JP2009283473A5 - - Google Patents
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- JP2009283473A5 JP2009283473A5 JP2009201785A JP2009201785A JP2009283473A5 JP 2009283473 A5 JP2009283473 A5 JP 2009283473A5 JP 2009201785 A JP2009201785 A JP 2009201785A JP 2009201785 A JP2009201785 A JP 2009201785A JP 2009283473 A5 JP2009283473 A5 JP 2009283473A5
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- Prior art keywords
- tert
- group
- lithium secondary
- butylbenzene
- secondary battery
- Prior art date
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- 239000011255 nonaqueous electrolyte Substances 0.000 claims description 34
- 239000002904 solvent Substances 0.000 claims description 26
- 229910052744 lithium Inorganic materials 0.000 claims description 25
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims description 23
- WHXSMMKQMYFTQS-UHFFFAOYSA-N lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 23
- RUOJZAUFBMNUDX-UHFFFAOYSA-N Propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 13
- YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 claims description 13
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 claims description 10
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims description 10
- 239000007774 positive electrode material Substances 0.000 claims description 9
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 8
- QCWXDVFBZVHKLV-UHFFFAOYSA-N 1-tert-butyl-4-methylbenzene Chemical group CC1=CC=C(C(C)(C)C)C=C1 QCWXDVFBZVHKLV-UHFFFAOYSA-N 0.000 claims description 7
- 239000003125 aqueous solvent Substances 0.000 claims description 7
- 239000003575 carbonaceous material Substances 0.000 claims description 7
- 239000003792 electrolyte Substances 0.000 claims description 7
- 239000007773 negative electrode material Substances 0.000 claims description 7
- IEJIGPNLZYLLBP-UHFFFAOYSA-N Dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 claims description 6
- 150000002430 hydrocarbons Chemical group 0.000 claims description 6
- -1 tert-butylbenzyl group Chemical group 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 4
- GUFMBISUSZUUCB-UHFFFAOYSA-N 1,3,5-tritert-butylbenzene Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(C(C)(C)C)=C1 GUFMBISUSZUUCB-UHFFFAOYSA-N 0.000 claims description 3
- ILNDSSCEZZFNGE-UHFFFAOYSA-N 1,3-ditert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1 ILNDSSCEZZFNGE-UHFFFAOYSA-N 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- VKSWWACDZPRJAP-UHFFFAOYSA-N 1,3-dioxepan-2-one Chemical compound O=C1OCCCCO1 VKSWWACDZPRJAP-UHFFFAOYSA-N 0.000 claims description 2
- VAYTZRYEBVHVLE-UHFFFAOYSA-N 1,3-dioxol-2-one Chemical compound O=C1OC=CO1 VAYTZRYEBVHVLE-UHFFFAOYSA-N 0.000 claims description 2
- VUVGFTPMYJWXIG-UHFFFAOYSA-N C1=CC(C(C)(C)C)(C(C)(C)C)CC=C1C1=CC=CC=C1 Chemical group C1=CC(C(C)(C)C)(C(C)(C)C)CC=C1C1=CC=CC=C1 VUVGFTPMYJWXIG-UHFFFAOYSA-N 0.000 claims description 2
- 150000005678 chain carbonates Chemical class 0.000 claims description 2
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 2
- 239000011651 chromium Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 229910052803 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 150000005676 cyclic carbonates Chemical class 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052748 manganese Inorganic materials 0.000 claims description 2
- 239000011572 manganese Substances 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium(0) Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims description 2
- 229910002804 graphite Inorganic materials 0.000 claims 1
- 239000010439 graphite Substances 0.000 claims 1
- 229910003455 mixed metal oxide Inorganic materials 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 description 15
- 239000000203 mixture Substances 0.000 description 12
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 10
- 229910052739 hydrogen Inorganic materials 0.000 description 10
- 239000001257 hydrogen Substances 0.000 description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 10
- 230000014759 maintenance of location Effects 0.000 description 9
- 229910013870 LiPF 6 Inorganic materials 0.000 description 7
- 229910012851 LiCoO 2 Inorganic materials 0.000 description 6
- 101700033034 LIPF Proteins 0.000 description 5
- 229910013872 LiPF Inorganic materials 0.000 description 5
- 229910021383 artificial graphite Inorganic materials 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 239000008151 electrolyte solution Substances 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 229910021382 natural graphite Inorganic materials 0.000 description 4
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 4
- 239000004810 polytetrafluoroethylene Substances 0.000 description 4
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 4
- 229910015643 LiMn 2 O 4 Inorganic materials 0.000 description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- WIXDSJRJFDWTNY-UHFFFAOYSA-N 1,3-ditert-butyl-5-methylbenzene Chemical compound CC1=CC(C(C)(C)C)=CC(C(C)(C)C)=C1 WIXDSJRJFDWTNY-UHFFFAOYSA-N 0.000 description 2
- UAGBDAUMTJRHBN-UHFFFAOYSA-N 1-tert-butyl-2,4-dimethylbenzene Chemical group CC1=CC=C(C(C)(C)C)C(C)=C1 UAGBDAUMTJRHBN-UHFFFAOYSA-N 0.000 description 2
- AXHVNJGQOJFMHT-UHFFFAOYSA-N 1-tert-butyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C(C)(C)C AXHVNJGQOJFMHT-UHFFFAOYSA-N 0.000 description 2
- 229920002943 EPDM rubber Polymers 0.000 description 2
- 229910013063 LiBF 4 Inorganic materials 0.000 description 2
- 229910015915 LiNi0.8Co0.2O2 Inorganic materials 0.000 description 2
- 229910013290 LiNiO 2 Inorganic materials 0.000 description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
