Solvent-controlled synthesis of Ni-PTA MOFs as high performance anode material for Li-ion batteries
Abstract Metal-organic frameworks are recognized as active electrode materials for rechargeable batteries due to their structural diversity, abundant electrochemical active sites and large ion diffusion channels. Herein, nickel-terephthalic acid metal-organic frameworks (Ni-PTA MOFs) with different...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Wang, Deping [verfasserIn] Hu, Wenming [verfasserIn] Gao, Yingxv [verfasserIn] Ma, Qian [verfasserIn] Xia, Xiaohong [verfasserIn] Liu, Hongbo [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2023 |
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| Schlagwörter: |
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| Anmerkung: |
© The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
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| Übergeordnetes Werk: |
Enthalten in: Journal of solid state electrochemistry - Springer Berlin Heidelberg, 1997, 28(2023), 7 vom: 26. Nov., Seite 2233-2241 |
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| Übergeordnetes Werk: |
volume:28 ; year:2023 ; number:7 ; day:26 ; month:11 ; pages:2233-2241 |
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| DOI / URN: |
10.1007/s10008-023-05723-3 |
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| Katalog-ID: |
SPR056480660 |
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| 520 | |a Abstract Metal-organic frameworks are recognized as active electrode materials for rechargeable batteries due to their structural diversity, abundant electrochemical active sites and large ion diffusion channels. Herein, nickel-terephthalic acid metal-organic frameworks (Ni-PTA MOFs) with different crystal and morphology structures are synthesized via a facile solvothermal method by simply adjusting the nature of solvent. Due to the fewest guest molecules and porous structure, the Ni-PTA resulting from the combinations of DMF and EtOH exhibits the comparatively higher chemical/thermal stability and shortened ion diffusion pathway. As a result, it exhibits a high discharge/charge capacity of 2196.4 and 1762.3 mAh $ g^{−1} $ at the first cycle and retains 1300 mAh $ g^{−1} $ after 50 cycles at 100 mA $ g^{−1} $ when tested as anode materials for Li-ion batteries. Even when the current density reaches 4000 mA $ g^{−1} $, it maintains a capacity of 452 mAh $ g^{−1} $. This work provides possibilities for regulating the crystal and morphology structure of MOFs as high performance anode materials for lithium ion batteries. | ||
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10.1007/s10008-023-05723-3 doi (DE-627)SPR056480660 (SPR)s10008-023-05723-3-e DE-627 ger DE-627 rakwb eng 540 VZ 35.14 bkl 35.90 bkl Wang, Deping verfasserin aut Solvent-controlled synthesis of Ni-PTA MOFs as high performance anode material for Li-ion batteries 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Metal-organic frameworks are recognized as active electrode materials for rechargeable batteries due to their structural diversity, abundant electrochemical active sites and large ion diffusion channels. Herein, nickel-terephthalic acid metal-organic frameworks (Ni-PTA MOFs) with different crystal and morphology structures are synthesized via a facile solvothermal method by simply adjusting the nature of solvent. Due to the fewest guest molecules and porous structure, the Ni-PTA resulting from the combinations of DMF and EtOH exhibits the comparatively higher chemical/thermal stability and shortened ion diffusion pathway. As a result, it exhibits a high discharge/charge capacity of 2196.4 and 1762.3 mAh $ g^{−1} $ at the first cycle and retains 1300 mAh $ g^{−1} $ after 50 cycles at 100 mA $ g^{−1} $ when tested as anode materials for Li-ion batteries. Even when the current density reaches 4000 mA $ g^{−1} $, it maintains a capacity of 452 mAh $ g^{−1} $. This work provides possibilities for regulating the crystal and morphology structure of MOFs as high performance anode materials for lithium ion batteries. Metal-organic frameworks (dpeaa)DE-He213 Solvent (dpeaa)DE-He213 Guest molecules (dpeaa)DE-He213 Lithium-ion batteries (dpeaa)DE-He213 Hu, Wenming verfasserin aut Gao, Yingxv verfasserin aut Ma, Qian verfasserin aut Xia, Xiaohong verfasserin (orcid)0000-0001-9753-8998 aut Liu, Hongbo verfasserin aut Enthalten in Journal of solid state electrochemistry Springer Berlin Heidelberg, 1997 28(2023), 7 vom: 26. Nov., Seite 2233-2241 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:28 year:2023 number:7 day:26 month:11 pages:2233-2241 https://dx.doi.org/10.1007/s10008-023-05723-3 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 VZ 35.90 VZ AR 28 2023 7 26 11 2233-2241 |
| spelling |
10.1007/s10008-023-05723-3 doi (DE-627)SPR056480660 (SPR)s10008-023-05723-3-e DE-627 ger DE-627 rakwb eng 540 VZ 35.14 bkl 35.90 bkl Wang, Deping verfasserin aut Solvent-controlled synthesis of Ni-PTA MOFs as high performance anode material for Li-ion batteries 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Metal-organic frameworks are recognized as active electrode materials for rechargeable batteries due to their structural diversity, abundant electrochemical active sites and large ion diffusion channels. Herein, nickel-terephthalic acid metal-organic frameworks (Ni-PTA MOFs) with different crystal and morphology structures are synthesized via a facile solvothermal method by simply adjusting the nature of solvent. Due to the fewest guest molecules and porous structure, the Ni-PTA resulting from the combinations of DMF and EtOH exhibits the comparatively higher chemical/thermal stability and shortened ion diffusion pathway. As a result, it exhibits a high discharge/charge capacity of 2196.4 and 1762.3 mAh $ g^{−1} $ at the first cycle and retains 1300 mAh $ g^{−1} $ after 50 cycles at 100 mA $ g^{−1} $ when tested as anode materials for Li-ion batteries. Even when the current density reaches 4000 mA $ g^{−1} $, it maintains a capacity of 452 mAh $ g^{−1} $. This work provides possibilities for regulating the crystal and morphology structure of MOFs as high performance anode materials for lithium ion batteries. Metal-organic frameworks (dpeaa)DE-He213 Solvent (dpeaa)DE-He213 Guest molecules (dpeaa)DE-He213 Lithium-ion batteries (dpeaa)DE-He213 Hu, Wenming verfasserin aut Gao, Yingxv verfasserin aut Ma, Qian verfasserin aut Xia, Xiaohong verfasserin (orcid)0000-0001-9753-8998 aut Liu, Hongbo verfasserin aut Enthalten in Journal of solid state electrochemistry Springer Berlin Heidelberg, 1997 28(2023), 7 vom: 26. Nov., Seite 2233-2241 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:28 year:2023 number:7 day:26 month:11 pages:2233-2241 https://dx.doi.org/10.1007/s10008-023-05723-3 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 VZ 35.90 VZ AR 28 2023 7 26 11 2233-2241 |
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10.1007/s10008-023-05723-3 doi (DE-627)SPR056480660 (SPR)s10008-023-05723-3-e DE-627 ger DE-627 rakwb eng 540 VZ 35.14 bkl 35.90 bkl Wang, Deping verfasserin aut Solvent-controlled synthesis of Ni-PTA MOFs as high performance anode material for Li-ion batteries 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Metal-organic frameworks are recognized as active electrode materials for rechargeable batteries due to their structural diversity, abundant electrochemical active sites and large ion diffusion channels. Herein, nickel-terephthalic acid metal-organic frameworks (Ni-PTA MOFs) with different crystal and morphology structures are synthesized via a facile solvothermal method by simply adjusting the nature of solvent. Due to the fewest guest molecules and porous structure, the Ni-PTA resulting from the combinations of DMF and EtOH exhibits the comparatively higher chemical/thermal stability