JPS60253165A - Non-aqueous electrolyte battery - Google Patents
Non-aqueous electrolyte batteryInfo
- Publication number
- JPS60253165A JPS60253165A JP59108066A JP10806684A JPS60253165A JP S60253165 A JPS60253165 A JP S60253165A JP 59108066 A JP59108066 A JP 59108066A JP 10806684 A JP10806684 A JP 10806684A JP S60253165 A JPS60253165 A JP S60253165A
- Authority
- JP
- Japan
- Prior art keywords
- aqueous electrolyte
- battery
- mixed solvent
- lithiumtrifluoromethanesulphonate
- dioxolane
- 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
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/14—Cells with non-aqueous electrolyte
- H01M6/16—Cells with non-aqueous electrolyte with organic electrolyte
- H01M6/162—Cells with non-aqueous electrolyte with organic electrolyte characterised by the electrolyte
- H01M6/164—Cells with non-aqueous electrolyte with organic electrolyte characterised by the electrolyte by the solvent
-
- 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
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Primary Cells (AREA)
Abstract
Description
【発明の詳細な説明】
(イ)産業上の利用分野
本発明はリチウム或いはリチウム合金を活物質とする負
極と、金属の酸化物、硫化物、ハロゲン化物などを活物
質とする正極と、溶媒と溶質とからなる非水電解液とを
備えた非水電解液電池に係り、特に非水電解液の改良に
関するものである。Detailed Description of the Invention (a) Field of Industrial Application The present invention relates to a negative electrode using lithium or a lithium alloy as an active material, a positive electrode using a metal oxide, sulfide, halide, etc. as an active material, and a solvent. The present invention relates to a non-aqueous electrolyte battery comprising a non-aqueous electrolyte comprising a solute and a solute, and particularly relates to improvements in the non-aqueous electrolyte.
(ロ)従来技術
この種電池に用いられる非水電解液を構成する溶媒及び
溶質として種々のものが提案されている。(B) Prior Art Various solvents and solutes have been proposed for forming the non-aqueous electrolyte used in this type of battery.
具体的には例えば特公昭57〜52866号公報に開示
されているように、溶媒としてプロピレンカーボネート
、r−グチロラクトン、ジメトキシエタン、ジオキソク
ン、テトラハイドミツランなど、又溶質として過塩素酸
リチクム、ホウフッ化すチクムなどが知られている。Specifically, as disclosed in Japanese Patent Publication No. 57-52866, propylene carbonate, r-gutyrolactone, dimethoxyethane, dioxocone, tetrahydromiturane, etc. are used as solvents, and lyticum perchlorate, borofluoride, etc. are used as solutes. Chikum is also known.
さて、近年に至ってはこの種電池の適用分野の拡大に伴
い電池特性の改善が要望されてお9.その一つとして保
存後の低温放電特性の向上がS−すれている。Now, in recent years, as the fields of application of this type of battery have expanded, there has been a demand for improvements in battery characteristics.9. One of the improvements is the improvement in low-temperature discharge characteristics after storage.
(ハ)発明の目的
本発明は非水電解液を改良して保存後の低温放電特性に
優れた非水電解液電池を提供することを目的とする。(c) Purpose of the Invention The object of the present invention is to provide a non-aqueous electrolyte battery that improves the non-aqueous electrolyte and has excellent low-temperature discharge characteristics after storage.
に)発明の構成
本発明はリチウム或いはリチウム合金を活物質とする負
極と、正極と、溶媒と溶質とからなる非水電解液とを備
えるものであって、前記溶媒がプロピレンカーボネート
と?):tキソランを含む混合溶媒であり、前記溶質が
リチウムトリフルオロメタンスルホネートであることを
特徴とする非水電解液電池にある。B) Structure of the Invention The present invention comprises a negative electrode using lithium or a lithium alloy as an active material, a positive electrode, and a non-aqueous electrolyte comprising a solvent and a solute, wherein the solvent is propylene carbonate or not. ): A mixed solvent containing t-xolane, and the solute is lithium trifluoromethanesulfonate.
