CA1327845C - Optical fibre with fluorescent additive - Google Patents

Optical fibre with fluorescent additive

Info

Publication number
CA1327845C
CA1327845C CA000580531A CA580531A CA1327845C CA 1327845 C CA1327845 C CA 1327845C CA 000580531 A CA000580531 A CA 000580531A CA 580531 A CA580531 A CA 580531A CA 1327845 C CA1327845 C CA 1327845C
Authority
CA
Canada
Prior art keywords
refractive index
dopant
core
region
glass composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
CA000580531A
Other languages
French (fr)
Inventor
Benjamin J. Ainslie
Susan P. Craig
Jonathan R. Armitage
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
British Telecommunications PLC
Original Assignee
British Telecommunications PLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by British Telecommunications PLC filed Critical British Telecommunications PLC
Priority to CA000616670A priority Critical patent/CA1334306C/en
Application granted granted Critical
Publication of CA1327845C publication Critical patent/CA1327845C/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C4/00Compositions for glass with special properties
    • C03C4/0071Compositions for glass with special properties for laserable glass
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B37/00Manufacture or treatment of flakes, fibres, or filaments from softened glass, minerals, or slags
    • C03B37/01Manufacture of glass fibres or filaments
    • C03B37/012Manufacture of preforms for drawing fibres or filaments
    • C03B37/014Manufacture of preforms for drawing fibres or filaments made entirely or partially by chemical means, e.g. vapour phase deposition of bulk porous glass either by outside vapour deposition [OVD], or by outside vapour phase oxidation [OVPO] or by vapour axial deposition [VAD]
    • C03B37/018Manufacture of preforms for drawing fibres or filaments made entirely or partially by chemical means, e.g. vapour phase deposition of bulk porous glass either by outside vapour deposition [OVD], or by outside vapour phase oxidation [OVPO] or by vapour axial deposition [VAD] by glass deposition on a glass substrate, e.g. by inside-, modified-, plasma-, or plasma modified- chemical vapour deposition [ICVD, MCVD, PCVD, PMCVD], i.e. by thin layer coating on the inside or outside of a glass tube or on a glass rod
    • C03B37/01807Reactant delivery systems, e.g. reactant deposition burners
    • C03B37/01838Reactant delivery systems, e.g. reactant deposition burners for delivering and depositing additional reactants as liquids or solutions, e.g. for solution doping of the deposited glass
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C13/00Fibre or filament compositions
    • C03C13/04Fibre optics, e.g. core and clad fibre compositions
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C13/00Fibre or filament compositions
    • C03C13/04Fibre optics, e.g. core and clad fibre compositions
    • C03C13/045Silica-containing oxide glass compositions
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01SDEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
    • H01S3/00Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range
    • H01S3/05Construction or shape of optical resonators; Accommodation of active medium therein; Shape of active medium
    • H01S3/06Construction or shape of active medium
    • H01S3/063Waveguide lasers, i.e. whereby the dimensions of the waveguide are of the order of the light wavelength
    • H01S3/067Fibre lasers
    • H01S3/06708Constructional details of the fibre, e.g. compositions, cross-section, shape or tapering
    • H01S3/06716Fibre compositions or doping with active elements
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B2201/00Type of glass produced
    • C03B2201/06Doped silica-based glasses
    • C03B2201/20Doped silica-based glasses doped with non-metals other than boron or fluorine
    • C03B2201/28Doped silica-based glasses doped with non-metals other than boron or fluorine doped with phosphorus
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B2201/00Type of glass produced
    • C03B2201/06Doped silica-based glasses
    • C03B2201/30Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi
    • C03B2201/31Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi doped with germanium
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B2201/00Type of glass produced
    • C03B2201/06Doped silica-based glasses
    • C03B2201/30Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi
    • C03B2201/34Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi doped with rare earth metals, i.e. with Sc, Y or lanthanides, e.g. for laser-amplifiers
    • C03B2201/36Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi doped with rare earth metals, i.e. with Sc, Y or lanthanides, e.g. for laser-amplifiers doped with rare earth metals and aluminium, e.g. Er-Al co-doped
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B2203/00Fibre product details, e.g. structure, shape
    • C03B2203/10Internal structure or shape details
    • C03B2203/22Radial profile of refractive index, composition or softening point
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01SDEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
    • H01S3/00Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range
    • H01S3/05Construction or shape of optical resonators; Accommodation of active medium therein; Shape of active medium
    • H01S3/06Construction or shape of active medium
    • H01S3/063Waveguide lasers, i.e. whereby the dimensions of the waveguide are of the order of the light wavelength
    • H01S3/067Fibre lasers
    • H01S3/06708Constructional details of the fibre, e.g. compositions, cross-section, shape or tapering
    • H01S3/0672Non-uniform radial doping
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01SDEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
    • H01S3/00Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range
    • H01S3/14Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range characterised by the material used as the active medium
    • H01S3/16Solid materials
    • H01S3/1691Solid materials characterised by additives / sensitisers / promoters as further dopants
    • H01S3/1693Solid materials characterised by additives / sensitisers / promoters as further dopants aluminium

Abstract

ABSTRACT

An optical fibre for use in fibre lasers has the lasing additive, eg Er3+, concentrated in centre of the core. Preferably the core has an inner region which contains the additive and an outer region which is dopant free. The concentration of the dopant reduces the pump threshold for a laser and improves the gain performance for a given pump power. The fibre is conveniently made by MCVD. The use of Al2O3 in the inner zone appears to reduce loss of dopant during tube collapse.

