JPS59173944A - Secondary battery - Google Patents
Secondary batteryInfo
- Publication number
- JPS59173944A JPS59173944A JP58047160A JP4716083A JPS59173944A JP S59173944 A JPS59173944 A JP S59173944A JP 58047160 A JP58047160 A JP 58047160A JP 4716083 A JP4716083 A JP 4716083A JP S59173944 A JPS59173944 A JP S59173944A
- Authority
- JP
- Japan
- Prior art keywords
- secondary battery
- battery
- film
- polyacetylene
- battery case
- 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.)
- Pending
Links
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims abstract description 18
- 229920001197 polyacetylene Polymers 0.000 claims abstract description 16
- 239000011347 resin Substances 0.000 claims abstract description 14
- 229920005989 resin Polymers 0.000 claims abstract description 14
- -1 Polyethylene Polymers 0.000 claims abstract description 9
- 229910052751 metal Inorganic materials 0.000 claims abstract description 7
- 239000002184 metal Substances 0.000 claims abstract description 7
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 6
- 150000001875 compounds Chemical class 0.000 claims abstract description 6
- 239000004698 Polyethylene Substances 0.000 claims abstract description 4
- 239000004743 Polypropylene Substances 0.000 claims abstract description 4
- 229920000573 polyethylene Polymers 0.000 claims abstract description 4
- 229920001155 polypropylene Polymers 0.000 claims abstract description 4
- 239000004677 Nylon Substances 0.000 claims abstract description 3
- 229920001778 nylon Polymers 0.000 claims abstract description 3
- 229920000515 polycarbonate Polymers 0.000 claims abstract description 3
- 239000004417 polycarbonate Substances 0.000 claims abstract description 3
- 229920000728 polyester Polymers 0.000 claims abstract description 3
- 239000010408 film Substances 0.000 claims description 22
- 239000010409 thin film Substances 0.000 claims description 8
- 229920000620 organic polymer Polymers 0.000 claims description 5
- 239000003792 electrolyte Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 8
- 229910052760 oxygen Inorganic materials 0.000 abstract description 8
- 239000001301 oxygen Substances 0.000 abstract description 8
- 230000003647 oxidation Effects 0.000 abstract description 2
- 238000007254 oxidation reaction Methods 0.000 abstract description 2
- 239000011149 active material Substances 0.000 abstract 1
- 230000035515 penetration Effects 0.000 abstract 1
- 238000010586 diagram Methods 0.000 description 6
- 239000003115 supporting electrolyte Substances 0.000 description 5
- 239000002019 doping agent Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 2
- 239000007772 electrode material Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- OJIJEKBXJYRIBZ-UHFFFAOYSA-N cadmium nickel Chemical compound [Ni].[Cd] OJIJEKBXJYRIBZ-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/10—Primary casings; Jackets or wrappings
- H01M50/116—Primary casings; Jackets or wrappings characterised by the material
- H01M50/124—Primary casings; Jackets or wrappings characterised by the material having a layered structure
- H01M50/126—Primary casings; Jackets or wrappings characterised by the material having a layered structure comprising three or more layers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/10—Primary casings; Jackets or wrappings
- H01M50/131—Primary casings; Jackets or wrappings characterised by physical properties, e.g. gas permeability, size or heat resistance
- H01M50/133—Thickness
-
- 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
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Secondary Cells (AREA)
- Sealing Battery Cases Or Jackets (AREA)
Abstract
Description
【発明の詳細な説明】
〔発明の利用分野〕
本発明は二次電池に係り、特に共役二重結合を有する有
機高分子化合物を少なくとも1方の電極とした充電過程
において電解質を消費する二次電化の改良に関するもの
でおる。[Detailed Description of the Invention] [Field of Application of the Invention] The present invention relates to a secondary battery, and particularly to a secondary battery that consumes electrolyte during the charging process using an organic polymer compound having a conjugated double bond as at least one electrode. This is related to improvements in electrification.
