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I -I 36 XCITON-LASER NPLIFIER(U) CORNELL UNIV ITHACA NYi/ RLLIBOFF ET AL. 01 DEC 92 R4-82 RFOSR-TR-83-9544 VI L RFOSR-78-3574 p NCLASSIFIED F/G 26/5 UL E4Khhhh

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I - I 36 XCITON-LASER NPLIFIER(U) CORNELL UNIV ITHACA NYi/

RLLIBOFF ET AL. 01 DEC 92 R4-82 RFOSR-TR-83-9544VI L RFOSR-78-3574

p NCLASSIFIED F/G 26/5 UL

E4Khhhh

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-• AFOSR-TR. 3 .544

/ A

A

p,"

Technical Report No. R-4-82

Project; Task No. 61102F; 2301/A3

Date: December 1, 1982

Title: Exciton-Laser Amplifier

Authors: Richard L. Liboff

K. C. Liu

Contractor: Cornell University

C) Principal Investigator: Richard L. Liboffc_.:

C-2

Research supported in part by the Air Force

office of Scientific Research under contract

* AFOSR-78-3574. Distribution of this report is unlimited.

Approv[

S 88 07 01 020

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SECURITY CLASSIFICVA I ' %'G, " DotEne) , READ INSTRUCTIONSREPORT DOCUMENTATION PAGE BEFORE COMPLETIG FORM

1. REPORT NUMBER 12. GOVT ACCESSION NO. 3. RECIPIENT'S CATALOG NUMBER

4. TITLE '(Ud rubl;t,5. TYPE OF REPORT & PERIOD COVERED

Exciton-Laser Amplifier Interim6. PERFORMING OqO. REPORT NUMBER

7. AUTHOR(s) 8. CONTRACT OR GRANT NUMBER(*)

Richard L. Liboff AFOSR 78-3574K.C. Liu

9. PERFORMING ORGANIZATION NAME AND ADDRESS 10. PROGRAM ELEMENT. PROJECT. TASKAREA & WORK UNIT NUMBERS

Cornell University 61102F

Ithaca, N.Y. 14853 2301/A3

I I. CONTROLLING OFFICE NAME AND ADDRESS 12. REPORT DATE

Directorate of Physics Dec. 1, 1982AFOSR 13. NUMBER OF PAGES

Bolling AF Base, D.C. 20332 Eight14. MONITORING AGENCY NAME & ADORESS(f different from Controlling Office) 15. SECURITY CLASS. (of this report)

UnclassifiedISa. DECLASSlFICATION/DOWNGRAOING

SCHEDULE

16. DISTRIBUTION STATEMENT (of this Report)

17. DISTRIBUTION STATEMENT (of the abstract entered in Block 30, it different from Report)

Approved for Public Release; Distribution Unlimited

IS. SUPPLEMENTARY NOTES

19. KEY WORDS (Continue on reverse side if necessary and identify by block number)

Laser. Laser amplifier, Excitons, Pure crystals. Semiconductors,Insulators, Gain. Suimulated decay. Non-bose like excitons.

20. ABSTRACT (Continue on reveres side if necessary and identify by block number)

A laser-amplifying device is described which is based on thesimulated decay of excitons in a pure crystal. An estimate is madeof the gain of the device. At a typical frequency the gain isfound to be appreciably large thus suggesting practical applicationof the laser amplifier.

DD ,JAI'1 1473 EOITIONOF 1 NOV 65 IS OBSOLETE

SECURITY CLASSIFICATION OF THIS PAGE (When Data Entered)

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0/

Abstract

A laser-amplifying device is described which is based on

the stimulated decay of excitons in a pure crystal. An estimate

is made of the gain of the device. At a typical frequency the

gain is found to be appreciably large thus suggesting practical

application of the laser amplifier.

j

-2-

0

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I

In a previous article by the authors [1], a lasing mechanism

was described based on stimulated decay of excitons. The process

depends critically on the non-boson quality of excitons, which in

turn may be assured by sufficiently high exciton density. This

criterion follows from the fact that the ideal bose commutation

relations [2] become increasingly invalid with growth ,f the

number of excited atoms in the crystal.

In the present paper a laser-amplifying device is proposed

based on the process described above. Namely, it is proposed

that excitons in a pure (insulator or semiconductor) crystal are

triggered by incident resonant laser radiation and that excitons

are created by an external intermittent radiative source.

Thus, for example [3], exciton decay wavelength in pure ZnSa

is 3201.71 A. The crystal could then be used to amplify radiation

stemming from a dye laser at the same wavelength. Other charac-

teristic wavelengths appropriate to this device are listed in

Table 1.

