TWI455341B - Method for manufacturing solar cells - Google Patents
Method for manufacturing solar cells Download PDFInfo
- Publication number
- TWI455341B TWI455341B TW100109539A TW100109539A TWI455341B TW I455341 B TWI455341 B TW I455341B TW 100109539 A TW100109539 A TW 100109539A TW 100109539 A TW100109539 A TW 100109539A TW I455341 B TWI455341 B TW I455341B
- Authority
- TW
- Taiwan
- Prior art keywords
- solar cell
- conductive type
- layer
- cell according
- type substrate
- Prior art date
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Landscapes
- Photovoltaic Devices (AREA)
Description
本發明是有關於一種太陽能電池的製造方法,特別是指一種以RIE技術進行表面粗糙化後之製程改良的太陽能電池的製造方法。The present invention relates to a method for producing a solar cell, and more particularly to a method for manufacturing a solar cell improved by a surface roughening by RIE technique.
已知太陽能電池結構中,其光照面通常具有凹凸結構,藉此降低太陽能電池表面對於光的反射率,提升太陽光入射比例。上述的表面凹凸結構,可以利用反應式離子蝕刻法(Reactive Ion Etching,簡稱RIE)蝕刻基板表面而形成。It is known that in a solar cell structure, the illuminating surface generally has a concave-convex structure, thereby reducing the reflectance of the surface of the solar cell to light and increasing the incident ratio of sunlight. The surface uneven structure described above can be formed by etching the surface of the substrate by reactive ion etching (RIE).
參閱圖1,雖然RIE製程能蝕刻基板11而達到基板11表面凹凸的需求,但此製程中的帶電粒子(電漿)也會因此與基板11材料反應,使基板11表面形成一電漿破壞層12,該電漿破壞層12的存在將增加載子的再結合率(Recombination),因而會降低太陽能電池的光電轉換效率,所以在RIE製程之後,必需再透過溼式蝕刻方式移除該電漿破壞層12,由於其材料是以矽(Si)、矽的氧化物(SiOx )為主,所以蝕刻液通常使用氫氧化鉀(KOH)、氫氟酸(HF)等溶液,當該電漿破壞層12移除後,後續再進行熱擴散(thermal diffusion)製程使該基板11表面形成p-n接面。Referring to FIG. 1, although the RIE process can etch the substrate 11 to meet the surface roughness of the substrate 11, the charged particles (plasma) in the process also react with the substrate 11 to form a plasma damage layer on the surface of the substrate 11. 12, the presence of the plasma destruction layer 12 will increase the recombination of the carrier, thereby reducing the photoelectric conversion efficiency of the solar cell, so after the RIE process, the plasma must be removed by wet etching. The destruction layer 12 is mainly composed of yttrium (Si) and lanthanum oxide (SiO x ). Therefore, a solution such as potassium hydroxide (KOH) or hydrofluoric acid (HF) is usually used as the etching solution. After the destruction layer 12 is removed, a thermal diffusion process is subsequently performed to form a pn junction on the surface of the substrate 11.
但是用於進行溼式蝕刻的儀器設備昂貴,而且在熱擴散製程之後還有另一次的溼式蝕刻必需進行,即是以HF移除基板11表面因高溫所產生的SiO2 ,所以如上述的太陽能 電池製造設備中,必需有兩組溼式蝕刻設備,造成設備及製造成本高,不利於工業量產。However, the apparatus for performing wet etching is expensive, and another wet etching is necessary after the thermal diffusion process, that is, HF is used to remove SiO 2 generated on the surface of the substrate 11 due to high temperature, so as described above. In the solar cell manufacturing equipment, two sets of wet etching equipment are required, resulting in high equipment and manufacturing cost, which is not conducive to industrial mass production.
因此,本發明之目的,即在提供一種降低設備成本、符合量產需求的太陽能電池的製造方法。Accordingly, it is an object of the present invention to provide a method of manufacturing a solar cell that reduces equipment costs and meets mass production requirements.
