JP2014531731A5 - - Google Patents
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- JP2014531731A5 JP2014531731A5 JP2014534590A JP2014534590A JP2014531731A5 JP 2014531731 A5 JP2014531731 A5 JP 2014531731A5 JP 2014534590 A JP2014534590 A JP 2014534590A JP 2014534590 A JP2014534590 A JP 2014534590A JP 2014531731 A5 JP2014531731 A5 JP 2014531731A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- phosphorus
- electrolyte solution
- pendant
- oxy
- 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
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- -1 phosphazene compound Chemical class 0.000 claims description 87
- 229910052698 phosphorus Inorganic materials 0.000 claims description 47
- 239000008151 electrolyte solution Substances 0.000 claims description 36
- 239000002608 ionic liquid Substances 0.000 claims description 31
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 27
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 26
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 26
- 239000011574 phosphorus Substances 0.000 claims description 26
- 125000004437 phosphorous atom Chemical group 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 21
- 125000001931 aliphatic group Chemical group 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 239000001257 hydrogen Substances 0.000 claims description 15
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 12
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 10
- 125000004149 thio group Chemical group *S* 0.000 claims description 10
- 125000002252 acyl group Chemical group 0.000 claims description 9
- 125000004442 acylamino group Chemical group 0.000 claims description 9
- 125000004423 acyloxy group Chemical group 0.000 claims description 9
- 125000003342 alkenyl group Chemical group 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 9
- 125000003282 alkyl amino group Chemical group 0.000 claims description 9
- 125000004947 alkyl aryl amino group Chemical group 0.000 claims description 9
- 125000005248 alkyl aryloxy group Chemical group 0.000 claims description 9
- 125000004414 alkyl thio group Chemical group 0.000 claims description 9
- 125000000304 alkynyl group Chemical group 0.000 claims description 9
- 125000000539 amino acid group Chemical group 0.000 claims description 9
- 125000003277 amino group Chemical group 0.000 claims description 9
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 9
- 125000001769 aryl amino group Chemical group 0.000 claims description 9
- 125000003118 aryl group Chemical group 0.000 claims description 9
- 125000005110 aryl thio group Chemical group 0.000 claims description 9
- 125000004104 aryloxy group Chemical group 0.000 claims description 9
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 9
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 9
- 125000000837 carbohydrate group Chemical group 0.000 claims description 9
- 238000003763 carbonization Methods 0.000 claims description 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 9
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 9
- 125000004986 diarylamino group Chemical group 0.000 claims description 9
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 9
- 125000003827 glycol group Chemical group 0.000 claims description 9
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 9
- 125000004475 heteroaralkyl group Chemical group 0.000 claims description 9
- 125000001072 heteroaryl group Chemical group 0.000 claims description 9
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 9
