Cycle deterioration analysis of 0.6 Ah-class lithium-ion cells with cell chemistry of LiNi0.6Co0.2Mn0.2O2-based/graphite
We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% a...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Kimura, Naoki [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2016transfer abstract |
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| Schlagwörter: |
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| Umfang: |
6 |
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| Übergeordnetes Werk: |
Enthalten in: Numerical modeling of wave–current forces acting on horizontal cylinder of marine structures by VOF method - Xiao, Hong ELSEVIER, 2013, the international journal on the science and technology of electrochemical energy systems, New York, NY [u.a.] |
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| Übergeordnetes Werk: |
volume:332 ; year:2016 ; day:15 ; month:11 ; pages:187-192 ; extent:6 |
| Links: |
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| DOI / URN: |
10.1016/j.jpowsour.2016.09.081 |
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ELV014161346 |
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| 245 | 1 | 0 | |a Cycle deterioration analysis of 0.6 Ah-class lithium-ion cells with cell chemistry of LiNi0.6Co0.2Mn0.2O2-based/graphite |
| 264 | 1 | |c 2016transfer abstract | |
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| 520 | |a We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. | ||
| 520 | |a We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. | ||
| 650 | 7 | |a Lithium ion battery |2 Elsevier | |
| 650 | 7 | |a Substitution |2 Elsevier | |
| 650 | 7 | |a Cathode material |2 Elsevier | |
| 650 | 7 | |a Molybdenum |2 Elsevier | |
| 650 | 7 | |a Cycle |2 Elsevier | |
| 700 | 1 | |a Seki, Eiji |4 oth | |
| 700 | 1 | |a Konishi, Hiroaki |4 oth | |
| 700 | 1 | |a Hirano, Tatsumi |4 oth | |
| 700 | 1 | |a Takahashi, Shin |4 oth | |
| 700 | 1 | |a Ueda, Atsushi |4 oth | |
| 700 | 1 | |a Horiba, Tatsuo |4 oth | |
| 773 | 0 | 8 | |i Enthalten in |n Elsevier |a Xiao, Hong ELSEVIER |t Numerical modeling of wave–current forces acting on horizontal cylinder of marine structures by VOF method |d 2013 |d the international journal on the science and technology of electrochemical energy systems |g New York, NY [u.a.] |w (DE-627)ELV00098745X |
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10.1016/j.jpowsour.2016.09.081 doi GBV00000000000213A.pica (DE-627)ELV014161346 (ELSEVIER)S0378-7753(16)31244-7 DE-627 ger DE-627 rakwb eng 620 620 DE-600 690 VZ 50.92 bkl Kimura, Naoki verfasserin aut Cycle deterioration analysis of 0.6 Ah-class lithium-ion cells with cell chemistry of LiNi0.6Co0.2Mn0.2O2-based/graphite 2016transfer abstract 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. Lithium ion battery Elsevier Substitution Elsevier Cathode material Elsevier Molybdenum Elsevier Cycle Elsevier Seki, Eiji oth Konishi, Hiroaki oth Hirano, Tatsumi oth Takahashi, Shin oth Ueda, Atsushi oth Horiba, Tatsuo oth Enthalten in Elsevier Xiao, Hong ELSEVIER Numerical modeling of wave–current forces acting on horizontal cylinder of marine structures by VOF method 2013 the international journal on the science and technology of electrochemical energy systems New York, NY [u.a.] (DE-627)ELV00098745X volume:332 year:2016 day:15 month:11 pages:187-192 extent:6 https://doi.org/10.1016/j.jpowsour.2016.09.081 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 50.92 Meerestechnik VZ AR 332 2016 15 1115 187-192 6 045F 620 |
| spelling |
10.1016/j.jpowsour.2016.09.081 doi GBV00000000000213A.pica (DE-627)ELV014161346 (ELSEVIER)S0378-7753(16)31244-7 DE-627 ger DE-627 rakwb eng 620 620 DE-600 690 VZ 50.92 bkl Kimura, Naoki verfasserin aut Cycle deterioration analysis of 0.6 Ah-class lithium-ion cells with cell chemistry of LiNi0.6Co0.2Mn0.2O2-based/graphite 2016transfer abstract 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. Lithium ion battery Elsevier Substitution Elsevier Cathode material Elsevier Molybdenum Elsevier Cycle Elsevier Seki, Eiji oth Konishi, Hiroaki oth Hirano, Tatsumi oth Takahashi, Shin oth Ueda, Atsushi oth Horiba, Tatsuo oth Enthalten in Elsevier Xiao, Hong ELSEVIER Numerical modeling of wave–current forces acting on horizontal cylinder of marine structures by VOF method 2013 the international journal on the science and technology of electrochemical energy systems New York, NY [u.a.] (DE-627)ELV00098745X volume:332 year:2016 day:15 month:11 pages:187-192 extent:6 https://doi.org/10.1016/j.jpowsour.2016.09.081 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 50.92 Meerestechnik VZ AR 332 2016 15 1115 187-192 6 045F 620 |
| allfields_unstemmed |
10.1016/j.jpowsour.2016.09.081 doi GBV00000000000213A.pica (DE-627)ELV014161346 (ELSEVIER)S0378-7753(16)31244-7 DE-627 ger DE-627 rakwb eng 620 620 DE-600 690 VZ 50.92 bkl Kimura, Naoki verfasserin aut Cycle deterioration analysis of 0.6 Ah-class lithium-ion cells with cell chemistry of LiNi0.6Co0.2Mn0.2O2-based/graphite 2016transfer abstract 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. Lithium ion battery Elsevier Substitution Elsevier Cathode material Elsevier Molybdenum Elsevier Cycle Elsevier Seki, Eiji oth Konishi, Hiroaki oth Hirano, Tatsumi oth Takahashi, Shin oth Ueda, Atsushi oth Horiba, Tatsuo oth Enthalten in Elsevier Xiao, Hong ELSEVIER Numerical modeling of wave–current forces acting on horizontal cylinder of marine structures by VOF method 2013 the international journal on the science and technology of electrochemical energy systems New York, NY [u.a.] (DE-627)ELV00098745X volume:332 year:2016 day:15 month:11 pages:187-192 extent:6 https://doi.org/10.1016/j.jpowsour.2016.09.081 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 50.92 Meerestechnik VZ AR 332 2016 15 1115 187-192 6 045F 620 |