共役二重結合を有する有機高分子化合物、例えば、アセ
チレン重合体(ポリアセチレン)は、電気化学的に(、
to4−、 PF5− 、 BF4−等のアニオン、ま
たは、L12. (’C4H3)4N+等のカチオン
をドーピングすることによp1p型およびn型の導電性
ポリアセチレンにすることが可能であることが知られテ
ィるC J、 C,S、 c:hem、 Comm、
、 (1979)pp594〜595 、 C,&EN
、す、39(1981):]。そしてこの電気化学的ド
ーピングを芯用すれば、ポリアセチレンを用いて充放電
可能な二次電池ができることが報告されている。このレ
ン膜を用い、電解質兼ドーパントとしてプロピレフ’j
)−ホネートに溶解させたテトラブチルアンモニウムの
過塩素酸塩C(C4Ht)4NCt04’l tJMイ
fC電池では、開/l18電圧2.5 V、短絡電流1
1.1mAが得られているC J、 C,S、 che
m、 comm。Organic polymer compounds having conjugated double bonds, such as acetylene polymers (polyacetylene), can be electrochemically (,
Anions such as to4-, PF5-, BF4-, or L12. It is known that it is possible to make p1p type and n type conductive polyacetylene by doping with cations such as ('C4H3)4N+. CJ, C,S, c:hem, Comm,
, (1979) pp594-595, C,&EN
, Su, 39 (1981): ]. It has been reported that if this electrochemical doping is used as a core, a rechargeable and dischargeable secondary battery can be made using polyacetylene. Using this membrane, propylev'j was used as an electrolyte and dopant.
) - perchlorate of tetrabutylammonium dissolved in honate C(C4Ht)4NCt04'l tJM IfC cell, open/l18 voltage 2.5 V, short circuit current 1
1.1 mA is obtained C J, C, S, che
m, comm.
(1981)I)I)317〜319)。(1981) I) I) 317-319).
ポリアセチレンは、チーグラー・ナツタ触媒を用いてア
セチレンを重合することによって得られる。そして直接
膜状とする方法およびゲルまたは粉末をプレス加工して
膜状とする方法によって製膜している。しかし、ポリア
セチレン膜を電極として二次電池を製作する場合、次の
ような問題がある。Polyacetylene is obtained by polymerizing acetylene using a Ziegler-Natsuta catalyst. Films are formed by directly forming a film or by pressing gel or powder into a film. However, when manufacturing a secondary battery using a polyacetylene film as an electrode, there are the following problems.
(1)電池の電圧が高いため、使用する有機溶媒が充電
時に電気分解を起し、そのとき発生する不純物が電池の
寿命に影響する。(1) Since the voltage of the battery is high, the organic solvent used causes electrolysis during charging, and the impurities generated at that time affect the life of the battery.
(2)電池の電圧が高いため、電解質溶液中に含まれて
いる水分が電気分解し、そのとき発生する酸素などがポ
リアセチレンを劣化させる。(2) Since the voltage of the battery is high, water contained in the electrolyte solution electrolyzes, and the oxygen generated at that time deteriorates polyacetylene.
(3) この電池の理論エネルギー密度は、電極活物
質となるポリアセチレンの比重が小さいため、従来のニ
ッケル・カドミウム電池や鉛電池にくらべて大きくなる
−1しかし、電池ケースや集電子材料等を考慮した実用
エネルギー密度は、従来技術では犬きくとれない。その
ため、ポリアセチレン膜を用いた電池の特性を生かすた
めには、電池パッケージ係数を小さくする必要がある。(3) The theoretical energy density of this battery is higher than that of conventional nickel-cadmium batteries or lead-acid batteries because the specific gravity of polyacetylene, which is the electrode active material, is low. The practical energy density achieved cannot be achieved using conventional technology. Therefore, in order to take advantage of the characteristics of a battery using a polyacetylene film, it is necessary to reduce the battery packaging factor.
(4) ポリアセチレンは、共役二重結合を持つため
酸化されやすい。したがって、電池ケースとしては酸素
および水分透過を防止できるものを用いる必要がある。(4) Polyacetylene is easily oxidized because it has conjugated double bonds. Therefore, it is necessary to use a battery case that can prevent oxygen and moisture from permeating.
(5) ポリアセチレンは膜状として用いるため、電
池ケースも薄膜形状のものが望ましい。(5) Since polyacetylene is used in the form of a film, it is desirable that the battery case also be in the form of a thin film.