- 239000002033 PVDF binder Substances 0.000 description 2
- WEVYAHXRMPXWCK-UHFFFAOYSA-N acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 2
- 239000006230 acetylene black Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive Effects 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- 239000006258 conductive agent Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N n-methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 230000002829 reduced Effects 0.000 description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- MJTFENDZXOFBLA-UHFFFAOYSA-N 1,2,3-tritert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1C(C)(C)C MJTFENDZXOFBLA-UHFFFAOYSA-N 0.000 description 1
- KOOZRCVIAJVLEQ-UHFFFAOYSA-N 1,2,4,5-tetratert-butylbenzene Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=C(C(C)(C)C)C=C1C(C)(C)C KOOZRCVIAJVLEQ-UHFFFAOYSA-N 0.000 description 1
- IHZGECPPAQDWKL-UHFFFAOYSA-N 1,2,4-tritert-butylbenzene Chemical compound CC(C)(C)C1=CC=C(C(C)(C)C)C(C(C)(C)C)=C1 IHZGECPPAQDWKL-UHFFFAOYSA-N 0.000 description 1
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- OOWNNCMFKFBNOF-UHFFFAOYSA-N 1,4-ditert-butylbenzene Chemical compound CC(C)(C)C1=CC=C(C(C)(C)C)C=C1 OOWNNCMFKFBNOF-UHFFFAOYSA-N 0.000 description 1
- GDXHBFHOEYVPED-UHFFFAOYSA-N 1-(2-butoxyethoxy)butane Chemical compound CCCCOCCOCCCC GDXHBFHOEYVPED-UHFFFAOYSA-N 0.000 description 1
- BQOBURPKVKFNKD-UHFFFAOYSA-N 1-butan-2-yl-4-tert-butylbenzene Chemical compound CCC(C)C1=CC=C(C(C)(C)C)C=C1 BQOBURPKVKFNKD-UHFFFAOYSA-N 0.000 description 1
- BDSMPLDBKOVNHW-UHFFFAOYSA-N 1-butyl-4-tert-butylbenzene Chemical compound CCCCC1=CC=C(C(C)(C)C)C=C1 BDSMPLDBKOVNHW-UHFFFAOYSA-N 0.000 description 1
- QRBAXYYNPFDZAX-UHFFFAOYSA-N 1-tert-butyl-2,3-dimethylbenzene Chemical group CC1=CC=CC(C(C)(C)C)=C1C QRBAXYYNPFDZAX-UHFFFAOYSA-N 0.000 description 1
- NKRAJTUTWBTQFT-UHFFFAOYSA-N 1-tert-butyl-2-ethylbenzene Chemical compound CCC1=CC=CC=C1C(C)(C)C NKRAJTUTWBTQFT-UHFFFAOYSA-N 0.000 description 1
- KNCZPLRYWQLPQT-UHFFFAOYSA-N 1-tert-butyl-2-propan-2-ylbenzene Chemical compound CC(C)C1=CC=CC=C1C(C)(C)C KNCZPLRYWQLPQT-UHFFFAOYSA-N 0.000 description 1
- FZSPYHREEHYLCB-UHFFFAOYSA-N 1-tert-butyl-3,5-dimethylbenzene Chemical group CC1=CC(C)=CC(C(C)(C)C)=C1 FZSPYHREEHYLCB-UHFFFAOYSA-N 0.000 description 1
- WYIXIYMLGZNHMJ-UHFFFAOYSA-N 1-tert-butyl-3-cyclohexylbenzene Chemical compound CC(C)(C)C1=CC=CC(C2CCCCC2)=C1 WYIXIYMLGZNHMJ-UHFFFAOYSA-N 0.000 description 1
- MUJPTTGNHRHIPH-UHFFFAOYSA-N 1-tert-butyl-3-ethylbenzene Chemical compound CCC1=CC=CC(C(C)(C)C)=C1 MUJPTTGNHRHIPH-UHFFFAOYSA-N 0.000 description 1
- JTIAYWZZZOZUTK-UHFFFAOYSA-N 1-tert-butyl-3-methylbenzene Chemical compound CC1=CC=CC(C(C)(C)C)=C1 JTIAYWZZZOZUTK-UHFFFAOYSA-N 0.000 description 1
- OWOLIQXOOMFSJE-UHFFFAOYSA-N 1-tert-butyl-3-propan-2-ylbenzene Chemical compound CC(C)C1=CC=CC(C(C)(C)C)=C1 OWOLIQXOOMFSJE-UHFFFAOYSA-N 0.000 description 1
- BNMPTGXSMLHHNS-UHFFFAOYSA-N 1-tert-butyl-4-(2-methylpropyl)benzene Chemical compound CC(C)CC1=CC=C(C(C)(C)C)C=C1 BNMPTGXSMLHHNS-UHFFFAOYSA-N 0.000 description 1
- CDKCEZNPAYWORX-UHFFFAOYSA-N 1-tert-butyl-4-(4-tert-butylphenyl)benzene Chemical group C1=CC(C(C)(C)C)=CC=C1C1=CC=C(C(C)(C)C)C=C1 CDKCEZNPAYWORX-UHFFFAOYSA-N 0.000 description 1
- KRMBVBPNWUBFBC-UHFFFAOYSA-N 1-tert-butyl-4-[(4-tert-butylphenyl)methyl]benzene Chemical compound C1=CC(C(C)(C)C)=CC=C1CC1=CC=C(C(C)(C)C)C=C1 KRMBVBPNWUBFBC-UHFFFAOYSA-N 0.000 description 1
- AGYWEUQFCAQALX-UHFFFAOYSA-N 1-tert-butyl-4-cyclohexylbenzene Chemical compound C1=CC(C(C)(C)C)=CC=C1C1CCCCC1 AGYWEUQFCAQALX-UHFFFAOYSA-N 0.000 description 1
- OYBFKZHDPTTWGE-UHFFFAOYSA-N 1-tert-butyl-4-ethylbenzene Chemical compound CCC1=CC=C(C(C)(C)C)C=C1 OYBFKZHDPTTWGE-UHFFFAOYSA-N 0.000 description 1
- JWUJQDFVADABEY-UHFFFAOYSA-N 2-Methyltetrahydrofuran Chemical compound CC1CCCO1 JWUJQDFVADABEY-UHFFFAOYSA-N 0.000 description 1
- IRMLULIFOFYBTI-UHFFFAOYSA-N 2-tert-butyl-1,4-dimethylbenzene Chemical group CC1=CC=C(C)C(C(C)(C)C)=C1 IRMLULIFOFYBTI-UHFFFAOYSA-N 0.000 description 1
- QRPPSTNABSMSCS-UHFFFAOYSA-N 4-tert-butyl-1,2-dimethylbenzene Chemical group CC1=CC=C(C(C)(C)C)C=C1C QRPPSTNABSMSCS-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229910000733 Li alloy Inorganic materials 0.000 description 1
- 229910013375 LiC Inorganic materials 0.000 description 1
- 229910013684 LiClO 4 Inorganic materials 0.000 description 1
- 229910013528 LiN(SO2 CF3)2 Inorganic materials 0.000 description 1
- 229910013385 LiN(SO2C2F5)2 Inorganic materials 0.000 description 1
- 229940017219 METHYL PROPIONATE Drugs 0.000 description 1
- RJUFJBKOKNCXHH-UHFFFAOYSA-N Methyl propionate Chemical compound CCC(=O)OC RJUFJBKOKNCXHH-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N Tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- OCKPCBLVNKHBMX-UHFFFAOYSA-N butylbenzene Chemical compound CCCCC1=CC=CC=C1 OCKPCBLVNKHBMX-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 239000011889 copper foil Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000003487 electrochemical reaction Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 238000006056 electrooxidation reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000001989 lithium alloy Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002296 pyrolytic carbon Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- YEJRWHAVMIAJKC-UHFFFAOYSA-N γ-lactone 4-hydroxy-butyric acid Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 1
Description
本発明は、電池のサイクル特性や電気容量、保存特性などの電池特性にも優れたリチウム二次電池に関する。 The present invention, the cycle characteristics and the electric capacity of the battery, regarding the lithium secondary battery is also excellent in battery characteristics such as storage characteristics.