於是,本發明太陽能電池的製造方法,包含:(A)利用乾式蝕刻法蝕刻一第一導電型基板,使其表面成為高低起伏狀,且該第一導電型基板的表面還形成一個電漿破壞層;(B)對該第一導電型基板進行熱擴散處理,使該第一導電型基板形成一個位於該電漿破壞層的下方的第二導電型摻雜層,並將該電漿破壞層氧化而轉變成一個氧化層,所述熱擴散處理包括一個沉積階段以及一個驅入階段,該驅入階段是在一驅入溫度下持續一驅入時間,該驅入溫度為800℃~950℃,該驅入時間為20分鐘~50分鐘;(C)利用溼式蝕刻法移除該氧化層,完成製作該太陽能電池的半成品;及(D)在該太陽能電池的半成品上形成電極。Therefore, the method for manufacturing a solar cell of the present invention comprises: (A) etching a first conductive type substrate by dry etching to have a surface having a high and low undulation, and a surface of the first conductive type substrate is further damaged by a plasma. (B) thermally diffusing the first conductive type substrate such that the first conductive type substrate forms a second conductive type doped layer under the plasma break layer, and the plasma damage layer is formed Oxidation and conversion into an oxide layer, the thermal diffusion process comprising a deposition phase and a drive-in phase, the drive-in phase being a drive-in time at a drive-in temperature of 800 ° C to 950 ° C The driving time is 20 minutes to 50 minutes; (C) removing the oxide layer by wet etching to complete the fabrication of the semi-finished product of the solar cell; and (D) forming an electrode on the semi-finished product of the solar cell.
當驅入溫度太低而小於800℃時,由於溫度不足,無法使反應氣體分子產生足夠的移動動能,因此擴散效果不好,不利於第二導電型摻雜層的形成,也無法將該電漿破壞層氧化;當驅入溫度太高而大於950℃時,超過第一導電型基板的耐溫範圍,會產生翹曲現象。而驅入時間過短時,反應氣體分子未能充分擴散,亦不利於形成該第二導電型 摻雜層,該電漿破壞層也無法充分氧化;驅入時間最多50分鐘就能達到效果,再增加時間只是造成能源浪費。When the driving temperature is too low and less than 800 ° C, the reaction gas molecules cannot generate sufficient moving kinetic energy due to insufficient temperature, so the diffusion effect is not good, which is disadvantageous for the formation of the second conductive type doped layer, and the electricity cannot be obtained. The slurry destruction layer is oxidized; when the driving temperature is too high and is greater than 950 ° C, the temperature resistance of the first conductive type substrate exceeds the temperature range, and warpage occurs. When the driving time is too short, the reaction gas molecules are not sufficiently diffused, which is not conducive to the formation of the second conductivity type. The doped layer, the plasma destruction layer can not be fully oxidized; the driving time can be up to 50 minutes to achieve the effect, and the additional time is only a waste of energy.
本發明之功效:透過改善熱擴散處理的驅入階段,使電漿破壞層氧化,並利用熱擴散處理之後的溼式蝕刻去除該氧化層,使本發明可以省略熱擴散處理前的溼式蝕刻,如此可以降低設備成本、有利於量產,而且製作出的太陽能電池仍然維持一定以上的轉換效率。The effect of the present invention is that the plasma destruction layer is oxidized by improving the driving-in stage of the thermal diffusion treatment, and the oxide layer is removed by wet etching after the thermal diffusion treatment, so that the present invention can omit the wet etching before the thermal diffusion treatment. This can reduce equipment costs, facilitate mass production, and the solar cells produced still maintain a certain conversion efficiency.
有關本發明之前述及其他技術內容、特點與功效,在以下配合參考圖式之一個較佳實施例及數個實驗例的詳細說明中,將可清楚的呈現。The above and other technical contents, features and advantages of the present invention will be apparent from the following detailed description of the preferred embodiments of the invention.
參閱圖2,本發明製造方法之較佳實施例,用於製造一太陽能電池,所述太陽能電池包括由下往上疊置的一第一導電型基板2、一第二導電型摻雜層4、一抗反射層5,以及二個各別位於該第一導電型基板2的下表面及抗反射層5的表面的電極6。Referring to FIG. 2, a preferred embodiment of the manufacturing method of the present invention is used to fabricate a solar cell comprising a first conductive type substrate 2 and a second conductive type doped layer 4 stacked from bottom to top. An anti-reflection layer 5 and two electrodes 6 respectively located on the lower surface of the first conductive substrate 2 and the surface of the anti-reflection layer 5.
