Zarach Zuzanna, Sawczak Mirosław, Dosche Carsten, Trzciński Konrad, Szkoda Mariusz, Graczyk-Zając Magdalena, Riedel Ralf, Wittstock Gunther, Nowak Andrzej P
Faculty of Chemistry, Gdansk University of Technology, Gdansk, 80-233, Poland.
Centre of Plasma and Laser Engineering, The Szewalski Institute of Fluid-Flow Machinery of Polish Academy of Sciences, Gdansk, 80-231, Poland.
Small. 2025 Sep;21(38):e04485. doi: 10.1002/smll.202504485. Epub 2025 Jul 31.
Developing robust and efficient anodes is essential for advancing sodium-ion battery technology. Herein, a systematic investigation of SnS@C composites prepared at different pyrolysis temperatures to elucidate how their structural, surface, and electrochemical properties govern sodium-ion storage is reported. The study reveals that a lower synthesis temperature traps extra sulfur within the carbon matrix, which hampers the complete SnS conversion reaction and Na intercalation processes. In contrast, pyrolysis at 800 °C facilitates more thorough sulfur release, yielding a defect-rich but stable carbon matrix that supports enhanced sodiation/desodiation reversibility. Operando Raman spectroscopy and X-ray photoelectron spectroscopy depth profiling confirm that the pyrolysis temperature strongly affects the formation and stability of the solid electrolyte interphase. The SnS@C material pyrolyzed at 800 °C not only possesses superior ion transport characteristics but also delivers enhanced electrochemical performance, maintaining a stable capacity of ≈500 mAh g at C/10 and retaining a substantial fraction of its capacity over 100 cycles, in contrast to the rapidly decaying capacity of the material pyrolyzed at 600 °C.
开发坚固且高效的阳极对于推进钠离子电池技术至关重要。在此,本文报道了对在不同热解温度下制备的SnS@C复合材料进行的系统研究,以阐明其结构、表面和电化学性质如何控制钠离子存储。研究表明,较低的合成温度会使额外的硫被困在碳基质中,这阻碍了SnS的完全转化反应和钠嵌入过程。相比之下,在800°C下热解有助于更彻底地释放硫,产生富含缺陷但稳定的碳基质,从而支持增强的 sodiation/desodiation 可逆性。原位拉曼光谱和X射线光电子能谱深度剖析证实,热解温度强烈影响固体电解质界面的形成和稳定性。在800°C下热解的SnS@C材料不仅具有优异的离子传输特性,还具有增强的电化学性能,在C/10下保持约500 mAh g的稳定容量,并在100次循环后保留其大部分容量,而在600°C下热解的材料容量则迅速衰减。