共 23 条
Na 3.8 [Sn 0.67 Si 0.33 ] 0.8 Sb 0.2 S 4: A quinary sodium fast ionic conductor for all -solid-state sodium battery
被引:21
|作者:
Jia, Huanhua
[1
,2
]
Peng, Linfeng
[1
,3
]
Zhang, Zhuoran
[1
,2
]
An, Tao
[1
,2
]
Xie, Jia
[1
]
机构:
[1] Huazhong Univ Sci & Technol, Sch Elect & Elect Engn, State Key Lab Adv Electromagnet Engn & Technol, Wuhan 430074, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Sch Mat Sci & Engn, State Key Lab Mat Proc & Die & Mould Technol, Wuhan 430074, Hubei, Peoples R China
[3] Huazhong Univ Sci & Technol, Sch Phys, Wuhan 430074, Hubei, Peoples R China
来源:
JOURNAL OF ENERGY CHEMISTRY
|
2020年
/
48卷
基金:
中国国家自然科学基金;
关键词:
SUPERIONIC CONDUCTOR;
CRYSTAL-STRUCTURE;
ELECTROLYTES;
TRANSPORT;
NA3SBS4;
D O I:
10.1016/j.jechem.2019.12.021
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
Strategy of Sb-substitution is carried out on the template structure Na4Sn0.67M0.33S4 (M = Si, Ge), which affords a series of quinary sulfide-based sodium fast ionic conductors formulated as Na4-x[Sn0.67M0.33]1-xSbxS4 (M = Si, x = 0.1, 0.2, 0.3; M = Ge, x = 0.2.). Among them, the highest ambient ionic conductivity (1.75 × 10−4 S cm−1) is achieved when M = Si and x = 0.2. The new fast ionic conductor Na3.8[Sn0.67Si0.33]0.8Sb0.2S4 is isostructural to its structure template Na4Sn0.67Si0.33S4 and thus crystallizes in the space group of I41/acd. It is shown that the incorporation of Sb improves the ionic conductivity. The study of lattice parameters shows that the improvement of the ion conductivity by Sb-substitution is mainly due to the enlarged crystal lattice. Furthermore, using Na3.8[Sn0.67Si0.33]0.8Sb0.2S4 as solid electrolytes, room temperature all-solid-state sodium battery of Se0.05S0.95@pPAN/Na3Sn is realized, which proves the novel fast ionic conductor a potential candidate to apply in sodium solid state battery. This work not only extends the scope of Na4[Sn0.67Si0.33]S4, the I41/acd space group template, but also deepens the understanding of the lattice size effect on the structure and property relationship by aliovalent substitution. © 2020
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页码:102 / 106
页数:5
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