Miao Zeqing, Gao Kesheng, Li Dazhi, Gao Ziwei, Zhao Wenxin, Li Zeyang, Sun Wei, Wang Xiaoguang, Zhang Haihang, Wang Xinyu, Sun Changlong, Zhu Yuanyuan, Li Zhenjiang
Shandong Engineering Laboratory for Preparation and Application of High-Performance Carbon-Materials, College of Electromechanical Engineering, Qingdao University of Science and Technology, Qingdao 266061, China.
College of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.
Molecules. 2023 Oct 1;28(19):6903. doi: 10.3390/molecules28196903.
The rational design of the heterogeneous interfaces enables precise adjustment of the electronic structure and optimization of the kinetics for electron/ion migration in energy storage materials. In this work, the built-in electric field is introduced to the iron-based anode material (FeO@TiO) through the well-designed heterostructure. This model serves as an ideal platform for comprehending the atomic-level optimization of electron transfer in advanced lithium-ion batteries (LIBs). As a result, the core-shell FeO@TiO delivers a remarkable discharge capacity of 1342 mAh g and an extraordinary capacity retention of 82.7% at 0.1 A g after 300 cycles. FeO@TiO shows an excellent rate performance from 0.1 A g to 4.0 A g. Further, the discharge capacity of FeO@TiO reached 736 mAh g at 1.0 A g after 2000 cycles, and the corresponding capacity retention is 83.62%. The heterostructure forms a conventional p-n junction, successfully constructing the built-in electric field and lithium-ion reservoir. The kinetic analysis demonstrates that FeO@TiO displays high pseudocapacitance behavior (77.8%) and fast lithium-ion reaction kinetics. The capability of heterointerface engineering to optimize electrochemical reaction kinetics offers novel insights for constructing high-performance iron-based anodes for LIBs.
异质界面的合理设计能够精确调整电子结构,并优化储能材料中电子/离子迁移的动力学。在这项工作中,通过精心设计的异质结构将内建电场引入铁基负极材料(FeO@TiO)。该模型为理解先进锂离子电池(LIBs)中电子转移的原子级优化提供了一个理想平台。结果,核壳结构的FeO@TiO在300次循环后,在0.1 A g的电流密度下具有1342 mAh g的显著放电容量和82.7%的优异容量保持率。FeO@TiO在0.1 A g至4.0 A g的电流密度范围内表现出优异的倍率性能。此外,FeO@TiO在1.0 A g的电流密度下经过2000次循环后,放电容量达到736 mAh g,相应的容量保持率为83.62%。这种异质结构形成了传统的p-n结,成功构建了内建电场和锂离子储存库。动力学分析表明,FeO@TiO表现出高赝电容行为(77.8%)和快速的锂离子反应动力学。异质界面工程优化电化学反应动力学的能力为构建高性能的LIBs铁基负极提供了新的见解。