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Title Technologies of Lithium Ion Polymer Battery Author(s) Roh, Young Bae Citation 電気材料技術雑誌. 14(2) P.143-P.148 Issue Date 2005-07-15 Text Version publisher URL http://hdl.handle.net/11094/76828 DOI rights Note Osaka University Knowledge Archive : OUKA Osaka University Knowledge Archive : OUKA https://ir.library.osaka-u.ac.jp/ Osaka University

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  • Title Technologies of Lithium Ion Polymer Battery

    Author(s) Roh, Young Bae

    Citation 電気材料技術雑誌. 14(2) P.143-P.148

    Issue Date 2005-07-15

    Text Version publisher

    URL http://hdl.handle.net/11094/76828

    DOI

    rights

    Note

    Osaka University Knowledge Archive : OUKAOsaka University Knowledge Archive : OUKA

    https://ir.library.osaka-u.ac.jp/

    Osaka University

  • 電気材料技術雑誌第14巻第2号J.Soc.Elect.Mat.Eng. Vol.14, No.2, 2005

    Technologies of Lithium Ion Polymer Battery

    Young Bae Roh

    £-square Technologies

    970-63, Wolchul-Dong, Buk-Gu, Gwangju-City, 500-460, Korea

    Te/:+ 82-62-973-7041, Fax:+ 82-62-9 73-7045

    E-mail: [email protected]

    Lithium Ion Battery(LIB) has been known to the general public as power source with

    higher energy density, longer cycle life, larger capacity and smaller self-discharge than

    those of commercial rechargeable batteries(Ni-MH, Ni-Cd and so on)[l -2]. Therefore,

    lithium ion battery has been used widely in the 3C market such as Mobile phone,

    Camcorder and Laptop since 1990's. Specially, Lithium Ion Polymer Batteries (LIPB)

    are in spotlight in secondary battery market because it is very light but has higher

    energy density than LIB and then is using the main power for Electric Vehicle (EV) in

    recent.

    Fig. 1 shows the technology tree of battery. LIPB is located in the top of battery

    technology and is at the cutting edge of secondary battery technology.

    Battery

    143/ [243]

  • 電気材料技術雑誌第14巻第2号J.Soc.Elect.Mat.Eng. Vol.14, No.2, 2005

    Fig. 1. Battery Technology Tree

    Fig. 2 explains about energy density comparison of several secondary batteries.

    The vertical line represents gravimetric energy density which means to be able to make

    battery light. LIPB system is to be lighter than other battery system. The horizontal line

    represents energy density per volume which means to be able to make battery small.

    LIPB system is to be smaller than other battery system. It is reasonable for LIPB

    system to be selected as the most powerful source of the secondary battery system in

    the world.

    5

    2 0

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    (W疋kg)Gravimet『icEnergy Density

    20

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    e

    如介且

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    0

    Fig. 2. Energy density comparison of various secondary batteries.

    Reaction mechanism of Li secondary battery is very simple as shown at the Fig. 3.

    Li ion battery consists of a carbon anode and a cathode of Li metal compound (LiCo02).

    Li metal is not in the battery. That means the safety of lithium ion battery is a good

    theoretically if manufacturing default is not generated in.

    Li ion in the crystal structure of lithium cobalt oxide (LiCo02) is only moving to the

    Graphite layer during the discharge and then return to the cathode during the charging.

    We call this mechanism as the rocking chair or shuttlecock [3-5].

    Li ion battery systems are divided into four parts according to the types of anode

    material or cathode material as shown at the Fig. 4. If liquid electrolyte and carbon

    anode is used, the system is defined as the lithium ion battery. Li Ion polymer battery

    system use carbon anode and polymer electrolyte.

    144/ [244]

  • 電気材料技術雑誌第 14巻第2号J.Soc.Elect.Mat.Eng. Vol.14, No.2, 2005

    charge e-

    -current collector

    separator

    +current collector

    REACTION

    ● Positive electrode LiCo02手Li1-xCo02+ xLi+ + xe―

    ● Negative electrode

    Cn + xLi+ + xe一手CnLix

    ● Overall discharge charge ~ LiCo02 + Cn d Li1-xCo02 + CnLix .

    Oxygen

    . Metal Atom L゚ithium

    . Carbon

    Fig. 3. Reaction mechanism of lithium ion battery.

    Li Metal Batte ry(LM B) Li-ion Battery(LIB)

    LI Metal

    ~HighCi甲a叫y Liquid Electrolyte tong町C給Ufe ►

    •· i.ow-Q四吐胆

    、◄ 8$d High Rate Capa.

    Polymer Electrolyte t.awt,a匹 ity,,

    High CO$l to make . •

    Carbon (Liーion)

    Li Polymer Battery(LPB) Li-ion Polymer Battery(LIPB)

    Fig. 4. Derivative systems of lithium ion battery.