(ホ)実施例 以下本発明の実施例について詳述する。(e) Examples Examples of the present invention will be described in detail below.
溶媒としてプロピレンカーボネート(pa)とジオキソ
クン(r)OXL)とを混合比1:1で混合した混合溶
媒を用い、この混合溶媒に溶質としてリチウ、ムトリフ
ルオロメタンスルホネート(L1075sOIs)を1
モル/l溶解したもの1電解液とする。A mixed solvent of propylene carbonate (pa) and dioxocune (r) OXL) mixed at a mixing ratio of 1:1 was used as a solvent, and lithium and mutrifluoromethanesulfonate (L1075sOIs) were added as a solute to this mixed solvent.
The solution dissolved in mol/l is considered as 1 electrolyte solution.
正極は550〜4′50℃の温度範囲で熱処理した二酸
化マンガンを活物質としこの二酸化マンガンと、導電剤
としてのカーボン粉末及び結着剤としてのフッ素樹脂粉
末とを85:10:5の重量比で混合した混合物を加圧
成形し250〜55[1℃で熱処理したものを用い、又
負極はリチウム圧延板を所定寸法に打抜いたものを用い
て径20.0−5厚み2.5IN、電池容量120mA
Hの本発明電池を得る。この電池をAとする。The positive electrode is made of manganese dioxide heat-treated at a temperature range of 550 to 4'50°C as an active material, and this manganese dioxide is mixed with carbon powder as a conductive agent and fluororesin powder as a binder in a weight ratio of 85:10:5. The mixture was pressure-molded and heat-treated at 250-55[1°C], and the negative electrode was a lithium rolled plate punched out to the specified dimensions, with a diameter of 20.0-5 and a thickness of 2.5 IN. Battery capacity 120mA
A battery of the present invention of H is obtained. This battery is called A.
次に本発明電池の優位性を調べるために溶質として過塩
素酸リチウム(Li0704)、ホクフツ化すチワム(
LiBF4)、リチウムへキサフルオロホスフェート(
LiP16)及びリチクムテトクグロロアルミネート(
LiAJC7a)@夫々用い。Next, in order to investigate the superiority of the battery of the present invention, lithium perchlorate (Li0704) was used as a solute.
LiBF4), lithium hexafluorophosphate (
LiP16) and lyticumtetoc gloroaluminate (
LiAJC7a) @ used respectively.
他の要素は実施例と同様の比較電池を作成した。A comparative battery was prepared in which the other elements were the same as in the example.
これらの電池IB、C,D及びEとする。Let these batteries be IB, C, D, and E.
$1図及び9j42図はこれらの電池の放電特性図であ
って、第1図は電池組立後、直ちに一20℃において6
にΩの定抵抗で放電した時の放電特性図、182図拡電
池組立後、60℃で5ケ月保存したのち、−20℃にお
いて5にΩの定抵抗で放電した時の放電特性図である。Figure 1 and Figure 9j42 are discharge characteristic diagrams of these batteries, and Figure 1 shows the discharge characteristics of these batteries.
Fig. 182 is a discharge characteristic diagram when discharging with a constant resistance of 5 Ω at -20 °C after being stored at 60 °C for 5 months after assembling the expanded battery. .
$1図及びs2図から明白なるように、電池組立直後の
低温放電特性では本発明電池の優位性はそれほど認めら
れないが、保存後の低温放電特性では本発明電池の優位
性がより顕著である。As is clear from Figure $1 and Figure s2, the superiority of the battery of the present invention is not so apparent in the low-temperature discharge characteristics immediately after battery assembly, but the superiority of the battery of the present invention is more pronounced in the low-temperature discharge characteristics after storage. be.
下表は本発明電池及び比較電池に夫々用いた各電解液の
調整直後の粘度と60℃で5ケ月保存した後の粘度とを
示す。The table below shows the viscosity of each electrolytic solution used in the batteries of the present invention and comparative batteries immediately after preparation and after storage at 60° C. for 5 months.
