectance difference spectroscopy) Linear polarized light source directed on the sample. Light is reflected from the sample. The reflection is monochromatized and a spectrum is detected. Only requirement for the system: transparent ambient and a window above the sample. easily fulfilled for MOVPE and MBE Bulk: isotropic signal Surface: reconstruction anisotropy in two directions (with square lattices) RAS signal: normalized change of polarization along two axes. Markus Pristovsek, Ph.D. Thesis, TU Berlin, 2001, berlin.de/diss/2000/pristovsek_markus.pdf)

22 Reflectance anisotropy spectroscopy (Reflectance difference spectroscopy) A RAS spectrum can be used to identify a surface, by comparing it to spectra measured on well-ordered reference surfaces with known reconstruction (measured at the same time, e.g., by RHEED in MBE). RAS spectra of a c(4x4) and a ß2(2x4) reconstruction on a GaAs (001) surface. Grey spectra are the spectra of a 33% c(4x4) /66% ß2(2x4) and 66% c(4x4) /33% ß2(2x4). (Markus Pristovsek, Ph.D. Thesis, TU Berlin, 2001, berlin.de/diss/2000/pristovsek_markus.pdf)

23 Exhaust system Pump and pressure controller Low pressure growth: mechanic pump and pressure controller control of growth pressure. The pump should be designed to handle large gas load (rotary pump). Waste gas treatment system The treatment of exhaust gas is a matter of safety concern. GaAs and InP: toxic materials like AsH 3 and PH 3. The exhaust gases still contain some not reacted AsH 3 and PH 3, Normally, the toxic gas need to be removed by using chemical scrubber. For GaN system, it is not a problem. AIXTOX system

24 Safety issues Concerns: Flammable gases (H 2 ) Toxic gases (AsH 3, PH 3 ) Safety measures: Lab underpressurization. Design of hydrides cylinders. Extensive gas monitoring systems placed in different locations, able to detect the presence of gas as small as parts per billion. Alarms located in different parts of the buildings + beeper calls to operators. Immediate shut down of the system to a failsafe condition in case of leakages and other severe failures. Alternatives: use of alternate gases N 2 carrier TBAs, TBP (toxic but liquid low vaopr pressure)

25 Analysis of the MOCVD growth process

26 MBE versus MOCVD growth rate T cell P v (T) Ballistic transport Sticking coefficient = 1 r = r (T) MBE MOCVD Flow rate f (total flow F, total pressure P, vapor pressure P v ) Diffusive mass transport Chemical reaction kinetics r = r (F, P, P v, mass transport, reaction kinetics)

27 3. At the same time: chemical reactions homogeneous, heterogeneous (parasitic deposit) reduction of reactant concentration, shift in alloy composition, reduced growth rate, epitaxial surface roughening. 4. (Partially decomposed) precursor diffusion to the surface reaction to form the desired material. 5. Simultaneous desorption of reaction products (hydrocarbons), surface diffusion of material to lattice sites. 1. Flow of reactant (precursors) to reactor tube, either by: Mixing in gas handling manifold, then enter the reactor Separate until the reactor (no premature side reactions) 2. In the reactor: establishment of gas layers governing transport of mass, energy and momentum: entry effects and possibly achievement of steady- state condition. Growth steps in (MO)CVD R. L. Moon and Y.-M. Houng, in Chemical vapor deposition - Principles and applications, edited by M. L. Hitchman and K. F. Jensen (Academic Press, London, 1993).

28 Reactive-flow conservation equations (Crosslight Procom Users manual) The state of the gas phase in a reactor can be completely described by the continuum mass density, the individual chemical species number density n i, the momentum density v, and the energy density E. The basic partial differential conservation equations are: total mass (continuity equation) individual species (precursors, intermediate species…) momentum (Navier-Stokes equation) energy (heat conduction equation) Total energy density Number density of species i Fluid velocity Number of chemical species present Pressure tensor Chemical production rate of species i Heat flux Radiative heat flux Diffusion velocity of species i Fluid mass density