and shortened ion diffusion pathway. As a result, it exhibits a high discharge/charge capacity of 2196.4 and 1762.3 mAh $ g^{−1} $ at the first cycle and retains 1300 mAh $ g^{−1} $ after 50 cycles at 100 mA $ g^{−1} $ when tested as anode materials for Li-ion batteries. Even when the current density reaches 4000 mA $ g^{−1} $, it maintains a capacity of 452 mAh $ g^{−1} $. This work provides possibilities for regulating the crystal and morphology structure of MOFs as high performance anode materials for lithium ion batteries. Metal-organic frameworks (dpeaa)DE-He213 Solvent (dpeaa)DE-He213 Guest molecules (dpeaa)DE-He213 Lithium-ion batteries (dpeaa)DE-He213 Hu, Wenming verfasserin aut Gao, Yingxv verfasserin aut Ma, Qian verfasserin aut Xia, Xiaohong verfasserin (orcid)0000-0001-9753-8998 aut Liu, Hongbo verfasserin aut Enthalten in Journal of solid state electrochemistry Springer Berlin Heidelberg, 1997 28(2023), 7 vom: 26. Nov., Seite 2233-2241 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:28 year:2023 number:7 day:26 month:11 pages:2233-2241 https://dx.doi.org/10.1007/s10008-023-05723-3 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 VZ 35.90 VZ AR 28 2023 7 26 11 2233-2241 |
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10.1007/s10008-023-05723-3 doi (DE-627)SPR056480660 (SPR)s10008-023-05723-3-e DE-627 ger DE-627 rakwb eng 540 VZ 35.14 bkl 35.90 bkl Wang, Deping verfasserin aut Solvent-controlled synthesis of Ni-PTA MOFs as high performance anode material for Li-ion batteries 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Metal-organic frameworks are recognized as active electrode materials for rechargeable batteries due to their structural diversity, abundant electrochemical active sites and large ion diffusion channels. Herein, nickel-terephthalic acid metal-organic frameworks (Ni-PTA MOFs) with different crystal and morphology structures are synthesized via a facile solvothermal method by simply adjusting the nature of solvent. Due to the fewest guest molecules and porous structure, the Ni-PTA resulting from the combinations of DMF and EtOH exhibits the comparatively higher chemical/thermal stability and shortened ion diffusion pathway. As a result, it exhibits a high discharge/charge capacity of 2196.4 and 1762.3 mAh $ g^{−1} $ at the first cycle and retains 1300 mAh $ g^{−1} $ after 50 cycles at 100 mA $ g^{−1} $ when tested as anode materials for Li-ion batteries. Even when the current density reaches 4000 mA $ g^{−1} $, it maintains a capacity of 452 mAh $ g^{−1} $. This work provides possibilities for regulating the crystal and morphology structure of MOFs as high performance anode materials for lithium ion batteries. Metal-organic frameworks (dpeaa)DE-He213 Solvent (dpeaa)DE-He213 Guest molecules (dpeaa)DE-He213 Lithium-ion batteries (dpeaa)DE-He213 Hu, Wenming verfasserin aut Gao, Yingxv verfasserin aut Ma, Qian verfasserin aut Xia, Xiaohong verfasserin (orcid)0000-0001-9753-8998 aut Liu, Hongbo verfasserin aut Enthalten in Journal of solid state electrochemistry Springer Berlin Heidelberg, 1997 28(2023), 7 vom: 26. Nov., Seite 2233-2241 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:28 year:2023 number:7 day:26 month:11 pages:2233-2241 https://dx.doi.org/10.1007/s10008-023-05723-3 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 VZ 35.90 VZ AR 28 2023 7 26 11 2233-2241 |