現在、−次電池であるマンガン電池やリチウム電池にお
いては、それの電池ケースについて種々考案されている
が、その技術のみでは上記したすべての問題を解決する
ことができない。Currently, various battery cases have been devised for negative batteries such as manganese batteries and lithium batteries, but these technologies alone cannot solve all of the above-mentioned problems.
本発明は上記に鑑みてなされたもので、その目的とする
ところは、有害な酸素や水分の侵入を防止することがで
き、電池の寿命を長くすることができる二次電池を提供
することにある。The present invention has been made in view of the above, and its purpose is to provide a secondary battery that can prevent harmful oxygen and moisture from entering and extend the life of the battery. be.
本発明は、ポリアセチレンなどの共役二重結合を有する
有機高分子化合物を電極とする二次電池の初期の電流効
率は優れているが、充放電サイクルを重ねると性能が低
下してしまい、その原因は有機溶媒中の不純物や水分に
あり、捷た、電池完成時に酸素が共存すると電極活物質
の酸化速度が増大して電極が劣化することを確認してな
されたもので、酸素や水分の侵入を防止するため、電池
ケースは金属薄膜を被覆もしくは挾み込んだ樹脂フィル
ムで構成したことを特徴としている。The present invention discloses that secondary batteries using organic polymer compounds with conjugated double bonds, such as polyacetylene, as electrodes have excellent initial current efficiency, but performance deteriorates with repeated charge/discharge cycles. This was done after confirming that impurities and moisture in organic solvents cause the oxidation rate of the electrode active material to increase and cause electrode deterioration if oxygen coexists with the battery when the battery is completed. In order to prevent this, the battery case is characterized by being constructed of a resin film covered with or sandwiched with a thin metal film.
以下本発明を第1図〜第3図に示した実施例および第4
図を用いて詳細に説明する。Examples of the present invention shown in FIGS. 1 to 3 and 4
This will be explained in detail using figures.
第1図は本発明の二次電池の一実施例を示す構造説明図
である。第1図に2いて、1はそれぞれ電極で、電極1
は比重0.91S厚さ236pm。FIG. 1 is a structural explanatory diagram showing an embodiment of the secondary battery of the present invention. In Figure 1, 2 and 1 are electrodes, and electrode 1
has a specific gravity of 0.91S and a thickness of 236pm.
大きさ4cniのボリア′セチレン膜の片面にスパッタ
IJング装置を用いて300人の厚みの金属薄膜を付け
た構成としである。2は支持電解質溶液で、アルミナウ
ールを厚さ200μmにプレスして作ったセパレータに
保持させてあシ、支持電解質溶液としては、支持電解質
兼ドーパントである(C*H5)4 NCtCh ’k
60 C、10−”mm)(gの条件下で24時間以
上脱水してこれtcan2で脱水後2回蒸留したアセト
ニトリル溶媒に1 mat / l溶解したものを用い
た。3はポリテトラフルオロエチレン製り電池保持体、
4は電池ケースである。A thin metal film having a thickness of 300 mm was attached to one side of a boria-cetylene film having a size of 4 cm by using a sputtering IJ apparatus. 2 is a supporting electrolyte solution, which is held in a separator made by pressing alumina wool to a thickness of 200 μm, and the supporting electrolyte solution is a supporting electrolyte and dopant (C*H5)4 NCtCh'k
60C, 10-"mm) (g) was dehydrated for over 24 hours, dehydrated with Tcan2, and then dissolved in twice-distilled acetonitrile solvent at a concentration of 1 mat/l. 3 is made of polytetrafluoroethylene. battery holder,
4 is a battery case.
ところで、本発明においては、電池ケース4は、第2図
に示すように、厚さ20μmのアルミニウム薄膜5を厚
さ100μmの樹脂フィルム6ではさみ込んだもので構
成し、端面は図示のように折り返して熱圧着して気密構
造とした。樹脂フィルム6としては、熱圧着性が良好な
ポリエチレン。By the way, in the present invention, as shown in FIG. 2, the battery case 4 is constructed by sandwiching an aluminum thin film 5 with a thickness of 20 μm between resin films 6 with a thickness of 100 μm, and the end faces are formed as shown in the figure. It was folded back and heat-pressed to create an airtight structure. The resin film 6 is made of polyethylene, which has good thermocompression bondability.
