TY - JOUR
T1 - Hollow Carbon Nanoballs Coupled with Ultrafine TiO2 Nanoparticles as Efficient Sulfur Hosts for Lithium-Sulfur Batteries
AU - Gu, Hangyu
AU - Wang, Hongkang
AU - Zhang, Rong
AU - Yao, Tianhao
AU - Liu, Ting
AU - Wang, Jinkai
AU - Han, Xiaogang
AU - Cheng, Yonghong
N1 - Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/10/2
Y1 - 2019/10/2
N2 - Lithium-sulfur (Li-S) batteries as among the most promising energy storage devices possess high theoretical capacity and energy density but suffer from the polysulfide dissolution, which hinders their practical application. Herein, we present a facile synthesis of hollow carbon nanoballs (HCNBs) anchored with ultrafine TiO2 nanoparticles (TiO2@HCNBs) in which the HCNBs with hollow interiors and graphitic crystallization accommodate the volume expansion of sulfur upon lithiation and improve the cathode conductivity, while the TiO2 nanoparticles effectively trap the polysulfides through strong chemical bonding. Notably, the S@TiO2@HCNBs with a high sulfur loading of ∼73 wt % demonstrate superior cycle performance at 0.5 C over 600 cycles with a slow capacity decay and deliver high specific capacities of 1217, 1013, 893, and 773 mA h/g at 0.1, 0.2, 0.5, and 1 C, respectively. The adsorption test clearly reveals the efficient suppression of the polysulfide shuttling owing to the spatial and chemical confinement of the TiO2@HCNBs host.
AB - Lithium-sulfur (Li-S) batteries as among the most promising energy storage devices possess high theoretical capacity and energy density but suffer from the polysulfide dissolution, which hinders their practical application. Herein, we present a facile synthesis of hollow carbon nanoballs (HCNBs) anchored with ultrafine TiO2 nanoparticles (TiO2@HCNBs) in which the HCNBs with hollow interiors and graphitic crystallization accommodate the volume expansion of sulfur upon lithiation and improve the cathode conductivity, while the TiO2 nanoparticles effectively trap the polysulfides through strong chemical bonding. Notably, the S@TiO2@HCNBs with a high sulfur loading of ∼73 wt % demonstrate superior cycle performance at 0.5 C over 600 cycles with a slow capacity decay and deliver high specific capacities of 1217, 1013, 893, and 773 mA h/g at 0.1, 0.2, 0.5, and 1 C, respectively. The adsorption test clearly reveals the efficient suppression of the polysulfide shuttling owing to the spatial and chemical confinement of the TiO2@HCNBs host.
UR - https://www.scopus.com/pages/publications/85072978882
U2 - 10.1021/acs.iecr.9b03393
DO - 10.1021/acs.iecr.9b03393
M3 - 文章
AN - SCOPUS:85072978882
SN - 0888-5885
VL - 58
SP - 18197
EP - 18204
JO - Industrial and Engineering Chemistry Research
JF - Industrial and Engineering Chemistry Research
IS - 39
ER -