CARRIER DYNAMICS IN SEMICONDUCTORS

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Transcription:

Chapter 4 CARRIER DYNAMICS IN SEMICONDUCTORS In this chapter we enclose gures that provide an overview of how electrons and holes respond to electric elds, concentration gradients, and optical radiation. We also discuss the nonradiative recombination of electrons and holes, the continuity equation, and diusion length.

TRANSPORT AND SCATTERING OF CARRIERS In a perfectly periodic material, electrons suffer no scattering and obey the equation h dk dt = Force If an electric field is applied the electrons will oscillate in k- space from the k=0 to zone edge k-value, as shown. Such oscillations are called Bloch Zener oscillations and can, in principle, generate terrahertz radiation. However, in real semiconductors scattering occurs and destroys the possibility of these oscillations. t = t 0 t = t 1 E F-field t = t 2 G The motion of an electron in a band in the absence of any scattering and in the presence of an electric field. The electron oscillates in k-space gaining and losing energy from the field.

SCATTERING OF ELECTRONS (HOLES) AND MOBILITY As electrons move in semiconductors they scatter from impurities, thermal vibrations of the atoms, and structural defects After a time τ sc, electrons, on average, lose coherence with their starting momentum. The average drift velocity in an electric field is t = 0 v = efτ sc m * t = τ sc The mobility of the mobile carriers: µ = eτ sc m * Conductivity σ = neµ n + peµ p Mobility is high if the effective mass is small. Loss scattering implies large τ sc and high mobility.

MOBILITIES OF SOME PURE SEMICONDUCTORS Mobility at 300 K (cm 2 /V s) Semiconductor Electrons Holes C 800 1200 Ge 3900 1900 Si 1500 450 α-sic 400 50 GaSb 5000 850 GaAs 8500 400 GaP 110 75 InAs 33000 460 InP 4600 150 CdTe 1050 100 As semiconductors are doped, electrons (holes) scatter from the dopants and mobility decreases. As temperature is lowered the atoms vibrate with smaller amplitude and thus cause less scattering. As a result, mobility increases as temperature is lowered.

HIGH FIELD TRANSPORT At low electric fields the drift velocity of electrons is proportional to the field v = µf At high electric fields the velocity tends to saturate. 10 8 CARRIER DRIFT VELOCITY (cm/s) 10 7 10 6 Ge GaAs Ge InP Si Electrons Holes 10 5 10 2 10 3 10 4 10 5 10 6 ELECTRIC FIELD (V/cm) At high electric fields, electrons gain energy from the electric field. Their energy is much larger than the zero field energy of 3/2 k B T. These hot electrons suffer increased scattering and the velocity saturates. The saturation velocity for most semiconductors is ~10 7 cm/s.

VERY HIGH FIELD TRANSPORT At very high electric fields electrons gain so much energy that they can excite an electron from the valence band into the conduction band. When this happens we get an extra electronhole pair. This process is called impact ionization or avalanche breakdown. BREAKDOWN ELECTRIC FIELDS IN MATERIALS Material Bandgap Breakdown electric (ev) field (V/cm) GaAs 1.43 4 x 10 5 Ge 0.664 10 5 InP 1.34 Si 1.1 3 x 10 5 In 0.53 Ga 0.47 As 0.8 2 x 10 5 C 5.5 10 7 SiC 2.9 2-3 x 106 SiO 2 9 ~10 7 Si 3 N 4 5 ~10 7 For high power devices avalanche breakdown limits the power output of the device, since beyond a certain bias the current runs away. Large bandgap material that can sustain a higher electric field are more suitable for high power devices. In a class of photodetectors called avalanche photodetectors the avalanche process is used to generate a high number of electrons and holes. This increases the gain of the device, i.e., the number of carriers generated for each photon.

BAND TO BAND TUNNELING AT HIGH ELECTRIC FIELDS At very high electric fields electrons can tunnel from the valence band to the conduction band (or vice versa). This tunneling causes a large current to flow. Electrons in conduction band Available empty states (holes) in valence band E v x 1 x 2 E v (a) E g x 1 0 x 2 x (b) Tunneling probability 3/2 4 2m* E T = exp g 3ehF F = electric field across the semiconductor. Tunneling is high in narrow bandgap materials. Band to band tunneling is exploited in Zener diode and Esaki diode.