ポリプロピレンが好ましく、条件によりポリエステル、
ポリカーボネート、ナイロンなども使用できる。第2図
においては、ポリエチレンを用いた。Polypropylene is preferred; depending on conditions, polyester,
Polycarbonate, nylon, etc. can also be used. In FIG. 2, polyethylene was used.
上記した二次電池を電流密度5mA/−で1時間充電し
、その後、電池電圧が1■になるまで5 In A /
cAの電流密度で放電し、各充放電サイクルでの電流
効率、すなわち、充電電荷量に対する放電電荷量の割合
(%)を測定し、その結果を第4図に大曲線で示した。The above-mentioned secondary battery was charged at a current density of 5 mA/- for 1 hour, and then charged at 5 In A/- until the battery voltage reached 1■.
The battery was discharged at a current density of cA, and the current efficiency in each charge/discharge cycle, that is, the ratio (%) of the amount of discharged charge to the amount of charged charge, was measured, and the results are shown as a large curve in FIG.
この場合、充放電を29回行ったが、29回目の電流効
率は94%で、また、29回目の充電終了後の電池電圧
は2.8■であった。また、電池の実用エネルギー密度
は、ドーパント(C2H5)4NC104のポリアセチ
レンへのドーピング率が6 m04%で45Whr/K
fであった。In this case, charging and discharging were performed 29 times, and the current efficiency at the 29th time was 94%, and the battery voltage after the completion of the 29th charge was 2.8 ■. In addition, the practical energy density of the battery is 45 Whr/K at a doping rate of dopant (C2H5)4NC104 to polyacetylene of 6 m04%.
It was f.
なお、比較のため、第1図において、金属ケース4のみ
をアルミニウム薄膜5を付与しない樹脂フィルムで構成
し、その他は上記と同様とした二次電池について、上記
と同様の充放電を行い、各充放電サイクルでの電流効率
を測定し、その結果を第4図に8曲線で示した。15回
目までの充放電サイクルにおいては高い電流効率を示し
たが、その後の充放電サイクルにおいては、それが徐々
に低下し、30回目においては、電流効率が30%まで
低下した。これは、電池ケース4(il−樹脂フィルム
としたため、空気中の酸素や水分が透過し、悪影響を及
ぼしたためである。For comparison, in FIG. 1, a secondary battery in which only the metal case 4 is made of a resin film without the aluminum thin film 5 and the other parts are the same as above was charged and discharged in the same manner as above, and each The current efficiency during charge/discharge cycles was measured, and the results are shown in eight curves in FIG. Although high current efficiency was shown in the 15th charge/discharge cycle, it gradually decreased in subsequent charge/discharge cycles, and at the 30th charge/discharge cycle, the current efficiency decreased to 30%. This is because the battery case 4 (made of an il-resin film) allows oxygen and moisture in the air to pass through and have an adverse effect.
また、電池ケース4を厚さ150μのS US 304
の薄板とし、他は上記実施例と同様とした二次電池につ
いて実験したところ、この電池の実用エネルギー密度は
、ドーパント(CzHs)4NC404のポリアセチレ
ンへのドーピング率が5m□7%で30W )1 r
7Kgと低かった。In addition, the battery case 4 is made of SUS 304 with a thickness of 150μ.
An experiment was conducted on a secondary battery made of a thin plate with the other parts being the same as in the above example, and the practical energy density of this battery was 30 W at a doping rate of dopant (CzHs)4NC404 to polyacetylene of 5 m □ 7%) 1 r
It was as low as 7kg.
これに対して、本発明に係る二次電池は、電池ケース4
を第2図に示す構成のものとしたので酸素や水分の透過
が防止され、上記したように電流効率が向上し、しかも
、それが充放電サイクルが多くなっても維持され、かつ
、実用エネルギー密度も向上する。In contrast, the secondary battery according to the present invention has a battery case 4
The configuration shown in Figure 2 prevents the permeation of oxygen and moisture, improves current efficiency as described above, maintains it even with many charge/discharge cycles, and reduces practical energy consumption. Density is also improved.
