TY - JOUR
T1 - Waste to Wealth
T2 - S,N-Codoped Si/C Anode Derived from Waste Tire Oil Exhibits Superior Performance in Lithium-Ion Batteries
AU - Ma, Xinlong
AU - Sun, Dong
AU - Wang, Meng
AU - Yang, Yin
AU - Zhang, Qi
AU - Ma, Zhuang
AU - Lu, Changbo
AU - Zhao, Kai
AU - Lu, Chun
AU - Xu, Chunming
AU - Xiao, Zhihua
AU - Li, Yongfeng
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/10/21
Y1 - 2024/10/21
N2 - Integrating silicon (Si) nanoparticles with carbonous materials has been regarded as an effective strategy to suppress the serious volume expansion and poor electrical conductivity of the Si anode in lithium-ion batteries (LIBs). Herein, the Si/C composite coated with a S,N-codoped graphene layer (Si@SNG) has been prepared via a facile and easily scale-up strategy that combines the vertical fluidized-bed-derived chemical vapor deposition in which the lightweight waste tire pyrolysis oil with high S content and pyridine is utilized as carbon source and dopants. The introduction of S,N-codoped graphene layer and graphite matrix can effectively increase Li+ storage room and conductivity, while buffering the volume expansion of pure Si. As result, the Si@SNG anode delivers a high initial Coulombic efficiency (ICE) of 86.91%, large specific capacity of 2446 mAh g-1 at 0.3 A g-1 and 90.3% capacity retention rate for 600 cycles within 0.01-1 V. In addition, the Si@SNG@G-P composite containing Si@SNG (10 wt %) and graphite matrix (90 wt %) has been prepared by ball milling and liquid-phase coating. As the anode, Si@SNG@G-P exhibits a high specific capacity of 695 mAh g-1 at 0.05 A g-1 coupled with 94.6% capacity retention rate for 500 cycles within 0.01-2 V. Moreover, the full cell assembled by Si@SNG@G-P anode and LiFePO4 cathode shows a high specific capacity of 157.7 and 128 mAh g-1 at 0.2 and 4 C, 93.1% capacity retention for 200 cycles along with a high energy density of 257.3 Wh kg-1. Therefore, this work offers a low-cost and high-efficiency preparation strategy for obtaining Si-based materials with outstanding electrochemical performance in LIBs.
AB - Integrating silicon (Si) nanoparticles with carbonous materials has been regarded as an effective strategy to suppress the serious volume expansion and poor electrical conductivity of the Si anode in lithium-ion batteries (LIBs). Herein, the Si/C composite coated with a S,N-codoped graphene layer (Si@SNG) has been prepared via a facile and easily scale-up strategy that combines the vertical fluidized-bed-derived chemical vapor deposition in which the lightweight waste tire pyrolysis oil with high S content and pyridine is utilized as carbon source and dopants. The introduction of S,N-codoped graphene layer and graphite matrix can effectively increase Li+ storage room and conductivity, while buffering the volume expansion of pure Si. As result, the Si@SNG anode delivers a high initial Coulombic efficiency (ICE) of 86.91%, large specific capacity of 2446 mAh g-1 at 0.3 A g-1 and 90.3% capacity retention rate for 600 cycles within 0.01-1 V. In addition, the Si@SNG@G-P composite containing Si@SNG (10 wt %) and graphite matrix (90 wt %) has been prepared by ball milling and liquid-phase coating. As the anode, Si@SNG@G-P exhibits a high specific capacity of 695 mAh g-1 at 0.05 A g-1 coupled with 94.6% capacity retention rate for 500 cycles within 0.01-2 V. Moreover, the full cell assembled by Si@SNG@G-P anode and LiFePO4 cathode shows a high specific capacity of 157.7 and 128 mAh g-1 at 0.2 and 4 C, 93.1% capacity retention for 200 cycles along with a high energy density of 257.3 Wh kg-1. Therefore, this work offers a low-cost and high-efficiency preparation strategy for obtaining Si-based materials with outstanding electrochemical performance in LIBs.
KW - Graphite matrix
KW - Lithium-ion battery
KW - S,N codoped graphene layer
KW - Si anode
KW - Waste tire pyrolysis oil
UR - http://www.scopus.com/inward/record.url?scp=85206526439&partnerID=8YFLogxK
U2 - 10.1021/acssuschemeng.4c04521
DO - 10.1021/acssuschemeng.4c04521
M3 - Article
AN - SCOPUS:85206526439
SN - 2168-0485
VL - 12
SP - 15447
EP - 15460
JO - ACS Sustainable Chemistry and Engineering
JF - ACS Sustainable Chemistry and Engineering
IS - 42
ER -