Hard carbon with an opened pore structure for enhanced sodium storage performance

被引:14
|
作者
You, Shunzhang [1 ]
Zhang, Qiaobao [2 ]
Liu, Junxiang [3 ]
Deng, Qiang [1 ]
Sun, Zhefei [2 ]
Cao, Dandan [1 ]
Liu, Tongchao [3 ]
Amine, Khalil [3 ]
Yang, Chenghao [1 ]
机构
[1] South China Univ Technol, New Energy Res Inst, Sch Environm & Energy, Guangzhou Key Lab Surface Chem Energy Mat, Guangzhou 510006, Peoples R China
[2] Xiamen Univ, Coll Mat, Dept Mat Sci & Engn, Xiamen 361005, Fujian, Peoples R China
[3] Argonne Natl Lab, Chem Sci & Engn Div, Lemont, IL 60439 USA
基金
国家重点研发计划;
关键词
D O I
10.1039/d4ee02519a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The pore structure of hard carbon has a significant impact on its Na+ storage capacity. Herein, a waste wood-derived hard carbon with opened pores (OP-HC) was fabricated with polyvinyl pyrrolidone (PVP) as an additive. Ex situ SAXS and HR-TEM testing results indicate that OP-HC with opened pores and enlarged d002 interlayer spacing facilitates the reversible (de)sodiation of Na+ ions. In situ TEM and XRD testing results demonstrate that OP-HC shows excellent structure stability during the (de)sodiation process. Thus, OP-HC delivers a high reversible charge capacity of 350.7 mA h g-1 at 0.05 C and an ultra-high initial Coulombic efficiency (ICE) of 94.9%. Moreover, OP-HC exhibits excellent cycling stability, and the assembled 18650 full cell with an OP-HC anode can achieve a high capacity retention of 94.5% after 400 cycles at 1.0 A. The excellent electrochemical performance and deep insights into OP-HC with opened pores and increased d002 interlayer spacing offer a new strategy to design high-performance HC anodes for SIBs. OP-HC shows a high specific capacity of 350.7 mA h g-1 with ultra-high ICE. These results are attributed to its opened pore and enlarged d002 interlayer spacing, which can enhance the reversibility of Na+ adsorption, intercalation and filling process.
引用
收藏
页码:8189 / 8197
页数:9
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