CARRIER CONCENTRATION TRANSPORT BY DIFFUSION If there is a concentration gradient in the carrier density in a material, carriers will flow from a region of high concentration to a region of low concentration. Direction of carrier flow mean free path n L n R L R x o x o x o + J(diffusion) = J n (diff) + J p (diff) x d = ed n n ed d p x d p d x D n D p µ n µ p (cm 2 /s) (cm 2 /s) (cm 2 /V s) (cm 2 /V s) Ge 100 50 3900 1900 Si 35 12.5 1350 480 GaAs 220 10 8500 400 Einstein relation D = µk B T e

QUASI-FERMI LEVELS In equilibrium a single energy band Fermi level describes the electron and hole densities. In nonequilibrium (i.e., if a field or radiation is present) separate Fermi levels are needed for the conduction band and valence band. E F Equilibrium for an n-type material (a) + + E Fn E v E Fp Excess electron injection (b) + + E Fn E v Excess electron and hole injection (c) E Fp + + + + + + + E v Electron quasi-fermi level, E Fn gives the electron occupation f e (E) = 1 EE exp Fn +1 k B T or f e (E) ~ exp EE Fn k B T A separate hole quasi-fermi level, E Fp describes the hole occupation f h (E) = 1 EE exp Fp +1 k B T or f h (E) ~ exp E Fp E k B T

ELECTRON-HOLE GENERATION AND RECOMBINATION Electrons and holes can be generated in a semiconductor by optical radiation and thermal energy. Electrons and holes can also recombine by emitting light or by emitting heat. electron-hole generation E v + + + donor ionization: free electron + ionized donor + electron-hole recombination + + electron recombination with a donor

OPTICAL ABSORPTION IN SEMICONDUCTORS When light shines on a semiconductor it can cause an electron in the valence band to go into the conduction band thus creating an e-h pair. Photon energy hω > E g Momentum must be conserved absorption is stornger in direct bandgap materials. ABSORPTION COEFFICIENT (cm 1 ) 10 6 10 5 10 4 10 3 10 2 3 2 Ge GaAs Si GaP Amorphous Si PHOTON ENERGY (ev) 1.5 1 InP 10 0.2 0.6 1 1.4 1.8 WAVELENGTH (µm) 0.7 Ga 0.3 In 0.7 As 0.64 P 0.36 InGaAs Rate of e-h pair generation (α: absorption coefficient; p: ~ optical power density) R G = αp ~ hω

ELECTRON-HOLE RECOMBINATION Electrons can recombine with holes and generate light this is called radiative recombination and is described by a recombination time τ r. Electrons can also recombine with holes via impurities as shown and simply emit heat this is nonradiative recombination and is described by a time τ nr. e e e e E v 1 2 Unoccupied Occupied 4 e (a) 3 e 1 2 Unoccupied Occupied 4 3 h h (b) Trap levels E v Nonradiative lifetime, τ nr.: average time for an electron-hole pair to recombine 1 = N t σ v th τ nr N t : impurity density σ : cross-section of the impurity v th : thermal velocity Total nonradiative recombination rate n p R R = ~ Schockley-Read-Hall τ nr (n+p) recombination Total recombination time τ 1 1 1 τ = + τ r τ nr

CONTINUITY EQUATION FOR CARRIERS IN SEMICONDUCTORS The continuity equation allows us to calculate the carrier distribution in the presence of generation and recombination. Continuity equation Conservation of electrons and hole densities Total rate of particle flow = Particle flow due to current Loss due to recombination rate = Gain due to generation rate Particle current Loss Gain (a) Area A J n (x) x x+ x J n (x+ x) (b) x R = recombination rate in volume A x G: generation rate L n : diffusion length for electrons = D n τ n L p : diffusion length for holes = D p τ p d 2 δ n d x 2 = δ n L n G d 2 δ p d2 x = δ p L2 p G

CARRIER INJECTION AND CARRIER DISTRIBUTION If excess carrier density is injected into a material, the carriers decay by recombination. If the carrier concentration is fixed at x = 0 and x = L we find the following: If L << L n : Carrier distribution is linear If L >> L n : Carrier distribution is exponential EXCESS CARRIER DENSITY L >> L n CARRIER DENSITY n(x) 0 L L << L n L 0 2 4 6 8 10 DISTANCE (a u) If carriers are injected across a region of width W and W << diffusion length, the transit time across the region is: t tr = W 2 2D