Description

1 327~45 OPTICAL FIBRE WITH FLUORESCENT ADDITIV~
BT PAT~NT CAS~ Z17-7 ~ ~0.09lOP) This invention relates to optical fibre with a fluorescent additive and in particular to fibre which is suitable for the construction of fibre lasers.
There is currently much technical interest in a wide range of devices in which radiation at wave lengths of 0.3 u~ to 4 ~m is generated in the core of an optical fibre. In these devic~s the fibre contains a fluorescent o additive which interacts with excitation radiation, usually identified as the "pump radiation", to produce the desired output. The devices take many forms, e.gO
broadband sources, super luminescent sources and temperature sensors, but devices which display laser activity are particularly important, especially in telecommunications. It should be realised that telecommunications uses laser activity in two distinct manners namely optical oscillators and optical amplifiers. However the same doped glass fibres are equally suitable for a plurality of such applications (and often for all such applications).
Stone and Nurrus in "~pplied Physics Lettersl' (Volume 23, No. 7, 1 October 137~ at pages 388 and 389) disclose lasers made of neodymium doped silica with end-pumped fibre geometry. One of their systems has an active core of fused SiO2 and Nd203 enclosed in a thin passive sleeve of SiO2 and Nb205 all enclosed in a fused jacket of SiO2. The diameter~of the active core was about 800 to 15~m and the length of the samples was lcm.
The function of the thin passive sleeve is to increase the guidance o~ the core and hence pump efficiency.

~` ''` 7 : ' ;: ' 1 3278~5 US Patent 3 ~08 549 describes an optical ~avsgulde light source having an active core surrounded by an inner cladding layer and an outer cladding layer. The refractive index of the outer cladding is lower than the refractive index of the inner cladding ~hich is lo~er than the refractive index of the core. Pump radiation is launched into the inner cladding layer to which it is confined by the outer cladding. The pump radiation makes many passes through the core whereby its absorption by the o core is increased. The signal is generated within the core.
It has long been recognised that the rare earth elements, e.g. Nd, ~r, and Yb, display fluorescent properties which make them suitable for use as fluorescent S additives in optical fibre. Their fluorescent properties make them particularly suitable ~or use in the laser devices mentioned above. The operation of a fluorescent device clearly depends on absorption of the pump photons in order to raise ions (or other fundamental particles) of dopant to an excited state for subsequent emission on a different transition. In a laser device, this emission is stimulated by the presence of a signal photon and, therefore, the operation of a laser device also depends on the interaction of radiation at signal wave length. It is an object of this invention to make efficient use of pump power launched into optical fibre. In the case of optical amplifiers this means achieving high gain for small launched pump powers whereas ~or optical oscillators it implies a 13w lasing threshold.
Fibre according the invention has a fluorescent additive unevenly distributed over the cross section of the core and having a higher concentration of the additive at the centre of the core than at the core/cladding ~ ~ 3 ~ 1 3278~5 boundary. The highest concentrations of additive should ideally be located in those regions of the fibre ~here, during pumping, the highest intensity of p~p radiation is to be expected. Lower or zero concentratiolls of the additive should be located where only low pl~p intensities are to be expected.
In most pumping schemes ~he highest intensity o~ the pump radiation will be located at the centre of the core and it is appropriate to provide the highest dopant o concentration at the centre of the core with zero concentration at its periphery. Preferably the core comprises two zones, namely an inner zone surrounded by an outer zone wherein the inner zone contains the dopant and the outer zone contains substantially no dopant. Suitably the inner zone constitutes less than a quarter, e.g. 5 to 15 /o, of the cross sectional area of the core.
The fibre may be implemented in any glass system which is compatible with the fluorescent dopants. Thus, for example, the fibre may be implemented in conventional silicate, phosphate and fluoride systems, eg. fluorides of Zr, Ba, La, Al, Na and Hf or in silica systems, eg. SiO2 with additives such as GeO2 to adjust the refractive index in the core.
In a specific embodiment silica fibre has (a) a cladding formed of SiO2 with P205 to reduce the melting point, and F to o~fset the increase in refractive index.
(b~ an outer core region formed of SiO2 with GeO2 ~o increased the refrac~ive inde~ and P205 to reduce the melting point; and (c) an inner core region formed of SiO2 with A1203 to increase the refractive index, P205 to decrease the melting point and prevent devitrification and a fluorescent dopant to interact with the pump radiation.

/ ~" " "' ~, " ''~' " ' ' ;

1 3278~5 The dimensions of the fibre are preferably such that it is single ~ode at signal wave le~gth. This lmplies that it may ba able to support several, e.g. up to 4 or 5, modes at pump frequency. ~h~ fluorescent dopants of major interest include the rare earth metals. Of these the most important are Er (which lases by the three level mechanis~) and Nd (which lases by the 3 and four level mechanism~
One method of making silica fibre according to the o invention utilises the modified chemical vapour deposition process usually identified as NCVD. MCVD is sometimes known as the inside deposition process because the glasses which eventually form the operative parts of the fibre are produced by converting the equivalent chlorides into the 1S desired oxides which are deposited, layer by layer, on the inner surface of a substrate tube. Usually a total of 10 to 30 layers are deposited. As initially deposited the glass is porous but the porous material is immediately fused to give a solid layer upon ~hich subsequent layers are deposited. When all the layers have been deposited the tube is collapsed to a rod which is dra~n into fibre.
To make fibre according to the invention this procedure is followed for the cladding and the outer core. The precursor of the inner core is deposited but left in the porous state. Dopants, including the fluorescent additive, are introduced as solution into the porous layer. After solvent removal and conversion to oxides as necessary, the porous layer is consolidated and the tubular configuration is collaped into a rod which is then drawn into fibre.
It will be appreciated that this, i.e. soaking a solution into a porous layer, is one of many known techniques of introducing dopants into optical fibre. It . , , , . . -.. . . .
~ ~, , . " ~ . ~
" .:

