Riemannian Surface on Carbon Anodes Enables Li-Ion Storage at-35 °C

被引:11
|
作者
Lu, Zongjing [1 ]
Wang, Jingnan [2 ]
Cheng, Xuechun [2 ]
Xie, Weiwei [3 ]
Gao, Zhiyi [1 ]
Zhang, Xuejing [1 ]
Xu, Yong [4 ]
Yi, Ding [5 ]
Yang, Yijun [5 ]
Wang, Xi [6 ]
Yao, Jiannian [7 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Mol Plus, Tianjin 300072, Peoples R China
[3] Karlsruhe Inst Technol, Inst Phys Chem, D-76131 Karlsruhe, Germany
[4] Innovat Lab Sci & Technol Energy Mat Fujian Prov, Xiamen 361005, Peoples R China
[5] Beijing Jiaotong Univ, Sch Sci, Dept Phys, Beijing 100044, Peoples R China
[6] Beijing Jiaotong Univ, Dept Phys, Sch Phys Sci & Engn, Beijing 100044, Peoples R China
[7] Chinese Acad Sci, Key Lab Photochem, Beijing Natl Lab Mol Sci, Inst Chem, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
DESOLVATION; BATTERY;
D O I
10.1021/acscentsci.2c00411
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Since sluggish Li+ desolvation leads to severe capacity degradation of carbon anodes at subzero temperatures, it is urgently desired to modulate electron configurations of surface carbon atoms toward high capacity for Li-ion batteries. Herein, a carbon-based anode material (O-DF) was strategically synthesized to construct the Riemannian surface with a positive curvature, which exhibits a high reversible capacity of 624 mAh g(-1) with an 85.9% capacity retention at 0.1 A g(-1) as the temperature drops to -20 degrees C. Even if the temperature drops to -35 degrees C, the reversible capacity is still effectively retained at 160 mAh g(-1) after 200 cycles. Various characterizations and theoretical calculations reveal that the Riemannian surface effectively tunes the low-temperature sluggish Li+ desolvation of the interfacial chemistry via locally accumulated charges of non-coplanar sp(x) (2 < x < 3) hybridized orbitals to reduce the rate-determining step of the energy barrier for the charge-transfer process. Ex-situ measurements further confirm that the sp(x)-hybridized orbitals of the pentagonal defect sites should denote more negative charges to solvated Li+ adsorbed on the Riemannian surface to form stronger Li-C coordinate bonds for Li+ desolvation, which not only enhances Li-adsorption on the curved surface but also results in more Li+ insertion in an extremely cold environment.
引用
收藏
页码:905 / 914
页数:10
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