The device is modeled as follows: Excitons in the pure

crystal are created by a flash lamp. The power supply to the

lamp has an on-off profile which is 7 radians out of phase with

the pulse frequency of the input laser. The duration between

peaks of this profile is of the order of the lifetime of an

exciton, -10- 6 sec.

We assume this modulation has the following effect. Exciton

density grows during the 'on' phase of the lamp to a peak value

-3-

IA

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I

and then suffers resonant stimulated decay by the input laser

-( radiation during the 'off' phase of the lamp.

During the amplification interval, radiative power flux,

S[W!m2], in the crystal satisfies the equation

dS = g s (1)

where g is the gain,

g = <(Pad-Poa) (2)

In this expression p is density of excited atoms, and P0o is density

of atoms in the general state. It follows that the total density

of atoms, PT' is given by

PT = P + Po

The absorption cross section is a and ad is the cross section

for stimulated decay. Finally K describes additional loss effects

such as, for example, that due to reflection, impurities, miss-

match between input and resonant frequencies, etc.

From the principle of microscopic reversibility [4] and

assuming non-degeneracy of excited and ground exciton levels, one

.A may set ad = a . Furthermore, for a we may write [5]

(2,T) 2e2WgL(w)d2

G(W) =3c (4)

Here d is the dipole matrix element between Wannier state functions.

At the site Z it is given by

d <cZ I (5)

-4-

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0!

Valence and conduction bands are denoted by v and c respectively.

-T This matrix element is relevant to a transition between the ground

and excited states of an exciton.

The term gL in (4) refers to the Lorentzian lineshape factor.

On resonance it reduces to [5]

L (6)

In this expression T denotes the decay time of the exciton. AsIpreviously noted, T 10-6 sec.

A rough estimate of the matrix element (5) may be constructed

as follows. We assume that the valence band is comprised of SO

atomic states and the conduction band is comprised of P atomic

states. With

s r-Z,

in the coordinate representation, the bra and ket vectors in (5)

become, respectively,

W v(s) 1 3/2 e-sa

-s/2a 3(7)

• Wc(S) _ s e cose

(2a)3/2 a vT/

where cos =-z-s/s, for an arbitrary z-axis. Furthermore,

* a =c a* = c fi /m*e0

where - is the dielectric constant.

-5-

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0

There results (2) 1 -s 7d - ai ds s4 e

(8)

S28- 35a

with (6) and (8), a as given by (4) becomes

S= 327 (11 ct wT a2 (9)

I where a is the fine structure constant.

Returning to (2), with (9) we write

g = 32 -r a 2 c (p-P o ) (10)

At 55% pumping efficiency, p = 0.55p T, po =0.45PT and (10)

reduces to

g-321r a w T a 0. KPT (11)

1 14 , -- 10_ 6 , .

At w -- l4 = , a 0.5 A we find

g 7.16xl0" 9 KPT (12)

Thus for pT> 1 g > I and the device may be expected to amplify

-0 the input laser pulse.

We have described a laser-amplifier device based on stimulated

decay of excitons in a pure crystal. An expression for the gain

O of the device together with a criterion for amplification were

obtained. These expressions suggest practical use of the Dro-

posed device. The device presumes a non-bose like quality of

excitons. This property is satisfied provided a sufficiently

large number of atoms are excited, i.e., p >

-6-

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This research was supported in part under contract AFOSR

78-3574.

References

[1] K.C. Liu and R.L. Liboff, "Criterion for Exciton Lasing inPure Crystals", submitted to J. Appl. Phys.

[2] J.J. Hopfield, "Theory of the Contribution of Excitons tothe Complex Dielectric Constant of Crystals", Phys. Rev.112 1555-1567, 1958.

[3] D.C. Reynolds and T.C. Collins, "Excitons: Their Propertiesand Uses", Academic Press, New York, 1981.

[4] R.L. Liboff, "Introductory Quantum Mechanics", Holden Day,Oakland, CA (1980).

[5] R.H. Pantell and H.E. Puthoff, "Fundamentals of QuantumElectronics", John Wiley, New York, 1969.

-

-7-

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Table 1

- Characteristic Exciton Properties in

Selected Crystals [3]

Energy gap Binding energy Photon energy 0Material Eg (meV) Eb (meV) E9-Eb (meV) Wavelength (A)

Si , 1112 14 1098 11290.5 (IR)

Ge 803 3.6 799.4 15507.9 (IR)

ZnO 3436 59 3377 3671.01 (V)

ZnS 3911 39 3872 3201.71 (UV)

ZnSe 2795 281 2514 4931.2 (0)

GaAs 1519 4.2 1514.8 8183.9 (IR)

CdS 2582 28 2554 4853.9 (0)

InSb 235.2 0.4 234.8 52798.1 (IR)

(IR, 0, V, UV) E (infrared, optical, violet, ultraviolet)

0

0

-8-

0

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