近年、リチウム二次電池は小型電子機器などの駆動用電源として広く使用されている。リチウム二次電池は、主に正極、非水電解液及び負極から構成されており、特に、LiCoO2などのリチウム複合酸化物を正極とし、炭素材料又はリチウム金属を負極としたリチウム二次電池が好適に使用されている。そして、そのリチウム二次電池用の非水電解液としては、エチレンカーボネート(EC)、プロピレンカーボネート(PC)などのカーボネート類が好適に使用されている。 In recent years, lithium secondary batteries have been widely used as driving power sources for small electronic devices and the like. A lithium secondary battery is mainly composed of a positive electrode, a non-aqueous electrolyte, and a negative electrode. In particular, a lithium secondary battery using a lithium composite oxide such as LiCoO 2 as a positive electrode and a carbon material or lithium metal as a negative electrode is used. It is preferably used. As the non-aqueous electrolyte for the lithium secondary battery, carbonates such as ethylene carbonate (EC) and propylene carbonate (PC) are preferably used.
しかしながら、電池のサイクル特性および電気容量などの電池特性について、さらに優れた特性を有する二次電池が求められている。
正極として、例えばLiCoO2、LiMn2O4、LiNiO2などを用いたリチウム二次電池は、非水電解液中の溶媒が充電時に局部的に一部酸化分解することにより、該分解物が電池の望ましい電気化学的反応を阻害するために電池性能の低下を生じる。これは正極材料と非水電解液との界面における溶媒の電気化学的酸化に起因するものと思われる。
また、負極として例えば天然黒鉛や人造黒鉛などの高結晶化した炭素材料を用いたリチウム二次電池は、非水電解液中の溶媒が充電時に負極表面で還元分解し、非水電解液溶媒として一般に広く使用されているECにおいても充放電を繰り返す間に一部還元分解が起こり、電池性能の低下が起こる。
このため、電池のサイクル特性および電気容量などの電池特性は必ずしも満足なものではないのが現状である。
非水電解液二次電池としては、例えば、特許文献1及び2が知られている。
However, there is a demand for a secondary battery having more excellent battery characteristics such as battery cycle characteristics and electric capacity.
A lithium secondary battery using, for example, LiCoO 2 , LiMn 2 O 4 , LiNiO 2 or the like as a positive electrode is partially decomposed by oxidation when a solvent in a non-aqueous electrolyte is locally charged. In order to inhibit the desired electrochemical reaction, the battery performance is degraded. This seems to be due to the electrochemical oxidation of the solvent at the interface between the positive electrode material and the non-aqueous electrolyte.
In addition, a lithium secondary battery using a highly crystallized carbon material such as natural graphite or artificial graphite as the negative electrode is reduced and decomposed on the negative electrode surface when the solvent in the non-aqueous electrolyte is charged. Even in EC that is generally widely used, reductive decomposition occurs partly during repeated charging and discharging, resulting in a decrease in battery performance.
For this reason, at present, battery characteristics such as battery cycle characteristics and electric capacity are not always satisfactory.
For example, Patent Documents 1 and 2 are known as non-aqueous electrolyte secondary batteries.
本発明は、前記のようなリチウム二次電池用非水電解液に関する課題を解決し、電池のサイクル特性に優れ、さらに電気容量や充電状態での保存特性などの電池特性にも優れたリチウム二次電池を提供することを目的とする。 The present invention solves the above-mentioned problems related to the non-aqueous electrolyte for a lithium secondary battery, has excellent battery cycle characteristics, and has excellent battery characteristics such as electric capacity and storage characteristics in a charged state. An object is to provide a secondary battery.
本発明は、正極、負極および非水溶媒に電解質が溶解されている非水電解液を含むリチウム二次電池であって、負極活物質が、格子面(002)の面間隔(d 002 )が0.335〜0.340nmである黒鉛型結晶構造を有する炭素材料であり、該非水電解液中に下記式(I) The present invention is a lithium secondary battery including a positive electrode, a negative electrode, and a non- aqueous electrolyte in which an electrolyte is dissolved in a non-aqueous solvent, wherein the negative electrode active material has a lattice spacing ( 002 ) spacing (d 002 ). A carbon material having a graphite-type crystal structure of 0.335 to 0.340 nm, and the following formula (I) in the non-aqueous electrolyte
(式中、R1、R2、R3、R4およびR5は、それぞれ独立して水素原子または炭素数1〜12の炭化水素基を示す。但し、R1、R2、R3、R4およびR5のうちの少なくとも一つは、炭素数1〜12の炭化水素基である。)で表されるtert−ブチルベンゼンまたはその誘導体が含有されていることを特徴とするリチウム二次電池を提供する。 (Wherein R 1 , R 2 , R 3 , R 4 and R 5 each independently represents a hydrogen atom or a hydrocarbon group having 1 to 12 carbon atoms, provided that R 1 , R 2 , R 3 , And at least one of R 4 and R 5 is a hydrocarbon group having 1 to 12 carbon atoms.) Tert-butylbenzene or a derivative thereof represented by Provide batteries.
本発明のリチウム二次電池を構成する非水電解液以外の構成部材については特に限定されず、従来使用されている種々の構成部材を使用できる。 Constituent members other than the non-aqueous electrolyte constituting the lithium secondary battery of the present invention are not particularly limited, and various conventionally used constituent members can be used.
本発明によれば、電池のサイクル特性、電気容量、保存特性などの電池特性に優れたリチウム二次電池を提供することができる。 According to the present invention, it is possible to provide a lithium secondary battery excellent in battery characteristics such as battery cycle characteristics, electric capacity, and storage characteristics.
