Facile solvothermal synthesis of NaTi2(PO4)3/C porous plates as electrode materials for high-performance sodium ion batteries

被引:37
|
作者
Huang, Zhifeng [1 ]
Liu, Li [1 ]
Yi, Lingguang [1 ]
Xiao, Wei [2 ]
Li, Min [1 ]
Zhou, Qian [1 ]
Guo, Guoxiong [1 ]
Chen, Xiaoying [1 ]
Shu, Hongbo [1 ]
Yang, Xiukang [1 ]
Wang, Xianyou [1 ]
机构
[1] Xiangtan Univ, Sch Chem, Key Lab Environm Friendly Chem & Applicat, Minist Educ, Xiangtan 411105, Hunan, Peoples R China
[2] Sany Heavy Ind Co Ltd, Changsha 410100, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Sodium titanium phosphate; Porous plates; Inductive agent; Sodium ion battery; SUPERIOR RATE CAPABILITY; HIGH-RATE ANODE; ELECTROCHEMICAL PERFORMANCE; ANATASE TIO2; LITHIUM; CATHODE; CARBON; NASICON; NA; COMPOSITE;
D O I
10.1016/j.jpowsour.2016.06.066
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
NaTi2(PO4)(3)/C porous plates have been successfully synthesized via solvothermal approach with ammonia as inductive agent combined in-situ carbon coating. It reveals that the inductive agent plays a critical role in morphology-controllable fabrication. The morphology, structure, and electrochemical properties of NaTi2(PO4)(3)/C composites with multilayered plates, single-layered plate, porous multilayered plates all have been investigated, which are prepared by using urea, triethylamine, and ammonia, respectively. Among these samples, NaTi2(PO4)(3)/C porous multilayered plates with ammonia addition exhibit the best electrochemical properties due to their uniquemesoporous structure. NaTi2(PO4)(3)/C porous multilayered plates deliver an initial specific capacity of 125 and 110 mAh g(-1) at 0.1 and 1 C, respectively. Furthermore, NaTi2(PO4)(3)/C porous multilayered plates show a good rate capability, whose capacity and corresponding capacity retention reach 85 mAh g(-1) and 82.4%, respectively, after 120 cycles under the high rate of 10 C. The excellent results indicate that the NaTi2(PO4)(3)/C porous multilayered plates are a promising electrode candidate for sodium ion battery. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:474 / 481
页数:8
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