Metal–Organic Framework-Derived Nanoconfinements of CoF2 and Mixed-Conducting Wiring for High-Performance Metal Fluoride-Lithium Battery
Metal fluoride (MF) conversion cathodes theoretically show higher gravimetric and volumetric capacities than Ni- or Co-based intercalation oxide cathodes, which makes metal fluoride–lithium batteries promising candidates for next-generation high-energy-density batteries. However, their high-energy c...
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Published in | ACS nano Vol. 15; no. 1; pp. 1509 - 1518 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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American Chemical Society
26.01.2021
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Abstract | Metal fluoride (MF) conversion cathodes theoretically show higher gravimetric and volumetric capacities than Ni- or Co-based intercalation oxide cathodes, which makes metal fluoride–lithium batteries promising candidates for next-generation high-energy-density batteries. However, their high-energy characteristics are clouded by low-capacity utilization, large voltage hysteresis, and poor cycling stability of transition MF cathodes. A variety of reasons is responsible for this: poor reaction kinetics, low conductivities, unstable MF/electrolyte interfaces and dissolution of active species upon cycling. Herein, we combine the synthesis of the metal–organic-framework (MOF) with the low-temperature fluorination to prepare MOF-shaped CoF2@C nanocomposites that exhibit confinement of the CoF2 nanoparticles and efficient mixed-conducting wiring in the produced architecture. The ultrasmall CoF2 nanoparticles (5–20 nm on average) are uniformly covered by graphitic carbon walls and embedded in the porous carbon framework. Within the CoF2@C nanocomposite, the cross-linked carbon wall and interconnected nanopores serve as electron- and ion-conducting pathways, respectively, enabling a highly reversible conversion reaction of CoF2. As a result, the produced CoF2@C composite cathodes successfully restrain the above-mentioned challenges and demonstrate high-capacity utilization of ∼500 mAh g–1 at 0.2C, good rate capability (up to 2C), and long-term cycle stability over 400 cycles. Overall, the presented study not only reports on a simple composite design to achieve high-energy characteristics in CoF2–Li batteries but also may provide a general solution for many other metal fluoride–lithium batteries. |
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AbstractList | Metal fluoride (MF) conversion cathodes theoretically show higher gravimetric and volumetric capacities than Ni- or Co-based intercalation oxide cathodes, which makes metal fluoride–lithium batteries promising candidates for next-generation high-energy-density batteries. However, their high-energy characteristics are clouded by low-capacity utilization, large voltage hysteresis, and poor cycling stability of transition MF cathodes. A variety of reasons is responsible for this: poor reaction kinetics, low conductivities, unstable MF/electrolyte interfaces and dissolution of active species upon cycling. Herein, we combine the synthesis of the metal–organic-framework (MOF) with the low-temperature fluorination to prepare MOF-shaped CoF2@C nanocomposites that exhibit confinement of the CoF2 nanoparticles and efficient mixed-conducting wiring in the produced architecture. The ultrasmall CoF2 nanoparticles (5–20 nm on average) are uniformly covered by graphitic carbon walls and embedded in the porous carbon framework. Within the CoF2@C nanocomposite, the cross-linked carbon wall and interconnected nanopores serve as electron- and ion-conducting pathways, respectively, enabling a highly reversible conversion reaction of CoF2. As a result, the produced CoF2@C composite cathodes successfully restrain the above-mentioned challenges and demonstrate high-capacity utilization of ∼500 mAh g–1 at 0.2C, good rate capability (up to 2C), and long-term cycle stability over 400 cycles. Overall, the presented study not only reports on a simple composite design to achieve high-energy characteristics in CoF2–Li batteries but also may provide a general solution for many other metal fluoride–lithium batteries. Metal fluoride (MF) conversion cathodes theoretically show higher gravimetric and volumetric capacities than Ni- or Co-based intercalation oxide cathodes, which makes metal fluoride-lithium batteries promising candidates for next-generation high-energy-density batteries. However, their high-energy characteristics are clouded by low-capacity utilization, large voltage hysteresis, and poor cycling stability of transition MF cathodes. A variety of reasons is responsible for this: poor reaction kinetics, low conductivities, unstable MF/electrolyte interfaces and dissolution of active species upon cycling. Herein, we combine the synthesis of the metal-organic-framework (MOF) with the low-temperature fluorination to prepare MOF-shaped CoF2@C nanocomposites that exhibit confinement of the CoF2 nanoparticles and efficient mixed-conducting wiring in the produced architecture. The ultrasmall CoF2 nanoparticles (5-20 nm on