第3図は本発明に係る二次電池の電池ケースの他の実施
例を示す構造図である。第3図においては、樹脂フィル
ム6の外側にアルミニウム薄膜5をラミネートした構成
としである。FIG. 3 is a structural diagram showing another embodiment of a battery case for a secondary battery according to the present invention. In FIG. 3, a thin aluminum film 5 is laminated on the outside of a resin film 6.
次に、本発明の二次電池の他の実施例について説明する
。第1図において、電極1としては上記した実施例と同
様のポリアセチレン膜を用い、集電子として金属薄膜を
スパッタする代シに100メツシユの5US304の金
鋼を用い、支持電解質溶液2を保持するセパレータはポ
リプロピレンで構成し、電池ケース4は第3図に示す構
成のものとした二次電池について、上記した実施例の場
合と同様の充放電を行い、各充放電サイクルでの電流効
率を測定し、その結果を第4図にC曲線で示した。本実
施例の場合は、29回目の充放電サイクルにおいては電
流効率81%と大曲線の場合に比較して多少低いが、大
曲線の場合と同様、充放電サイクル数によって電流効率
が低下することはない。また、29回目の充電終了後の
電池電圧は3.1vであった。Next, other embodiments of the secondary battery of the present invention will be described. In FIG. 1, the same polyacetylene film as in the above embodiment is used as the electrode 1, 100 mesh 5US304 gold steel is used as the current collector for sputtering a metal thin film, and the separator holds the supporting electrolyte solution 2. A secondary battery made of polypropylene and a battery case 4 having the configuration shown in FIG. 3 was charged and discharged in the same manner as in the above example, and the current efficiency in each charge and discharge cycle was measured. The results are shown in FIG. 4 by curve C. In the case of this example, the current efficiency was 81% at the 29th charge/discharge cycle, which is somewhat lower than in the case of the large curve, but as in the case of the large curve, the current efficiency decreases depending on the number of charge/discharge cycles. There isn't. Further, the battery voltage after the 29th charge was 3.1V.
以上説明したように、本発明によれば、有害な酸素や水
分の侵入を防止することができ、電池の寿命を長くする
ことができるとともに、軽量化によって実用エネルギー
密度の向上をはかることができるという効果がある。As explained above, according to the present invention, it is possible to prevent the intrusion of harmful oxygen and moisture, extend the life of the battery, and improve the practical energy density by reducing the weight. There is an effect.
第1図は本発明の二次電池の一実施例を示す構造説明図
、第2図は第1図の電池ケースの一実施例を示す構造図
、第3図は電池ケースの他の実施例を示す構造図、第4
図は本発明の詳細な説明するための充放電サイクルと電
流効率との関係線図である。
1・・・電極、2・・・支持電解質溶液、4・・・電池
ケース、訃・・アルミニウム薄膜、6・・・樹脂フィル
ム。
N ノ 図
Vt21
苓 4 図
充方丈電すイクツb数(回p
第1頁の続き
■出 願 人 昭和電工株式会社
東京都港区芝大門1丁目13番5Fig. 1 is a structural diagram showing one embodiment of the secondary battery of the present invention, Fig. 2 is a structural diagram showing one embodiment of the battery case of Fig. 1, and Fig. 3 is another embodiment of the battery case. Structure diagram showing 4th
The figure is a relationship diagram between charge/discharge cycles and current efficiency for detailed explanation of the present invention. DESCRIPTION OF SYMBOLS 1... Electrode, 2... Supporting electrolyte solution, 4... Battery case, Death... Aluminum thin film, 6... Resin film. N No Figure Vt21 蓓 4 Figure Jōdensu Ikutsu b number (Continuation of page 1) Applicant Showa Denko Co., Ltd. 1-13-5 Shiba Daimon, Minato-ku, Tokyo
Claims (1)
高分子化合物で構成しである充電過程において電解質を
消費する二次電池において、電池ケースは金属薄膜を被
覆もしくは挾み込んだ樹脂フィルムで構成しであること
を特徴とする二次電池。 2 前記金属薄膜はアルミニウム薄膜である特許請求の
範囲第1項記載の二次電池。 13、
前記樹脂フィルムはポリエチレン、ポリプロ ′ピ
レン、ポリエステル、ポリカーボネートあるいはナイロ
ンよりなる特許請求の範囲第1項または第2項記載の二
次電池。 4、 前記電池ケースは端面において前記樹脂フィルム
を圧着して気密構造としである特許請求の範囲第1項ま
たは第2項または第3項記載の二次電池。
j5、前記有機高分子
化合物がポリアセチレンであ項または第4項記載の二次
電池。[Claims] 1. In a secondary battery in which at least one electrode is composed of an organic polymer compound having a conjugated double bond and which consumes electrolyte during the charging process, the battery case covers or sandwiches a metal thin film. A secondary battery characterized in that it is made of a resin film containing a resin film. 2. The secondary battery according to claim 1, wherein the metal thin film is an aluminum thin film. 13,
3. The secondary battery according to claim 1, wherein said resin film is made of polyethylene, polypropylene, polyester, polycarbonate, or nylon. 4. The secondary battery according to claim 1, 2, or 3, wherein the battery case has an airtight structure by pressure-bonding the resin film on the end face.
