TY - JOUR
T1 - Embedding antimony nanoparticles into metal–organic framework derived TiO2@carbon nanotablets for high-performance sodium storage
AU - Yao, Tianhao
AU - Li, Li
AU - Wang, Hongkang
N1 - Publisher Copyright:
© 2023
PY - 2023/10
Y1 - 2023/10
N2 - Titanium dioxide (TiO2) has been widely investigated as a candidate for anode materials of sodium-ion batteries (SIBs) due to its low cost and high abundance. However, the intrinsic sluggish ion/electron transfer rate hinders its practical applications for high energy density storage devices. In contrast, antimony (Sb) shows high specific theoretical capacity (660 mAh/g) as well as excellent electron conductivity, but the large volume variation upon cycling usually leads to severe capacity fading. Herein, with the objective of achieving high-performance sodium storage anode materials, TiO2@C-Sb nanotablets with a small amount of Sb content (6.4 wt%) are developed through calcination Ti-metal–organic framework (MIL-125) derived TiO2@C/SbCl3 mixture under reductive atmosphere. Benefitting from the synergetic effect of well-dispersed Sb nanoparticles as well as robust porous TiO2@C substrate, the TiO2@C-Sb shows enhanced electron/ion transfer rate and predominantly pseudocapacitive sodium storage behavior, delivering a reversible capacity of 219 mAh/g at 0.5 A/g even after 1000 cycles. More significantly, this method may be commonly used to incorporate other alloy-based high-theoretical materials into MIL-125-derived TiO2@C, which is promising for developing high-energy-density TiO2-based energy storage devices.
AB - Titanium dioxide (TiO2) has been widely investigated as a candidate for anode materials of sodium-ion batteries (SIBs) due to its low cost and high abundance. However, the intrinsic sluggish ion/electron transfer rate hinders its practical applications for high energy density storage devices. In contrast, antimony (Sb) shows high specific theoretical capacity (660 mAh/g) as well as excellent electron conductivity, but the large volume variation upon cycling usually leads to severe capacity fading. Herein, with the objective of achieving high-performance sodium storage anode materials, TiO2@C-Sb nanotablets with a small amount of Sb content (6.4 wt%) are developed through calcination Ti-metal–organic framework (MIL-125) derived TiO2@C/SbCl3 mixture under reductive atmosphere. Benefitting from the synergetic effect of well-dispersed Sb nanoparticles as well as robust porous TiO2@C substrate, the TiO2@C-Sb shows enhanced electron/ion transfer rate and predominantly pseudocapacitive sodium storage behavior, delivering a reversible capacity of 219 mAh/g at 0.5 A/g even after 1000 cycles. More significantly, this method may be commonly used to incorporate other alloy-based high-theoretical materials into MIL-125-derived TiO2@C, which is promising for developing high-energy-density TiO2-based energy storage devices.
KW - Electrochemical properties
KW - Metal–organic framework
KW - Sb/TiO
KW - Sodium storage behavior
KW - Sodium-ion batteries
UR - https://www.scopus.com/pages/publications/85165031132
U2 - 10.1016/j.cclet.2023.108186
DO - 10.1016/j.cclet.2023.108186
M3 - 文章
AN - SCOPUS:85165031132
SN - 1001-8417
VL - 34
JO - Chinese Chemical Letters
JF - Chinese Chemical Letters
IS - 10
M1 - 108186
ER -