Li Yuanjian, Feng Xiang, Yang Gaoliang, Lieu Wei Ying, Fu Lin, Zhang Chang, Xing Zhenxiang, Ng Man-Fai, Zhang Qianfan, Liu Wei, Lu Jun, Seh Zhi Wei
Institute of Materials Research and Engineering (IMRE), Agency for Science, Technology and Research (A*STAR), 2 Fusionopolis Way, Innovis #08-03, Singapore, 138634, Republic of Singapore.
School of Materials Science and Engineering, Beihang University, 100191, Beijing, P. R. China.
Nat Commun. 2024 Oct 30;15(1):9364. doi: 10.1038/s41467-024-53796-z.
Magnesium (Mg) metal is a promising anode candidate for high-energy and cost-effective multivalent metal batteries, but suffers from severe surface passivation in conventional electrolytes, especially aqueous solutions. Here, we uncover that MgH, in addition to the well-known MgO and Mg(OH), can be formed during the passivation of Mg by water. The formation mechanism and spatial distribution of MgH, and its detrimental effect on interfacial dynamics and stability of Mg anode are revealed by comprehensive experimental and theoretical investigations. Furthermore, a graphite-based hydrophobic and Mg-permeable water-tolerant interphase is drawn using a pencil on the surface of Mg anodes, allowing them to cycle stably in symmetric (> 900 h) and full cells (> 500 cycles) even after contact with water. The mechanistic understanding of MgH-involved Mg passivation and the design of pencil-drawn waterproof Mg anodes may inspire the further development of Mg metal batteries with high water resistance.
镁(Mg)金属是用于高能且经济高效的多价金属电池的一种很有前景的负极候选材料,但在传统电解质中,尤其是在水溶液中,会遭受严重的表面钝化。在此,我们发现,除了众所周知的MgO和Mg(OH)₂之外,Mg在被水钝化过程中还会形成MgH₂。通过全面的实验和理论研究,揭示了MgH₂的形成机制、空间分布及其对Mg负极界面动力学和稳定性的有害影响。此外,用铅笔在Mg负极表面绘制了一种基于石墨的疏水且Mg可渗透的耐水界面层,使它们即使在与水接触后仍能在对称电池(> 900小时)和全电池(> 500次循环)中稳定循环。对涉及MgH₂的Mg钝化的机理理解以及铅笔绘制的防水Mg负极的设计可能会激发具有高耐水性的Mg金属电池的进一步发展。