參閱圖3、4,本發明太陽能電池的製造方法包含:Referring to Figures 3 and 4, the method of manufacturing a solar cell of the present invention comprises:
(1)進行步驟71:準備該第一導電型基板2,本實施例為p型半導體矽(Si)基板,實施時不限於此,也可以使用n型基板。(1) Step 71: The first conductive type substrate 2 is prepared. This embodiment is a p-type semiconductor germanium (Si) substrate, and is not limited thereto, and an n-type substrate may be used.
(2)進行步驟72:利用乾式蝕刻法蝕刻該第一導電型基板2的一表面,本實施例是使用反應式離子蝕刻法(Reactive Ion Etching,簡稱RIE),並以SF6 、Cl2 及O2 混合作為反應氣體,使第一導電型基板2的表面成為高低起伏狀,也就 是形成凹凸狀的粗糙微結構(Texturing)。而且因為該第一導電型基板2的表面會與電漿產生反應,因此會在此凹凸狀的粗糙微結構表面形成一個電漿破壞層3,該電漿破壞層3材料主要為矽及矽的氧化物(SiOx )。(2) performing step 72: etching a surface of the first conductive type substrate 2 by dry etching, in this embodiment, using reactive ion etching (Reactive Ion Etching, RIE for short), and using SF 6 , Cl 2 and O 2 is mixed as a reaction gas, and the surface of the first-conductivity-type substrate 2 is made to have a high and low undulation, that is, a rough texture in which irregularities are formed. Moreover, since the surface of the first conductive type substrate 2 reacts with the plasma, a plasma damage layer 3 is formed on the surface of the uneven rough microstructure, and the material of the plasma damage layer 3 is mainly tantalum and niobium. Oxide (SiO x ).
(3)進行步驟73:對該第一導電型基板2進行熱擴散處理,所述熱擴散處理包括一個沉積階段以及一個驅入(drive-in)階段。首先為沉積階段,將該第一導電型基板2置入一高溫爐管,爐管內的溫度約為750℃~800℃,並且在爐管內通入一反應氣體,本實施例為N2 -POCl3 (三氯氧磷)、O2 及N2 的混合氣體,但不限於此,並進一步於該第一導電型基板2表面沉積磷(P)。(3) Performing step 73: performing thermal diffusion processing on the first conductive type substrate 2, the heat diffusion processing including a deposition stage and a drive-in stage. First, in the deposition stage, the first conductive substrate 2 is placed in a high temperature furnace tube, the temperature in the furnace tube is about 750 ° C ~ 800 ° C, and a reaction gas is introduced into the furnace tube, which is N 2 in this embodiment. -POCl 3 (phosphorus oxychloride), a mixed gas of O 2 and N 2 , but is not limited thereto, and further deposits phosphorus (P) on the surface of the first conductive substrate 2 .
接著進行驅入階段,該驅入階段是在一驅入溫度下持續一驅入時間,該驅入溫度為800℃~950℃,較佳地為810℃~950℃,更佳地為850℃~900℃;該驅入時間為20分鐘~50分鐘,較佳地為25分鐘~37.5分鐘,使該第一導電型基板2表面的磷(P)進入該第一導電型基板2的表層,進而在該電漿破壞層3下方形成n型的第二導電型摻雜層4,其材料主要為磷玻璃(PSG);本步驟亦相當於是在該第一導電型基板2內靠近該表面(該表面是指經過步驟72之乾式蝕刻法蝕刻的表面)處形成該第二導電型摻雜層4。Then, the driving in phase is continued for a driving time at a driving temperature of 800 ° C to 950 ° C, preferably 810 ° C to 950 ° C, more preferably 850 ° C. ~900 ° C; the driving time is 20 minutes to 50 minutes, preferably 25 minutes to 37.5 minutes, so that the phosphorus (P) on the surface of the first conductive substrate 2 enters the surface layer of the first conductive substrate 2, Further, an n-type second conductive type doped layer 4 is formed under the plasma destruction layer 3, and the material thereof is mainly phosphorus glass (PSG); this step is also equivalent to being close to the surface in the first conductive type substrate 2 ( The surface means that the second conductive type doped layer 4 is formed at the surface etched by the dry etching method of step 72.
