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Sommaire du brevet 1164734 

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L'apparition de différences dans le texte et l'image des Revendications et de l'Abrégé dépend du moment auquel le document est publié. Les textes des Revendications et de l'Abrégé sont affichés :

  • lorsque la demande peut être examinée par le public;
  • lorsque le brevet est émis (délivrance).
(12) Brevet: (11) CA 1164734
(21) Numéro de la demande: 375170
(54) Titre français: METHODE DE DEPOSITION D'UN ENDUIT ANTIREFLECHISSEMENT A LA SURFACE D'UNE PILE SOLAIRE
(54) Titre anglais: METHOD FOR APPLYING AN ANTI-REFLECTION COATING TO A SOLAR CELL
Statut: Périmé
Données bibliographiques
(52) Classification canadienne des brevets (CCB):
  • 117/64
(51) Classification internationale des brevets (CIB):
  • H01L 31/18 (2006.01)
  • H01L 21/288 (2006.01)
  • H01L 31/0224 (2006.01)
(72) Inventeurs :
  • SCHNEIDER, MICHAEL (Etats-Unis d'Amérique)
(73) Titulaires :
  • EXXON RESEARCH AND ENGINEERING COMPANY (Etats-Unis d'Amérique)
(71) Demandeurs :
(74) Agent: BORDEN LADNER GERVAIS LLP
(74) Co-agent:
(45) Délivré: 1984-04-03
(22) Date de dépôt: 1981-04-10
Licence disponible: S.O.
(25) Langue des documents déposés: Anglais

Traité de coopération en matière de brevets (PCT): Non

(30) Données de priorité de la demande:
Numéro de la demande Pays / territoire Date
167,417 Etats-Unis d'Amérique 1980-07-11

Abrégés

Abrégé anglais




ABSTRACT OF THE DISCLOSURE

The present invention teaches a method for
applying an anti-reflection coating 14 to solar cells
shown in Figure 3 whereby the coating is interdispersed
among the cell's electrodes 20 on the cell's junction
surface. The method includes coating the solar cell's
surface 12 with an anti-reflection layer 14, selectively
etching a pattern through the anti-reflection layer,
which corresponds to the desired electrode pattern 18
and electrolessly plating a layer of nickel 18 onto the
cell's surface.

Revendications

Note : Les revendications sont présentées dans la langue officielle dans laquelle elles ont été soumises.



THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A method of applying an anti-reflective
coating and an electrode pattern to a solar cell sur-
face, said method comprising:
coating at least said surface with an anti-
reflection layer of a metal oxide;
masking a portion of said coated surface to
form an electrode pattern in at least a portion of said
surface which remains unmasked;
etching said coating in the unmasked portion
of said surface to remove said oxide coating;
sensitizing at least said etched region of
said solar cell surface;
electrolessly plating a layer comprising nickel
onto at least said sensitized region of said solar cell
surface;
removing said masking from said solar cell
surface whereby said nickel layer remains only in said
electrode pattern;
coating said nickel layer with a layer of
conduction supporting metal.

2. The method of claim 1 wherein said anti-
reflection coating comprises an oxide of titanium/
silica.

3. The method of claim 2 wherein said anti-
reflection oxide is formed by spin-on coating said
surface with a solution of titanium/silica in an
alcohol based solvent.

4. The method of claim 3 wherein said spin-on
coating is subsequently heat treated at a temperature
ranging from about 200°C to about 400° C for a period
ranging from about 15 minutes to about 30 minutes.




5. The method of claim 2 wherein said oxide
coating is formed by spraying a solution of titanium/
silica in an alcohol based solvent onto a heated cell
surface.

6. The method of claim 1 wherein said mask-
ing comprises screening an asphalt based ink coating
a portion of at least one surface of said solar cell,
patterned to expose an area of said surface which
corresponds to an electrode pattern for said solar
cell.

7. The method of claim 1 wherein said elec-
troless nickel plating comprises contacting at least
said etched surface and a bottom surface of said solar
cell with an electroless plating solution comprising
ammonium acetate, ammonium chloride, nickel chloride
and sodium hypophosphate.

8. The method of claim 7 wherein said plat-
ing produces a layer of nickel ranging in thickness
from about 0.08 microns to about 1.2 microns.

9. The method set forth in claim 8 wherein
said nickel layer is heat treated at a temperature
ranging from about 250°C to about 350°C for a time period
ranging from about 10 minutes to about 30 minutes.