,:,., `
, _ 5 _ 1 3 2 7 8 4 5 has been adapted, in accordance with the invention, to provide a small, doped centre region in a larger core. One difficulty inherent in MCVD is that there is a tendency t:o lose dopant by S evaporation from the exposed inner surface. This is not acceptable since the invention requires a high concentration of dopant at the axis. The depleted zone can be removed, e.g.
by etching, just before final collapse. Although there appears to be a risk that further losses could occur during the final stage o~ the collapse, this does not happen to any noticeable extent because: -(1) The exposed surface is so small that the rate of loss is minimal~
(2) The final stage only takes a time which is too brief for noticeable loss to occur.
However we have most surprisingly discovered that,when aluminum is used to adjust the refractive index of the core, the losses of fluorescent dopant are not noticeable.
The aluminum can be introduced at the same time as the fluorescent dopant, e.g. as Al(NO3~3 in alcoholic solution.
During heating the Al(N03) 3 iS converted to A12O3.
In accordance with an embodiment of the invention, an optical fibre, suitable for forming fluorescent devices, which contains a fluorescent dopant in its core, is characterized in that the concentration of the dopant is greater on the core axis than at the interface between the core and the cladding.
The fibre according to the invention can be used to make conventional fibre devices which include a pump for providing excitation radiation for the fluorescent additive.
The invention will now be described by way of example with reference to the accompanying drawing which is a cross-section through a fibre according to the invention.
The drawing shows a fibre according to the invention prepared by the MCVD process. This fibr~ has a residual layer 10 which is the residue of the substrate tube used in the MCVD process. The layer 10 has no optical .l .~,.
.

. .

: :
,~

func~ion. The fibre also ha~ a conventional cladding 11, a core which is generally indicat~d by the numeral 14, having an (undoped) outer region 12 an inner region 1~ '~
whi~h contains a fluorescent dopant, e.g. Er, at a concentration of .001 - 10.0 wt /o Er.
Fibre as descri~ed above was prepared by a substantially conventional ~CVD process in which a substate tube was rotated in a glass blowing lathe while a reactant gas was passed through its bore. In the course of the preparation three different reactant mixtures, to be specified below, were used.
A short segment of tube, about 2cm long, was heated to reaction temperature by a travelling flame. In this segment chlorides were converted into oxides which ; deposited as a porous ring downstream of the flame. As the flame traversed, in the case of cladding and outer core, the deposit was fused to form a thin layer on the inner surface of the substrate tube. In the case of inner core, a lower temperature was used so that the deposit did ~ not fuse whereby it remained porous.
The reaction mixture used to form the cladding precursor was obtained by bubbling:-700ml/min f 2 through SiC14, 90ml/min f 2 through POC130 The mixture of these two gas streams was diluted with 1.5 litre/min 2 and 1.0 litre/min Ne. In addition, 6 ml/min of CC12F2 were included in the mixture. The maximum temperature in the hot zone was 1600C and the flame travelled at 18cm/min.
Five cladding layers were thus deposited on a substrate tube of lOmm inner diameter. These fused together to form a cladding layer of SiO2 doped with P205 and fluorine.

, ;

(The P205, which is derived from the PCC'13, is incorporated to reduce the melting point of the sio2 ~hich makes the fusion eas1er. The P205 slightly increases the refractive index of the silica but the fluorine slightly reduces the refractive index. By balancing the two concentrations the refractive index of the five cladding layers is sunstantially equal to that of pure silica. Thus the POC13 and C C12F2 are processing aids which have little or no effect on the o performance of the final product which, therefore, consists essentially of SiO2).
Eight layers to form the outer core were deposited next. The reaction mixture used for each layer was obtained by bubbling:-200 ml/min at 2 through SiC14 200 ml/min f 2 through GeC14 10 ml/min f 2 through PGC13.
The mixture of these three gas streams was diluted with 1.5 litres/min f 2 These eight layers were fused together at 1500C and the flame travelled at 16 cm/min. This formed the outer core region which consisted essentially of SiO2 doped with GeO2 to increase the refractive index and P205 to facilitate processing by lowering the melting point of the glass.
The precursor at the inner core was deposited in two porous layers. The reaction mi~ture was obtained by bubbling:-200 ml/min f 2 through SiC14 10 mltmin f 2 through POC13 and diluting with 1.5 litres/min f 2~ The torch traverse rate was 17 cm/min and the ma~imum temperature was at 1300C ~which is too low to fuse the deposit).

.. . ..

: , ; ' ' , ' ~ "

~ - 8 1 3278~5 (Note. In all bubbling operations th~ liquid ~as at 25C~ At this point the tube ~as removed from the lathe and dopants were introduced into the porous layers by immersion for 1 hour in an ethanolic solution of s lN Al(N03)3 0.08M ErC13.
After soaking, the tub~ was drained, blown dry with N2 for one hour, and returned to the lathe where it was heated at about 800 - 1000C for a few minutes. This completed solvent evaporation. The temperature was raised to about 1900C for collapse to a rod. This also ensured conversion of Rl(N03)3 to A1203 and ErC13 to Er203. The tube was flushed with 02/He mixture during all of these stages (about 10 /O
(volume) of C12 could be introduced into the 02/He mix i~ a very dry product were required.) The resulting perform had a core about 2mm diameter.
Analysis (using disperive X-ray techniques) confirmed that Al and Er3 were confined to the central region. The reason for choosing a large core will be briefly explained.
The ultimate objective is a fibre having the dopant, Er3 , contained in a very small inner core, e.g. with a diameter of 1 to 3~m. It ~as decided to achieve this by means of a fat outer core ~8 layers), a thin inner core (2 layers) and a high overall draw ratio, i.e. length extension of about 1:105.
The fatness of the preform made it difficult to handle and it was drawn in two stages. First the e~ternal diameter was reduced from 7.0mm to 3.2mm, i.e. an axial draw of 1:4.8. The drawn rod was sleeved with a silica tube and then drawn 1: 2.5x104 to give the product fibre.
(There is a well known problem that dopants are lost during collapse from the inner layers of the preform.