29 Simplified model of (MO)CVD reaction kinetics Simplified deposition process of a film, starting from a molecule AB in the gas phase (L. Vescan, in Handbook of thin film process technology, edited by D. A. Glocker and S. I. Shah (Institute of Physics Publishing, Bristol, 1995), p. B1.4:1) AB(g) A(s) + B(g) J 1 : molecular flux from the gas phase to the substrate surface, J 2 : consumption flux of AB corresponding to the surface reaction: J 1 h G (C G – C S ) (~supersaturation) J 2 k S C S with h G = gas diffusion rate constant, C G = gas-phase concentration of AB, C S = surface concentration of AB, k S = heterogeneous rate constant J1J1 J2J2

30 Simplified model of (MO)CVD reaction kinetics Steady-state conditions: Growth rate r = J 0 (with 0 = unit volume of the crystal) r mole fraction of the species AB in the gas phase, and determined by the smaller of the rate constants h G, k S. Limiting cases: r k S C G 0 surface kinetics control r h G C G 0 mass transport control

31 Interpretation in terms of supersaturation Driving force: supersaturation (chemical potential difference between gas phase and solid) out-of-equilibrium process; equilibrium at the vapor- solid interface The relative importance of surface kinetics and mass transport can be interpreted as a function of the chemical potential dependence on the reaction coordinate. If most of the chemical potential drop occurs in the boundary layer (red line), the growth is controlled by mass transport; if it occurs at the interface (green line), the growth is kinetically limited Input gas phase Boundary layer InterfaceSolid Chemical potential Reaction coordinate Mass transport Reaction kinetics R. L. Moon and Y.-M. Houng, in Chemical vapor deposition - Principles and applications, edited by M. L. Hitchman and K. F. Jensen (Academic Press, London, 1993).

32 Mass transport Fundamental and very complex aspect in reactor design Factors influencing gas flow in a reactor: temperature concentration and momentum gradients gravity ( convection) homogeneous, heterogeneous chemical reactions ( parasitic nucleation) Simplified (2 regions) picture in a horizontal reactor: Upper region: turbulence or vorticity good mixing and heat transfer Close to the susceptor: region of laminar flow (boundary or stagnant layer) molecular diffusional transport to the hot substrate, where the transverse velocity is zero.

33 Mass transport Assuming a gas velocity U = U in the bulk gas phase, and U = 0 at the growth surface calculation of boundary layer width ( D. W. Kisker and T. F. Kuech, in Handbook of crystal growth, edited by D. T. J. Hurle (Elsevier Science, Amsterdam, 1994), Vol. 3, p. 93) ~ (PU ) -1/2, where P is the total reactor pressure. If the molecular transport in the boundary layer proceeds by diffusion alone, the rate constant h G can be written as where D ~ P -1 is the diffusion coefficient mass-transport-limited growth rate where C G ~ p AB = AB partial pressure growth rate is practically independent of the growth temperature, and depends linearly on the species partial pressure.

34 Reaction kinetics Two kinds of thermally-activated reactions Reactions in the gas phase (homogeneous reactions) Reactions at the surface (heterogeneous reactions) Forward and reverse rates are characterized by rate constants that can be expressed in an Arrhenius form: k = A exp (-E/k B T), where E is the activation energy for the process. Surface kinetics are poorly known processes, in which a number of sub-processes can be identified. Among them: adsorption of reactant species, heterogeneous decomposition reactions, surface migration, incorporation and desorption of products.

35 Reaction kinetics In the most simplified picture, the chemistry of heterogeneous reactions can be modeled by taking into account only adsorption and desorption: where is a vacant surface site, A is an adsorbed state, k ads and k des are the adsorption and desorption rate constants Assumptions: no interaction between absorbed species; equivalence among all the adsorption sites. G. B. Stringfellow, Organometallic vapor phase epitaxy: theory and practice (Academic Press, Boston, 1989).

36 Reaction kinetics Steady state (adsorption rate = desorption rate): adsorption coefficient with = fraction of occupied lattice sites assumes the form of a Langmuir isotherm: G. B. Stringfellow, Organometallic vapor phase epitaxy: theory and practice (Academic Press, Boston, 1989).