10. The method of claim 1 wherein said conduc-
tion supporting metal comprises solder.
11

Description

Note : Les descriptions sont présentées dans la langue officielle dans laquelle elles ont été soumises.


`i 1 6'173~1

-- 1 --


1 BACKGROUND OF THE INVENTION
2 The present invention relates to solar cells and
3 in particular to solar cells having an anti-reflection
4 coating which is applied to the solar cell prior to elec-
troding.
6 Photovoltaic devices such as silicon solar
7 cells promise a viable alternative to non-replenishable
8 fossil fuel energy generation. Light energy (photons)
9 incident on a solar cell's surface must enter and be ab-
sorbed within the cell to be converted to electrical
11 energy. The efficiency of the solar cell is directly pro-
12 portional to the amount of light absorbed by the cell.
13 Depending upon the particular cell fabrication
14 process, the surface of the solar cell may be substa~-
tially reflective of light energy, reducing the solar
16 cell's efficiency. Polished silicon, for example, may
17 have a reflectivity of 40~ in the spectral region of 0.35
18 and 1.2 microns. The problem is well recognized in the
19 art and numerous solutions have been employed. A known
effective technique for reducing the unwanted reflection
21 is an anti-reflection layer in contact with the solar
22 cell's surface. The anti-reflection (hereinafter A-R)
23 layer is selected to coordinate its index of refraction,
24 thickness and transmittance characteristics to surface re-
flection characteristics and the spectral region of in-
26 terest. For silicon solar cells having a principal spec-
27 tral absorbance between 0.35 and 1.2 microns, metal
28 oxides such as tin oxide, titanium dioxide and magnesium
29 fluoride are known anti-reflective coatings. Typically
these oxide layers are applied to the cell's surface
31 after the cell fabrication has been completed, coating
32 virtually the entire cell surface including the cell's
33 electrodes. Applying the A-R coating after the comple-
34 tion of the cell restricts the temperature at which the


~. ~

" i 1 6~7.~


1 A-R coating may be applied or treated. In contrast to
2 the typical coating sequence, the present invention
3 teaches an A-R coating method where an A-R la~er precedes
4 the electroding of the solar cell, avoiding the tempera-
ture limitations of the aforedescribed p~ior art process.
6 The process is of further advantage in permitting elec-
7 trical contact to the cell's electrode after the A-R
8 coating, facilitating automated production of solar cells
9 and solar panel assembly.
The art has generally recognized the advantage
11 of exposing at least a portion of the solar cell's elec-
12 trodes through the A-R coating. In U.S. Patent 3,949,463,
13 for example, Lindmayer et al teach a method for applying
14 an A-R coating ~o a silicon solar cell where the A-R
coating does not overcoat the cell's current collecting
16 electrode. The technique is further exemplified in U.S.
17 Patent 3,904,453 where Revesz et al use photolithographic
18 techniques in the formation of solar cell electrodes which
19 are not overcoated with the cell's A-R coating.
SUr~A~Y OF THE IN~ENTION
21 The present invention teaches an improved solar
22 cell having an A-~ coating which is applied to the cell
23 prior to constructing the cell's electrodes. Junction
24 diffused silicon wafers are coated with an A-R layer by
either spin-on coating or spray deposition, both tech-
26 niques employing a heating of the cell at about 200C to
27 about 300C. An electrode pattern is masked onto the
28 A-R coa~ed surface and the oxide is removed from the un-
29 masked regions by chemical etching means to expose the
solar cell's surface. The etched region is contacted with
31 an electroless nickel sensitizer and plated with a layer
32 of electroless nickel plating. The electrode pattern
33 mask is then removed and the nickel plated electrodes are
34 contacted with solder flux and molten solder which forms
a layered nic]cel/solder electrode interdispersed through
36 the A-R coating. The process taught herein permits heat


