Ultrastable Bioderived Organic Anode Induced by Synergistic Coupling of Binder/Carbon-Network for Advanced Potassium-Ion Storage

被引:24
作者
Qu, Zexi [1 ]
Zhang, Xixue [1 ]
Huang, Ruling [1 ]
Wu, Shumeng [1 ]
Chen, Renjie [1 ,2 ]
Wu, Feng [1 ,2 ,3 ]
Li, Li [1 ,2 ,3 ]
机构
[1] Beijing Inst Technol, Beijing Key Lab Environm Sci & Engn, Sch Mat Sci & Engn, Beijing 100081, Peoples R China
[2] Beijing Inst Technol, Adv Technol Res Inst, Jinan 250300, Peoples R China
[3] Guangzhou Inst Energy Testing, Guangdong Key Lab Battery Safety, Guangzhou 511447, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
potassium-ion batteries; organic anode; bioderived molecular; juglone; in situ FTIR; PI-PI STACKING; BATTERY; JUGLONE; CHEMISTRY; BINDER; LIFE;
D O I
10.1021/acs.nanolett.2c00847
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bioderived molecules have been identified as viable anodes for organic potassium-ion batteries (OPIBs) due to the abundance of the necessary natural resources, their high capacity, and their sustainability. However, the high solubility and the inherent nonconductivity cause serious capacity decay and large voltage hysteresis. Here, the biomass molecule juglone was cross-linked with a carbon nanotube network, coupling and cooperating with sodium alginate binder (J@CNT-SA), and was proposed to inhibit small molecule dissolution via weak intermolecular interactions. The synergistic effect of hydrogen bonding and pi-pi stacking is proven for its outstanding reversible high capacities (262 mA h g(-1) at 0.05 A g(-1)), and a remarkable long life span with capacity retention of 77% over 5000 cycles. Further in situ Fourier transform infrared spectroscopy (FTIR) was performed to reveal the electrochemical mechanism. The feasibility of juglone as an anode for PIBs paves the way for other natural organic small molecules to be investigated as potential energy storage materials.
引用
收藏
页码:4115 / 4123
页数:9
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