非水溶媒に電解質が溶解されている非水電解液に含有される前記一般式(I)で表されるtert−ブチルベンゼン誘導体において、R1、R2、R3、R4、R5はそれぞれ独立して、水素原子、メチル基、エチル基、プロピル基、ブチル基などの直鎖状のアルキル基や、iso−プロピル基、iso−ブチル基、sec−ブチル基、tert−ブチル基などの分枝状のアルキル基が好ましい。また、シクロプロピル基、シクロヘキシル基などのように炭素数3〜6のシクロアルキル基であってもよい。更には、フェニル基、ベンジル基や、トシル基、tert−ブチルベンゼン基、tert−ブチルベンジル基などのアルキル置換されたフェニル基、ベンジル基であっても良い。このような、炭素数1〜12の炭化水素基を有することが好ましい。 In the tert-butylbenzene derivative represented by the above general formula (I) contained in a nonaqueous electrolytic solution in which an electrolyte is dissolved in a nonaqueous solvent, R 1 , R 2 , R 3 , R 4 , R 5 are: Independently, a linear alkyl group such as a hydrogen atom, a methyl group, an ethyl group, a propyl group or a butyl group, an iso-propyl group, an iso-butyl group, a sec-butyl group or a tert-butyl group Branched alkyl groups are preferred. Further, it may be a cycloalkyl group having 3 to 6 carbon atoms such as a cyclopropyl group or a cyclohexyl group. Further, it may be a phenyl group, a benzyl group, an alkyl-substituted phenyl group such as a tosyl group, a tert-butylbenzene group, or a tert-butylbenzyl group, or a benzyl group. It is preferable to have such a hydrocarbon group having 1 to 12 carbon atoms.
前記一般式(I)で表されるtert−ブチルベンゼン誘導体の具体例としては、例えば、tert−ブチルベンゼン〔R1=R2=R3=R4=R5=水素原子〕、2−tert−ブチルトルエン〔R1=メチル基、R2=R3=R4=R5=水素原子〕、3−tert−ブチルトルエン〔R2=メチル基、R1=R3=R4=R5=水素原子〕、4−tert−ブチルトルエン〔R3=メチル基、R1=R2=R4=R5=水素原子〕、1−(tert−ブチル)−2−エチルベンゼン〔R1=エチル基、R2=R3=R4=R5=水素原子〕、1−(tert−ブチル)−3−エチルベンゼン〔R2=エチル基、R1=R3=R4=R5=水素原子〕、1−(tert−ブチル)−4−エチルベンゼン〔R3=エチル基、R1=R2=R4=R5=水素原子〕、3−tert−ブチル−o−キシレン〔R1=R2=メチル基、R3=R4=R5=水素原子〕、4−tert−ブチル−o−キシレン〔R2=R3=メチル基、R1=R4=R5=水素原子〕、4−tert−ブチル−m−キシレン〔R1=R3=メチル基、R2=R4=R5=水素原子〕、5−tert−ブチル−m−キシレン〔R2=R4=メチル基、R1=R3=R5=水素原子〕、2−tert−ブチル−p−キシレン〔R1=R4=メチル基、R2=R3=R5=水素原子〕、3−iso−プロピル−1−tert−ブチルベンゼン〔R2=iso−プロピル基、R1=R3=R4=R5=水素原子〕、4−iso−プロピル−1−tert−ブチルベンゼン〔R3=iso−プロピル基、R1=R2=R4=R5=水素原子〕、4−n−ブチル−1−tert−ブチルベンゼン〔R3=n−ブチル基、R1=R2=R4=R5=水素原子〕、4−iso−ブチル−1−tert−ブチルベンゼン〔R3=iso−ブチル基、R1=R2=R4=R5=水素原子〕、4−sec−ブチル−1−tert−ブチルベンゼン〔R3=sec−ブチル基、R1=R2=R4=R5=水素原子〕、3−シクロヘキシル−1−tert−ブチルベンゼン〔R2=シクロヘキシル基、R1=R3=R4=R5=水素原子〕、4−シクロヘキシル−1−tert−ブチルベンゼン〔R3=シクロヘキシル基、R1=R2=R4=R5=水素原子〕、4,4’−ジ−tert−ブチルジフェニルメタン〔R3=4−tert−ブチルフェニル基、R1=R2=R4=R5=水素原子〕、4,4’−ジ−tert−ブチルビフェニル〔R3=4−tert−ブチルベンゼン基、R1=R2=R4=R5=水素原子〕、1,3−ジ−tert−ブチルベンゼン〔R2=tert−ブチル基、R1=R3=R4=R5=水素原子〕、1,4−ジ−tert−ブチルベンゼン〔R3=tert−ブチル基、R1=R2=R4=R5=水素原子〕、1,2,4−トリ−tert−ブチルベンゼン〔R1=R3=tert−ブチル基、R2=R4=R5=水素原子〕、1,2,3−トリ−tert−ブチルベンゼン〔R1=R2=tert−ブチル基、R3=R4=R5=水素原子〕、1,3,5−トリ−tert−ブチルベンゼン〔R2=R4=tert−ブチル基、R1=R3=R5=水素原子〕、1,2,3,5−テトラ−tert−ブチルベンゼン〔R1=R2=R4=tert−ブチル基、R3=R5=水素原子〕、1,2,3,4−テトラ−tert−ブチルベンゼン〔R1=R2=R3=tert−ブチル基、R4=R5=水素原子〕、1,2,4,5−テトラ−tert−ブチルベンゼン〔R1=R3=R4=tert−ブチル基、R2=R5=水素原子〕、3,5−ジ−tert−ブチルトルエン〔R2=メチル、R4=tert−ブチル基、R1=R3=R5水素原子〕などが挙げられる。 Specific examples of the tert-butylbenzene derivative represented by the general formula (I) include, for example, tert-butylbenzene [R 1 = R 2 = R 3 = R 4 = R 5 = hydrogen atom], 2-tert - butyl toluene [R 1 = methyl, R 2 = R 3 = R 4 = R 5 = hydrogen], 3-tert-butyl toluene [R 2 = methyl, R 1 = R 3 = R 4 = R 5 = Hydrogen atom], 4-tert-butyltoluene [R 3 = methyl group, R 1 = R 2 = R 4 = R 5 = hydrogen atom], 1- (tert-butyl) -2-ethylbenzene [R 1 = ethyl Group, R 2 = R 3 = R 4 = R 5 = hydrogen atom], 1- (tert-butyl) -3-ethylbenzene [R 2 = ethyl group, R 1 = R 3 = R 4 = R 5 = hydrogen atom] ], 1-(tert-butyl) -4-ethylbenzene [R 3 = ethyl, R 1 = R 2 = 4 = R 5 = hydrogen], 3-tert-butyl -o- xylene [R 1 = R 2 = methyl, R 3 = R 4 = R 5 = hydrogen], 4-tert-butyl -o- xylene [R 2 = R 3 = methyl group, R 1 = R 4 = R 5 = hydrogen atom], 4-tert-butyl-m-xylene [R 1 = R 3 = methyl group, R 2 = R 4 = R 5 = Hydrogen atom], 5-tert-butyl-m-xylene [R 2 = R 4 = methyl group, R 1 = R 3 = R 5 = hydrogen atom], 2-tert-butyl-p-xylene [R 1 = R 4 = methyl group, R 2 = R 3 = R 5 = hydrogen atom], 3-iso-propyl-1-tert-butylbenzene [R 2 = iso-propyl group, R 1 = R 3 = R 4 = R 5 = hydrogen], 4-an iso-propyl -1-tert-butylbenzene [R 3 = an iso-propyl group, R 1 = R 2 R 4 = R 5 = hydrogen], 4-n-butyl -1-tert-butylbenzene [R 3 = n-butyl group, R 1 = R 2 = R 4 = R 5 = hydrogen], 4-iso - butyl -1-tert-butylbenzene [R 3 = an iso-butyl group, R 1 = R 2 = R 4 = R 5 = hydrogen], 4-sec-butyl -1-tert-butylbenzene [R 3 = sec-butyl group, R 1 = R 2 = R 4 = R 5 = hydrogen atom], 3-cyclohexyl-1-tert-butylbenzene [R 2 = cyclohexyl group, R 1 = R 3 = R 4 = R 5 = Hydrogen atom], 4-cyclohexyl-1-tert-butylbenzene [R 3 = cyclohexyl group, R 1 = R 2 = R 4 = R 5 = hydrogen atom], 4,4′-di-tert-butyldiphenylmethane [R 3 = 4-tert-butylphenyl group, R 1 = R 2 = R 4 = R 5 = hydrogen atom], 4,4′-di-tert-butylbiphenyl [R 3 = 4-tert-butylbenzene group, R 1 = R 2 = R 4 = R 5 = hydrogen atom], 1,3 - di -tert- butyl benzene [R 2 = tert-butyl group, R 1 = R 3 = R 4 = R 5 = hydrogen], 1,4-di -tert- butyl benzene [R 3 = tert-butyl group R 1 = R 2 = R 4 = R 5 = hydrogen atom], 1,2,4-tri-tert-butylbenzene [R 1 = R 3 = tert-butyl group, R 2 = R 4 = R 5 = Hydrogen atom], 1,2,3-tri-tert-butylbenzene [R 1 = R 2 = tert-butyl group, R 3 = R 4 = R 5 = hydrogen atom], 1,3,5-tri-tert - butylbenzene [R 2 = R 4 = tert- butyl, R 1 = R 3 = R 5 = hydrogen], 1,2,3, - tetra -tert- butyl benzene [R 1 = R 2 = R 4 = tert- butyl, R 3 = R 5 = hydrogen], 1,2,3,4 -tert- butyl benzene [R 1 = R 2 = R 3 = tert-butyl group, R 4 = R 5 = hydrogen atom], 1,2,4,5-tetra-tert-butylbenzene [R 1 = R 3 = R 4 = tert-butyl group, R 2 = R 5 = hydrogen atom], 3,5-di-tert-butyltoluene [R 2 = methyl, R 4 = tert-butyl group, R 1 = R 3 = R 5 hydrogen atom] and the like.
非水電解液中に含有される前記式(I)で表されるtert−ブチルベンゼン誘導体の含有量は、過度に多いと電池性能が低下することがあり、また、過度に少ないと期待した十分な電池性能が得られない。したがって、その含有量は非水電解液の重量に対して0.1〜20重量%、好ましく0.2〜10重量%、特に好ましくは0.5〜5重量%の範囲がサイクル特性が向上するのでよい。 When the content of the tert-butylbenzene derivative represented by the formula (I) contained in the non-aqueous electrolyte is excessively large, the battery performance may be deteriorated. Battery performance is not obtained. Therefore, the cycle characteristics are improved when the content is in the range of 0.1 to 20% by weight, preferably 0.2 to 10% by weight, particularly preferably 0.5 to 5% by weight, based on the weight of the non-aqueous electrolyte. So good.
本発明で使用される非水溶媒としては、高誘電率溶媒と低粘度溶媒とからなるものが好ましい。
高誘電率溶媒としては、例えば、エチレンカーボネート(EC)、プロピレンカーボネート(PC)、ブチレンカーボネート(BC)、ビニレンカーボネート(VC)などの環状カーボネート類が好適に挙げられる。これらの高誘電率溶媒は、1種類で使用してもよく、また2種類以上組み合わせて使用してもよい。
As the non-aqueous solvent used in the present invention, a solvent composed of a high dielectric constant solvent and a low viscosity solvent is preferable.
Preferred examples of the high dielectric constant solvent include cyclic carbonates such as ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate (BC), and vinylene carbonate (VC). These high dielectric constant solvents may be used alone or in combination of two or more.
低粘度溶媒としては、例えば、ジメチルカーボネート(DMC)、メチルエチルカーボネート(MEC)、ジエチルカーボネート(DEC)などの鎖状カーボネート類、テトラヒドロフラン、2−メチルテトラヒドロフラン、1,4−ジオキサン、1,2−ジメトキシエタン、1,2−ジエトキシエタン、1,2−ジブトキシエタンなどのエーテル類、γ−ブチロラクトンなどのラクトン類、アセトニトリルなどのニトリル類、プロピオン酸メチルなどのエステル類、ジメチルホルムアミドなどのアミド類が挙げられる。これらの低粘度溶媒は1種類で使用してもよく、また2種類以上組み合わせて使用してもよい。
高誘電率溶媒と低粘度溶媒とはそれぞれ任意に選択され組み合わせて使用される。なお、前記の高誘電率溶媒および低粘度溶媒は、容量比(高誘電率溶媒:低粘度溶媒)で通常1:9〜4:1、好ましくは1:4〜7:3の割合で使用される。
Examples of the low viscosity solvent include chain carbonates such as dimethyl carbonate (DMC), methyl ethyl carbonate (MEC), and diethyl carbonate (DEC), tetrahydrofuran, 2-methyltetrahydrofuran, 1,4-dioxane, 1,2- Ethers such as dimethoxyethane, 1,2-diethoxyethane, 1,2-dibutoxyethane, lactones such as γ-butyrolactone, nitriles such as acetonitrile, esters such as methyl propionate, amides such as dimethylformamide Kind. These low viscosity solvents may be used alone or in combination of two or more.
