TY - JOUR
T1 - Polyacrylonitrile@metal organic frameworks composite-derived heteroatoms doped carbon@encapsulated cobalt sulfide as superb sodium ion batteries anode
AU - Wang, Junling
AU - Wu, Na
AU - Han, Longfei
AU - Liao, Can
AU - Mu, Xiaowei
AU - Kan, Yongchun
AU - Hu, Yuan
N1 - Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2021/1/1
Y1 - 2021/1/1
N2 - Considering the finite resources of nonrenewable fossil fuels and urgent demands of modern society, sodium ion batteries (SIBs) featuring low cost, considerable natural supply and environmental friendless, show huge prospects in energy storage field, especially in constructing massive energy storage networks. Here, we propose a facile polyacrylonitrile@metal organic frameworks composite-derived sulfuration method, for acquiring heteroatoms doped carbon@encapsulated CoS2 nanoparticles (NSPCFS@CoS2) as SIBs anode. This electrode shows long and steady cycling process at 1 A g−1. After running 2095 cycles, it maintains a capacity of 546.3 mA h g−1. An exceedingly low capacity fading ratio of 0.013% per cycle can be acquired. Also, it gives high discharge capacities of 540.7 and 493.6 mA h g−1, even at 4 and 8 A g−1, separately. In addition, NSPCFS@CoS2 possesses a comparative or even better rate capability than other CoS2 based materials and other types of metal sulfides. Overall, this electrode exhibits superior cycling and rate performances. Additionally, its Na+ reaction kinetics and storage mechanism are deeply investigated.
AB - Considering the finite resources of nonrenewable fossil fuels and urgent demands of modern society, sodium ion batteries (SIBs) featuring low cost, considerable natural supply and environmental friendless, show huge prospects in energy storage field, especially in constructing massive energy storage networks. Here, we propose a facile polyacrylonitrile@metal organic frameworks composite-derived sulfuration method, for acquiring heteroatoms doped carbon@encapsulated CoS2 nanoparticles (NSPCFS@CoS2) as SIBs anode. This electrode shows long and steady cycling process at 1 A g−1. After running 2095 cycles, it maintains a capacity of 546.3 mA h g−1. An exceedingly low capacity fading ratio of 0.013% per cycle can be acquired. Also, it gives high discharge capacities of 540.7 and 493.6 mA h g−1, even at 4 and 8 A g−1, separately. In addition, NSPCFS@CoS2 possesses a comparative or even better rate capability than other CoS2 based materials and other types of metal sulfides. Overall, this electrode exhibits superior cycling and rate performances. Additionally, its Na+ reaction kinetics and storage mechanism are deeply investigated.
KW - Metal organic frameworks
KW - Pseudocapacitive behavior
KW - Sodium storage performance
KW - Transition metal chalcogenides
UR - http://www.scopus.com/inward/record.url?scp=85089388680&partnerID=8YFLogxK
U2 - 10.1016/j.jcis.2020.08.015
DO - 10.1016/j.jcis.2020.08.015
M3 - 文章
C2 - 32805672
AN - SCOPUS:85089388680
SN - 0021-9797
VL - 581
SP - 552
EP - 565
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
ER -