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 9
- 125000005740 oxycarbonyl group Chemical group [*:1]OC([*:2])=O 0.000 claims description 9
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 9
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 claims description 9
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims description 9
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 claims description 9
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 9
- 125000003375 sulfoxide group Chemical group 0.000 claims description 9
- 125000004950 trifluoroalkyl group Chemical group 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 claims description 6
- 150000001350 alkyl halides Chemical class 0.000 claims description 6
- 150000001450 anions Chemical class 0.000 claims description 6
- 150000004982 aromatic amines Chemical class 0.000 claims description 6
- RPXKKUZDTAOVEQ-UHFFFAOYSA-N boric acid;oxalic acid Chemical group OB(O)O.OC(=O)C(O)=O.OC(=O)C(O)=O RPXKKUZDTAOVEQ-UHFFFAOYSA-N 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 6
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical group OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 claims description 6
- 238000004146 energy storage Methods 0.000 claims description 4
- 229910003002 lithium salt Inorganic materials 0.000 claims description 4
- 159000000002 lithium salts Chemical class 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 150000003512 tertiary amines Chemical class 0.000 claims description 4
- QGHDLJAZIIFENW-UHFFFAOYSA-N 4-[1,1,1,3,3,3-hexafluoro-2-(4-hydroxy-3-prop-2-enylphenyl)propan-2-yl]-2-prop-2-enylphenol Chemical group C1=C(CC=C)C(O)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(O)C(CC=C)=C1 QGHDLJAZIIFENW-UHFFFAOYSA-N 0.000 claims description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 3
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 3
- YUWBVKYVJWNVLE-UHFFFAOYSA-N [N].[P] Chemical group [N].[P] YUWBVKYVJWNVLE-UHFFFAOYSA-N 0.000 claims description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 3
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 3
- 150000004820 halides Chemical class 0.000 claims description 3
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 3
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 3
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 3
- 150000003139 primary aliphatic amines Chemical class 0.000 claims description 3
- 150000003141 primary amines Chemical class 0.000 claims description 3
- 150000005619 secondary aliphatic amines Chemical class 0.000 claims description 3
- 150000003335 secondary amines Chemical class 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- 150000003573 thiols Chemical class 0.000 claims description 3
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims description 2
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 claims description 2
- 150000005677 organic carbonates Chemical group 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 6
- 125000005521 carbonamide group Chemical group 0.000 claims 2
- GKTNLYAAZKKMTQ-UHFFFAOYSA-N n-[bis(dimethylamino)phosphinimyl]-n-methylmethanamine Chemical class CN(C)P(=N)(N(C)C)N(C)C GKTNLYAAZKKMTQ-UHFFFAOYSA-N 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13/253,707 US9206210B2 (en) | 2011-10-05 | 2011-10-05 | Ionic liquids, electrolyte solutions including the ionic liquids, and energy storage devices including the ionic liquids |
| US13/253,707 | 2011-10-05 | ||
