TY - JOUR
T1 - Advanced anode for sodium-ion battery with promising long cycling stability achieved by tuning phosphorus-carbon nanostructures
AU - Yu, Zhaoxin
AU - Song, Jiangxuan
AU - Wang, Daiwei
AU - Wang, Donghai
N1 - Funding Information:
This work was supported by U.S. National Science Foundation (NSF) with Grant No. DMR-1610430 and partially supported by the National Natural Science Foundation of China ( 51602250 ) and Thousand Youth Talents Plan Project of China.
Publisher Copyright:
© 2017
PY - 2017/10
Y1 - 2017/10
N2 - Phosphorus is considered as a promising anode for Na-ion battery because of its high theoretical capacity of 2595 mAh g−1. In this study, two phosphorus-carbon (P-C) composites with well-controlled compositions and nanostructures of P and C have been developed: P@YP composite with P confined within porous structure of YP-80F carbon and P@CNT with unconfined P deposited on the surface of carbon nanotube. The structure and electrochemical performance of these two composites have been studied to illustrate the effect of nanostructures of both C and P. P@YP composite with appropriate amount of P confined in nanopores can accommodate its large volume change upon sodiation/desodiation and enable a stable solid-electrolyte interphase (SEI), ensuring an excellent long-term cycling stability with superior capacity retention of 92% after 100 cycles and 46% after 1000 cycles. In contrast, the P@CNT composite with unconfined P nanostructures shows a rapid capacity decay with capacity retention of ~ 40.6% after 100 cycles, most likely due to unstable SEI during cycling, caused by the large volume changes of unconfined P in the P@CNT composite. The well-designed nanostructured P-C composite with P confined within porous structure of carbon is demonstrated to greatly enhance the electrochemical performance, leading to promising long-term cycling stability.
AB - Phosphorus is considered as a promising anode for Na-ion battery because of its high theoretical capacity of 2595 mAh g−1. In this study, two phosphorus-carbon (P-C) composites with well-controlled compositions and nanostructures of P and C have been developed: P@YP composite with P confined within porous structure of YP-80F carbon and P@CNT with unconfined P deposited on the surface of carbon nanotube. The structure and electrochemical performance of these two composites have been studied to illustrate the effect of nanostructures of both C and P. P@YP composite with appropriate amount of P confined in nanopores can accommodate its large volume change upon sodiation/desodiation and enable a stable solid-electrolyte interphase (SEI), ensuring an excellent long-term cycling stability with superior capacity retention of 92% after 100 cycles and 46% after 1000 cycles. In contrast, the P@CNT composite with unconfined P nanostructures shows a rapid capacity decay with capacity retention of ~ 40.6% after 100 cycles, most likely due to unstable SEI during cycling, caused by the large volume changes of unconfined P in the P@CNT composite. The well-designed nanostructured P-C composite with P confined within porous structure of carbon is demonstrated to greatly enhance the electrochemical performance, leading to promising long-term cycling stability.
UR - http://www.scopus.com/inward/record.url?scp=85028950657&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85028950657&partnerID=8YFLogxK
U2 - 10.1016/j.nanoen.2017.08.019
DO - 10.1016/j.nanoen.2017.08.019
M3 - Article
AN - SCOPUS:85028950657
SN - 2211-2855
VL - 40
SP - 550
EP - 558
JO - Nano Energy
JF - Nano Energy
ER -