Fang Xiang Xiang, Jiang Chaoyan, Yue Chuang, Hu Fang
Department of Microelectronics Science and Engineering, School of Physical Science and Technology, Ningbo University, Ningbo, 315211, China.
School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, 315211, China.
Chemistry. 2024 May 17;30(28):e202400063. doi: 10.1002/chem.202400063. Epub 2024 Mar 22.
Three-dimensional (3D) self-supported Ge anode is one of the promising candidates to replace the traditional graphite anode material for high-performance binder-free lithium-ion batteries (LIBs). The enlarged surface area and the shortened ions/electrons transporting distance of the 3D electrode would greatly facilitate the rapid transfer of abundant lithium ions during cycling, thus achieve enhanced energy and power density during cycling. Cycle stability of the 3D self-supported Ge electrode would be improved due to the obtained enough space could effectively accommodate the large volume expansion of the Ge anode. In this review, we first describe the electrochemical properties and Li ions storage mechanism of Ge anode. Moreover, the recent advances in the 3D self-supported Ge anode architectures design are majorly illustrated and discussed. Challenges and prospects of the 3D self-supported Ge electrode are finally provided, which shed light on ways to design more reliable 3D Ge-based electrodes in energy storage systems.
三维(3D)自支撑锗阳极是有望替代传统石墨阳极材料用于高性能无粘结剂锂离子电池(LIB)的候选材料之一。3D电极增大的表面积和缩短的离子/电子传输距离将极大地促进循环过程中大量锂离子的快速转移,从而在循环过程中提高能量和功率密度。由于获得了足够的空间可以有效容纳锗阳极的大体积膨胀,3D自支撑锗电极的循环稳定性将得到改善。在本综述中,我们首先描述了锗阳极的电化学性质和锂离子存储机制。此外,主要阐述和讨论了3D自支撑锗阳极结构设计的最新进展。最后给出了3D自支撑锗电极面临的挑战和前景,这为在储能系统中设计更可靠的3D锗基电极指明了方向。