A hierarchical porous hard carbon@Si@soft carbon material for advanced lithium-ion batteries

被引:6
|
作者
Lv, Dan [1 ]
Yang, Lili [1 ]
Song, Runfeng [1 ]
Yuan, Hongyan [1 ]
Luan, Jingyi [1 ]
Liu, Jie [1 ]
Hu, Wenbin [1 ,2 ]
Zhong, Cheng [1 ,3 ]
机构
[1] Tianjin Univ, Sch Mat Sci & Engn, Key Lab Adv Ceram & Machining Technol, Minist Educ, Tianjin 300072, Peoples R China
[2] Int Campus Tianjin Univ, Joint Sch Natl Univ Singapore & Tianjin Univ, Fuzhou 350207, Peoples R China
[3] Tianjin Univ, Dept Mat Sci & Engn, Tianjin Key Lab Composite & Funct Mat, Tianjin 300072, Peoples R China
关键词
Lithium-ion batteries; Anode; Silicon; Hard carbon; Soft carbon; ANODE MATERIAL; SILICON; SHELL; COMPOSITE;
D O I
10.1016/j.jcis.2024.09.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Silicon (Si) is considered as one of the most potential commercial materials for the next-generation lithium-ion batteries (LIBs) owing to its high theoretical capacity and low voltage platform. However, the severe volume expansion and poor electric conductivity of Si anodes limit the practical application. Herein, a hierarchical porous hard carbon@Si@soft carbon (PHC@Si@SC) material was prepared by a chemical vapor deposition (CVD) and following calcination process. The differences in capacities and initial Coulombic efficiencies (ICEs) resulting from variations in silane deposition are demonstrated using PHC@Si as a model. To improve the cycling performance, a cheap pitch-derived soft carbon was introduced to protect the nano-Si to suppress the volume expansion. The formed PHC@Si@SC anode delivers a high capacity of 1625 mAh g(-1) and a high ICE of 86.8%, attributed to the excellent cooperation of hard and soft carbon. The capacity retention is 55% after 100 cycles with a harsh N/P ratio of 1.1 in a PHC@Si@SC||NCM811 full cell. This work provides a strategy, which is easy to scale up for practical application.
引用
收藏
页码:336 / 342
页数:7
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