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Suppressed Volume Change of a Spray-Dried 3D Spherical-like Si/Graphite Composite Anode for High-Rate and Long-Term Lithium-Ion Batteries

Jeng-Ywan ShihDepartment of Chemical Engineering, Ming Chi University of Technology, New Taipei City 24301, Taiwan, R.O.CYing-Ru ChenBattery Research Center of Green Energy, Ming Chi University of Technology, New Taipei City 24301, Taiwan, R.O.CYing-Jeng James LiBattery Research Center of Green Energy, Ming Chi University of Technology, New Taipei City 24301, Taiwan, R.O.CTai‐Feng HungBattery Research Center of Green Energy, Ming Chi University of Technology, New Taipei City 24301, Taiwan, R.O.CLi-Fan HsuBattery Research Center of Green Energy, Ming Chi University of Technology, New Taipei City 24301, Taiwan, R.O.CYi-De TsaiBattery Research Center of Green Energy, Ming Chi University of Technology, New Taipei City 24301, Taiwan, R.O.CSayee Kannan RamarajRajan JoseNanostructured Renewable Energy Materials Laboratory, Faculty of Industrial Sciences and Technology, University Malaysia Pahang, Kuantan 26300, MalaysiaChelladurai KaruppiahBattery Research Center of Green Energy, Ming Chi University of Technology, New Taipei City 24301, Taiwan, R.O.CChun‐Chen YangBattery Research Center of Green Energy, Ming Chi University of Technology, New Taipei City 24301, Taiwan, R.O.C
2022en
ABI

Аннотация

Morphology plays a vital role in controlling the volume variation in Si-based anode materials and enhances lithium-ion battery performances. Here, we demonstrated advanced techniques that combine electrostatic self-assembly and spray-drying methods to form 3D spherical-like silicon/graphite (denoted “Si/G”) composite anode materials. This spherical morphology alleviates issues relating to silicon volume changes that occur in high-rate lithium-ion batteries. Commercial graphite (G) flakes were initially mixed with silicon nanoparticles (ca. 50 nm) to form a bare-Si/G composite through electrostatic interaction; spherical-like composite particles were then obtained through single and double spray-drying processes, giving samples SD1-Si/G and SD2-Si/G, respectively. We examined the charge/discharge characteristics of the fabricated electrodes (CR2032-type coin cells) in the voltage range 0.02–1.5 V (vs Li/Li+). The as-fabricated bare-Si/G, SD1-Si/G, and SD2-Si/G half-cells provided initial discharge specific capacities of 897, 866, and 1020 mA h g–1, respectively. The SD2-Si/G half-cell shows better cycling stability at a high current rate of 400 mA g–1 than the SD1-Si/G and bare-Si/G half-cells due to effective inhibition of the volume change in the more stable spherical structure of the SD2-Si/G composite, as evidenced through in situ dilatometry. Thus, the spherical Si/G composite material produced through this simple spray-drying process had structural characteristics that could effectively resist silicon’s high expansion rate, lower the production rate of broken silicon particles, and improve the electrochemical performance of the anode.

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