Co-catalyzed nitridation of silicon and in-situ growth of α-Si3N4 nanorods

被引:60
作者
Huang, Juntong [1 ,2 ]
Zhang, Shaowei [2 ]
Huang, Zhaohui [1 ]
Fang, Minghao [1 ]
Liu, Yan'gai [1 ]
Chen, Kai [1 ]
机构
[1] China Univ Geosci, Sch Mat Sci & Technol, Beijing 100083, Peoples R China
[2] Univ Exeter, Coll Engn Math & Phys Sci, Exeter EX4 4QF, Devon, England
基金
中国国家自然科学基金;
关键词
alpha-Si3N4; Nanorods; Nitridation of silicon; Cobalt catalyst; Growth mechanisms; TEMPERATURE; MECHANISM; NITROGEN; KINETICS; METALS; FE;
D O I
10.1016/j.ceramint.2014.03.122
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The catalytic effects of cobalt (Co) on the direct nitridation of silicon (Si) and morphologies of the nitridation products were investigated, and the relevant reaction mechanisms were proposed. The overall conversion of Si to silicon nitride (Si3N4) was dramatically improved with increasing the nitridation temperature from 1300 to 1350 degrees C. Co played an important role in accelerating the Si nitridation as well as the in-situ growth of alpha-Si3N4 nanorods, via the formation of Co Si liquid phase. At 1350 degrees C, the overall conversion in the reference sample without Co was only 54%, whereas it exceeded 90% in the sample containing 1.25 wt% Co. When the Co addition was more than 7.5 wt%, alpha-Si3N4 nanorods of 80-120 nm in diameter and 800-1600 nm in length became the main product phase. The growth processes of the nanorods with and without nanoparticles (caps) at their tips were governed respectively by vapor-liquid-solid and vapor-vapor-solid mechanisms. (C) 2014 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:11063 / 11070
页数:8
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