': : ,:.,, '.~ ' ,.`' ~ " .' "'"':' .
':

' ~ ' :~ ' `' This results in a thin axial depletion zone. In the process above described A1203 was present and in the presence of this compound no loss of ~r3 + occurred.) The product fibre had the following measurements.
Claddinq (11) OD 7~m ID 4~m RI match~d to silica C _ Outer Region 12 o OD 4~m ID 1.5~m Er3 NONE
Core Inner Region 13 Diameter 1.5~m S Er3 1 wt ~o General Properties OD 125~m ~Pll Cut Off790 nm RI step 0.01 ~RI step" denotes the difference between the RI of the core and the RI of the cladding.
A possible theory of the operation of this fibre will now be briefly indicated.
The considerations set out above are particularly pertinant to dopants which lase as a three level syste~.
The three levels are:-(a~ The ground state, (b) the pump level, (c) upper laser level, (also known as ~he metastable level~.
The absorption of pump photon by a ground state ion transfers tha~ ion to the upper pump Ievel from where it decays non-radiatively to the upper laser level. That ion - ~
... ... , ,.,, ~ .

:. ,... ~ , can then return to the ground state via the lasing transition, i.e. gives out a signal photon. In order to achieve the population inversion essential for laser operation it is necessary to pump more than half the dopant ions from the ground state to the upper laser level. Thus it is i~portant to note that, cl~ a particular point in space, if ~ewer than half the ions have been pumped to the upper laser level then the signal beam will be attenuated at that point.
It is there~ore extremely desirable to preferentially locate the fluoresence additive where the pump intensity is highest, i.e. on the axis and to revent there being any dopant ions in the regions where the pump intensity is lower.
S The signal beam, which being single mode also has its maximum intensity on the axis, overlaps well with the excited dopant ions and thus e~fectively depopulates the upper laser level.
In order to illustrate the benefit of the invention comparative measurements ~ere made on two very similar fibres hoth of which used Er3 ions as the fluorescent specles. The fibre, identified as ''~'l, had the Er3 ions located in a centre core Region 13 as shown in Fiqure 1. The comparative fibre, identified as "X", had the more standard Er3+ distribution, i.e. uniformly distributed over the whole of the core. Details of both fibres are given in Table lo Dia~eters (~m) a x r Total 125 125 To Cladding ~11) 6.0 6.0 To Core (12) 3.5 3.5 Inner Region (133 1.0 NONE
RI Step 0.0100~0.005 0.0095+0.005 LP11 Mode cut off (n~ 790 790 ,. ~

': .
., :

: : :

In the case of fibre A the dopant was contained only in the inner region 13. Based on this region alone theconcentration of ~r3+ was 0.45/o wt or 0.037/o wt based on the total core 14. For fibre X l:he concentration of Er3 was 0O05O/o wt based Oll the total core 14.
The performances of the two fibres were compared by measuring the "transparency power~ of each.
To measure the transparency power a short length o~
lO fibre is used so that pump power does not change significantly along the length. The test co~prises launching the signal at wave length 1.54 ~m and pump at wave length 528.7nm into the opposite ends of the fibre.
The input and output po~ers of the signal are measured for several values of pump power. There exists a specific pump power at which the signal is neither amplified or attenuated and this power is known as the "transparency power". This name is considered appropriate because, at this pump power, the ~ibre simulates a perfectly transparent window. At higher pump powers than the transparency power, the fibre ampliries the signal beam ~hereas at lower pump powers the fibre attenuates the signal beam. The transparency power is a direct measure of the performance of the invention and the lo~er the transparency power the better ~he performance. The transparency powers of the two fibres was Fibre A 0.8mW
Fibre X 1.4mW
Ratio 1 : 1.75 Thus the fibre according to the invention gave gain at much lower pump power than the co~parative fibre.

, . . .
: ,~ .

Claims (15)

