共 36 条
Construction of NaTi2(PO4)3 3D heterostructure by double modification strategy of F substitution and PEDOT derived carbon nanotube cross-linking for efficient capacitive deionization
被引:0
|作者:
Jin, Ying
Wang, Yue
[1
]
Fang, Rongli
Huang, Shunjiang
Guo, Kaiwen
Li, Bingying
机构:
[1] Tianjin Univ, Chem Engn Res Ctr, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
来源:
关键词:
Capacitive deionization;
NaTi2(PO4)3;
PEDOT derived carbon nanotubes;
3D heterostructure;
F-;
doping;
SODIUM-ION BATTERY;
POROUS CARBON;
PERFORMANCE;
DESALINATION;
NANOCRYSTALS;
SURFACE;
DESIGN;
D O I:
10.1016/j.desal.2024.118473
中图分类号:
TQ [化学工业];
学科分类号:
0817 ;
摘要:
NaTi2(PO4)3 (NTP) is a promising capacitive deionization (CDI) electrode material due to large theoretical capacity and excellent structural stability. However, the existence of insulating [PO4] tetrahedron and large particle sizes result in low intrinsic conductivity and unfavorable ion diffusion distances, greatly limit application in CDI. Herein, PCN@NTP-F0.05 three-dimensional (3D) heterostructure was prepared by double modification strategy. Using F- with small ionic radius to partially replace PO43- effectively reduces the size of NTP particles from submicron to nanoscale and significantly increases the portion of macropores and mesopores. Additionally, the unique 3D heterostructure constructed by introducing PEDOT-derived carbon nanotubes as the supporting network of NTP-F0.05 nanoparticles remarkably improves conductivity of PCN@NTP-F0.05, from 1.42 x 104 to 1.05 x 102 S2 center dot cm, and increases specific surface area from 22.11 to 80.18 m2 g-1. The resulting PCN@NTP-F0.05 has a larger specific capacitance of 304.34 F g- 1, which is 7.93 times that of NTP. In addition, PCN//PCN@NTPF0.05 CDI cell exhibits excellent desalination capacity of 45.43 mg g-1, fast desalination rate of 16.10 mg g- 1 min- 1 and high charging efficiency of 90.79 %. Therefore, the double modification strategy provides a feasible solution for the development of highly efficient CDI electrode materials.
引用
收藏
页数:16
相关论文