期刊
CERAMICS INTERNATIONAL
卷 47, 期 16, 页码 22839-22853出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.ceramint.2021.04.303
关键词
SiBCN; Soluble polyborosilazanes; Electrochemical performance
资金
- National Natural Science Foundation of China [52002092, 51832002]
- National Key Research and Development Program of China [2017YFB0310400]
- China Postdoctoral Science Foundation [BX20190095, 2019M660072, LBH-Z19141]
- Advanced Space Propulsion Laboratory of BICE and Beijing Engineering Research center of Efficient and Green Aerospace Propulsion Technology [LabASP-2019-08]
A novel method for synthesizing polyborosilazanes was proposed and demonstrated to exhibit stable performance in the preparation of SiBCN ceramics, showing a high reversible capacity in the initial cycle.
Tris(dichloromethylsilylethyl)borane is a compound containing a B-C bond and Cl and H elements. Herein, we propose a novel method to synthesize polyborosilazanes using tris(dichloromethylsilylethyl)borane and boron trichlorosilane as boron sources and hexamethyldisilazane as a nitrogen source. The microstructure and chemical composition of the as-synthesized polyborosilazanes and as-annealed SiBCN ceramics were investigated using Fourier transform infrared spectroscopy, nuclear magnetic resonance spectroscopy, Raman spectroscopy, scanning electron microscope, and transmission electron microscope methods. The organic precursors were converted entirely into inorganic ceramics at 800 degrees C, and the ceramic yield of the polyborosilazanes was 88% at 1000 degrees C. SiBCN ceramics with irregular shapes contained chemical bonds of B-N, Si-N, and Si-C at 1500 degrees C and retained an amorphous structure below 1600 degrees C. After the first cycle, the fabricated SiBCN ceramic anodes exhibited a reversible capacity of 261.3 mA h/g, which was 2.6 times that reported in the literature (101 mA h/g). The discharge capacity decreased to 157.6 mA h/g after 30 cycles. The satisfactory electrochemical performance of the resulting SiBCN ceramic anodes can be attributed to the formation of conductive carbon species favoring the transport properties of lithium ion.
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