Readily useable bulk phenoxazine-based covalent organic framework cathode materials with superior kinetics and high redox potentials

被引:28
作者
Meng, Zhiying [1 ]
Zhang, Ying [2 ]
Dong, Mengqing [1 ]
Zhang, Yue [1 ]
Cui, Fengmin [1 ]
Loh, Teck-Peng [1 ,3 ]
Jin, Yinghua [4 ]
Zhang, Wei [4 ]
Yang, Haishen [2 ]
Du, Ya [1 ]
机构
[1] Nanjing Tech Univ, Sch Chem & Mol Engn, Inst Adv Synth, Nanjing 211816, Peoples R China
[2] Shanghai Univ Elect Power, Shanghai Key Lab Mat Protect & Adv Mat Elect Powe, Shanghai 200090, Peoples R China
[3] Nanyang Technol Univ, Sch Phys & Math Sci, Div Chem & Biol Chem, Singapore 637616, Singapore
[4] Univ Colorado, Dept Chem, Boulder, CO 80309 USA
基金
中国国家自然科学基金;
关键词
LITHIUM STORAGE; ENERGY; POLYMER; CRYSTALLINE; NANOSHEETS; CARBON;
D O I
10.1039/d0ta10785a
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
Redox-active covalent organic frameworks (COFs) with dense redox sites are promising electrical energy storage materials with robust architectures, high surface areas, insolubility in electrolytes, and open pores for electrolyte transportation. However, low redox potentials and poor electrical conductivity of pristine COFs often result in low accessibilities of redox-active sites and slow redox kinetics, greatly limiting their practical applications. Herein, we report the design and synthesis of two novel p-type phenoxazine-based COFs (DAPO-COFs) with high redox potentials (similar to 3.6 V vs. Li/Li+) and excellent electrical conductivities. Simply blended with conductive additives (CAs) and binders, pristine bulk DAPO-COFs without pre-composition with CAs or extra exfoliation are readily useable as cathode materials for lithium-ion batteries. Both as-synthesized DAPO-COF powders displayed superior active-site accessibility, ultrafast redox kinetics, and remarkable cycling stability. This work provides new perspectives on the development of readily useable COF-based cathode materials, and contributes to the advancement of eco-friendly and sustainable organic-based energy storage devices.
引用
收藏
页码:10661 / 10665
页数:5
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