Fe
Magnetite (Fe3O4) has become a potential anode material in lithium ion batteries (LIBs) because of its high theoretical capacity and low cost, but is impeded for application by its low conductivity and large volume change during cycling. Herein, the Fe3O4C-500 composite was fabricated via the one-st...
Ausführliche Beschreibung
Autor*in: |
Li, Min [verfasserIn] Ma, Wensheng [verfasserIn] Tan, Fuquan [verfasserIn] Yu, Bin [verfasserIn] Cheng, Guanhua [verfasserIn] Gao, Hui [verfasserIn] Zhang, Zhonghua [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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Übergeordnetes Werk: |
Enthalten in: Journal of power sources - New York, NY [u.a.] : Elsevier, 1976, 574 |
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Übergeordnetes Werk: |
volume:574 |
DOI / URN: |
10.1016/j.jpowsour.2023.233146 |
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Katalog-ID: |
ELV009786368 |
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520 | |a Magnetite (Fe3O4) has become a potential anode material in lithium ion batteries (LIBs) because of its high theoretical capacity and low cost, but is impeded for application by its low conductivity and large volume change during cycling. Herein, the Fe3O4C-500 composite was fabricated via the one-step pyrolytic carbonization of commercial ammonium ferric citrate (AFC), which is simple and environmentally friendly. As an anode in LIBs, the Fe3O4@C-500 electrode shows superior specific capacity, long cycling stability and excellent rate performance. Such remarkable performance can be attributed to the formation of the architecture with carbon (C) matrix, not only buffering the volume change and inhibiting the aggregation of internal Fe3O4 nanoparticles during (de)lithiation, but also elevating the electron conductivity. In situ X-ray diffraction (XRD) results demonstrate that the (de)lithiated mechanism of the Fe3O4@C-500 electrode involves a full electrochemically-driven amorphization upon cycling. Furthermore, the full cell assembled with Fe3O4@C-500 and LiFePO4 (LFP) electrodes shows outstanding electrochemical performance, demonstrating its practical energy storage application. | ||
650 | 4 | |a Lithium ion batteries | |
650 | 4 | |a Fe | |
650 | 4 | |a Pyrolytic carbonization | |
650 | 4 | |a Ammonium ferric citrate | |
650 | 4 | |a In situ X-ray diffraction | |
700 | 1 | |a Ma, Wensheng |e verfasserin |4 aut | |
700 | 1 | |a Tan, Fuquan |e verfasserin |4 aut | |
700 | 1 | |a Yu, Bin |e verfasserin |4 aut | |
700 | 1 | |a Cheng, Guanhua |e verfasserin |4 aut | |
700 | 1 | |a Gao, Hui |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Zhonghua |e verfasserin |4 aut | |
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10.1016/j.jpowsour.2023.233146 doi (DE-627)ELV009786368 (ELSEVIER)S0378-7753(23)00521-9 DE-627 ger DE-627 rda eng 620 VZ 52.57 bkl 53.36 bkl Li, Min verfasserin aut Fe 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Magnetite (Fe3O4) has become a potential anode material in lithium ion batteries (LIBs) because of its high theoretical capacity and low cost, but is impeded for application by its low conductivity and large volume change during cycling. Herein, the Fe3O4C-500 composite was fabricated via the one-step pyrolytic carbonization of commercial ammonium ferric citrate (AFC), which is simple and environmentally friendly. As an anode in LIBs, the Fe3O4@C-500 electrode shows superior specific capacity, long cycling stability and excellent rate performance. Such remarkable performance can be attributed to the formation of the architecture with carbon (C) matrix, not only buffering the volume change and inhibiting the aggregation of internal Fe3O4 nanoparticles during (de)lithiation, but also elevating the electron conductivity. In situ X-ray diffraction (XRD) results demonstrate that the (de)lithiated mechanism of the Fe3O4@C-500 electrode involves a full electrochemically-driven amorphization upon cycling. Furthermore, the full cell assembled with Fe3O4@C-500 and LiFePO4 (LFP) electrodes shows outstanding electrochemical performance, demonstrating its practical energy storage application. Lithium ion batteries Fe Pyrolytic carbonization Ammonium ferric citrate In situ X-ray diffraction Ma, Wensheng verfasserin aut Tan, Fuquan verfasserin aut Yu, Bin verfasserin aut Cheng, Guanhua verfasserin aut Gao, Hui verfasserin aut Zhang, Zhonghua verfasserin aut Enthalten in Journal of power sources New York, NY [u.a.] : Elsevier, 1976 574 Online-Ressource (DE-627)302718923 (DE-600)1491915-1 (DE-576)259483958 1873-2755 nnns volume:574 GBV_USEFLAG_U SYSFLAG_U GBV_ELV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 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_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 52.57 Energiespeicherung VZ 53.36 Energiedirektumwandler elektrische Energiespeicher VZ AR 574 |