而且在驅入階段中,反應氣體分子也會擴散進入該電漿破壞層3,並因較高的溫度與時間之設定,使其氧化而轉變成為一個氧化層3’,該氧化層3’材料主要為二氧化矽、磷與矽的氧化物等;該氧化層3’相當於是形成於該第一導電型基 板2上靠近該表面(該表面是指經過步驟72之乾式蝕刻法蝕刻的表面)側。Moreover, in the driving-in stage, the reactive gas molecules also diffuse into the plasma destruction layer 3, and are oxidized to become an oxide layer 3' due to a higher temperature and time setting, and the oxide layer 3' material Mainly oxides of cerium oxide, phosphorus and cerium; the oxide layer 3' is equivalent to being formed on the first conductive type The side of the board 2 is adjacent to the surface (the surface refers to the surface etched by the dry etching of step 72).
需要說明的是,若第一導電型基板2使用n型半導體,則熱擴散處理而形成的第二導電型摻雜層4為p型半導體。In addition, when the n-type semiconductor is used for the first conductive type substrate 2, the second conductive type doped layer 4 formed by thermal diffusion treatment is a p-type semiconductor.
(4)進行步驟74:利用溼式蝕刻法移除該氧化層3’,使該第二導電型摻雜層4露出。本實施例使用氫氟酸(HF)等溶液作為蝕刻液。(4) Step 74 is performed: the oxide layer 3' is removed by wet etching to expose the second conductivity type doping layer 4. This embodiment uses a solution such as hydrofluoric acid (HF) as an etching solution.
(5)進行步驟75:在該第二導電型摻雜層4的表面形成氮化矽之抗反射層5,抗反射層5能降低太陽光反射,提升光線入射比例。於實施上,可以利用濺鍍(Sputtering)或電漿輔助化學氣相沉積(PECVD)等技術進行。(5) Step 75 is performed to form an anti-reflection layer 5 of tantalum nitride on the surface of the second conductive type doped layer 4, and the anti-reflection layer 5 can reduce the reflection of sunlight and increase the incident ratio of light. In practice, it can be carried out by techniques such as sputtering or plasma assisted chemical vapor deposition (PECVD).
此時已完成製作該太陽能電池的半成品,但須注意的是,形成抗反射層5並非必要步驟,因此太陽能電池的半成品中,也可以不包含該抗反射層5。At this time, the semi-finished product of the solar cell has been completed, but it should be noted that the formation of the anti-reflection layer 5 is not an essential step, and therefore the anti-reflection layer 5 may not be included in the semi-finished product of the solar cell.
(6)進行步驟76:在該太陽能電池的半成品上形成電極6,電極6主要是透過網印的方式,形成於抗反射層5的上表面及該第一導電型基板2的下表面。其中圖3中電極6之型態僅為示意而非限定,亦可為其他設計之態樣。(6) Step 76: An electrode 6 is formed on the semi-finished product of the solar cell, and the electrode 6 is formed on the upper surface of the anti-reflection layer 5 and the lower surface of the first conductive substrate 2 mainly by screen printing. The shape of the electrode 6 in FIG. 3 is merely illustrative and not limiting, and may be in other designs.
(7)進行步驟77:將進行完步驟76的樣品置於高溫的燒結爐中,燒結爐內有複數個溫度不同的高溫區域,爐內的滾輪帶動樣品持續前進並且受到不同高溫的燒結,電極6因此能牢固地附著,如此即完成太陽能電池的製作。(7) Performing step 77: placing the sample subjected to step 76 in a high temperature sintering furnace, wherein the sintering furnace has a plurality of high temperature regions having different temperatures, and the rollers in the furnace drive the sample to continue to advance and are sintered at different high temperatures, the electrodes 6 Therefore, it can be firmly attached, thus completing the fabrication of the solar cell.
