MOF-Derived ZnS Nanodots/Ti3C2T x MXene Hybrids Boosting Superior Lithium Storage Performance
Abstract ZnS has great potentials as an anode for lithium storage because of its high theoretical capacity and resource abundance; however, the large volume expansion accompanied with structural collapse and low conductivity of ZnS cause severe capacity fading and inferior rate capability during lit...
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Published in | Nano-micro letters Vol. 13; no. 1; pp. 1 - 17 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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SpringerOpen
01.12.2021
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ISSN | 2311-6706 2150-5551 |
DOI | 10.1007/s40820-021-00728-x |
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Abstract | Abstract ZnS has great potentials as an anode for lithium storage because of its high theoretical capacity and resource abundance; however, the large volume expansion accompanied with structural collapse and low conductivity of ZnS cause severe capacity fading and inferior rate capability during lithium storage. Herein, 0D-2D ZnS nanodots/Ti3C2T x MXene hybrids are prepared by anchoring ZnS nanodots on Ti3C2T x MXene nanosheets through coordination modulation between MXene and MOF precursor (ZIF-8) followed with sulfidation. The MXene substrate coupled with the ZnS nanodots can synergistically accommodate volume variation of ZnS over charge–discharge to realize stable cyclability. As revealed by XPS characterizations and DFT calculations, the strong interfacial interaction between ZnS nanodots and MXene nanosheets can boost fast electron/lithium-ion transfer to achieve excellent electrochemical activity and kinetics for lithium storage. Thereby, the as-prepared ZnS nanodots/MXene hybrid exhibits a high capacity of 726.8 mAh g−1 at 30 mA g−1, superior cyclic stability (462.8 mAh g−1 after 1000 cycles at 0.5 A g−1), and excellent rate performance. The present results provide new insights into the understanding of the lithium storage mechanism of ZnS and the revealing of the effects of interfacial interaction on lithium storage performance enhancement. |
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AbstractList | Abstract ZnS has great potentials as an anode for lithium storage because of its high theoretical capacity and resource abundance; however, the large volume expansion accompanied with structural collapse and low conductivity of ZnS cause severe capacity fading and inferior rate capability during lithium storage. Herein, 0D-2D ZnS nanodots/Ti3C2T x MXene hybrids are prepared by anchoring ZnS nanodots on Ti3C2T x MXene nanosheets through coordination modulation between MXene and MOF precursor (ZIF-8) followed with sulfidation. The MXene substrate coupled with the ZnS nanodots can synergistically accommodate volume variation of ZnS over charge–discharge to realize stable cyclability. As revealed by XPS characterizations and DFT calculations, the strong interfacial interaction between ZnS nanodots and MXene nanosheets can boost fast electron/lithium-ion transfer to achieve excellent electrochemical activity and kinetics for lithium storage. Thereby, the as-prepared ZnS nanodots/MXene hybrid exhibits a high capacity of 726.8 mAh g−1 at 30 mA g−1, superior cyclic stability (462.8 mAh g−1 after 1000 cycles at 0.5 A g−1), and excellent rate performance. The present results provide new insights into the understanding of the lithium storage mechanism of ZnS and the revealing of the effects of interfacial interaction on lithium storage performance enhancement. |
Author | Lianli Wang Huan Liu Xin Zhang Huiling Du Qizhen Zhu Peng Zhang Rupeng Zhang Bin Xu Bin Cao |
Author_xml | – sequence: 1 fullname: Bin Cao organization: State Key Laboratory of Organic–Inorganic Composites, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology – sequence: 2 fullname: Huan Liu organization: State Key Laboratory of Organic–Inorganic Composites, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology – sequence: 3 fullname: Xin Zhang organization: State Key Laboratory of Organic–Inorganic Composites, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology – sequence: 4 fullname: Peng Zhang organization: State Key Laboratory of Organic–Inorganic Composites, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology – sequence: 5 fullname: Qizhen Zhu organization: State Key Laboratory of Organic–Inorganic Composites, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology – sequence: 6 fullname: Huiling Du organization: College of Materials Science and Engineering, Xi’an University of Science and Technology – sequence: 7 fullname: Lianli Wang organization: College of Materials Science and Engineering, Xi’an University of Science and Technology – sequence: 8 fullname: Rupeng Zhang organization: State Key Laboratory of Organic–Inorganic Composites, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology – sequence: 9 fullname: Bin Xu organization: State Key Laboratory of Organic–Inorganic Composites, Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology |
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SubjectTerms | Heterointerface Interfacial interaction Lithium-ion batteries MOF Ti3C2T x MXene ZnS |
Title | MOF-Derived ZnS Nanodots/Ti3C2T x MXene Hybrids Boosting Superior Lithium Storage Performance |
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