期刊
NEW JOURNAL OF CHEMISTRY
卷 40, 期 8, 页码 7034-7042出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5nj03723a
关键词
-
资金
- National Natural Science Foundation of China [51321061, 51472059, 51272300]
- China National Funds for Distinguished Young Scientists [51225203]
Here, we demonstrated a novel synthesis of a polyborosilazane (PBSN) precursor using hydroboration and aminolysis reaction synergies to modify polysilazane (PSN). Specifically, borane-tetrahydrofuran and boron trichloridehexane were used as dual boron sources, which not only reacted with Si Vi and Si N H functionality respectively to modify multiple active sites of PSN resulting in boron-rich silicon boron carbide nitride (SiBCN) ceramics, but also improved controllability on composition, molecular structure, as well as final features. The resulting structures were characterized by FTIR, solid-state 11B and 29Si magic-angle spinning NMR and inductively coupled plasma emission spectral (ICP) analysis. These polymers were found to be structurally complex networks composed of tri-coordinate BCxN3-x and tetra-coordinate BCxN4-x bridges. The resulting polyborosilazanes contained similar to 11 wt% higher boron contents than that in the starting polymer. The structural evolution of the resulting polymers was evaluated by means of XPS, FTIR and XRD, and TGA-DSC-QMS was utilized to detail the precursor-to-ceramic conversion.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据