| PCT/US2012/056838 WO2013052294A1 (en) | 2011-10-05 | 2012-09-24 | Ionic liquids, electrolyte solutions including the ionic liquids, and energy storage devices including the ionic liquids |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2014531731A JP2014531731A (ja) | 2014-11-27 |
| JP2014531731A5 true JP2014531731A5 (https=) | 2015-11-05 |
Family
ID=48042294
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014534590A Pending JP2014531731A (ja) | 2011-10-05 | 2012-09-24 | イオン性液体、イオン性液体を含む電解質溶液、およびイオン性液体を含むエネルギー貯蔵装置 |
Country Status (6)
| Country | Link |
|---|---|
| US (3) | US9206210B2 (https=) |
| EP (1) | EP2764003B1 (https=) |
| JP (1) | JP2014531731A (https=) |
| KR (1) | KR20140072880A (https=) |
| CN (1) | CN103842367A (https=) |
| WO (1) | WO2013052294A1 (https=) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8153435B1 (en) | 2005-03-30 | 2012-04-10 | Tracer Detection Technology Corp. | Methods and articles for identifying objects using encapsulated perfluorocarbon tracers |
| US9206210B2 (en) * | 2011-10-05 | 2015-12-08 | Battelle Energy Alliance, Llc | Ionic liquids, electrolyte solutions including the ionic liquids, and energy storage devices including the ionic liquids |
| US20140342240A1 (en) * | 2013-05-14 | 2014-11-20 | Mason Kurt Harrup | Fluorinated phosphazenes for use as electrolyte additives and co-solvents in lithium ion batteries |
| WO2015179831A1 (en) * | 2014-05-23 | 2015-11-26 | Battelle Energy Alliance, Llc | Electrolyte solutions including a phosphoranimine compound, and energy storage devices including same |
| US20160141727A1 (en) * | 2014-11-13 | 2016-05-19 | Basf Corporation | Electrolytes and Metal Hydride Batteries |
| US10243240B2 (en) | 2014-11-13 | 2019-03-26 | Basf Corporation | Electrolytes and metal hydride batteries |
| CN104485454A (zh) * | 2014-12-10 | 2015-04-01 | 天能电池集团有限公司 | 铅酸蓄电池正极铅膏 |
| JP6437392B2 (ja) * | 2015-02-06 | 2018-12-12 | デクセリアルズ株式会社 | 磁気記録媒体用潤滑剤、及び磁気記録媒体 |
| US10587012B2 (en) * | 2015-03-26 | 2020-03-10 | Basf Corporation | Electrolyte compositions comprising ionic liquids and metal hydride batteries comprising same |
| WO2016160703A1 (en) * | 2015-03-27 | 2016-10-06 | Harrup Mason K | All-inorganic solvents for electrolytes |
| US10367229B2 (en) | 2015-08-04 | 2019-07-30 | Battelle Energy Alliance, Llc | Phosphoranimine compounds, electrolyte solutions including a phosphoranimine compound, and energy storage devices including same |
| CN105161764B (zh) * | 2015-09-25 | 2018-07-27 | 江苏华东锂电技术研究院有限公司 | 锂硫电池电解液及其制备方法，以及锂硫电池 |
| US10868332B2 (en) | 2016-04-01 | 2020-12-15 | NOHMs Technologies, Inc. | Modified ionic liquids containing phosphorus |
| US10707531B1 (en) | 2016-09-27 | 2020-07-07 | New Dominion Enterprises Inc. | All-inorganic solvents for electrolytes |
| JP7296893B2 (ja) | 2017-07-17 | 2023-06-23 | ノームズ テクノロジーズ インコーポレイテッド | リン含有電解質 |
| CN109935904B (zh) * | 2017-12-15 | 2021-08-20 | 华为技术有限公司 | 一种电解液添加剂、锂二次电池电解液和锂二次电池 |
| GB2571910A (en) * | 2017-12-21 | 2019-09-18 | Continental automotive systems inc | Laser ablation for wire bonding on organic solderability preservative surface |
| CN109776613A (zh) * | 2019-01-15 | 2019-05-21 | 顺德职业技术学院 | 具有β晶诱导成核作用的环三磷腈阻燃剂及其合成方法 |
| CN110204731B (zh) * | 2019-05-27 | 2021-06-29 | 台州学院 | 一种含离子液体的纳米磷腈微球及其制备方法和应用 |
| CN113121602B (zh) * | 2019-12-30 | 2023-03-24 | 北京卫蓝新能源科技有限公司 | 一种磷腈基磷酸酯添加剂和制备方法及锂电池电解液 |
| CN115315840A (zh) * | 2020-03-31 | 2022-11-08 | 三井化学株式会社 | 电池用非水电解液、锂二次电池前体、锂二次电池的制造方法、锂二次电池、磷腈化合物、及电池用添加剂 |
| WO2022051152A1 (en) * | 2020-09-03 | 2022-03-10 | The Regents Of The University Of California | Pressure sensor device with organic electrochemical transistors |
