High-crystallinity and high-rate Prussian Blue analogues synthesized at the oil-water interface

被引:33
|
作者
Duan, Ceheng [1 ]
Meng, Yan [1 ]
Wang, Yujue [2 ]
Zhang, Zhaokun [3 ]
Ge, Yunchen [2 ]
Li, Xiaopeng [1 ]
Guo, Yong [2 ,3 ]
Xiao, Dan [1 ,2 ,3 ]
机构
[1] Sichuan Univ, Sch Chem Engn, Chengdu 610065, Peoples R China
[2] Sichuan Univ, Inst New Energy & Low Carbon Technol INELT, Chengdu 610207, Peoples R China
[3] Sichuan Univ, Coll Chem, Chengdu 610064, Peoples R China
基金
中国国家自然科学基金;
关键词
SUPERIOR CATHODE; POSITIVE ELECTRODE; OPEN FRAMEWORK; SODIUM; BEHAVIOR; BATTERY; NANOCRYSTALS; DEFECTS; STORAGE; WHITE;
D O I
10.1039/d0qi01361g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Prussian blue (PB) and its analogues (PBAs) are considered to be cathode materials for practical applications in sodium-ion batteries due to their open three-dimensional structure and low cost. However, PBAs synthesized by traditional methods generally have poor crystallinity and a high content of [Fe(CN)(6)] vacancy defects and coordinate water, which not only affect the Na+-storage capacity of PBAs, but also hinder Na+ transportation in the bulk phase and lead to a deterioration in electrochemical performance. Therefore, we propose an unconventional two-phase method to synthesize PBAs. Due to the unique reaction environment of the two-phase method, the reaction time lasts long, which is advantageous to control the synthesis of PBAs to ensure high crystallinity, low defects, and a suitable size. The as-prepared PBA at optimal condition delivers a high initial discharge specific capacity of 152 mA h g(-1) at 0.2 C (1 C = 170 mA h g(-1)), 110 and 105 mA h g(-1) even at high current densities of 10 C and 20 C,respectively, as well as a capacity retention of 84% after 200 cycles at 2 C. In particular, superior electrochemical performances also suggested that the two-phase method could be extended to the synthesis of other types of PBAs, such as Mn-PBAs and Co-PBAs, or even more materials with poor crystallinity due to rapid nucleation and growth.
引用
收藏
页码:2008 / 2016
页数:9
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