spelling |
10.1016/j.jpowsour.2023.233146 doi (DE-627)ELV009786368 (ELSEVIER)S0378-7753(23)00521-9 DE-627 ger DE-627 rda eng 620 VZ 52.57 bkl 53.36 bkl Li, Min verfasserin aut Fe 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Magnetite (Fe3O4) has become a potential anode material in lithium ion batteries (LIBs) because of its high theoretical capacity and low cost, but is impeded for application by its low conductivity and large volume change during cycling. Herein, the Fe3O4C-500 composite was fabricated via the one-step pyrolytic carbonization of commercial ammonium ferric citrate (AFC), which is simple and environmentally friendly. As an anode in LIBs, the Fe3O4@C-500 electrode shows superior specific capacity, long cycling stability and excellent rate performance. Such remarkable performance can be attributed to the formation of the architecture with carbon (C) matrix, not only buffering the volume change and inhibiting the aggregation of internal Fe3O4 nanoparticles during (de)lithiation, but also elevating the electron conductivity. In situ X-ray diffraction (XRD) results demonstrate that the (de)lithiated mechanism of the Fe3O4@C-500 electrode involves a full electrochemically-driven amorphization upon cycling. Furthermore, the full cell assembled with Fe3O4@C-500 and LiFePO4 (LFP) electrodes shows outstanding electrochemical performance, demonstrating its practical energy storage application. Lithium ion batteries Fe Pyrolytic carbonization Ammonium ferric citrate In situ X-ray diffraction Ma, Wensheng verfasserin aut Tan, Fuquan verfasserin aut Yu, Bin verfasserin aut Cheng, Guanhua verfasserin aut Gao, Hui verfasserin aut Zhang, Zhonghua verfasserin aut Enthalten in Journal of power sources New York, NY [u.a.] : Elsevier, 1976 574 Online-Ressource (DE-627)302718923 (DE-600)1491915-1 (DE-576)259483958 1873-2755 nnns volume:574 GBV_USEFLAG_U SYSFLAG_U GBV_ELV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 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_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 52.57 Energiespeicherung VZ 53.36 Energiedirektumwandler elektrische Energiespeicher VZ AR 574 |
allfields_unstemmed |
10.1016/j.jpowsour.2023.233146 doi (DE-627)ELV009786368 (ELSEVIER)S0378-7753(23)00521-9 DE-627 ger DE-627 rda eng 620 VZ 52.57 bkl 53.36 bkl Li, Min verfasserin aut Fe 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Magnetite (Fe3O4) has become a potential anode material in lithium ion batteries (LIBs) because of its high theoretical capacity and low cost, but is impeded for application by its low conductivity and large volume change during cycling. Herein, the Fe3O4C-500 composite was fabricated via the one-step pyrolytic carbonization of commercial ammonium ferric citrate (AFC), which is simple and environmentally friendly. As an anode in LIBs, the Fe3O4@C-500 electrode shows superior specific capacity, long cycling stability and excellent rate performance. Such remarkable performance can be attributed to the formation of the architecture with carbon (C) matrix, not only buffering the volume change and inhibiting the aggregation of internal Fe3O4 nanoparticles during (de)lithiation, but also elevating the electron conductivity. In situ X-ray diffraction (XRD) results demonstrate that the (de)lithiated mechanism of the Fe3O4@C-500 electrode involves a full electrochemically-driven amorphization upon cycling. Furthermore, the full cell assembled with Fe3O4@C-500 and LiFePO4 (LFP) electrodes shows outstanding electrochemical performance, demonstrating its practical energy storage application. Lithium ion batteries Fe Pyrolytic carbonization Ammonium ferric citrate In situ X-ray diffraction Ma, Wensheng verfasserin aut Tan, Fuquan verfasserin aut Yu, Bin verfasserin aut Cheng, Guanhua verfasserin aut Gao, Hui verfasserin aut Zhang, Zhonghua verfasserin aut Enthalten in Journal of power sources New York, NY [u.a.] : Elsevier, 1976 574 Online-Ressource (DE-627)302718923 (DE-600)1491915-1 (DE-576)259483958 1873-2755 nnns volume:574 GBV_USEFLAG_U SYSFLAG_U GBV_ELV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 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_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 52.57 Energiespeicherung VZ 53.36 Energiedirektumwandler elektrische Energiespeicher VZ AR 574 |