| CN115160371B (zh) * | 2022-08-11 | 2024-05-17 | 华润化学材料科技股份有限公司 | 一种氮磷协同的离子型阻燃剂及其制备方法与应用 |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4314503B2 (ja) | 1999-08-04 | 2009-08-19 | 株式会社豊田中央研究所 | リチウム二次電池 |
| ATE444944T1 (de) | 2000-04-20 | 2009-10-15 | Mitsui Chemicals Inc | Verfahren zur herstellung substituierter aromatischer verbindungen |
| JP4512233B2 (ja) | 2000-05-26 | 2010-07-28 | ソニー株式会社 | 非水電解液電池 |
| JPWO2002076924A1 (ja) | 2001-03-26 | 2004-07-15 | 日清紡績株式会社 | イオン性液体、蓄電デバイス用電解質塩、蓄電デバイス用電解液、電気二重層キャパシタ、および二次電池 |
| DE60314433T2 (de) | 2002-09-20 | 2008-02-14 | Nisshinbo Industries, Inc. | Zusammensetzung für polyelektrolyte,polyelektrolyte,elektrische doppelschichtkondensatoren und sekundärzellen mit wasserfreiem elektrolyt |
| AU2003901144A0 (en) | 2003-03-13 | 2003-03-27 | Monash University School Of Chemistry | Room temperature ionic liquid electrolytes for lithium secondary batteries |
| IL162078A0 (en) * | 2003-06-12 | 2005-11-20 | Mitsui Chemicals Inc | Method for producing organic compound by substituted halogen atoms |
| US7824800B1 (en) | 2004-04-08 | 2010-11-02 | Electrochemical Systems, Inc. | Lithium-ion cell with a wide operating temperature range |
| US7582380B1 (en) | 2004-04-08 | 2009-09-01 | Electrochemical Systems, Inc. | Lithium-ion cell with a wide operating temperature range |
| US7285362B2 (en) | 2004-05-17 | 2007-10-23 | Battelle Energy Alliance, Llc | Safe battery solvents |
| JP4599107B2 (ja) | 2004-07-28 | 2010-12-15 | 三井化学株式会社 | イオン液体 |
| JP4939836B2 (ja) | 2005-11-08 | 2012-05-30 | 株式会社ブリヂストン | イオン性化合物 |
| WO2007074609A1 (ja) * | 2005-12-26 | 2007-07-05 | Bridgestone Corporation | 電池用非水電解液及びそれを備えた非水電解液電池、並びに電気二重層キャパシタ用電解液及びそれを備えた電気二重層キャパシタ |
| JP5134783B2 (ja) * | 2005-12-26 | 2013-01-30 | 株式会社ブリヂストン | 電池用非水電解液及びそれを備えた非水電解液電池 |
| JP4435113B2 (ja) | 2006-05-30 | 2010-03-17 | 株式会社東芝 | 非水電解質電池 |
| FR2917537B1 (fr) | 2007-06-15 | 2009-09-25 | Saft Groupe Sa | Accumulateur lithium-ion contenant un electrolyte comprenant un liquide ionique |
| KR101351698B1 (ko) | 2007-06-26 | 2014-02-11 | 삼성에스디아이 주식회사 | 고체 고분자 전해질 및 이를 이용한 리튬 이차전지 |
| JP2010027007A (ja) | 2008-07-24 | 2010-02-04 | Canon Inc | 処理装置、要求装置、及びそれらの処理方法 |
| JP5639344B2 (ja) | 2009-05-22 | 2014-12-10 | 株式会社ブリヂストン | イオン液体及びその製造方法 |
| KR20110094106A (ko) | 2009-09-02 | 2011-08-19 | 파나소닉 주식회사 | 비수 용매, 및 그것을 이용한 비수 전해액 및 비수계 2차 전지 |
| US8524388B2 (en) | 2010-01-20 | 2013-09-03 | Ut-Battelle, Llc | Superbase-derived protic ionic liquids |
| US9206210B2 (en) * | 2011-10-05 | 2015-12-08 | Battelle Energy Alliance, Llc | Ionic liquids, electrolyte solutions including the ionic liquids, and energy storage devices including the ionic liquids |
| US20140342240A1 (en) * | 2013-05-14 | 2014-11-20 | Mason Kurt Harrup | Fluorinated phosphazenes for use as electrolyte additives and co-solvents in lithium ion batteries |
-
2011
- 2011-10-05 US US13/253,707 patent/US9206210B2/en not_active Expired - Fee Related
-
2012
- 2012-09-24 WO PCT/US2012/056838 patent/WO2013052294A1/en not_active Ceased
- 2012-09-24 JP JP2014534590A patent/JP2014531731A/ja active Pending
- 2012-09-24 CN CN201280048753.9A patent/CN103842367A/zh active Pending
- 2012-09-24 KR KR1020147008631A patent/KR20140072880A/ko not_active Ceased
- 2012-09-24 EP EP12838450.0A patent/EP2764003B1/en active Active
-
2015
- 2015-11-02 US US14/930,248 patent/US20160056506A1/en not_active Abandoned
-
2017
- 2017-03-09 US US15/454,166 patent/US20170179530A1/en not_active Abandoned
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