| allfieldsGer |
10.1016/j.jpowsour.2016.09.081 doi GBV00000000000213A.pica (DE-627)ELV014161346 (ELSEVIER)S0378-7753(16)31244-7 DE-627 ger DE-627 rakwb eng 620 620 DE-600 690 VZ 50.92 bkl Kimura, Naoki verfasserin aut Cycle deterioration analysis of 0.6 Ah-class lithium-ion cells with cell chemistry of LiNi0.6Co0.2Mn0.2O2-based/graphite 2016transfer abstract 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. Lithium ion battery Elsevier Substitution Elsevier Cathode material Elsevier Molybdenum Elsevier Cycle Elsevier Seki, Eiji oth Konishi, Hiroaki oth Hirano, Tatsumi oth Takahashi, Shin oth Ueda, Atsushi oth Horiba, Tatsuo oth Enthalten in Elsevier Xiao, Hong ELSEVIER Numerical modeling of wave–current forces acting on horizontal cylinder of marine structures by VOF method 2013 the international journal on the science and technology of electrochemical energy systems New York, NY [u.a.] (DE-627)ELV00098745X volume:332 year:2016 day:15 month:11 pages:187-192 extent:6 https://doi.org/10.1016/j.jpowsour.2016.09.081 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 50.92 Meerestechnik VZ AR 332 2016 15 1115 187-192 6 045F 620 |
| allfieldsSound |
10.1016/j.jpowsour.2016.09.081 doi GBV00000000000213A.pica (DE-627)ELV014161346 (ELSEVIER)S0378-7753(16)31244-7 DE-627 ger DE-627 rakwb eng 620 620 DE-600 690 VZ 50.92 bkl Kimura, Naoki verfasserin aut Cycle deterioration analysis of 0.6 Ah-class lithium-ion cells with cell chemistry of LiNi0.6Co0.2Mn0.2O2-based/graphite 2016transfer abstract 6 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. Lithium ion battery Elsevier Substitution Elsevier Cathode material Elsevier Molybdenum Elsevier Cycle Elsevier Seki, Eiji oth Konishi, Hiroaki oth Hirano, Tatsumi oth Takahashi, Shin oth Ueda, Atsushi oth Horiba, Tatsuo oth Enthalten in Elsevier Xiao, Hong ELSEVIER Numerical modeling of wave–current forces acting on horizontal cylinder of marine structures by VOF method 2013 the international journal on the science and technology of electrochemical energy systems New York, NY [u.a.] (DE-627)ELV00098745X volume:332 year:2016 day:15 month:11 pages:187-192 extent:6 https://doi.org/10.1016/j.jpowsour.2016.09.081 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U 50.92 Meerestechnik VZ AR 332 2016 15 1115 187-192 6 045F 620 |
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Enthalten in Numerical modeling of wave–current forces acting on horizontal cylinder of marine structures by VOF method New York, NY [u.a.] volume:332 year:2016 day:15 month:11 pages:187-192 extent:6 |
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Enthalten in Numerical modeling of wave–current forces acting on horizontal cylinder of marine structures by VOF method New York, NY [u.a.] volume:332 year:2016 day:15 month:11 pages:187-192 extent:6 |
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Numerical modeling of wave–current forces acting on horizontal cylinder of marine structures by VOF method |
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Kimura, Naoki @@aut@@ Seki, Eiji @@oth@@ Konishi, Hiroaki @@oth@@ Hirano, Tatsumi @@oth@@ Takahashi, Shin @@oth@@ Ueda, Atsushi @@oth@@ Horiba, Tatsuo @@oth@@ |
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cycle deterioration analysis of 0.6 ah-class lithium-ion cells with cell chemistry of lini0.6co0.2mn0.2o2-based/graphite |
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Cycle deterioration analysis of 0.6 Ah-class lithium-ion cells with cell chemistry of LiNi0.6Co0.2Mn0.2O2-based/graphite |
| abstract |
We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. |
| abstractGer |
We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. |
| abstract_unstemmed |
We applied a thermally stabilized LiNi0.6Co0.2Mn0.2O2-based cathode active material for lithium-ion batteries, which we had developed by partial substitution of molybdenum for the transition metal, to 0.6 Ah-class single cells. Cycling test of the cell unexpectedly showed capacity retention of 87% after 3000 cycles, which is better than a cell using cathode active material without molybdenum-substitution. Disassembled analyses of the cells cycled for 3000 times definitely demonstrated that no degradation in both the cathodes and anodes of the molybdenum-substituted and non-substituted. However, there was definite potential slippage in both the cells; that of the non-substituted cell was larger than the molybdenum-substituted cell. Analysis showed that very small amount of molybdenum, in the molybdenum-substituted cell, eluted from the cathode and deposited on the surface of the anode. It is speculated that the deposition might suppress the SEI growth on the anode, and restrain the slippage of the operating potentials for the cathode and anode. |
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