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I 3 6473~


1 treatment/heat processing of the A-R coating and facili-
2 tates electrical connections to the A-R coated cell.
3 BRIEF DESCRIPTION OF THE DRAWING
4 In the drawing, where like components are com-
monly designated, Figures 1 through 3 illustrate cross-
6 sectional views of the solar cell during successive steps
7 in the fabrication tectmique of the present invention.
8 DETAILED DESCRIPTION OF THE INVENTION
9 In Figure 1, a silicon wafer 8 having a first
type conductivity region 10 which may comprise P-type or
11 N-type silicon,is diffused to form a region 12 of con-
12 ductivity type opposite to that of region 10, forming a
13 semiconductor junction otherw;se termed a P-N (or N-P)
14 junction in the region of the interface between regions
10 and 12. The diffusion and junction forming processes
16 are well known in the art. Furthermore, the present in- `
17 ventive A-R coating is operable for either N on P or P
18 on N type cells. In a preferred embodiment, diffused
19 layer 12 extends a relatively short distance into the
wafer to form a shallow junction, less than about 0.5
21 microns in depth.
22 The diffused cell is then optionally etched in
23 a buffered solution of hydrofluoric acid to remove sur-
24 face oxidation and possible adsorbed contaminants. The
cell is then coated with an A-R layer 14 comprising a
26 metal oxide selected from the group consisting of titan-
27 ium dioxide (TioX), silicon dioxide (SiOx), magnesium
28 fluoride, and silicon nitride. As recognized by those
29 of the art, the precise oxidation state of the A-R
layer 14 may vary dependent upon the metal oxide used and
31 its preparation conditions; however, oxidation state
32 variations are compensated for in adjusting the thickness
33 of the layer to provide the desired optical properties
34 of the A-R layer.
The formation of A-R layer 14 is, itself, known
36 in the art, and may comprise the alternate techniques


~..~

i ~ fi~73~1



1 described hereinbelow. The thickr.ess and refractive in-
2 dex of the particular A-R coating utilized are approxi-
3 mated by the theoretical relationship for constructive
4 interference in the A-R coating; d = ~/4n where d is
the approximate thickness of the A-R layer, ,~ is wave
6 length, and n is the refractive index of the A-R coating
7 material.
8 Spin-On Coating: ~ayer 14 may be formed by
9 applying an amount of spin-on coating material such as a
solution of titanium and silica in alcohol based solvent,
ll commercially available from Emulsiton Corporation under
12 the trade name of "Titanium Silica Film C". The coating
13 is applied by the known technique of contacting the cell
14 surface with the coating li~uid and spinning the cell in
commercial photoresist spinner means. Layer thickness
16 is controlled by regulating the amount of liquid applied
17 to the surface and the spinning speed which controls the
18 centrifugal liquid soreading force. ~pproximate regula-
l9 tion of the layer thickness may be provided by monitor-
ing the interference color of the layer, whereby a deep
21 blue reflection color is indicia of an appropriate thick-
22 ness for the A-R coating. The soin-on coated layer is
23 then densified by heat treating the cell at a temperature
24 ranging from about 200C to about 400C for a time rang-
ing from about 15 min. to about 30 min.
26 Spray Deposition: The A-~ layer may be fabri-
27 cated by thermal decomposition of a solution containing
28 a metal solute wnich will decompose to the desired metal
29 oxide upon heating. Spraying (or misting) the solution
onto a heated cell is a conventional deposition tech-
31 nique which provides a controlled growth of the metal
32 oxide A-R layer. Particular spray solution compositions,
33 spray rates and decomposition temperatures are known in
34 the art and, as is the case with each of the A-R layer
compositions recited herein, constitute no part of the
36 present invention.

~ I 6473~
..~



1 Vacuum Deposition: Several alternate vacuum
2 deposition techniques are known for depositing metal
3 oxide for forming the A-R coating including sputtering,
4 electron beam and ion beam deposition. Although general-
ly more costly, vacuum deposition techniques generally
6 facilitate accurate control over layer thickness.
7 Each A-R layer construction technique taught
8 herein re~uires elevated temperature processing which,
9 for cells having electrodes previously constructed onto
the cell's surface, may cause tem?erature damage to the
11 electrode itself or migration of the electrode material
12 into and through the junction barrier, particularly when
13 the junction is of the shallow type where junction
14 regions are relatively near the electrode surface.
The A-R coated surface is then masked to expose
16 only that area of the cell sur_ace which corresponds to
17 the desired electrode pattern. Accordingly a layer 16
18 may alternatively comprise a silk screened asphalt based
19 ink mask patterned onto A-R layer 14 or a photoresist
material which has been patterned by photolithographic
21 means to provide a masking layer exposing a region of
22 A-R layer 14 which corresponds to the desired electrode
23 pattern. The masked surface is then contacted with an
24 etchant chosen to provide selective etching of the pa~ti-
cular A-R coating composition employed. For example,
26 where A-R coating 14 comprises a layer of TiOX, fabri-
27 cated by heat treated spin-on deposition, an etching solu-
28 tion of buffered hydrofluoric acid is used to selective-
29 ly remove the A-R coating in the unmasked regions of the
cell surface. Referring to Figure 2, it is to be recog-
31 nized that the etching solution is chosen to selectively
32 etch the A-R coating in preference to the underlying sili-
33 con layer 12. Furthermore, the solution concentration
34 of the etchant is selected to minimize etchant under-
cutting of the mask. Accordingly, the etching solution
36 removes the unmasked regions of A-R layer 14 which




... .... . .

