Luo Junlong, Cai Jun, Gong De, Guo Aoping, Wang Jaw-Kai, Zhang Jiangtao
School of Mechanical Engineering and Automation, Beihang University, Beijing 100191, China.
College of Chemistry, Beijing Normal University, Beijing 100083, China.
Materials (Basel). 2024 Sep 12;17(18):4473. doi: 10.3390/ma17184473.
Pursuing improved electrode materials is essential for addressing the challenges associated with large-scale Li-ion battery applications. Specifically, silicon oxide (SiO) has emerged as a promising alternative to graphite anodes, despite issues related to volume expansion and rapid capacity degradation. In this study, we synthesized carbon-coated SiO using diatom biomass derived from artificially cultured diatoms. However, the inherent carbon content from diatoms poses a significant challenge for the electrochemical performance of diatom-based anodes in large-scale applications. Subsequently, we conducted further research and demonstrated excellent performance with a carbon content of 33 wt.% as anodes. Additionally, real-time characterization of the carbonization process was achieved using thermogravimetry coupled with infrared spectroscopy and gas chromatography mass spectrometry (TG-FTIR-GCMS), revealing the emission of CO and CO during carbonization. Furthermore, electrochemical tests of the processed diatom and carbon (PD@C) anode exhibited outstanding rate capability (~500 mAh g at 2 A g), high initial Coulomb efficiency (76.95%), and a D diffusion rate of 1.03 × 10 cm s. Moreover, structural characterization techniques such as HRTEM-SAED were employed, along with DFT calculations, to demonstrate that the lithium storage process involves not only reversible transport in LiSiO and LiSi, but also physical adsorption between the PD and C layers. Exploring the integration of diatom frustules with the intrinsic carbon content in the fabrication of battery anodes may contribute to a deeper understanding of the mechanisms behind their successful application.
追求改进的电极材料对于应对大规模锂离子电池应用相关的挑战至关重要。具体而言,氧化硅(SiO)已成为石墨负极的一种有前景的替代材料,尽管存在与体积膨胀和快速容量衰减相关的问题。在本研究中,我们使用源自人工培养硅藻的硅藻生物质合成了碳包覆的SiO。然而,硅藻固有的碳含量对基于硅藻的负极在大规模应用中的电化学性能构成了重大挑战。随后,我们进行了进一步研究,并证明当碳含量为33 wt.% 作为负极时具有优异的性能。此外,通过热重分析结合红外光谱和气相色谱 - 质谱联用(TG - FTIR - GCMS)实现了碳化过程的实时表征,揭示了碳化过程中CO和CO的排放。此外,对处理后的硅藻和碳(PD@C)负极的电化学测试显示出出色的倍率性能(在2 A g时约为500 mAh g)、高初始库仑效率(76.95%)以及1.03×10 cm s的D扩散速率。此外,采用了诸如高分辨率透射电子显微镜 - 选区电子衍射(HRTEM - SAED)等结构表征技术以及密度泛函理论(DFT)计算,以证明锂存储过程不仅涉及在LiSiO和LiSi中的可逆传输,还涉及PD和C层之间的物理吸附。探索在电池负极制造中硅藻壳与固有碳含量的整合可能有助于更深入地理解其成功应用背后的机制。