Bai Yunfei, Liu Ting, Peng Huayu, Zhao Han, Fan Qingchen, Pan Xiaobo, Zhou Lian, Zhao Hao
State Key Laboratory of Applied Organic Chemistry, Key Laboratory of Nonferrous Metal Chemistry and Resources Utilization of Gansu Province, College of Chemistry and Chemical Engineering, Lanzhou University Lanzhou 730000 P. R. China
School of Physics and Electronic Information, Yantai University Yantai 264005 People's Republic of China
RSC Adv. 2024 Feb 28;14(10):7215-7220. doi: 10.1039/d3ra06060h. eCollection 2024 Feb 21.
Polymer electrodes are drawing widespread attention to the future generation of lithium-ion battery materials. However, weak electrochemical performance of organic anode materials still exists, such as low capacity, low rate performance, and low cyclability. Herein, we successfully constructed a donor-acceptor thiophene-based polymer (PBT-1) by introducing an organoboron unit. The charge delocalization and lower LUMO energy level due to the unique structure enabled good performance in electrochemical tests with a reversible capacity of 405 mA h g at 0.5 A g and over 10 000 cycles at 1 A g. Moreover, electron paramagnetic resonance (EPR) spectra revealed that the unique stable spin system in the PBT-1 backbone during cycling provides a fundamental explanation for the highly stable electrochemical performance. This work offers a reliable reference for the design of organic anode materials and expands the potential application directions of organoboron chemistry.
聚合物电极正引起人们对下一代锂离子电池材料的广泛关注。然而,有机负极材料的电化学性能仍然较弱,例如容量低、倍率性能差和循环稳定性低。在此,我们通过引入有机硼单元成功构建了一种供体-受体噻吩基聚合物(PBT-1)。由于其独特的结构,电荷离域和较低的最低未占分子轨道(LUMO)能级使得该聚合物在电化学测试中表现出色,在0.5 A g下可逆容量为405 mA h g,在1 A g下循环超过10000次。此外,电子顺磁共振(EPR)光谱表明,PBT-1主链在循环过程中独特的稳定自旋系统为其高度稳定的电化学性能提供了根本解释。这项工作为有机负极材料的设计提供了可靠的参考,并拓展了有机硼化学的潜在应用方向。