` ~ Jfi~734


1 correspond to the desired electrode pattern, exposing the
2 underlying silicon surface 12'.
3 The cell is then prepared for plating by con-
4 tacting at least the exposed silicon regions 12' with an
electroless nickel sensiti~er such as gold cyanide or
6 gold chloride, for example. The cell is then subjected
7 to electroless nickel plating which comprises contacting
8 at least the sensitized exposed silicon regions with an
9 electroless nickel plating solution to electrolessly
plate a layer of nickel 18 onto at least the sensitized
11 exposed silicon surface 12'. Nickel layer 18 in the re-
12 gion contacting the formerly exposed silicon surface is
13 about 0.1 microns in thickness.
14 Subsequent to the electroless nickel deposition,
masr~ing layer16 is removed using a suitable solvent. The
16 removal of masking layer 16 further removes stray nickel
17 deposition which may at least partially overcoat masking
18 layer 16. Referring to Figure 3, the removal of masking
19 layer 16 produces a cell having an A-R coating 14 and an
inter-dispersed electrode 18. In a preferred embodiment,
21 the cell is heat treated at a temperature ranging from
22 about 250C to about 350C to improve the adherence of
23 the electroless nickel layer 18 to the underlying sili-
24 con 12.
Electrolessly deposited nickel layer 18 is in-
26 sufficiently conductive to serve as a suitable current
27 carrying electrode for most solar cell applications.
28 Accordingly, a conduction supportive electrode layer 20
29 comprising a relatively high electroconductivity metal
may be formed by solder dipping, electroplating or the
31 like. In a preferred embodiment, the surface area of the
32 cell comprising at least the nickel electrode 18 is con-
33 tacted first with a solder flux agent and then with
34 molten solder to form layer 20 comprising solder. In an
alternate embodiment prior to the aforedescribed addition
36 of a conduction supporting electrode layer, a generally




, . . .

- `' '

`I 1 64734
... .


1 circular outer circumferential region of both surfaces
2 of the silicon cell is etched using an etchant comprising
3 a mixture of hydrofluoric and nitric acids. This pro-
4 cess of edge region etching reduces the probability of
edge region leakage currents and is well known in the art.
6 A suitable masking pattern, generally circular and
7 slightly less is diameter than the generally circular
8 solar cell may be used to confine the etching to the
9 outer circumferential edge regions of the cell.
An ohmic electrode generally designated 22 may
11 be formed concurrent to the formation of layer~ 18 and
12 20 comprising a first region 18' layer of electroless
13 nickel and a second region layer 20' comprising solder
14 for example. As taught with respect to layer 18, layer
22 may preferably be heat treated to increase its ad-
16 herence to silicon layer 10.
17 As readily recognized from the teaching of the
18 present specification, this invention is of advantage in
19 permitting heat treatment of the cell after application
of the A-R coating and of further advantage in facili-
21 tating electrical connection to the A-R coated cell. To
22 assist one skilled in the art, the following examples
23 detail a particular embodiment of the present invention.
24 Example 1
A 5.6 cm diameter N-type single crystal sili-
26 con wafer was diffused to form a P-N junction having a
27 relatively shallow junction depth of about 0.3 microns.
28 The diffused wafer was then cleaned in a solution of hydro-
29 fluoric acid to remove surface oxidation, rinsed in dis-
tilled deionized water, and blown dry. The cleaned cell
31 was then placed on a photoresist spinner and, using an
32 eye dropper, an amount of a solution of titanium/silica,
33 commercially available from the Emulsitone Corporation
34 located in Whippany, New Jersey, was applied to the cell's
junction surface. The solution was spin coated at approxi-
36 mately 3,500 rpm for about 10 seconds. The cell was then


~,~


..... .

