摘要
采用等离子体源离子渗氮,即低能(1-3keV)、超大剂量(10^(19)~10^(20)ions.cm^(-2))氮离子注入-同步热扩散技术,在300~500℃处理碳化硼薄膜,合成了硼碳氮三元薄膜.俄歇电子能谱和漫反射富氏变换红外光谱分析表明,合成的硼碳氮薄膜是碳硼比固定,氮含量可控的非晶态薄膜.300℃渗氮的薄膜由sp^2型的硼、碳、氮微区构成,而500℃渗氮的薄膜则由sp^3和sP^2型复合的微区组成.较高的渗氮工艺温度促进sP^3型结构的形成,渗氮工艺时间对薄膜结构的影响不显著.
An amorphous boron-carbon-nitrogen film was syathesized by plasma source ion nitriding,that is nitrogen ion implantation at low energy (1-3 keV) and superhigh dose (1019-1020ions. cm(-2)) and simultaneously indiffusion. Auger electron spectroscopy and diffuse reflectanceFourier transform infrared spectra showed that the films are mainly composed of sp2 and sp3 plain(graphite- and Pyridine-like) microdomains with a fixed B/C ratio and a controllable nitrogencontent at a nitriding temperature of 500℃ for a nitriding time from 2 to 6 h. The formation ofsp3 plain microdomains strongly depends on the nitriding temperature and softly on the nitridingtime.
出处
《无机材料学报》
SCIE
EI
CAS
CSCD
北大核心
1999年第1期189-192,共4页
Journal of Inorganic Materials
基金
国家自然科学基金!59402009
关键词
等离子体源
离子渗氮
硼碳氮薄膜
plasma source ion nitriding, boron-carbon-nitrogen film