j5, the secondary battery according to item 4, wherein the organic polymer compound is polyacetylene;
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58047160A JPS59173944A (en) | 1983-03-23 | 1983-03-23 | Secondary battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58047160A JPS59173944A (en) | 1983-03-23 | 1983-03-23 | Secondary battery |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS59173944A true JPS59173944A (en) | 1984-10-02 |
Family
ID=12767325
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58047160A Pending JPS59173944A (en) | 1983-03-23 | 1983-03-23 | Secondary battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59173944A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63259961A (en) * | 1987-04-16 | 1988-10-27 | Sanyo Electric Co Ltd | Cell case |
JPH05325924A (en) * | 1992-05-26 | 1993-12-10 | Kanebo Ltd | Organic electrolyte battery |
JPH05325925A (en) * | 1992-05-26 | 1993-12-10 | Kanebo Ltd | Organic electrolyte battery |
JPH05325926A (en) * | 1992-05-26 | 1993-12-10 | Kanebo Ltd | Organic electrolyte battery |
FR2770032A1 (en) * | 1997-10-16 | 1999-04-23 | Alsthom Cge Alcatel | WATERPROOF MULTI-LAYERED ENCLOSURE |
US6242131B1 (en) * | 1998-08-29 | 2001-06-05 | Samsung Sdi Co., Ltd. | Case of lithium secondary battery based on a polymer coated aluminum material |
US7022391B2 (en) | 2000-10-13 | 2006-04-04 | Showa Denko Packaging Co. | Packaging material for electronic-part case, and others |
-
1983
- 1983-03-23 JP JP58047160A patent/JPS59173944A/en active Pending
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63259961A (en) * | 1987-04-16 | 1988-10-27 | Sanyo Electric Co Ltd | Cell case |
JPH05325924A (en) * | 1992-05-26 | 1993-12-10 | Kanebo Ltd | Organic electrolyte battery |
JPH05325925A (en) * | 1992-05-26 | 1993-12-10 | Kanebo Ltd | Organic electrolyte battery |
JPH05325926A (en) * | 1992-05-26 | 1993-12-10 | Kanebo Ltd | Organic electrolyte battery |
FR2770032A1 (en) * | 1997-10-16 | 1999-04-23 | Alsthom Cge Alcatel | WATERPROOF MULTI-LAYERED ENCLOSURE |
EP0913874A1 (en) * | 1997-10-16 | 1999-05-06 | Alcatel | Sealed storage battery with multilayered jacket |
US6146785A (en) * | 1997-10-16 | 2000-11-14 | Alcatel | Sealed cell having a multilayer case |
US6242131B1 (en) * | 1998-08-29 | 2001-06-05 | Samsung Sdi Co., Ltd. | Case of lithium secondary battery based on a polymer coated aluminum material |
US7022391B2 (en) | 2000-10-13 | 2006-04-04 | Showa Denko Packaging Co. | Packaging material for electronic-part case, and others |
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