The high dielectric constant solvent and the low viscosity solvent are arbitrarily selected and used in combination. The high dielectric constant solvent and the low viscosity solvent are usually used in a volume ratio (high dielectric constant solvent: low viscosity solvent) of 1: 9 to 4: 1, preferably 1: 4 to 7: 3. The
本発明で使用される電解質としては、例えば、LiPF6、LiBF4、LiClO4、LiN(SO2CF3)2、LiN(SO2C2F5)2、LiC(SO2CF3)3、LiPF3(CF3)3、LiPF3(C2F5)3、LiPF4(C2F5)2、LiPF3(iso−C3F7)3、LiPF5(iso−C3F7)などが挙げられる。これらの電解質は、1種類で使用してもよく、2種類以上組み合わせて使用してもよい。これら電解質は、前記の非水溶媒に通常0.1〜3M、好ましくは0.5〜1.5Mの濃度で溶解されて使用される。 Examples of the electrolyte used in the present invention include LiPF 6 , LiBF 4 , LiClO 4 , LiN (SO 2 CF 3 ) 2 , LiN (SO 2 C 2 F 5 ) 2 , LiC (SO 2 CF 3 ) 3 , LiPF 3 (CF 3 ) 3 , LiPF 3 (C 2 F 5 ) 3 , LiPF 4 (C 2 F 5 ) 2 , LiPF 3 (iso-C 3 F 7 ) 3 , LiPF 5 (iso-C 3 F 7 ) Etc. These electrolytes may be used alone or in combination of two or more. These electrolytes are used by being dissolved in the non-aqueous solvent usually at a concentration of 0.1 to 3M, preferably 0.5 to 1.5M.
本発明で使用される非水電解液は、例えば、前記の高誘電率溶媒や低粘度溶媒を混合し、これに前記の電解質を溶解し、前記式(I)で表されるtert−ブチルベンゼン誘導体を溶解することにより得られる。 The non-aqueous electrolyte used in the present invention is, for example, a mixture of the above-mentioned high dielectric constant solvent or low-viscosity solvent, dissolves the above-mentioned electrolyte therein, and tert-butylbenzene represented by the above formula (I). It is obtained by dissolving the derivative.
例えば、正極活物質としてはコバルト、マンガン、ニッケル、クロム、鉄およびバナジウムからなる群より選ばれる少なくとも一種類の金属とリチウムとの複合金属酸化物が使用される。このような複合金属酸化物としては、例えば、LiCoO2、LiMn2O4、LiNiO2、LiNi0.8CO0.2O2などが挙げられる。これらの正極活物質は、1種類だけを選択して使用しても良いし、2種類以上を組み合わせて用いても良い。 For example, a composite metal oxide of at least one metal selected from the group consisting of cobalt, manganese, nickel, chromium, iron, and vanadium and lithium is used as the positive electrode active material. Examples of such composite metal oxides include LiCoO 2 , LiMn 2 O 4 , LiNiO 2 , LiNi 0.8 CO 0.2 O 2 and the like. Only one type of these positive electrode active materials may be selected and used, or two or more types may be used in combination.
正極は、前記の正極活物質をアセチレンブラック、カーボンブラックなどの導電剤、ポリテトラフルオロエチレン(PTFE)、ポリフッ化ビニリデン(PVDF)などの結着剤および溶剤と混練して正極合剤とした後、この正極材料を集電体としてのアルミニウム箔やステンレス製のラス板に塗布して、乾燥、加圧成型後、50℃〜250℃程度の温度で2時間程度真空下で加熱処理することにより作製される。 The positive electrode is obtained by kneading the positive electrode active material with a conductive agent such as acetylene black or carbon black, a binder such as polytetrafluoroethylene (PTFE) or polyvinylidene fluoride (PVDF), and a solvent to form a positive electrode mixture. By applying this positive electrode material to an aluminum foil or stainless steel lath plate as a current collector, and after drying and pressure molding, heat treatment is performed under vacuum at a temperature of about 50 ° C. to 250 ° C. for about 2 hours. Produced.
負極活物質としては、リチウム金属やリチウム合金、およびリチウムを吸蔵・放出可能な黒鉛型結晶構造を有する炭素材料〔熱分解炭素類、コークス類、グラファイト類(人造黒鉛、天然黒鉛など)、有機高分子化合物燃焼体、炭素繊維〕や複合スズ酸化物などの物質が使用される。特に、格子面(002)の面間隔(d002)が0.335〜0.340nmである黒鉛型結晶構造を有する炭素材料を使用することが好ましい。これらの負極活物質は、1種類だけを選択して使用しても良いし、2種類以上を組み合わせて用いても良い。なお、炭素材料のような粉末材料はエチレンプロピレンジエンターポリマー(EPDM)、ポリテトラフルオロエチレン(PTFE)、ポリフッ化ビニリデン(PVDF)などの結着剤と混練して負極合剤として使用される。負極の製造方法は、特に限定されず、上記の正極の製造方法と同様な方法により製造することができる。 Examples of the negative electrode active material include lithium metal and lithium alloy, and carbon materials having a graphite-type crystal structure capable of occluding and releasing lithium (pyrolytic carbons, cokes, graphites (artificial graphite, natural graphite, etc.), Materials such as molecular compound combustor, carbon fiber] and composite tin oxide are used. In particular, it is preferable to use a carbon material having a graphite-type crystal structure in which a lattice spacing ( 002 ) (d 002 ) is 0.335 to 0.340 nm. Only one kind of these negative electrode active materials may be selected and used, or two or more kinds may be used in combination. A powder material such as a carbon material is kneaded with a binder such as ethylene propylene diene terpolymer (EPDM), polytetrafluoroethylene (PTFE), or polyvinylidene fluoride (PVDF) and used as a negative electrode mixture. The manufacturing method of a negative electrode is not specifically limited, It can manufacture with the method similar to the manufacturing method of said positive electrode.
リチウム二次電池の構造は特に限定されるものではなく、正極、負極および単層又は複層のセパレータを有するコイン型電池、さらに、正極、負極およびロール状のセパレータを有する円筒型電池や角型電池などが一例として挙げられる。なお、セパレータとしては公知のポリオレフィンの微多孔膜、織布、不織布などが使用される。 The structure of the lithium secondary battery is not particularly limited, and a coin-type battery having a positive electrode, a negative electrode, and a single-layer or multi-layer separator, and a cylindrical battery or a square type having a positive electrode, a negative electrode, and a roll separator. An example is a battery. A known polyolefin microporous film, woven fabric, non-woven fabric or the like is used as the separator.
次に、実施例および比較例を挙げて、本発明を具体的に説明する。
実施例1
〔非水電解液の調製〕
EC:PC:DEC(容量比)=30:5:65の非水溶媒を調製し、これにLiPF6を1Mの濃度になるように溶解して非水電解液を調製した後、さらに4−tert−ブチルトルエンを非水電解液に対して2.0重量%となるように加えた。
Next, an Example and a comparative example are given and this invention is demonstrated concretely.
