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...
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Autor*in:	Li, Min [verfasserIn] Ma, Wensheng [verfasserIn] Tan, Fuquan [verfasserIn] Yu, Bin [verfasserIn] Cheng, Guanhua [verfasserIn] Gao, Hui [verfasserIn] Zhang, Zhonghua [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2023

Schlagwörter:	Lithium ion batteries Fe Pyrolytic carbonization Ammonium ferric citrate In situ X-ray diffraction

Übergeordnetes Werk:	Enthalten in: Journal of power sources - New York, NY [u.a.] : Elsevier, 1976, 574
Übergeordnetes Werk:	volume:574

DOI / URN:	10.1016/j.jpowsour.2023.233146

Katalog-ID:	ELV009786368

Internformat


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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
773	0	8	\|i Enthalten in \|t Journal of power sources \|d New York, NY [u.a.] : Elsevier, 1976 \|g 574 \|h Online-Ressource \|w (DE-627)302718923 \|w (DE-600)1491915-1 \|w (DE-576)259483958 \|x 1873-2755 \|7 nnns
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912			\|a GBV_ILN_370
912			\|a GBV_ILN_602
912			\|a GBV_ILN_702
912			\|a GBV_ILN_2001
912			\|a GBV_ILN_2003
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912			\|a GBV_ILN_2007
912			\|a GBV_ILN_2008
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912			\|a GBV_ILN_2010
912			\|a GBV_ILN_2011
912			\|a GBV_ILN_2014
912			\|a GBV_ILN_2015
912			\|a GBV_ILN_2020
912			\|a GBV_ILN_2021
912			\|a GBV_ILN_2025
912			\|a GBV_ILN_2026
912			\|a GBV_ILN_2027
912			\|a GBV_ILN_2034
912			\|a GBV_ILN_2044
912			\|a GBV_ILN_2048
912			\|a GBV_ILN_2049
912			\|a GBV_ILN_2050
912			\|a GBV_ILN_2055
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912			\|a GBV_ILN_2059
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912			\|a GBV_ILN_2088
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912			\|a GBV_ILN_2110
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912			\|a GBV_ILN_4251
912			\|a GBV_ILN_4305
912			\|a GBV_ILN_4306
912			\|a GBV_ILN_4307
912			\|a GBV_ILN_4313
912			\|a GBV_ILN_4322
912			\|a GBV_ILN_4323
912			\|a GBV_ILN_4324
912			\|a GBV_ILN_4325
912			\|a GBV_ILN_4326
912			\|a GBV_ILN_4333
912			\|a GBV_ILN_4334
912			\|a GBV_ILN_4338
912			\|a GBV_ILN_4393
912			\|a GBV_ILN_4700
936	b	k	\|a 52.57 \|j Energiespeicherung \|q VZ
936	b	k	\|a 53.36 \|j Energiedirektumwandler \|j elektrische Energiespeicher \|q VZ
951			\|a AR
952			\|d 574

Indexfelder

author_variant	m l ml w m wm f t ft b y by g c gc h g hg z z zz
matchkey_str	article:18732755:2023----::
hierarchy_sort_str	2023
bklnumber	52.57 53.36
publishDate	2023
allfields	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
allfieldsSound	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
language	English
source	Enthalten in Journal of power sources 574 volume:574
sourceStr	Enthalten in Journal of power sources 574 volume:574
format_phy_str_mv	Article
bklname	Energiespeicherung Energiedirektumwandler elektrische Energiespeicher
institution	findex.gbv.de
topic_facet	Lithium ion batteries Fe Pyrolytic carbonization Ammonium ferric citrate In situ X-ray diffraction
dewey-raw	620
isfreeaccess_bool	false
container_title	Journal of power sources
authorswithroles_txt_mv	Li, Min @@aut@@ Ma, Wensheng @@aut@@ Tan, Fuquan @@aut@@ Yu, Bin @@aut@@ Cheng, Guanhua @@aut@@ Gao, Hui @@aut@@ Zhang, Zhonghua @@aut@@
publishDateDaySort_date	2023-01-01T00:00:00Z
hierarchy_top_id	302718923
dewey-sort	3620
id	ELV009786368
language_de	englisch
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author	Li, Min
spellingShingle	Li, Min ddc 620 bkl 52.57 bkl 53.36 misc Lithium ion batteries misc Fe misc Pyrolytic carbonization misc Ammonium ferric citrate misc In situ X-ray diffraction Fe
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topic_title	620 VZ 52.57 bkl 53.36 bkl Fe Lithium ion batteries Pyrolytic carbonization Ammonium ferric citrate In situ X-ray diffraction
topic	ddc 620 bkl 52.57 bkl 53.36 misc Lithium ion batteries misc Fe misc Pyrolytic carbonization misc Ammonium ferric citrate misc In situ X-ray diffraction
topic_unstemmed	ddc 620 bkl 52.57 bkl 53.36 misc Lithium ion batteries misc Fe misc Pyrolytic carbonization misc Ammonium ferric citrate misc In situ X-ray diffraction
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doi_str_mv	10.1016/j.jpowsour.2023.233146
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title_auth	Fe
abstract	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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title_short	Fe
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author2	Ma, Wensheng Tan, Fuquan Yu, Bin Cheng, Guanhua Gao, Hui Zhang, Zhonghua
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doi_str	10.1016/j.jpowsour.2023.233146
up_date	2024-07-07T00:21:02.224Z
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score	7.4005365

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