allfieldsGer |
10.1016/j.jpowsour.2023.233146 doi (DE-627)ELV009786368 (ELSEVIER)S0378-7753(23)00521-9 DE-627 ger DE-627 rda eng 620 VZ 52.57 bkl 53.36 bkl Li, Min verfasserin aut Fe 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Magnetite (Fe3O4) has become a potential anode material in lithium ion batteries (LIBs) because of its high theoretical capacity and low cost, but is impeded for application by its low conductivity and large volume change during cycling. Herein, the Fe3O4C-500 composite was fabricated via the one-step pyrolytic carbonization of commercial ammonium ferric citrate (AFC), which is simple and environmentally friendly. As an anode in LIBs, the Fe3O4@C-500 electrode shows superior specific capacity, long cycling stability and excellent rate performance. Such remarkable performance can be attributed to the formation of the architecture with carbon (C) matrix, not only buffering the volume change and inhibiting the aggregation of internal Fe3O4 nanoparticles during (de)lithiation, but also elevating the electron conductivity. In situ X-ray diffraction (XRD) results demonstrate that the (de)lithiated mechanism of the Fe3O4@C-500 electrode involves a full electrochemically-driven amorphization upon cycling. Furthermore, the full cell assembled with Fe3O4@C-500 and LiFePO4 (LFP) electrodes shows outstanding electrochemical performance, demonstrating its practical energy storage application. Lithium ion batteries Fe Pyrolytic carbonization Ammonium ferric citrate In situ X-ray diffraction Ma, Wensheng verfasserin aut Tan, Fuquan verfasserin aut Yu, Bin verfasserin aut Cheng, Guanhua verfasserin aut Gao, Hui verfasserin aut Zhang, Zhonghua verfasserin aut Enthalten in Journal of power sources New York, NY [u.a.] : Elsevier, 1976 574 Online-Ressource (DE-627)302718923 (DE-600)1491915-1 (DE-576)259483958 1873-2755 nnns volume:574 GBV_USEFLAG_U SYSFLAG_U GBV_ELV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 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_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 52.57 Energiespeicherung VZ 53.36 Energiedirektumwandler elektrische Energiespeicher VZ AR 574 |
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10.1016/j.jpowsour.2023.233146 doi (DE-627)ELV009786368 (ELSEVIER)S0378-7753(23)00521-9 DE-627 ger DE-627 rda eng 620 VZ 52.57 bkl 53.36 bkl Li, Min verfasserin aut Fe 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Magnetite (Fe3O4) has become a potential anode material in lithium ion batteries (LIBs) because of its high theoretical capacity and low cost, but is impeded for application by its low conductivity and large volume change during cycling. Herein, the Fe3O4C-500 composite was fabricated via the one-step pyrolytic carbonization of commercial ammonium ferric citrate (AFC), which is simple and environmentally friendly. As an anode in LIBs, the Fe3O4@C-500 electrode shows superior specific capacity, long cycling stability and excellent rate performance. Such remarkable performance can be attributed to the formation of the architecture with carbon (C) matrix, not only buffering the volume change and inhibiting the aggregation of internal Fe3O4 nanoparticles during (de)lithiation, but also elevating the electron conductivity. In situ X-ray diffraction (XRD) results demonstrate that the (de)lithiated mechanism of the Fe3O4@C-500 electrode involves a full electrochemically-driven amorphization upon cycling. Furthermore, the full cell assembled with Fe3O4@C-500 and LiFePO4 (LFP) electrodes shows outstanding electrochemical performance, demonstrating its practical energy storage application. Lithium ion batteries Fe Pyrolytic carbonization Ammonium ferric citrate In situ X-ray diffraction Ma, Wensheng verfasserin aut Tan, Fuquan verfasserin aut Yu, Bin verfasserin aut Cheng, Guanhua verfasserin aut Gao, Hui verfasserin aut Zhang, Zhonghua verfasserin aut Enthalten in Journal of power sources New York, NY [u.a.] : Elsevier, 1976 574 Online-Ressource (DE-627)302718923 (DE-600)1491915-1 (DE-576)259483958 1873-2755 nnns volume:574 GBV_USEFLAG_U SYSFLAG_U GBV_ELV GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 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_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 52.57 Energiespeicherung VZ 53.36 Energiedirektumwandler elektrische Energiespeicher VZ AR 574 |