Example 1
(Preparation of non-aqueous electrolyte)
A nonaqueous solvent of EC: PC: DEC (volume ratio) = 30: 5: 65 was prepared, and LiPF 6 was dissolved therein to a concentration of 1 M to prepare a nonaqueous electrolytic solution. Tert-butyltoluene was added so that it might become 2.0 weight% with respect to a non-aqueous electrolyte.
〔リチウム二次電池の作製および電池特性の測定〕
LiCoO2(正極活物質)を80重量%、アセチレンブラック(導電剤)を10重量%、ポリフッ化ビニリデン(結着剤)を10重量%の割合で混合し、これに1−メチル−2−ピロリドン溶剤を加えて混合したものをアルミニウム箔上に塗布し、乾燥、加圧成型、加熱処理して正極を調製した。人造黒鉛(負極活物質)を90重量%、ポリフッ化ビニリデン(結着剤)を10重量%の割合で混合し、これに1−メチル−2−ピロリドン溶剤を加え、混合したものを銅箔上に塗布し、乾燥、加圧成型、加熱処理して負極を調製した。そして、ポリプロピレン微多孔性フィルムのセパレータを用い、上記の非水電解液を注入させてコイン電池(直径20mm、厚さ3.2mm)を作製した。
このコイン電池を用いて、室温(20℃)下、0.8mAの定電流及び定電圧で、終止電圧4.2Vまで5時間充電し、次に0.8mAの定電流下、終止電圧2.7Vまで放電し、この充放電を繰り返した。初期充放電容量は、4−tert−ブチルトルエン無添加の1M LiPF6−EC/PC/DEC(容量比30/5/65)を非水電解液として用いた場合(比較例1)と比較して相対値で1.03であり、50サイクル後の電池特性を測定したところ、初期放電容量を100%としたときの放電容量維持率は92.2%であった。また、低温特性も良好であった。コイン電池の作製条件および電池特性を表1に示す。
[Production of lithium secondary battery and measurement of battery characteristics]
80% by weight of LiCoO 2 (positive electrode active material), 10% by weight of acetylene black (conductive agent), and 10% by weight of polyvinylidene fluoride (binder) are mixed, and this is mixed with 1-methyl-2-pyrrolidone. What mixed and added the solvent was apply | coated on the aluminum foil, and it dried, press-molded, and heat-processed, and prepared the positive electrode. 90% by weight of artificial graphite (negative electrode active material) and 10% by weight of polyvinylidene fluoride (binder) were mixed, and 1-methyl-2-pyrrolidone solvent was added to this, and the resulting mixture was added to the copper foil. The negative electrode was prepared by drying, pressure molding, and heat treatment. And using the separator of a polypropylene microporous film, said nonaqueous electrolyte solution was inject | poured and the coin battery (diameter 20mm, thickness 3.2mm) was produced.
Using this coin battery, it was charged at a constant current and a constant voltage of 0.8 mA at room temperature (20 ° C.) for 5 hours to a final voltage of 4.2 V, and then at a constant current of 0.8 mA and a final voltage of 2. The battery was discharged to 7 V, and this charge / discharge was repeated. The initial charge / discharge capacity is compared with the case where 1M LiPF 6 -EC / PC / DEC (capacity ratio 30/5/65) without addition of 4-tert-butyltoluene is used as the non-aqueous electrolyte (Comparative Example 1). The relative value was 1.03, and the battery characteristics after 50 cycles were measured, and the discharge capacity retention rate was 92.2% when the initial discharge capacity was 100%. Also, the low temperature characteristics were good. The production conditions and battery characteristics of the coin battery are shown in Table 1.
実施例2
添加剤として、4−tert−ブチルトルエンを非水電解液に対して5.0重量%使用したほかは実施例1と同様に非水電解液を調製してコイン電池を作製し、50サイクル後の電池特性を測定したところ、放電容量維持率は91.7%であった。コイン電池の作製条件および電池特性を表1に示す。
Example 2
A coin battery was prepared by preparing a non-aqueous electrolyte in the same manner as in Example 1 except that 4-tert-butyltoluene was used as an additive at 5.0% by weight based on the non-aqueous electrolyte. When the battery characteristics were measured, the discharge capacity retention rate was 91.7%. The production conditions and battery characteristics of the coin battery are shown in Table 1.
実施例3
添加剤として、4−tert−ブチルトルエンを非水電解液に対して0.5重量%使用したほかは実施例1と同様に非水電解液を調製してコイン電池を作製し、50サイクル後の電池特性を測定したところ、放電容量維持率は90.1%であった。コイン電池の作製条件および電池特性を表1に示す。
Example 3
A coin battery was prepared by preparing a non-aqueous electrolyte in the same manner as in Example 1 except that 4-tert-butyltoluene was used as an additive in an amount of 0.5% by weight based on the non-aqueous electrolyte. When the battery characteristics of were measured, the discharge capacity retention rate was 90.1%. The production conditions and battery characteristics of the coin battery are shown in Table 1.
比較例1
EC:PC:DEC(容量比)=30:5:65の非水溶媒を調製し、これにLiPF6を1Mの濃度になるように溶解した。このときtert−ブチルベンゼン誘導体は全く添加しなかった。この非水電解液を使用して実施例1と同様にコイン電池を作製し、電池特性を測定した。初期放電容量に対し、50サイクル後の放電容量維持率は82.6%であった。コイン電池の作製条件および電池特性を表1に示す。
Comparative Example 1
A non-aqueous solvent of EC: PC: DEC (volume ratio) = 30: 5: 65 was prepared, and LiPF 6 was dissolved therein to a concentration of 1M. At this time, no tert-butylbenzene derivative was added. Using this non-aqueous electrolyte, a coin battery was produced in the same manner as in Example 1, and the battery characteristics were measured. The discharge capacity retention ratio after 50 cycles was 82.6% with respect to the initial discharge capacity. The production conditions and battery characteristics of the coin battery are shown in Table 1.