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10.1007/s10008-023-05723-3 doi (DE-627)SPR056480660 (SPR)s10008-023-05723-3-e DE-627 ger DE-627 rakwb eng 540 VZ 35.14 bkl 35.90 bkl Wang, Deping verfasserin aut Solvent-controlled synthesis of Ni-PTA MOFs as high performance anode material for Li-ion batteries 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. Abstract Metal-organic frameworks are recognized as active electrode materials for rechargeable batteries due to their structural diversity, abundant electrochemical active sites and large ion diffusion channels. Herein, nickel-terephthalic acid metal-organic frameworks (Ni-PTA MOFs) with different crystal and morphology structures are synthesized via a facile solvothermal method by simply adjusting the nature of solvent. Due to the fewest guest molecules and porous structure, the Ni-PTA resulting from the combinations of DMF and EtOH exhibits the comparatively higher chemical/thermal stability and shortened ion diffusion pathway. As a result, it exhibits a high discharge/charge capacity of 2196.4 and 1762.3 mAh $ g^{−1} $ at the first cycle and retains 1300 mAh $ g^{−1} $ after 50 cycles at 100 mA $ g^{−1} $ when tested as anode materials for Li-ion batteries. Even when the current density reaches 4000 mA $ g^{−1} $, it maintains a capacity of 452 mAh $ g^{−1} $. This work provides possibilities for regulating the crystal and morphology structure of MOFs as high performance anode materials for lithium ion batteries. Metal-organic frameworks (dpeaa)DE-He213 Solvent (dpeaa)DE-He213 Guest molecules (dpeaa)DE-He213 Lithium-ion batteries (dpeaa)DE-He213 Hu, Wenming verfasserin aut Gao, Yingxv verfasserin aut Ma, Qian verfasserin aut Xia, Xiaohong verfasserin (orcid)0000-0001-9753-8998 aut Liu, Hongbo verfasserin aut Enthalten in Journal of solid state electrochemistry Springer Berlin Heidelberg, 1997 28(2023), 7 vom: 26. Nov., Seite 2233-2241 (DE-627)271175400 (DE-600)1478940-1 1433-0768 nnns volume:28 year:2023 number:7 day:26 month:11 pages:2233-2241 https://dx.doi.org/10.1007/s10008-023-05723-3 X:SPRINGER Resolving-System lizenzpflichtig Volltext SYSFLAG_0 GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 VZ 35.90 VZ AR 28 2023 7 26 11 2233-2241 |
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Wang, Deping @@aut@@ Hu, Wenming @@aut@@ Gao, Yingxv @@aut@@ Ma, Qian @@aut@@ Xia, Xiaohong @@aut@@ Liu, Hongbo @@aut@@ |
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Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Metal-organic frameworks are recognized as active electrode materials for rechargeable batteries due to their structural diversity, abundant electrochemical active sites and large ion diffusion channels. Herein, nickel-terephthalic acid metal-organic frameworks (Ni-PTA MOFs) with different crystal and morphology structures are synthesized via a facile solvothermal method by simply adjusting the nature of solvent. Due to the fewest guest molecules and porous structure, the Ni-PTA resulting from the combinations of DMF and EtOH exhibits the comparatively higher chemical/thermal stability and shortened ion diffusion pathway. As a result, it exhibits a high discharge/charge capacity of 2196.4 and 1762.3 mAh $ g^{−1} $ at the first cycle and retains 1300 mAh $ g^{−1} $ after 50 cycles at 100 mA $ g^{−1} $ when tested as anode materials for Li-ion batteries. Even when the current density reaches 4000 mA $ g^{−1} $, it maintains a capacity of 452 mAh $ g^{−1} $. 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Wang, Deping |
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Wang, Deping ddc 540 bkl 35.14 bkl 35.90 misc Metal-organic frameworks misc Solvent misc Guest molecules misc Lithium-ion batteries Solvent-controlled synthesis of Ni-PTA MOFs as high performance anode material for Li-ion batteries |
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540 VZ 35.14 bkl 35.90 bkl Solvent-controlled synthesis of Ni-PTA MOFs as high performance anode material for Li-ion batteries Metal-organic frameworks (dpeaa)DE-He213 Solvent (dpeaa)DE-He213 Guest molecules (dpeaa)DE-He213 Lithium-ion batteries (dpeaa)DE-He213 |
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solvent-controlled synthesis of ni-pta mofs as high performance anode material for li-ion batteries |
| title_auth |
Solvent-controlled synthesis of Ni-PTA MOFs as high performance anode material for Li-ion batteries |
| abstract |