1. An optical fibre, suitable for forming fluorescent devices, which contains a fluorescent dopant in its core, characterised in that the concentration of the dopant is greater on the core axis than at the interface between the core and the cladding.
2. A fibre according to Claim 1 wherein the core comprises an inner region and an outer region surrounding the inner region wherein substantially all of the dopant is contained in the inner region.
3. A fibre according to claim 2, wherein the inner region constitutes not more than a quarter of the total cross sectional area of the core.
4. A fibre according to claim 3, wherein the inner region constitutes 5% to 15% of the cross sectional area of the core.
5. A fibre according to claim 2, wherein the dopant is substantially uniformly distributed in the inner region of the core.
6. A fibre according to claim 1,which is monomode at signal wave length.
7. A fibre according to claim 1,wherein the dopant is capable of lasing transition.
8. A fibre according to Claim 7, wherein the dopant is a three level lasing element.
9. A fibre according to claim 1, wherein the dopant is a rare earth element.
10. A fibre according to Claim 9, wherein the dopant is selected from Er, Nd, Pr, Ho, Yb and Tm.
11. A fibre according to claim 10, wherein the dopant is Er3+.
12. An optical fibre which comprises (a) a cladding region formed of a first glass composition having a first refractive index;
(b) an outer core region surrounded by said cladding region and formed of a second glass composition having a second refractive index said second refractive index being higher than said first refractive index;
(c) an inner core region surrounded by said outer core region and formed of a third glass composition having a refractive index substantially equal to said second refractive index wherein said third glass composition contains a dopant which is capable of undergoing lasing transitions wherein the concentration of said dopant is 0.001 to 10% by weight based on the total third glass composition.
13. An optical fibre which comprises (a) a cladding region formed of a first glass composition having a first refractive index;
(b) an outer core region surrounded by said cladding region and formed of a second glass composition having a second refractive index said second refractive index being higher than said first refractive index;
(c) an inner core region surrounded by said outer core region and formed of a third glass composition having a refractive index substantially equal to said second refractive index wherein said third glass composition contains a dopant which provides a rare earth element in a form capable of undergoing lasing transitions wherein the concentration of said dopant is such as to provide 0.001 to 10% by weight of said rare earth element based on the total third glass composition.
14. An optical fibre which comprises (a) a cladding region formed of a first glass composition having a first refractive index;
(b) an outer core region surrounded by said cladding region and formed of a second glass composition having a second refractive index said second refractive index being higher than said first refractive index;
(c) an inner core region surrounded by said outer core region and formed of a third glass composition having a refractive index substantially equal to said second refractive index wherein said third glass composition contains a dopant which provides an element selected from Er, Nd, Pr, Ho, Yb and Tm in a form capable of undergoing lasing transitions wherein the concentration of said dopant is such as to provide 0.001 to 10% by weight of said element based on the total third glass composition.
15. An optical fibre which comprises (a) a cladding region consisting essentially of SiO2;
(b) an outer core region surrounded by said cladding region and consisting essentially of SiO2 and an additive which increases the refractive index of the SiO2;
(c) an inner core region surrounded by said outer core region and consisting essentially of SiO2, an additive which increases the refractive index of the SiO2 so that the refractive indices of the inner and outer core regions are substantially equal, and a dopant which is capable of undergoing lasing transitions wherein the mole ratio of Si to dopant is between 1:10-4 and 1:10.
CA000580531A 1987-10-22 1988-10-18 Optical fibre with fluorescent additive Expired - Lifetime CA1327845C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CA000616670A CA1334306C (en) 1987-10-22 1993-05-28 Optical fibre with fluorescent additive

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8724736 1987-10-22
GB878724736A GB8724736D0 (en) 1987-10-22 1987-10-22 Optical fibre

Related Child Applications (1)

Application Number Title Priority Date Filing Date
CA000616670A Division CA1334306C (en) 1987-10-22 1993-05-28 Optical fibre with fluorescent additive

Publications (1)

Publication Number Publication Date
CA1327845C true CA1327845C (en) 1994-03-15

Family

ID=10625717

Family Applications (2)

Application Number Title Priority Date Filing Date
CA000580531A Expired - Lifetime CA1327845C (en) 1987-10-22 1988-10-18 Optical fibre with fluorescent additive
CA000616670A Expired - Lifetime CA1334306C (en) 1987-10-22 1993-05-28 Optical fibre with fluorescent additive

Family Applications After (1)

Application Number Title Priority Date Filing Date
CA000616670A Expired - Lifetime CA1334306C (en) 1987-10-22 1993-05-28 Optical fibre with fluorescent additive

Country Status (11)

Country Link
US (2) US4923279A (en)
EP (2) EP0313209B1 (en)
JP (3) JPH07118558B2 (en)
AT (2) ATE161664T1 (en)
CA (2) CA1327845C (en)
DE (2) DE3856092T2 (en)
ES (2) ES2111006T3 (en)
GB (1) GB8724736D0 (en)
GR (2) GR3006615T3 (en)
HK (2) HK128796A (en)
SG (1) SG47966A1 (en)