" i 1 6~73~
-- 8 --

1 heat treated at a temperature of about 200C to cure and
2 densify the A-R coating. After cooling, tlle cell's coat-
3 ing was visually observed to be deep blue in color having
4 a relatively hard, mar-resistant surface. The A-R coated
5 c211 was then masked by silk screening an asphalt based
6 ink, patterned to expose the A-~ layer only in a region
7 to correspond to the desired electrode pattern. The mask
8 pattern was baked at about 100C to cure the asphalt based
9 ink and assure the adherence of the mask during the sub-
sequent processing steps. The desired electrode pattern
11 was a central, tapered wldth bus, tapering from about 4 mm
12 near one circumference of the cell to about 2 mm near the
13 diametrically opposed circumference of the cell. Eighteen
14 grid line electrodes, generally perpendicular to the bus
15 and approximately equally spaced, were about 0.3 mm in
16 width. The masked surface was then immersed in a dilute,
17 buffered hydrofluoric acid etch comprising a well known
18 etchant mixture of 15 parts by weight of ammonium fluoride
19 and eight parts water, this being mixed in a ratio of 4 to
1 with hydrofluoric acid. The etchant removed the TiOX
21 A-R layer in the exposed (unmasked) areas,exposing the
22 underlying silicon layer. Visual observance of the sur-
23 face revealed virtually no undercutting or lifting of the
24 mask. The cell was then immersed in an electroless gold
sensitizer comprising 50 ml hydrofluoric acid, 50 ml of
26 0.5% w/v of gold chloride and 900 ml of water which solu-
27 tion coated both the etched surface and the back of the
28 cell (the N-type surface). The sensitized cell was then
29 immersed in an electroless nickel plating solution com-
prising 65 gm ammonium acetate, 50 gm of ammonium chloride,
31 30 ml of nickel chloride and 10 gm of sodium hypophos-
32 phate. Electroless plating continued for about 10 min-
33 utes, whereafter the cell was rinsed in distilled de-
34 ionized water and blo~m dry. The masking layer was then
removed from the cell in a chloronated solvent such as
36 I~hibisol, a trade ~ of the Pentone Corporation of

`-`` i 16~73~
_ 9 _

1 Tenafly, ~ew Jersey. The removal of the mask also re-
2 moved any stray nickel deposit, leaving essentially the
3 desired grid pattern on the cell's top surface and an
4 approximately full surface coverage of the bottom (N-
type) surface. The outer circumferential region of each
6 surface was then ground to minimize leakage current paths
7 through the cell's edge. The cell was then heat treated
8 at about 300C for about 15 minutes to improve the ad-
9 herence of the nickel to the silicon and alleviate edge
grinding work damage. The cell was then immersed in
11 solder flux and dipped into a molten solder bath which
12 adhered to the nickel plated electrode areas of both sur-
13 faces, completing the fabrication of the cell.
14 The cell's reflectivity characteristics were
determined using a Beckman Model ',DX-la spectrometer fitted
16 with an integrating sphere for measuring total spectral
17 and diffuse reflection. The cell having an A-R coating
18 in accordance with the present invention had an average
19 reflectance of about 3~ in the spectral region of about.4
microns to about 1.1 microns as compared to a typical re-
21 flectance of 30% for conventionally prepared cells.

Dessin représentatif

Désolé, le dessin représentatatif concernant le document de brevet no 1164734 est introuvable.

États administratifs

Pour une meilleure compréhension de l'état de la demande ou brevet qui figure sur cette page, la rubrique Mise en garde , et les descriptions de Brevet , États administratifs , Taxes périodiques et Historique des paiements devraient être consultées.

États administratifs

Titre Date
Date de délivrance prévu 1984-04-03
(22) Dépôt 1981-04-10
(45) Délivré 1984-04-03
Expiré 2001-04-03

Historique d'abandonnement

Il n'y a pas d'historique d'abandonnement

Historique des paiements

Type de taxes Anniversaire Échéance Montant payé Date payée
Le dépôt d'une demande de brevet 0,00 $ 1981-04-10
Titulaires au dossier

Les titulaires actuels et antérieures au dossier sont affichés en ordre alphabétique.

Titulaires actuels au dossier
EXXON RESEARCH AND ENGINEERING COMPANY
Titulaires antérieures au dossier
S.O.
Les propriétaires antérieurs qui ne figurent pas dans la liste des « Propriétaires au dossier » apparaîtront dans d'autres documents au dossier.
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Description du
Document 
Date
(yyyy-mm-dd) 
Nombre de pages   Taille de l'image (Ko) 
Dessins 1994-03-15 1 13
Revendications 1994-03-15 2 66
Abrégé 1994-03-15 1 14
Page couverture 1994-03-15 1 15
Description 1994-03-15 9 411