実施例4
EC:PC:DEC(容量比)=30:5:65の非水溶媒を調製し、これにLiPF6を1Mの濃度になるように溶解して非水電解液を調整した後、さらにtert−ブチルベンゼンを非水電解液に対して2.0重量%となるように加えた。この非水電解液を使用して実施例1と同様にコイン電池を作製し、電池特性を測定したところ、初期放電容量は4−tert−ブチルベンゼン誘導体無添加の1M LiPF6−EC/PC/DEC(容量比30/5/65)を非水電解液として用いた場合(比較例1)と比較して相対値で1.02であり、50サイクル後の電池特性を測定したところ、初期放電容量を100%としたときの放電容量維持率は91.8%であった。また、低温特性も良好であった。コイン電池の作製条件および電池特性を表1に示す。
Example 4
A non-aqueous solvent of EC: PC: DEC (volume ratio) = 30: 5: 65 was prepared, and LiPF 6 was dissolved therein to a concentration of 1 M to prepare a non-aqueous electrolyte solution. Butylbenzene was added to 2.0 wt% with respect to the non-aqueous electrolyte. Using this non-aqueous electrolyte, a coin battery was prepared in the same manner as in Example 1, and the battery characteristics were measured. The initial discharge capacity was 1M LiPF 6 -EC / PC / without the 4-tert-butylbenzene derivative added. When DEC (capacity ratio 30/5/65) was used as a non-aqueous electrolyte (Comparative Example 1), the relative value was 1.02, and the battery characteristics after 50 cycles were measured. The discharge capacity retention rate when the capacity was 100% was 91.8%. Also, the low temperature characteristics were good. The production conditions and battery characteristics of the coin battery are shown in Table 1.
実施例5
添加剤として、4−tert−ブチル−m−キシレンを非水電解液に対して2.0重量%使用したほかは実施例1と同様に非水電解液を調製してコイン電池を作製し、50サイクル後の電池特性を測定したところ、放電容量維持率は91.6%であった。コイン電池の作製条件および電池特性を表1に示す。
Example 5
A non-aqueous electrolyte was prepared in the same manner as in Example 1 except that 4-tert-butyl-m-xylene was used in an amount of 2.0% by weight based on the non-aqueous electrolyte. When the battery characteristics after 50 cycles were measured, the discharge capacity retention rate was 91.6%. The production conditions and battery characteristics of the coin battery are shown in Table 1.
実施例6
非水溶媒として、EC/PC/DEC/DMC(容量比30/5/30/35)を使用し、負極活物質として、人造黒鉛に代えて天然黒鉛を使用したほかは実施例1と同様に非水電解液を調製してコイン電池を作製し、50サイクル後の電池特性を測定したところ、放電容量維持率は92.6%であった。コイン電池の作製条件および電池特性を表1に示す。
Example 6
As in Example 1, except that EC / PC / DEC / DMC (capacity ratio 30/5/30/35) was used as the nonaqueous solvent and natural graphite was used as the negative electrode active material instead of artificial graphite. A coin battery was prepared by preparing a nonaqueous electrolytic solution, and the battery characteristics after 50 cycles were measured. The discharge capacity retention rate was 92.6%. The production conditions and battery characteristics of the coin battery are shown in Table 1.
実施例7
非水電解液として、1M LiPF6−EC/PC/MEC/DMC(容量比30/5/50/15)を使用し、正極活物質として、LiCoO2に代えてLiNi0.8Co0.2O2を使用したほかは実施例1と同様に非水電解液を調製してコイン電池を作製し、50サイクル後の電池特性を測定したところ、放電容量維持率は90.8%であった。コイン電池の作製条件および電池特性を表1に示す。
Example 7
1M LiPF 6 -EC / PC / MEC / DMC (capacity ratio 30/5/50/15) is used as the non-aqueous electrolyte, and LiNi 0.8 Co 0.2 O 2 is used instead of LiCoO 2 as the positive electrode active material. In the same manner as in Example 1, a non-aqueous electrolyte was prepared to produce a coin battery, and the battery characteristics after 50 cycles were measured. The discharge capacity retention rate was 90.8%. The production conditions and battery characteristics of the coin battery are shown in Table 1.
実施例8
非水電解液として、1M LiBF4−EC/PC/DEC/DMC(容量比30/5/30/35)を使用し、正極活物質として、LiCoO2に代えてLiMn2O4を使用したほかは実施例1と同様に非水電解液を調製してコイン電池を作製し、50サイクル後の電池特性を測定したところ、放電容量維持率は92.3%であった。コイン電池の作製条件および電池特性を表1に示す。
Example 8
1M LiBF 4 -EC / PC / DEC / DMC (capacity ratio 30/5/30/35) was used as the non-aqueous electrolyte, and LiMn 2 O 4 was used instead of LiCoO 2 as the positive electrode active material. Prepared a coin battery by preparing a non-aqueous electrolyte in the same manner as in Example 1 and measured the battery characteristics after 50 cycles. As a result, the discharge capacity retention rate was 92.3%. The production conditions and battery characteristics of the coin battery are shown in Table 1.
実施例9〜実施例11
4−tert−ブチルトルエンに代えて、各実施例において、4,4−ジ−tert−ブチルビフェニル、1,3−ジ−tert−ブチルベンゼン、1,3,5−トリ−tert−ブチルベンゼンを使用したほかは実施例1と同様に非水電解液を調製してコイン電池を作製し、50サイクル後の電池特性を測定した。コイン電池の作製条件および電池特性を表1に示す。
Example 9 to Example 11
Instead of 4-tert-butyltoluene, in each example, 4,4-di-tert-butylbiphenyl, 1,3-di-tert-butylbenzene, 1,3,5-tri-tert-butylbenzene was used. A coin battery was prepared by preparing a nonaqueous electrolytic solution in the same manner as in Example 1 except that it was used, and the battery characteristics after 50 cycles were measured. The production conditions and battery characteristics of the coin battery are shown in Table 1.
実施例12
4−tert−ブチルトルエンに代えて、3,5−ジ−tert−ブチルトルエンを使用し、負極活物質として、人造黒鉛に代えて天然黒鉛を使用したほかは実施例1と同様に非水電解液を調製してコイン電池を作製し、50サイクル後の電池特性を測定した。コイン電池の作製条件および電池特性を表1に示す。
Example 12
Non-aqueous electrolysis as in Example 1 except that 3,5-di-tert-butyltoluene was used instead of 4-tert-butyltoluene and natural graphite was used as the negative electrode active material instead of artificial graphite. The liquid was prepared to prepare a coin battery, and the battery characteristics after 50 cycles were measured. The production conditions and battery characteristics of the coin battery are shown in Table 1.
なお、本発明は記載の実施例に限定されず、発明の趣旨から容易に類推可能な様々な組み合わせが可能である。特に、上記実施例の溶媒の組み合わせは限定されるものではない。更には、上記実施例はコイン電池に関するものであるが、本発明は円筒形、角柱形の電池にも適用される。 In addition, this invention is not limited to the Example described, The various combination which can be easily guessed from the meaning of invention is possible. In particular, the combination of solvents in the above examples is not limited. Furthermore, although the said Example is related with a coin battery, this invention is applied also to a cylindrical and prismatic battery.
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