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Li, Min @@aut@@ Ma, Wensheng @@aut@@ Tan, Fuquan @@aut@@ Yu, Bin @@aut@@ Cheng, Guanhua @@aut@@ Gao, Hui @@aut@@ Zhang, Zhonghua @@aut@@ |
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620 VZ 52.57 bkl 53.36 bkl Fe Lithium ion batteries Pyrolytic carbonization Ammonium ferric citrate In situ X-ray diffraction |
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Magnetite (Fe3O4) has become a potential anode material in lithium ion batteries (LIBs) because of its high theoretical capacity and low cost, but is impeded for application by its low conductivity and large volume change during cycling. Herein, the Fe3O4C-500 composite was fabricated via the one-step pyrolytic carbonization of commercial ammonium ferric citrate (AFC), which is simple and environmentally friendly. As an anode in LIBs, the Fe3O4@C-500 electrode shows superior specific capacity, long cycling stability and excellent rate performance. Such remarkable performance can be attributed to the formation of the architecture with carbon (C) matrix, not only buffering the volume change and inhibiting the aggregation of internal Fe3O4 nanoparticles during (de)lithiation, but also elevating the electron conductivity. In situ X-ray diffraction (XRD) results demonstrate that the (de)lithiated mechanism of the Fe3O4@C-500 electrode involves a full electrochemically-driven amorphization upon cycling. Furthermore, the full cell assembled with Fe3O4@C-500 and LiFePO4 (LFP) electrodes shows outstanding electrochemical performance, demonstrating its practical energy storage application. |
abstractGer |
Magnetite (Fe3O4) has become a potential anode material in lithium ion batteries (LIBs) because of its high theoretical capacity and low cost, but is impeded for application by its low conductivity and large volume change during cycling. Herein, the Fe3O4C-500 composite was fabricated via the one-step pyrolytic carbonization of commercial ammonium ferric citrate (AFC), which is simple and environmentally friendly. As an anode in LIBs, the Fe3O4@C-500 electrode shows superior specific capacity, long cycling stability and excellent rate performance. Such remarkable performance can be attributed to the formation of the architecture with carbon (C) matrix, not only buffering the volume change and inhibiting the aggregation of internal Fe3O4 nanoparticles during (de)lithiation, but also elevating the electron conductivity. In situ X-ray diffraction (XRD) results demonstrate that the (de)lithiated mechanism of the Fe3O4@C-500 electrode involves a full electrochemically-driven amorphization upon cycling. Furthermore, the full cell assembled with Fe3O4@C-500 and LiFePO4 (LFP) electrodes shows outstanding electrochemical performance, demonstrating its practical energy storage application. |
abstract_unstemmed |
Magnetite (Fe3O4) has become a potential anode material in lithium ion batteries (LIBs) because of its high theoretical capacity and low cost, but is impeded for application by its low conductivity and large volume change during cycling. Herein, the Fe3O4C-500 composite was fabricated via the one-step pyrolytic carbonization of commercial ammonium ferric citrate (AFC), which is simple and environmentally friendly. As an anode in LIBs, the Fe3O4@C-500 electrode shows superior specific capacity, long cycling stability and excellent rate performance. Such remarkable performance can be attributed to the formation of the architecture with carbon (C) matrix, not only buffering the volume change and inhibiting the aggregation of internal Fe3O4 nanoparticles during (de)lithiation, but also elevating the electron conductivity. In situ X-ray diffraction (XRD) results demonstrate that the (de)lithiated mechanism of the Fe3O4@C-500 electrode involves a full electrochemically-driven amorphization upon cycling. Furthermore, the full cell assembled with Fe3O4@C-500 and LiFePO4 (LFP) electrodes shows outstanding electrochemical performance, demonstrating its practical energy storage application. |
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