Families Citing this family (76)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2638854B1 (en) * 1988-11-10 1992-09-04 Comp Generale Electricite DOPED FIBER OPTIC LASER AMPLIFIER
JP2546711B2 (en) * 1988-12-22 1996-10-23 国際電信電話株式会社 Er-doped optical fiber laser device
DE69031571T2 (en) * 1989-10-31 1998-02-26 Fujitsu Ltd Method of making an optical fiber preform
US5005175A (en) * 1989-11-27 1991-04-02 At&T Bell Laboratories Erbium-doped fiber amplifier
US5121450A (en) * 1989-12-22 1992-06-09 Gte Laboratories Incorporated Fiber optical Y-junction
US5638204A (en) * 1990-01-22 1997-06-10 Pirelli Cavi S.P.A. Optical power amplifier with Al2 O3 and erbium doped active fiber
IT1237980B (en) * 1990-02-12 1993-06-19 Pirelli Cavi Spa CURVED SINGLE-MODE ACTIVE FIBER OPTICAL AMPLIFIER
WO1991013038A1 (en) * 1990-02-28 1991-09-05 Otc Limited A rare-earth doped fibre
US5040186A (en) * 1990-03-13 1991-08-13 At&T Bell Laboratories InP-based quantum-well laser
FR2659755B1 (en) * 1990-03-16 1992-05-29 Alcatel Nv ERBIUM DOPED FIBER OPTICAL AMPLIFIER.
GB9010943D0 (en) * 1990-05-16 1990-07-04 British Telecomm Wave-guiding structure with lasing properties
US5109463A (en) * 1990-06-25 1992-04-28 Lee Ho Shang Fiber optic lamp
US5155621A (en) * 1990-07-31 1992-10-13 Fujitsu Limited Optical fiber amplifier
US5074633A (en) * 1990-08-03 1991-12-24 At&T Bell Laboratories Optical communication system comprising a fiber amplifier
US5058976A (en) * 1990-08-03 1991-10-22 At&T Bell Laboratories System comprising Er-doped optical fiber
JP2888616B2 (en) * 1990-08-08 1999-05-10 住友電気工業株式会社 Optical amplifier and optical oscillator
US5039190A (en) * 1990-09-07 1991-08-13 At&T Bell Laboratories Apparatus comprising an optical gain device, and method of producing the device
GB2249660B (en) * 1990-11-09 1994-07-06 Stc Plc Amplified optical fibre systems
DE4036938A1 (en) * 1990-11-20 1992-05-21 Drescher Ruediger Solar power generator tower - has inexpensive reflectors e.g. inner surfaces of waste drink cartons for diffuse light reflection
JP3292729B2 (en) * 1990-11-26 2002-06-17 三菱電機株式会社 Optical fiber type optical amplifier
US5121460A (en) * 1991-01-31 1992-06-09 The Charles Stark Draper Lab., Inc. High-power mode-selective optical fiber laser
US5107538A (en) * 1991-06-06 1992-04-21 At&T Bell Laboratories Optical waveguide system comprising a rare-earth Si-based optical device
JP2959877B2 (en) * 1991-06-24 1999-10-06 古河電気工業株式会社 Optical fiber manufacturing method
US5268910A (en) * 1991-07-18 1993-12-07 General Instrument Corporation Superluminescent optical source
US5191586A (en) * 1991-07-18 1993-03-02 General Instrument Corporation Narrow band incoherent optical carrier generator
FR2679548B1 (en) * 1991-07-25 1994-10-21 Alsthom Cge Alcatel METHOD FOR MANUFACTURING ACTIVE OPTICAL FIBERS.
US5227913A (en) * 1991-09-11 1993-07-13 Wisconsin Alumni Research Foundation Co-deposition of erbium and titanium into lithium niobate and optical amplifier produced thereby
JP2766420B2 (en) * 1992-04-07 1998-06-18 株式会社フジクラ Method for producing erbium-doped quartz
US5299210A (en) * 1992-04-28 1994-03-29 Rutgers University Four-level multiply doped rare earth laser system
US5259046A (en) * 1992-10-01 1993-11-02 At&T Bell Laboratories Article comprising an optical waveguide containing a fluorescent dopant
US5296012A (en) * 1992-12-28 1994-03-22 Corning Incorporated Method of making optical waveguide preforms
US5337375A (en) * 1992-12-31 1994-08-09 At&T Bell Laboratories Depolarizer using unpumped, doped optical fiber and method using same
JP3301275B2 (en) * 1994-09-27 2002-07-15 日本電信電話株式会社 Optical fiber amplifier
JPH08278523A (en) 1995-04-05 1996-10-22 Hitachi Ltd Light amplifier
US5588084A (en) * 1995-04-28 1996-12-24 Johnson; Kurtis F. Scintillating optical fibers containing non-uniformly distributed dopants and process for preparing same
CN1087432C (en) * 1995-08-31 2002-07-10 住友电气工业株式会社 Dispersion-compensating fiber and method of fabricating the same
FR2740563B1 (en) * 1995-10-31 1997-11-21 Alcatel Submarcom FIBER OPTIC COMPRISING A FLUORESCENT DOPANT
JP3298799B2 (en) * 1995-11-22 2002-07-08 ルーセント テクノロジーズ インコーポレイテッド Cladding pump fiber and its manufacturing method
US5854865A (en) * 1995-12-07 1998-12-29 The United States Of America As Represented By The Secretary Of The Navy Method and apparatus for side pumping an optical fiber
JPH1011022A (en) 1996-06-18 1998-01-16 Sharp Corp Driving circuit of display device
US6289698B1 (en) * 1996-08-02 2001-09-18 Corning Incorporated Method of making a fiber preform with increases in alumina concentration at radial distances
US5729645A (en) * 1996-08-13 1998-03-17 The Trustees Of The University Of Pennsylvania Graded index optical fibers
US5708669A (en) * 1996-09-24 1998-01-13 Lucent Technologies Inc. Article comprising a cladding-pumped optical fiber laser
EP0947064A1 (en) * 1996-12-19 1999-10-06 Corning Incorporated Distributed fiber amplifier for solitons
US7576909B2 (en) * 1998-07-16 2009-08-18 Imra America, Inc. Multimode amplifier for amplifying single mode light
US5832163A (en) * 1997-07-18 1998-11-03 Mcdonnell Douglas Corporation Single mode optical waveguide with expanded rare-earth doped region
FR2778751B1 (en) 1998-05-14 2000-06-16 Alsthom Cge Alcatel OPTICAL FIBER FOR FLAT GAIN OPTICAL AMPLIFIER
US6620748B1 (en) * 1998-10-20 2003-09-16 Asahi Glass Co Ltd Light-amplifying glass, light-amplifying medium and resin-coated light-amplifying medium
US6275512B1 (en) 1998-11-25 2001-08-14 Imra America, Inc. Mode-locked multimode fiber laser pulse source
US6982996B1 (en) * 1999-12-06 2006-01-03 Weatherford/Lamb, Inc. Large diameter optical waveguide, grating, and laser
JP2000252558A (en) * 1999-02-26 2000-09-14 Sumitomo Electric Ind Ltd Light amplifying optical fiber and manufacture thereof
AU6865300A (en) 1999-09-10 2001-04-17 Nikon Corporation Light source and wavelength stabilization control method, exposure apparatus andexposure method, method for producing exposure apparatus, and device manufactur ing method and device
KR100352373B1 (en) 1999-12-03 2002-09-11 한국전자통신연구원 Complex rare - earths doped optical waveguide
US20020071647A1 (en) * 1999-12-08 2002-06-13 Tariq Manzur Multi-clad optical fiber and amplifier
US6353497B1 (en) 2000-03-03 2002-03-05 Optical Coating Laboratory, Inc. Integrated modular optical amplifier
FR2805899B1 (en) * 2000-03-03 2003-01-31 Cit Alcatel C-STRIP MULTIMODE SHEATH FIBER OPTICAL AMPLIFICATION
JP2001267665A (en) * 2000-03-16 2001-09-28 Sumitomo Electric Ind Ltd Optical fiber for light amplification and optical fiber amplifier and optical fiber laser oscillator
JP2002009376A (en) * 2000-06-23 2002-01-11 Furukawa Electric Co Ltd:The Optical fiber for light amplification
US6836607B2 (en) * 2001-03-14 2004-12-28 Corning Incorporated Cladding-pumped 3-level fiber laser/amplifier
US7085461B2 (en) * 2001-04-30 2006-08-01 Verrillon, Inc. Optical fiber with visualization features
US6819846B2 (en) * 2001-08-02 2004-11-16 Corning Incorporated High absorption erbium doped amplifying optical fiber
GB2379279B (en) * 2001-08-31 2005-10-26 Gsi Lumonics Ltd Laser processing system and optical fibres
US7058269B2 (en) * 2001-10-24 2006-06-06 Institut National D'optique Reconstructed glass for fiber optic applications
US6995900B2 (en) 2003-01-21 2006-02-07 Jds Uniphase Corporation Method of making a short-pass fiber with controlled cut-off wavelength
WO2003077381A2 (en) * 2002-03-08 2003-09-18 Lightwave Electronics Amplifiers and light sources employing s-band erbium-doped fiber and l-band thulium-doped fiber with distributed suppression of amplified spontaneous emission (ase)
US20030200771A1 (en) * 2002-04-30 2003-10-30 Burke Gerald E. Method of manufacturing phosphosilicate optical fibers and optical fibers formed therefrom
JP2004250251A (en) * 2003-02-18 2004-09-09 Sumitomo Electric Ind Ltd Fluorescent glass, waveguide for optical amplification and optical amplification module
JP2005039126A (en) * 2003-07-17 2005-02-10 Sumitomo Electric Ind Ltd Wide-band light source
US7046902B2 (en) * 2003-09-30 2006-05-16 Coractive High-Tech Inc. Large mode field diameter optical fiber
WO2006120663A2 (en) * 2005-05-13 2006-11-16 Heye Research And Development Limited Soda lime glass compositions and process for manufacturing containers from said compositions
CN101688949B (en) * 2007-02-05 2012-01-18 Ofs菲特尔有限责任公司 Preventing dielectric breakdown in optical fibers
DE102016111730B3 (en) * 2016-06-27 2017-12-28 Leica Microsystems Cms Gmbh Lighting device and microscope with such a lighting device
EP3526560A4 (en) 2016-10-11 2020-07-08 Victoria Link Limited A spectrometer apparatus for measuring spectra of a liquid sample using an integrating cavity
JP6833611B2 (en) * 2017-05-25 2021-02-24 株式会社クラレ Plastic wavelength conversion fiber and its manufacturing method
WO2021192783A1 (en) * 2020-03-27 2021-09-30 株式会社フジクラ Optical fiber having added active element, base material for optical fiber having added active element, resonator, and fiber laser device
CN111548005A (en) * 2020-05-25 2020-08-18 上海大学 Preparation method of laser-drawn silicon germanium core optical fiber