average) are uniformly covered by graphitic carbon walls and embedded in the porous carbon framework. Within the CoF2@C nanocomposite, the cross-linked carbon wall and interconnected nanopores serve as electron- and ion-conducting pathways, respectively, enabling a highly reversible conversion reaction of CoF2. As a result, the produced CoF2@C composite cathodes successfully restrain the above-mentioned challenges and demonstrate high-capacity utilization of ∼500 mAh g-1 at 0.2C, good rate capability (up to 2C), and long-term cycle stability over 400 cycles. Overall, the presented study not only reports on a simple composite design to achieve high-energy characteristics in CoF2-Li batteries but also may provide a general solution for many other metal fluoride-lithium batteries.Metal fluoride (MF) conversion cathodes theoretically show higher gravimetric and volumetric capacities than Ni- or Co-based intercalation oxide cathodes, which makes metal fluoride-lithium batteries promising candidates for next-generation high-energy-density batteries. However, their high-energy characteristics are clouded by low-capacity utilization, large voltage hysteresis, and poor cycling stability of transition MF cathodes. A variety of reasons is responsible for this: poor reaction kinetics, low conductivities, unstable MF/electrolyte interfaces and dissolution of active species upon cycling. Herein, we combine the synthesis of the metal-organic-framework (MOF) with the low-temperature fluorination to prepare MOF-shaped CoF2@C nanocomposites that exhibit confinement of the CoF2 nanoparticles and efficient mixed-conducting wiring in the produced architecture. The ultrasmall CoF2 nanoparticles (5-20 nm on average) are uniformly covered by graphitic carbon walls and embedded in the porous carbon framework. Within the CoF2@C nanocomposite, the cross-linked carbon wall and interconnected nanopores serve as electron- and ion-conducting pathways, respectively, enabling a highly reversible conversion reaction of CoF2. As a result, the produced CoF2@C composite cathodes successfully restrain the above-mentioned challenges and demonstrate high-capacity utilization of ∼500 mAh g-1 at 0.2C, good rate capability (up to 2C), and long-term cycle stability over 400 cycles. Overall, the presented study not only reports on a simple composite design to achieve high-energy characteristics in CoF2-Li batteries but also may provide a general solution for many other metal fluoride-lithium batteries. |
Author | Wu, Feixiang Maier, Joachim Zhang, Mingyu Srot, Vesna Chen, Shuangqiang Yu, Yan van Aken, Peter A Wang, Yong |
AuthorAffiliation | Department of Chemical Engineering, School of Environmental and Chemical Engineering School of Metallurgy and Environment, Engineering Research Center of the Ministry of Education for Advanced Battery Materials State Key Laboratory of Powder Metallurgy Dalian National Laboratory for Clean Energy (DNL), Chinese Academy of Sciences (CAS) State Key Laboratory of Fire Science and Hefei National Laboratory for Physical Sciences at the Microscale, Department of Materials Science and Engineering, CAS Key Laboratory of Materials for Energy Conversion |
AuthorAffiliation_xml | – name: State Key Laboratory of Powder Metallurgy – name: Department of Chemical Engineering, School of Environmental and Chemical Engineering – name: Dalian National Laboratory for Clean Energy (DNL), Chinese Academy of Sciences (CAS) – name: State Key Laboratory of Fire Science and Hefei National Laboratory for Physical Sciences at the Microscale, Department of Materials Science and Engineering, CAS Key Laboratory of Materials for Energy Conversion – name: School of Metallurgy and Environment, Engineering Research Center of the Ministry of Education for Advanced Battery Materials |
Author_xml | – sequence: 1 givenname: Feixiang orcidid: 0000-0002-9688-2428 surname: Wu fullname: Wu, Feixiang email: feixiang.wu@csu.edu.cn organization: School of Metallurgy and Environment, Engineering Research Center of the Ministry of Education for Advanced Battery Materials – sequence: 2 givenname: Vesna orcidid: 0000-0001-8864-0931 surname: Srot fullname: Srot, Vesna – sequence: 3 givenname: Shuangqiang orcidid: 0000-0002-9111-1691 surname: Chen fullname: Chen, Shuangqiang email: chensq@shu.edu.cn organization: Department of Chemical Engineering, School of Environmental and Chemical Engineering – sequence: 4 givenname: Mingyu orcidid: 0000-0001-7907-3971 surname: Zhang fullname: Zhang, Mingyu organization: State Key Laboratory of Powder Metallurgy – sequence: 5 givenname: Peter A surname: van Aken fullname: van Aken, Peter A – sequence: 6 givenname: Yong orcidid: 0000-0003-3489-7672 surname: Wang fullname: Wang, Yong organization: Department of Chemical Engineering, School of Environmental and Chemical Engineering – sequence: 7 givenname: Joachim surname: Maier fullname: Maier, Joachim – sequence: 8 givenname: Yan orcidid: 0000-0002-3685-7773 surname: Yu fullname: Yu, Yan email: yanyumse@ustc.edu.cn organization: Dalian National Laboratory for Clean Energy (DNL), Chinese Academy of Sciences (CAS) |
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