本發明相對於現有製程而言,主要是省略熱擴散處理前的溼式蝕刻,並且改良熱擴散處理的驅入階段,藉由驅 入溫度及驅入時間的配合,能夠在形成該第二導電型摻雜層4時,還使該電漿破壞層3氧化,其優點在於:現有太陽能電池製程中,在熱擴散處理之後原本就必需進行溼式蝕刻,又因為氫氟酸溶液對於氧化物有良好的蝕刻效果,所以本發明直接利用此溼式蝕刻步驟移除該氧化層3’,而且氧化層3’是透過氧化該電漿破壞層3而得,所以氧化層3’的厚度原則上相對於電漿破壞層3更厚,較容易控制將其完全蝕刻,並避免傷害該第二導電型摻雜層4。Compared with the prior art process, the present invention mainly omits the wet etching before the thermal diffusion treatment, and improves the driving stage of the thermal diffusion treatment by driving The combination of the temperature and the driving time can also oxidize the plasma destruction layer 3 when the second conductive type doping layer 4 is formed. The advantage is that in the existing solar cell process, after the thermal diffusion treatment, the original Wet etching is necessary, and because the hydrofluoric acid solution has a good etching effect on the oxide, the present invention directly removes the oxide layer 3' by using the wet etching step, and the oxide layer 3' is oxidized by the plasma. Destruction of the layer 3, so that the thickness of the oxide layer 3' is in principle thicker relative to the plasma destruction layer 3, it is easier to control to completely etch it, and to avoid damage to the second conductivity type doping layer 4.
參閱表一,以下透過實驗例證明本發明製造出的太陽能電池仍然具有良好的性能。表一的Voc 代表開路電壓,Jsc 代表短路電流,F.F值代表fill factor,Eff.為轉換效率。在本發明實驗例1~8所限定的驅入溫度及驅入時間範圍內,各樣品的短路電流、F.F值及轉換效率都能達到一定的標準。反觀比較例1,其驅入溫度為780℃而低於800℃,反應氣體分子的移動動能不足、擴散效果不好,不利於第二導電型摻雜層4的形成,其電漿破壞層3也無法充分氧化及完全移除,造成比較例1的短路電流及轉換效率較差。Referring to Table 1, the following experimental examples demonstrate that the solar cell produced by the present invention still has good performance. Table 1 V oc represents the open circuit voltage, J sc represents the short circuit current, FF value represents the fill factor, and Eff. is the conversion efficiency. In the range of the driving temperature and the driving time defined in Experimental Examples 1 to 8, the short-circuit current, the FF value, and the conversion efficiency of each sample can reach a certain standard. In contrast, in Comparative Example 1, the driving temperature is 780 ° C and lower than 800 ° C, the moving kinetic energy of the reaction gas molecules is insufficient, and the diffusion effect is not good, which is disadvantageous for the formation of the second conductive type doped layer 4, and the plasma destruction layer 3 thereof Also, it was not sufficiently oxidized and completely removed, resulting in poor short-circuit current and conversion efficiency of Comparative Example 1.
綜上所述,本發明改善熱擴散處理中的驅入階段,並且省略傳統方法在熱擴散處理前的溼式蝕刻,因此本發明製程中只需要一組溼式蝕刻設備,進而降低設備成本、有利於量產,而且製作出的太陽能電池仍然維持一定以上的轉換效率,因此本發明兼顧量產的可行性及太陽能電池品質。In summary, the present invention improves the driving-in stage in the thermal diffusion process, and omits the wet etching of the conventional method before the thermal diffusion process. Therefore, only one set of wet etching equipment is required in the process of the present invention, thereby reducing equipment cost, It is advantageous for mass production, and the produced solar cells still maintain a certain conversion efficiency. Therefore, the present invention takes into consideration the feasibility of mass production and the quality of solar cells.
惟以上所述者,僅為本發明之較佳實施例而已,當不能以此限定本發明實施之範圍,即大凡依本發明申請專利範圍及發明說明內容所作之簡單的等效變化與修飾,皆仍屬本發明專利涵蓋之範圍內。The above is only the preferred embodiment of the present invention, and the scope of the invention is not limited thereto, that is, the simple equivalent changes and modifications made by the scope of the invention and the description of the invention are All remain within the scope of the invention patent.