表
本発明電池が保存後の低温放電特性に優れる理由を考察
するに、上表かられかるように、比較電池に用いた電解
液は保存に伴いゲル化して粘度が高くなり電導度が低下
するのに対し1本発明電池に用いた電解液では保存後も
初期の粘度を維持し電導度の低下がないことが重要な要
因であると考えられる。Table Considering the reason why the battery of the present invention has excellent low-temperature discharge characteristics after storage, as can be seen from the table above, the electrolyte used in the comparative battery gels with storage, increases viscosity, and decreases conductivity. On the other hand, an important factor is considered to be that the electrolytic solution used in the battery of the present invention maintains its initial viscosity even after storage and does not exhibit a decrease in electrical conductivity.
第3図は本発明電池における混合溶媒の混合比D O×
L/P O比が20〜80/B □〜2 (1f) 範
囲カ好tしい。Figure 3 shows the mixing ratio DO× of the mixed solvent in the battery of the present invention.
The L/PO ratio is preferably in the range of 20 to 80/B to 2 (1f).
(へ)発明の効果
上述した如く1本発明によれば保存後の低温放電特性に
優れた非水電解液電池を得ることができるものであり、
この種電池の用途拡大に資するところ極めて犬である。(F) Effects of the Invention As mentioned above, according to the present invention, a non-aqueous electrolyte battery with excellent low-temperature discharge characteristics after storage can be obtained.
This is extremely helpful in expanding the uses of this type of battery.
第1図及び@2図は低温下における電池の放電特性図で
あり、!1図は初期放電特性図、@2図は60℃で6ケ
月保存後の放電特性図である。第5図は本発明電池にお
ける混合溶媒の混合比と。
60℃で5ケ月保存後の電池の放電容量との関係を示す
図である。
k・・・本発明電池、■)(C)の)(E)・・・比較
電池。
出願人 三洋電″aa式会社
代理人 弁理士 佐 野 静 夫
第1図
第2図
第3図
PC100806040200
混@; f4r>艦な比Figures 1 and 2 are discharge characteristic diagrams of batteries at low temperatures. Figure 1 is an initial discharge characteristic diagram, and Figure 2 is a discharge characteristic diagram after storage at 60°C for 6 months. FIG. 5 shows the mixing ratio of the mixed solvent in the battery of the present invention. It is a figure which shows the relationship with the discharge capacity of the battery after storage at 60 degreeC for 5 months. k...Battery of the present invention, ■)(C))(E)...Comparison battery. Applicant Sanyo Denki AA company agent Patent attorney Shizuo Sano Figure 1 Figure 2 Figure 3 PC100806040200 Mixed @; f4r>Kan ratio
Claims (1)
、正極と、溶媒と溶質とからなる非水電解液とを備える
ものであって、前記溶媒がプロピレンカーボネートとジ
オキソクンを含む混合溶媒であり、前記溶質がリチウム
トリフルオロメタンスルホネートであることを特徴とす
る非水電解液電池。(2) A device comprising nine electrodes using lithium or a lithium alloy as an active material, a positive electrode, and a non-aqueous electrolyte consisting of a solvent and a solute, wherein the solvent is a mixed solvent containing propylene carbonate and dioxocane; A nonaqueous electrolyte battery characterized in that the solute is lithium trifluoromethanesulfonate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59108066A JPS60253165A (en) | 1984-05-28 | 1984-05-28 | Non-aqueous electrolyte battery |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59108066A JPS60253165A (en) | 1984-05-28 | 1984-05-28 | Non-aqueous electrolyte battery |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS60253165A true JPS60253165A (en) | 1985-12-13 |
Family
ID=14475020
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59108066A Pending JPS60253165A (en) | 1984-05-28 | 1984-05-28 | Non-aqueous electrolyte battery |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60253165A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63307669A (en) * | 1987-06-08 | 1988-12-15 | Sanyo Electric Co Ltd | Nonaqueous electrolyte cell |
-
1984
- 1984-05-28 JP JP59108066A patent/JPS60253165A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63307669A (en) * | 1987-06-08 | 1988-12-15 | Sanyo Electric Co Ltd | Nonaqueous electrolyte cell |
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