Kim Dong Ki, Suh Joo Hyeong, Hong Yoojin, Kim Daeun, Park Min-Sik, Kim Jung Ho
Department of Advanced Materials Engineering for Information and Electronics, Integrated Education Institute for Frontier Science & Technology (BK21 Four), Kyung Hee University, Republic of Korea.
Institute for Superconducting & Electronic Materials (ISEM), Faculty of Engineering and Information Sciences, University of Wollongong, North Wollongong, NSW, Australia.
Sci Technol Adv Mater. 2025 Jan 31;26(1):2455371. doi: 10.1080/14686996.2025.2455371. eCollection 2025.
Using a lithium (Li) metal anode is essential for high-energy batteries, however, dendritic Li growth is unavoidable during Li plating and stripping processes. Strategically, a porous carbon structure derived from a metal-organic framework is suggested for directly storing metallic Li, although problems still exist with plating Li from the core to the surface and with stripping Li from the surface. Herein, we strategically utilize the carbon structure of zeolitic imidazolate framework-8 as an anode and replace the inactive residual Zn with Ag through galvanic displacement. The strong affinity of Ag for Li ions facilitates the transfer of plating from the surface of the carbon structure to its interior. After determining the optimal conditions for galvanic displacement by varying reaction times and temperatures, we carefully evaluate the electrochemical performance.
使用锂(Li)金属阳极对于高能电池至关重要,然而,在锂电镀和剥离过程中,树枝状锂生长是不可避免的。从策略上讲,有人提出源自金属有机框架的多孔碳结构可用于直接存储金属锂,尽管从核心到表面电镀锂以及从表面剥离锂仍存在问题。在此,我们策略性地利用沸石咪唑酯骨架-8的碳结构作为阳极,并通过电化置换用银取代惰性残余锌。银对锂离子的强亲和力促进了电镀从碳结构表面转移到其内部。在通过改变反应时间和温度确定电化置换的最佳条件后,我们仔细评估了电化学性能。