Abstract Metal-organic frameworks are recognized as active electrode materials for rechargeable batteries due to their structural diversity, abundant electrochemical active sites and large ion diffusion channels. Herein, nickel-terephthalic acid metal-organic frameworks (Ni-PTA MOFs) with different crystal and morphology structures are synthesized via a facile solvothermal method by simply adjusting the nature of solvent. Due to the fewest guest molecules and porous structure, the Ni-PTA resulting from the combinations of DMF and EtOH exhibits the comparatively higher chemical/thermal stability and shortened ion diffusion pathway. As a result, it exhibits a high discharge/charge capacity of 2196.4 and 1762.3 mAh $ g^{−1} $ at the first cycle and retains 1300 mAh $ g^{−1} $ after 50 cycles at 100 mA $ g^{−1} $ when tested as anode materials for Li-ion batteries. Even when the current density reaches 4000 mA $ g^{−1} $, it maintains a capacity of 452 mAh $ g^{−1} $. This work provides possibilities for regulating the crystal and morphology structure of MOFs as high performance anode materials for lithium ion batteries. © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
| abstractGer |
Abstract Metal-organic frameworks are recognized as active electrode materials for rechargeable batteries due to their structural diversity, abundant electrochemical active sites and large ion diffusion channels. Herein, nickel-terephthalic acid metal-organic frameworks (Ni-PTA MOFs) with different crystal and morphology structures are synthesized via a facile solvothermal method by simply adjusting the nature of solvent. Due to the fewest guest molecules and porous structure, the Ni-PTA resulting from the combinations of DMF and EtOH exhibits the comparatively higher chemical/thermal stability and shortened ion diffusion pathway. As a result, it exhibits a high discharge/charge capacity of 2196.4 and 1762.3 mAh $ g^{−1} $ at the first cycle and retains 1300 mAh $ g^{−1} $ after 50 cycles at 100 mA $ g^{−1} $ when tested as anode materials for Li-ion batteries. Even when the current density reaches 4000 mA $ g^{−1} $, it maintains a capacity of 452 mAh $ g^{−1} $. This work provides possibilities for regulating the crystal and morphology structure of MOFs as high performance anode materials for lithium ion batteries. © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
| abstract_unstemmed |
Abstract Metal-organic frameworks are recognized as active electrode materials for rechargeable batteries due to their structural diversity, abundant electrochemical active sites and large ion diffusion channels. Herein, nickel-terephthalic acid metal-organic frameworks (Ni-PTA MOFs) with different crystal and morphology structures are synthesized via a facile solvothermal method by simply adjusting the nature of solvent. Due to the fewest guest molecules and porous structure, the Ni-PTA resulting from the combinations of DMF and EtOH exhibits the comparatively higher chemical/thermal stability and shortened ion diffusion pathway. As a result, it exhibits a high discharge/charge capacity of 2196.4 and 1762.3 mAh $ g^{−1} $ at the first cycle and retains 1300 mAh $ g^{−1} $ after 50 cycles at 100 mA $ g^{−1} $ when tested as anode materials for Li-ion batteries. Even when the current density reaches 4000 mA $ g^{−1} $, it maintains a capacity of 452 mAh $ g^{−1} $. This work provides possibilities for regulating the crystal and morphology structure of MOFs as high performance anode materials for lithium ion batteries. © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. |
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Solvent-controlled synthesis of Ni-PTA MOFs as high performance anode material for Li-ion batteries |
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Hu, Wenming Gao, Yingxv Ma, Qian Xia, Xiaohong Liu, Hongbo |
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| score |
7.399727 |