    Li Ion polymer battery has many advantages in aspects of battery performance,

    comparing with lithium ion battery. LIPB is able to be thinner, lighter, cheaper and more

    flexible design than LIB. Specially, a safety of LIPB is better than LIB so that LIPB

    system is apt to use power source of Electric Vehicle and is popular to the high power

    system to derive motor such as electric tools and R/C appliances.

    145/ [245]

  • 電気材料技術雑誌第 14巻第2号J.Soc.Elect.Mat.Eng. Vol.14, No.2, 2005

    However, It is necessary for us to solve swelling problem to apply LIPE to

    commercial electronic appliances. The swelling problem is to be main defect and

    affects on the change of cell thickness as shown at the Fig. 5.

    7.5

    7.06

    7.0 トーー 1-.Ave『agel

    ---一--Max ---一— ·Min

    5

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    5

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    6

    5

    (EE) ssau)I0!4l.

    4.5

    5.0 ... -------~ ---------------------------------------------------

    Assembly Formation Charge Standard Charge 90'C, 6hr

    E-Square Tech

    Fig. 5. Cell thickness variation of LPB on the storage test condition under 90℃.

    When the battery starts a redox reaction, gas is generally generated in the battery, the

    exterior of the Li polymer battery is made of Aluminum laminated film (Pouch) instead

    of aluminum can like lithium ion battery. The pouch is inclined to swell easily and to

    make cell thickness changed due to weakness of material.

    In facts, there are several factors influenced on swelling in battery system. A special

    solution which prevents gas from being generated in the battery is added additive

    material to electrolyte in the LIPB.

    It has been paid close attention to search for functional electrolyte with additive

    material. Functional electrolyte is designed to generate a dense film called solid

    electrolyte interface (SEI) on the surface of carbon anode during the first charging

    process. We expect functional electrolyte to protect a continuous gas evolution for the

    cycle running. We calculated HOMO (highest occupied molecular orbital) and LUMO

    (lowest unoccupied molecular orbital) level of additive materials like as much as 150EA

    to select promising additive materials as shown at the Fig. 6.

    146/ [246]

  • 電気材料技術雑誌第 14巻第2号

    J.Soc.Elect.Mat.Eng. Vol.14, No.2, 2005

    -14

    oxidation

    resistance

    ゜ー

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    -12

    -8

    -6

    -3

    Additive Selection

    ❖ physical property

    ❖ electrochemical

    property

    (LSV & CV)

    ❖ molecular structure

    ❖optimizing

    molecular orbital

    function (HOMO /

    LUMO)

    -2 -1 1 2

    LUMO (eV) • ゜3

    reduction

    『esistance

    Fig. 6. An extent of redox reaction on HOMO and RUMO value.

    Fig. 7 shows variation of cyclic voltammetic profiles between general electrolyte and

    functional electrolyte with additive material, SEI formation due to the decomposition of

    functional electrolyte is appearing at the lower voltage than one of general electrolyte.

    The research of quantitative and qualitative analysis on SEI film is now on progressing

    in our laboratory.

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    147 / [247]

  • 電気材料技術雑誌第 14巻第2号

    J.Soc.Elect.Mat.Eng. Vol.14, No.2, 2005

    Fig. 7. Variation of cyclic volammetric profiles between general E/L and additive E/L.

    Fig. 8 shows the effect of functional electrolyte. Test condition of cell is designed to

    show clearly the change of cell thickness under 85℃ . Functional electrolyte decreases

    effectively the cell thickness by 30% after 7 days, comparing with general electrolyte.

    Swelling in terms of the change of initial thickness is controlled by 3% in the functional

    electrolyte. SBACA (2-Sulfobenzoic acid cyclic anhydride) shows a good characteristic

    to control cell thickness as the additive material in electrolyte.

    SBACA is now in pending on international patent as the material of swelling restraint.

    ,40•,ti

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    '皿 .fllR IDAヽぞ 7DAY

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    Fig. 8. Effect on swelling restraint under 85℃ standing for 4hrs, lday and 7days.

    References

    [l] Y.B. Roh, T. Kawai, H. Araki and K. Yoshino, Jpn. J. Appl. Phys, Vol. 33 (1994) 5917.

    [2] N. Takami. A. Satoh. M. Hara and T. Ohsaki, J. Electrochem.Soc,142 (1995) 2564.

    [3] Y.B. Roh, K.M. Jeong, H.G. Cho and H.Y. Kang, J. Power Sources, 68 (1997) 271.

    [ 4] K. Sato, M. Noguchi, A. Demachi, N. Oki and M. Endo, Science, 264 (1994) 556.

    [5] J.R. Dahn, T. Zheng, Y. Liu and J.S. Xue, Science, 270 (1995) 590.

    148/ [248]