Efficient thermal energy harvesting using phase change materials (PCMs) has great potential for thermal energy storage and thermal management applications. Benefiting from these merits of pore structure diversity, convenient controllability, and excellent thermophysical stability, SiO-based composite PCMs have comparatively shown more promising prospect. In this regard, the microstructure-thermal property correlation of SiO-based composite PCMs is still unclear despite the significant achievements in structural design. To enrich the fundamental understanding on the correlations between the microstructure and the thermal properties, we systematically summarize the state-of-the-art advances in SiO-based composite PCMs for tuning thermal energy storage from the perspective of tailoring chemistry strategies. In this review, the tailoring chemistry influences of surface functional groups, pore sizes, dopants, single shell, and hybrid shells on the thermal properties of SiO-based composite PCMs are systematically summarized and discussed. This review aims to provide in-depth insights into the correlation between structural designs and thermal properties, thus showing better guides on the tailor-made construction of high-performance SiO-based composite PCMs. Finally, the current challenges and future recommendations for the tailoring chemistry are also highlighted.
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http://dx.doi.org/10.1016/j.isci.2020.101606 | DOI Listing |
J Colloid Interface Sci
February 2025
Key Laboratory of Advanced Ceramics and Machining Technology (Ministry of Education), and Tianjin Key Laboratory of Composite and Functional Materials, School of Materials Science and Engineering, Tianjin University, Tianjin 300072, China. Electronic address:
Due to its high theoretical specific capacity, micron-sized silicon monoxide (SiO) is regarded as one of the most competitive anode materials for lithium-ion batteries with high specific energy density. However, originating from the low initial Coulombic efficiency (ICE) and large volume expansion, its large-scale application is seriously hindered. Herein, an easy-to-implement solid-state pre-lithiation method synergized with the magnesiothermic reduction process was performed to enhance the ICE of SiO and a common bimetallic hydride was used as a prelithiation reagent.
View Article and Find Full Text PDFChempluschem
October 2024
Faculty of Materials Science and Engineering, Kunming University of Science and Technology, Kunming, 650093, P. R. China.
Lithium-ion batteries (LIBs) are widely used in electric vehicles, portable electronic devices, clean energy storage, and other fields due to their long service life, high energy density, and low self-discharge rate, which also puts forward higher requirements for the performance of lithium-ion batteries. As an anode for lithium-ion batteries, SiO materials have garnered significant attention from researchers due to its high specific capacity (2400 mAh g), abundance of raw materials, and simple preparation. However, its large volume change (~200 %) and poor electrical conductivity hinder its large-scale commercial application.
View Article and Find Full Text PDFChemistryOpen
March 2021
Department of Research and Development, Shanghai Power and Energy Storage Battery System Engineering Technology Research Center, Shanghai, 200245, China.
Silicon monoxide (SiO) is considered as one of the most promising alternative anode materials thanks to its high theoretical capacity, satisfying operating voltage and low cost. However, huge volume change, poor electrical conductivity, and poor cycle performance of SiO dramatically hindered its commercial application. In this work, we report an affordable and simple way for manufacturing carbon-coated SiO-C composites with good electrochemical performance on kilogram scales.
View Article and Find Full Text PDFFront Chem
May 2020
Guangdong Provincial Key Laboratory of Advanced Energy Storage Materials, School of Materials Science and Engineering, South China University of Technology, Guangzhou, China.
The SiO-based composites containing different carbon structures were prepared from asphalt and graphite by the milling, spray drying, and pyrolysis. In the obtained near-spherical composite particles, the refined amorphous SiO plates, which are coated with an amorphous carbon layer, are aggregated with the binding of graphite sheets. The SiO/C/Graphite composites present a maximum initial charge capacity of 963 mAh g at 100 mA g, excellent cyclic stability (~950 mAh g over 100 cycles), and rate capability with the charge capacity of 670 mAh g at 1,000 mA g.
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