Yegamkulov Mukagali, Bakhytzhanova Zhansaya, Bekmakhanova Ayazhan, Issatayev Nurbolat, Nurpeissova Arailym, Bakenov Zhumabay, Mukanova Aliya
National Laboratory Astana, Nazarbayev University Kabanbay Batyr Ave. 53 Astana 010000 Kazakhstan
Institute of Batteries LLC Kabanbay Batyr Ave. 53 Astana 010000 Kazakhstan.
RSC Adv. 2025 Sep 11;15(39):32810-32820. doi: 10.1039/d5ra05444c. eCollection 2025 Sep 5.
The continuous demand for high-performance lithium-ion batteries (LIBs) has accelerated the development of microscale energy storage systems with improved specific and volumetric capacities. Tin oxide (SnO) is a promising anode material due to its high theoretical capacity and favorable lithiation properties; however, its practical application is hindered by significant volume changes and unstable electrode-electrolyte interfaces during cycling. Here, we systematically investigate the impact of thin film morphology and artificial interface engineering on the electrochemical performance of radio frequency (RF) magnetron-sputtered SnO anodes. By optimizing deposition and annealing parameters, we achieve porous SnO architectures with enhanced cycling stability. A subsequent carbon coating reduces electrolyte contact and buffers volume expansion, while the incorporation of 5 wt% vinylene carbonate (VC) into the electrolyte enables the formation of a robust, elastic solid electrolyte interphase (SEI). The dual approach - combining engineered porosity with interfacial stabilization - significantly improved capacity retention, suppressed polarization, and ensured high coulombic efficiency over 200 cycles. Post-mortem scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS) analyses confirm that the carbon coating and VC worked synergistically to preserve structural integrity, minimized side reactions, and promoted favorable SEI composition. These results highlight an effective strategy for designing durable, high-capacity SnO-based thin film anodes for next-generation LIBs.
对高性能锂离子电池(LIBs)的持续需求加速了具有更高比容量和体积容量的微尺度储能系统的发展。氧化锡(SnO)因其高理论容量和良好的锂化性能而成为一种有前景的负极材料;然而,其实际应用受到循环过程中显著的体积变化和不稳定的电极 - 电解质界面的阻碍。在此,我们系统地研究了薄膜形态和人工界面工程对射频(RF)磁控溅射SnO负极电化学性能的影响。通过优化沉积和退火参数,我们实现了具有增强循环稳定性的多孔SnO结构。随后的碳涂层减少了与电解质的接触并缓冲了体积膨胀,同时在电解质中加入5 wt%的碳酸亚乙烯酯(VC)能够形成坚固、有弹性的固体电解质界面(SEI)。这种将工程孔隙率与界面稳定相结合的双重方法显著提高了容量保持率,抑制了极化,并确保了在200次循环中具有高库仑效率。事后扫描电子显微镜(SEM)和X射线光电子能谱(XPS)分析证实,碳涂层和VC协同作用以保持结构完整性,最小化副反应,并促进有利的SEI组成。这些结果突出了一种为下一代LIBs设计耐用、高容量SnO基薄膜负极的有效策略。