Suppressing the P2–OP4 phase transition of single-crystal P2-type Ni/Zn/Mn-based layered oxide for advanced sodium-ion batteries
P2-type layered Na0.66Ni0.26Zn0.07Mn0.67O2 (NNZM) is expected to be a competitive alternative to lithium layered oxide due to its high-energy-density, low production cost, and high-speed Na+ ion transport channels. However, it is still necessary to further improve its air stability and cycle life to...
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Published in | Powder technology Vol. 448; p. 120314 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.12.2024
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Abstract | P2-type layered Na0.66Ni0.26Zn0.07Mn0.67O2 (NNZM) is expected to be a competitive alternative to lithium layered oxide due to its high-energy-density, low production cost, and high-speed Na+ ion transport channels. However, it is still necessary to further improve its air stability and cycle life to meet the needs of practical applications. Single crystals with micron-scale have smaller specific surface area and greater packing density, which can improve air stability and cycle life compared to the traditional polycrystalline. Herein, single-crystal Na0.66Ni0.26Zn0.07Mn0.67O2 (SC-NNZM) is prepared by using Na2MoO4 as the molten salt. Driven by molten salt Na2MoO4, regular hexagonal prism morphology SC-NNZM with a median diameter (D50) of 7.86 μm and the (001) plane-dominated structure is obtained, larger than that (5.05 μm) of single-crystal C-NNZM without Na2MoO4, implying that specific surface area of SC-NNZM is smaller than that of C-NNZM, thereby reducing the contact area of SC-NNZM with the electrolyte, which is good for suppressing both harmful interface side-reactions and phase transitions at high voltages. Therefore, SC-NNZM exhibits 95.44 % capacity retention at 100 mA g−1 after 100 cycles, higher than C-NNZM (86.09 %). Moreover, rate capability of SC-NNZM is also higher than that of C-NNZM. This study provides a new strategy for inducing crystal plane growth that is conducive to the structure stability of single-crystal layered oxide at high voltages.
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•Single-crystal P2-type layered Na0.66Ni0.26Zn0.07Mn0.67O2 (SC-NNZM) has (001) plane-dominated structure.•SC-NNZM has smaller specific surface area and faster Na+ ion diffusion kinetics.•SC-NNZM has larger the (002) interplanar spacing and smaller lattice strain.•P2–OP4 phase transition of SC-NNZM at high voltage is restrained.•SC-NNZM can delivers excellent cycling stability and rate capability. |
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AbstractList | P2-type layered Na0.66Ni0.26Zn0.07Mn0.67O2 (NNZM) is expected to be a competitive alternative to lithium layered oxide due to its high-energy-density, low production cost, and high-speed Na+ ion transport channels. However, it is still necessary to further improve its air stability and cycle life to meet the needs of practical applications. Single crystals with micron-scale have smaller specific surface area and greater packing density, which can improve air stability and cycle life compared to the traditional polycrystalline. Herein, single-crystal Na0.66Ni0.26Zn0.07Mn0.67O2 (SC-NNZM) is prepared by using Na2MoO4 as the molten salt. Driven by molten salt Na2MoO4, regular hexagonal prism morphology SC-NNZM with a median diameter (D50) of 7.86 μm and the (001) plane-dominated structure is obtained, larger than that (5.05 μm) of single-crystal C-NNZM without Na2MoO4, implying that specific surface area of SC-NNZM is smaller than that of C-NNZM, thereby reducing the contact area of SC-NNZM with the electrolyte, which is good for suppressing both harmful interface side-reactions and phase transitions at high voltages. Therefore, SC-NNZM exhibits 95.44 % capacity retention at 100 mA g−1 after 100 cycles, higher than C-NNZM (86.09 %). Moreover, rate capability of SC-NNZM is also higher than that of C-NNZM. This study provides a new strategy for inducing crystal plane growth that is conducive to the structure stability of single-crystal layered oxide at high voltages.
[Display omitted]
•Single-crystal P2-type layered Na0.66Ni0.26Zn0.07Mn0.67O2 (SC-NNZM) has (001) plane-dominated structure.•SC-NNZM has smaller specific surface area and faster Na+ ion diffusion kinetics.•SC-NNZM has larger the (002) interplanar spacing and smaller lattice strain.•P2–OP4 phase transition of SC-NNZM at high voltage is restrained.•SC-NNZM can delivers excellent cycling stability and rate capability. |
ArticleNumber | 120314 |
Author | Song, Miaoyan Chen, Ming Wu, Wenwei Xie, Junzhou Tan, Zhaohong Wu, Xuehang Xu, Lin Qiu, Shiming |
Author_xml | – sequence: 1 givenname: Lin surname: Xu fullname: Xu, Lin organization: School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, PR China – sequence: 2 givenname: Miaoyan surname: Song fullname: Song, Miaoyan organization: School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, PR China – sequence: 3 givenname: Junzhou surname: Xie fullname: Xie, Junzhou organization: School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, PR China – sequence: 4 givenname: Ming surname: Chen fullname: Chen, Ming organization: School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, PR China – sequence: 5 givenname: Wenwei surname: Wu fullname: Wu, Wenwei email: gxuwuwenwei@aliyun.com, wuwenwei@gxu.edu.cn organization: School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, PR China – sequence: 6 givenname: Zhaohong surname: Tan fullname: Tan, Zhaohong organization: School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, PR China – sequence: 7 givenname: Shiming surname: Qiu fullname: Qiu, Shiming organization: Chongzuo Key Laboratory of Comprehensive Utilization Technology of Manganese Resources, Guangxi Key Laboratory for High-value Utilization of Manganese Resources, College of Chemistry and Biological Engineering, Guangxi Minzu Normal University, Chongzuo 532200, PR China – sequence: 8 givenname: Xuehang surname: Wu fullname: Wu, Xuehang email: xhwu@gxu.edu.cn organization: School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, PR China |
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