| Orientation-Dependent Lithium Miscibility Gap in LiFePO4 |
| Li, ZJ; Yang, JX; Li, CJ; Wang, SC; Zhang, L; Zhu, KJ; Wang, XH; Wang, XH (reprint author), Chinese Acad Sci, Shenyang Natl Lab Mat Sci, Inst Met Res, Shenyang 110016, Liaoning, Peoples R China.
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| 2018-02-13
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发表期刊 | CHEMISTRY OF MATERIALS
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ISSN | 0897-4756
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卷号 | 30期号:3页码:874-878 |
摘要 | [100](Pnma) is believed to be a tough diffusion direction for Li+ in LiFePO4, leading to the belief that the rate performance of [100]-oriented LiFePO4 is poor. Recent work revealed that reducing the dimension of the LiFePO4 phase to 12 nm in the [100] direction increased the extent of Li solid solution between LiFePO4 and FePO4, which produced an increase in the active population and excellent rate performance, but the lithiation/delithiation mechanism for this interesting phenomenon remains to be unraveled. Here we report, by using operando X-ray diffraction, the phase transition path involved in the lithiation/delithiation process is single-phase featured. This work presents one of the first experimental demonstrations that decreasing the dimension of LiFePO4 in the [100] direction to the LiFePO4/FePO4 equilibrium phase boundary width can improve the solid solubility of both the end solid solutions (Li alpha FePO4 and Li1-beta FePO4) and decrease the miscibility gap of LiFePO4, demonstrating a highly orientation-dependent lithium miscibility gap.; [100](Pnma) is believed to be a tough diffusion direction for Li+ in LiFePO4, leading to the belief that the rate performance of [100]-oriented LiFePO4 is poor. Recent work revealed that reducing the dimension of the LiFePO4 phase to 12 nm in the [100] direction increased the extent of Li solid solution between LiFePO4 and FePO4, which produced an increase in the active population and excellent rate performance, but the lithiation/delithiation mechanism for this interesting phenomenon remains to be unraveled. Here we report, by using operando X-ray diffraction, the phase transition path involved in the lithiation/delithiation process is single-phase featured. This work presents one of the first experimental demonstrations that decreasing the dimension of LiFePO4 in the [100] direction to the LiFePO4/FePO4 equilibrium phase boundary width can improve the solid solubility of both the end solid solutions (Li alpha FePO4 and Li1-beta FePO4) and decrease the miscibility gap of LiFePO4, demonstrating a highly orientation-dependent lithium miscibility gap. |
部门归属 | [li, zhaojin
; yang, jinxing
; li, changji
; wang, sucheng
; zhang, lei
; wang, xiaohui] chinese acad sci, shenyang natl lab mat sci, inst met res, shenyang 110016, liaoning, peoples r china
; [li, zhaojin] univ chinese acad sci, beijing 100039, peoples r china
; [yang, jinxing] univ sci & technol china, sch mat sci & engn, shenyang 110016, liaoning, peoples r china
; [zhu, kongjun] nanjing univ aeronaut & astronaut, state key lab mech & control mech struct, nanjing 210016, jiangsu, peoples r china
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关键词 | Phase-transition
Room-temperature
Li-insertion/extraction
Coherency Strain
Solid-solution
Lixfepo4
Fepo4
Nanoparticles
Electrodes
Kinetics
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学科领域 | Chemistry, Physical
; Materials Science, Multidisciplinary
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资助者 | Youth Innovation Promotion Association; Chinese Academy of Sciences (CAS) [2011152]; Shenyang National Laboratory for Materials Science, Institute of Metal Research, CAS; Special Program for Applied Research on Super Computation of the NSFC-Guangdong Joint Fund [U1501501]
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收录类别 | SCI
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语种 | 英语
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WOS记录号 | WOS:000425840500037
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引用统计 |
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文献类型 | 期刊论文
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条目标识符 | http://ir.imr.ac.cn/handle/321006/79504
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专题 | 中国科学院金属研究所
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通讯作者 | Wang, XH (reprint author), Chinese Acad Sci, Shenyang Natl Lab Mat Sci, Inst Met Res, Shenyang 110016, Liaoning, Peoples R China. |
推荐引用方式 GB/T 7714 |
Li, ZJ,Yang, JX,Li, CJ,et al. Orientation-Dependent Lithium Miscibility Gap in LiFePO4[J]. CHEMISTRY OF MATERIALS,2018,30(3):874-878.
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APA |
Li, ZJ.,Yang, JX.,Li, CJ.,Wang, SC.,Zhang, L.,...&Wang, XH .(2018).Orientation-Dependent Lithium Miscibility Gap in LiFePO4.CHEMISTRY OF MATERIALS,30(3),874-878.
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MLA |
Li, ZJ,et al."Orientation-Dependent Lithium Miscibility Gap in LiFePO4".CHEMISTRY OF MATERIALS 30.3(2018):874-878.
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