Family Cites Families (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3254031A (en) * 1962-06-27 1966-05-31 Eastman Kodak Co Borate glass for laser use
US3503764A (en) * 1967-01-20 1970-03-31 Bendix Corp Core glass for fiber-optic structures having high index of refraction
US3571737A (en) * 1968-06-07 1971-03-23 Bell Telephone Labor Inc Transmission line
DE1928947A1 (en) * 1968-06-29 1970-01-02 Philips Nv Glass for a fiber optic element
US3894857A (en) * 1968-07-06 1975-07-15 Nippon Selfoc Co Ltd Process for exchanging alkali ions for thallium ions in a glass fiber
US3599106A (en) * 1968-11-06 1971-08-10 American Optical Corp High intensity-high coherence laser system
US3636473A (en) * 1969-03-06 1972-01-18 American Optical Corp Composite glass laser rod
US3808549A (en) * 1972-03-30 1974-04-30 Corning Glass Works Optical waveguide light source
US3785834A (en) * 1972-06-09 1974-01-15 Owens Illinois Inc Glasses,glass-ceramics and process for making same
US3938974A (en) * 1973-04-27 1976-02-17 Macedo Pedro B Method of producing optical wave guide fibers
FR2238679B1 (en) * 1973-07-26 1978-06-30 Auzel Francois
US3864113A (en) * 1973-10-19 1975-02-04 Corning Glass Works Method of Producing Glass by Flame Hydrolysis
DE2417963B1 (en) * 1974-04-11 1975-08-07 Max Planck Gesellschaft Light guide
US4040890A (en) * 1975-06-27 1977-08-09 Bell Telephone Laboratories, Incorporated Neodymium oxide doped yttrium aluminum garnet optical fiber
US3971645A (en) * 1975-09-12 1976-07-27 Bell Telephone Laboratories, Incorporated Method of making compound-glass optical waveguides fabricated by a metal evaporation technique
US4149772A (en) * 1975-09-22 1979-04-17 Northern Electric Company Limited Optical fibre having low mode dispersion
FR2339266A1 (en) * 1976-01-26 1977-08-19 Commissariat Energie Atomique Multi-layer light amplifying system - has glass amplifying medium with active centres of trivalent ions of neodymium increasing in concentration away from optical pump
US4283213A (en) * 1979-10-22 1981-08-11 International Telephone And Telegraph Corporation Method of fabrication of single mode optical fibers or waveguides
US4419115A (en) * 1981-07-31 1983-12-06 Bell Telephone Laboratories, Incorporated Fabrication of sintered high-silica glasses
US4715679A (en) * 1981-12-07 1987-12-29 Corning Glass Works Low dispersion, low-loss single-mode optical waveguide
US4516826A (en) * 1983-04-21 1985-05-14 At&T Technologies, Inc. Single mode lightguide fiber having a trapezoidal refractive index profile
US4618211A (en) * 1984-03-12 1986-10-21 At&T Bell Laboratories Optical fiber tap with activatable chemical species
JPS60200208A (en) * 1984-03-23 1985-10-09 Fujitsu Ltd Optical fiber
US4637025A (en) * 1984-10-22 1987-01-13 Polaroid Corporation Super radiant light source
US4597787A (en) * 1984-11-13 1986-07-01 Ispra Fibroptics Industries Herzlia Ltd. Manufacture of optical fibre preforms
JPS61151034A (en) * 1984-12-26 1986-07-09 Nippon Sekiei Glass Kk Quartz laser glass for amplifying infrared light
JPS62502748A (en) * 1985-06-03 1987-10-22 ヒユ−ズ・エアクラフト・カンパニ− How to introduce dovants into optical fiber preforms
US4780877A (en) * 1985-07-26 1988-10-25 Polaroid Corporation Optical fiber laser
GB2199029B (en) * 1985-08-13 1990-09-05 Simon Blanchette Poole Fabrication of optical fibres
US4666486A (en) * 1985-09-24 1987-05-19 Hutta Joseph J Process for making bulk heavy metal fluoride glasses
JPS62111208A (en) * 1985-11-11 1987-05-22 Nippon Telegr & Teleph Corp <Ntt> Optical fiber
JPS62158135A (en) * 1985-12-28 1987-07-14 Hoya Corp Single mode optical fiber having faraday rotation effect
JPS63184386A (en) * 1986-09-18 1988-07-29 Furukawa Electric Co Ltd:The Optical fiber and optical fiber type light emitting material