37 Reaction kinetics MOCVD of binary compound semiconductors: two molecules AB and CD are transported to the surface, and are adsorbed on cation and anion sites, respectively. For this noncompetitive process, the growth rate of the bimolecular reaction is proportional to the anion and cation surface coverages (Langmuir-Hinshelwood isotherm): III-V semiconductors: tipically V/III ratio ~ 100 AB << 1; CD 1 r K p AB, with K a typical rate constant for the process, temperature- dependent. growth rate depends only on temperature and on the group-III precursor partial pressure, and not on the group-V one.

38 Reaction kinetics for GaAs Overall reactions: TMGa + AsH 3 :AsH 3 + Ga (CH 3 ) 3 GaAs + 3CH 4 TEGa + AsH 3 :AsH 3 + Ga (C 2 H 5 ) 3 GaAs + 3C 2 H 4 + 3H 2 Lower activation energies for decomposition for TEGa than for TMGa ~200K lower temperature for 50% decomposition. (Markus Pristovsek, Ph.D. Thesis, TU Berlin, 2001, berlin.de/diss/2000/pristovsek_markus.pdf)

39 Reaction kinetics for GaAs Overall reactions: TMGa + AsH 3 :AsH 3 + Ga (CH 3 ) 3 GaAs + 3CH 4 TEGa + AsH 3 :AsH 3 + Ga (C 2 H 5 ) 3 GaAs + 3C 2 H 4 + 3H 2 TMGa decomposition is strongly enhanced at the onset of the AsH 3 de-composition. This is most likely due to hydrogen radicals produced by AsH 3 decomposition. (Markus Pristovsek, Ph.D. Thesis, TU Berlin, 2001, berlin.de/diss/2000/pristovsek_markus.pdf)

40 Reaction kinetics for GaAs Proposed mechanisms (TMGa + AsH 3 ): Complex series of decomposition steps in the gas phase and on the surface, each with its own characteristic reaction constant and activation energy. K. F. Jensen, Adv. Chem. Ser. 245, 397 (1995)

41 Growth modes in MOCVD

42 Growth mode: studies on GaAs from TMGa and AsH 3 Studies for atmospheric pressure (AP = 10 5 Pa = 1000mbar) and for low pressure (LP = 10 4 Pa = 100mbar), and different surface orientations. Three regimes: Low T: kinetically limited growth strong T dependence, low P dependence (r K p TMGa ), with K dependent on T. Mid T: mass transport-limited growth r does not depend appreciably on T and surface orientation, but increases with decreasing P (r p TMGa P -1/2 ). High T: increasingly low growth rates, probably due to homogeneous reactions in the gas phase, causing a depletion of reactants, or surface re-evaporation. G. B. Stringfellow, Organometallic vapor phase epitaxy: theory and practice (Academic Press, Boston, 1989). Effect of substrate temperature

43 Growth mode: studies on GaAs from TMGa and AsH 3 Studies for T = 650°C and V/III ratio 100 Two regimes: P > 100mbar, growth is limited by mass transport, and r ~ P -1/2 After a transition region, at P < 20mbar, the growth rate becomes independent on P, and growth becomes kinetically limited. Effect of reactor pressure G. B. Stringfellow, Organometallic vapor phase epitaxy: theory and practice (Academic Press, Boston, 1989).

44 Growth mode: studies on GaAs from TMGa and AsH 3 Studies for different T and substrate orientations Three regimes: T = 700 o C: r p TMGa at all TMGa pressures and substrate orientations (mass transport limited) T = 500 o C: r saturates for high TMGa pressures and depends on orientation (kinetically limited). Evidence for (orientation-dependent) incomplete AsH 3 decomposition (with TMGa completely pyrolized). T = 1000 o C: decreased growth rate: gas- phase reactions ( reduction of gas-phase nutrients) and surface desorption ( orientation dependence) Effect of TMGa partial pressure R. L. Moon and Y.-M. Houng, in Chemical vapor deposition - Principles and applications, edited by M. L. Hitchman and K. F. Jensen (Academic Press, London, 1993). 500°C 700°C 1000°C


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