Mechanisms and Performances of Na1.5Fe0.5Ti1.5(PO4)3/C Composite as Electrode Material for Na-Ion Batteries

被引:36
作者
Difi, Siham [1 ,2 ]
Saadoune, Ismael [2 ]
Sougrati, Moulay Tahar [1 ,3 ]
Hakkou, Rachid [2 ]
Edstrom, Kristina [4 ]
Lippens, Pierre-Emmanuel [1 ,3 ]
机构
[1] Univ Montpellier, CNRS, Inst Charles Gerhardt, UMR 5253, F-34095 Montpellier 5, France
[2] Univ Cadi Ayyad, Lab Chim Mat & Environm, Marrakech, Morocco
[3] CNRS, FR 3459, Reseau Stockage Electrochim Energie RS2E, F-80039 Amiens, France
[4] Uppsala Univ, Dept Chem, Angstrom Lab, SE-75121 Uppsala, Sweden
基金
瑞典研究理事会;
关键词
TITANIUM PHOSPHATES; MOSSBAUER RESONANCE; SODIUM INSERTION; RAMAN; INTERCALATION; SPECTROSCOPY; NATI2(PO4)3; LI; TI; LI3FE2(PO4)(3);
D O I
10.1021/acs.jpcc.5b07931
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
The properties, insertion mechanisms, and electrochemical performances of the Na1.5Fe0.5Ti1.5(PO4)(3)/C composite as electrode material for Na-ion batteries are reported. The composite was obtained by solid-state reaction and consists of porous secondary particles of submicron-sized particles coated by carbon. Detailed characterizations were performed by combining theoretical and experimental tools. This includes the determination of the crystal structure of Na1.5Fe0.5Ti1.5(PO4)(3) from both first-principles calculations and X-ray diffraction providing Na distribution over M1 and M2 interstitial sites, which is of importance for ionic conductivity. Na1.5Fe0.5Ti1.5(PO4)(3)/C was used as an electrode material at 2.2 V versus Na+/Na-0, exhibiting good Na-storage ability with a specific capacity of 125 mAh g(-1), close to the theoretical value, for the first discharge at C/10, good capacity retention, and Coulombic efficiency of 95% and 99.5% at the 60th cycle, respectively, and high power rate with a decrease of the specific capacity of only 14% from C/10 to 2C. These good performances have been related to the morphology of the composite and substitution of Fe for Ti, leading to an insertion mechanism that differs from that of NaTi2(PO4)(3). This mechanism was quantitatively analyzed from operand Fe-57 Mossbauer spectroscopy used for the first time in both galvanostatic and GITT modes.
引用
收藏
页码:25220 / 25234
页数:15
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