Also Published As

Publication number Publication date
HK1008761A1 (en) 1999-05-14
JPH01145881A (en) 1989-06-07
JPH07118558B2 (en) 1995-12-18
EP0490881A3 (en) 1993-04-07
JPH11195832A (en) 1999-07-21
EP0490881A2 (en) 1992-06-17
SG47966A1 (en) 1998-04-17
DE3856092D1 (en) 1998-02-05
EP0490881B1 (en) 1997-12-29
GR3025787T3 (en) 1998-03-31
CA1334306C (en) 1995-02-07
HK128796A (en) 1996-07-26
USRE35946E (en) 1998-11-03
DE3875582T2 (en) 1993-04-15
EP0313209A1 (en) 1989-04-26
ES2111006T3 (en) 1998-03-01
ATE161664T1 (en) 1998-01-15
US4923279A (en) 1990-05-08
DE3875582D1 (en) 1992-12-03
EP0313209B1 (en) 1992-10-28
GR3006615T3 (en) 1993-06-30
DE3856092T2 (en) 1998-05-14
GB8724736D0 (en) 1987-11-25
ES2052736T3 (en) 1994-07-16
JPH05283789A (en) 1993-10-29
ATE81925T1 (en) 1992-11-15

Similar Documents

Publication Publication Date Title
CA1327845C (en) Optical fibre with fluorescent additive
US5262365A (en) Quartz glass doped with rare earth element and production thereof
US4787927A (en) Fabrication of optical fibers
EP0528946B1 (en) Wave-guiding structure with lasing properties
US6889528B2 (en) Process of making rare earth doped optical fiber
Tumminelli et al. Fabrication of high-concentration rare-earth doped optical fibers using chelates
KR20040075318A (en) A process of making rare earth doped optical fibre
CA2436579C (en) A process for making rare earth doped optical fibre
CA1325121C (en) Optical wave guides
NZ229482A (en) Optical amplifier using doped optical fibre
CA2481204C (en) A method of fabricating rare earth doped optical fibre
DiGiovanni Fabrication of rare-earth-doped optical fiber
JPH038744A (en) Rare earth element-doped quartz glass fiber preform and preparation thereof
Dhar et al. Tm-Yb doped optical fiber performance with variation of host-glass composition
JPH04271329A (en) Partially erbium-added optical fiber coupler and production thereof
Simpson Rare Earth Doped Fiber Fabrication: Techniques and Physical Properties
Hua et al. The Fabrication And Optical Properties Of Neodymium And Erbium Doped Silica-Based Fibres

Legal Events

Date Code Title Description
MKEX Expiry

Effective date: 20110315