2‧‧‧第一導電型基板2‧‧‧First Conductive Substrate
3‧‧‧電漿破壞層3‧‧‧plasma damage layer
3’‧‧‧氧化層3'‧‧‧Oxide
4‧‧‧第二導電型摻雜層4‧‧‧Second conductive doped layer
5‧‧‧抗反射層5‧‧‧Anti-reflective layer
6‧‧‧電極6‧‧‧Electrode
71~77‧‧‧步驟71~77‧‧‧Steps
圖1是一種已知太陽能電池的示意圖;圖2是一示意圖,顯示本發明太陽能電池的製造方法之較佳實施例製造出的太陽能電池;圖3是該較佳實施例各步驟進行時的示意圖;及圖4是該較佳實施例的步驟流程圖。1 is a schematic view of a known solar cell; FIG. 2 is a schematic view showing a solar cell manufactured by a preferred embodiment of the method for fabricating a solar cell of the present invention; and FIG. 3 is a schematic view showing the steps of the preferred embodiment. And Figure 4 is a flow chart of the steps of the preferred embodiment.
71~77‧‧‧步驟71~77‧‧‧Steps
Claims (8)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TW100109539A TWI455341B (en) | 2011-03-21 | 2011-03-21 | Method for manufacturing solar cells |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TW100109539A TWI455341B (en) | 2011-03-21 | 2011-03-21 | Method for manufacturing solar cells |
Publications (2)
Publication Number | Publication Date |
---|---|
TW201240127A TW201240127A (en) | 2012-10-01 |
TWI455341B true TWI455341B (en) | 2014-10-01 |
Family
ID=47599714
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW100109539A TWI455341B (en) | 2011-03-21 | 2011-03-21 | Method for manufacturing solar cells |
Country Status (1)
Country | Link |
---|---|
TW (1) | TWI455341B (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW200836353A (en) * | 2006-09-06 | 2008-09-01 | Univ Illinois | Controlled buckling structures in semiconductor interconnects and nanomembranes for stretchable electronics |
-
2011
- 2011-03-21 TW TW100109539A patent/TWI455341B/en not_active IP Right Cessation
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW200836353A (en) * | 2006-09-06 | 2008-09-01 | Univ Illinois | Controlled buckling structures in semiconductor interconnects and nanomembranes for stretchable electronics |
Also Published As
Publication number | Publication date |
---|---|
TW201240127A (en) | 2012-10-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR101225978B1 (en) | Sollar Cell And Fabrication Method Thereof | |
US20100037952A1 (en) | Selective Emitter Solar Cell and Fabrication Method Thereof | |
TW201003934A (en) | Method for manufacturing solar cell | |
TW200910618A (en) | Solar cell and method for manufacturing the same | |
US20130291935A1 (en) | Optical anti-reflection structure and solar cell including the same, and method for making the optical anti-reflection structure | |
CN102270688A (en) | Solar cell | |
TWI518937B (en) | Manufacture of solar cells | |
JP2013165160A (en) | Method for manufacturing solar cell, and solar cell | |
WO2024012162A1 (en) | Manufacturing method for p-type ibc battery | |
CN101339966A (en) | Post produced velvet production process of solar cell | |
JP5408009B2 (en) | Manufacturing method of solar cell | |
CN114447142B (en) | N-type TOPCON solar cell and manufacturing method thereof | |
WO2009157052A1 (en) | Method for manufacturing photovoltaic system | |
JP5817046B2 (en) | Manufacturing method of back contact type crystalline silicon solar cell | |
JP2012038852A (en) | Solar cell and method for manufacturing the same | |
CN104134706B (en) | Graphene silicon solar cell and manufacturing method thereof | |
CN105244417A (en) | Crystalline silicon solar cell and preparation method thereof | |
TWI455341B (en) | Method for manufacturing solar cells | |
CN103367526A (en) | Method for manufacturing rear side local contact silicon solar cell | |
JP2012256713A (en) | Manufacturing method of solar cell | |
KR102049604B1 (en) | Solar cell and Method of manufacturing the same | |
CN102956742B (en) | Manufacturing method of solar cell | |
CN103904168B (en) | The manufacture method of solar battery cell | |
TWI574425B (en) | Solar cell and manufacturing method thereof | |
TWI568012B (en) | Bifacial solar cell manufacturing method |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Annulment or lapse of patent due to non-payment of fees |