氢环境下TiO2层的低压化学气相沉积

S. Yamauchi, K. Ishibashi, S. Hatakeyama
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引用次数: 10

摘要

研究了锐钛矿型TiO2在3 mtorr压力下的低压化学气相沉积(LPCVD),并与TTIP和O2的低压化学气相沉积(LPCVD)进行了比较。TTIP在H2中的解离能高于O2,但沉积在H2中的层的电阻率显著降低至0.2 Ω cm,而沉积在O2中的层的电阻率高于100 Ω cm。紫外-可见透射光谱显示,由于Urbach尾的增加,TTIP + H2沉积层在2.2 eV左右的吸收增加,禁能隙减小。在100 K以下的低温电阻率表明,在h2环境下沉积的层由于高电子密度而退化,但在100 K以上的温度下电阻率下降,活化能约为100 meV。基于核、晶界和表面陷阱的可能的电子传导模型可以澄清温度相关电阻率,表明层的电阻率受到从表面延伸的晶界耗尽区限制,层内形成了10-3 Ω cm量级的显著低电阻率核。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low Pressure Chemical Vapor Deposition of TiO2 Layer in Hydrogen-Ambient
Low pressure chemical vapor deposition (LPCVD) of anatase TiO2 as a reduction gas was demonstrated at pres- sure of 3 mtorr in comparison to that using TTIP and O2 with study for the property of the layers. Dissociation energy of TTIP in H2 was higher than that in O2 but resistivity of the layer deposited in H2 was significantly decreased to 0.2 Ω cm in contrast to the high resistivity beyond 100 Ω cm of the layer deposited in O2. UV-Vis optical transmission spectra showed absorption around 2.2 eV was increased in the layer deposited by TTIP + H2 in addition to decrease of forbidden energy gap due to increase of Urbach tail. Resistivity at low temperature below 100 K indicating the layer deposited in H2-ambient was degenerated by the high electron density but the resistivity was decreased with temperature above 100 K with the activation energy about 100 meV. A possible electronic conduction model based on kernel, grain boundary and surface trap to clarify the temperature dependent resistivity suggesting resistivity of the layer was limited by depletion region in the grain-boundary extended from the surface and the kernel with significantly low resistivity in 10-3 Ω cm order was formed in the layer.
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