Maslar James E, Hoang John, Kimes William A, Sperling Brent A
Material Measurement Laboratory, National Institute of Standards and Technology, 100 Bureau Drive, Stop 8320, Gaithersburg, MD 20899-8320 USA.
Appl Spectrosc. 2015 Mar;69(3):332-41. doi: 10.1366/14-07695. Epub 2015 Feb 1.
A nondispersive infrared (NDIR) gas analyzer that utilizes a mid-infrared light emitting diode (LED) source was demonstrated for monitoring the metal alkylamide compound tetrakis(dimethylamido) titanium (TDMAT), Ti[N(CH3)2]4. This NDIR gas analyzer was based on direct absorption measurement of TDMAT vapor in the C-H stretching spectral region, a spectral region accessed using a LED with a nominal emission center wavelength of 3.65 μm. The sensitivity of this technique to TDMAT was determined by comparing the absorbance measured using this technique to the TDMAT density as determined using in situ Fourier transform IR (FT-IR) spectroscopy. Fourier transform IR spectroscopy was employed because this technique could be used to (1) quantify TDMAT density in the presence of a carrier gas (the presence of which precludes the use of a capacitance manometer to establish TDMAT density) and (2) distinguish between TDMAT and other gas-phase species containing IR-active C-H stretching modes (allowing separation of the signal from the LED-based optical system into fractions due to TDMAT and other species, when necessary). During TDMAT-only delivery, i.e., in the absence of co-reactants and deposition products, TDMAT minimum detectable molecular densities as low as ≈4 × 10(12) cm(-3) were demonstrated, with short measurement times and appropriate signal averaging. Reactions involving TDMAT often result in the evolution of the reaction product dimethylamine (DMA), both as a thermal decomposition product in a TDMAT ampoule and as a deposition reaction product in the deposition chamber. Hence, the presence of DMA represents a significant potential interference for this technique, and therefore, the sensitivity of this technique to DMA was also determined by measuring DMA absorbance as a function of pressure. The ratio of the TDMAT sensitivity to the DMA sensitivity was determined to be ≈6.0. To further examine the selectivity of this technique, measurements were also performed during atomic layer deposition (ALD) of titanium dioxide using TDMAT and water. During ALD, potential interferences were expected from the evolution of DMA due to deposition reactions and the deposition on the windows of species containing IR-active C-H stretching modes. It was found that the interfering effects of the evolution of DMA and deposition of species on the windows corresponded to a maximum of only ≈6% of the total observed TDMAT density. However, this level of interference likely is relatively low compared to a typical chemical vapor deposition process in which co-reactants are introduced into the chamber at the same time.
展示了一种利用中红外发光二极管(LED)源的非色散红外(NDIR)气体分析仪,用于监测金属烷基酰胺化合物四(二甲基氨基)钛(TDMAT),即Ti[N(CH3)2]4。该NDIR气体分析仪基于在C-H伸缩光谱区域对TDMAT蒸气的直接吸收测量,该光谱区域可通过标称发射中心波长为3.65μm的LED来实现。通过将该技术测量的吸光度与使用原位傅里叶变换红外(FT-IR)光谱法测定的TDMAT密度进行比较,确定了该技术对TDMAT的灵敏度。采用傅里叶变换红外光谱法是因为该技术可用于:(1)在存在载气的情况下定量TDMAT密度(载气的存在排除了使用电容式压力计来确定TDMAT密度);(2)区分TDMAT和其他含有红外活性C-H伸缩模式的气相物种(必要时可将基于LED的光学系统的信号分离为由于TDMAT和其他物种产生的部分)。在仅输送TDMAT时,即在没有共反应物和沉积产物的情况下,展示了TDMAT的最低可检测分子密度低至≈4×10(12) cm(-3),测量时间短且进行了适当的信号平均。涉及TDMAT的反应通常会产生反应产物二甲胺(DMA),它既作为TDMAT安瓿中的热分解产物,也作为沉积室中的沉积反应产物。因此,DMA的存在对该技术构成了重大潜在干扰,所以,也通过测量DMA吸光度随压力的变化来确定该技术对DMA的灵敏度。确定TDMAT灵敏度与DMA灵敏度之比约为6.0。为了进一步研究该技术的选择性,还在使用TDMAT和水进行二氧化钛原子层沉积(ALD)过程中进行了测量。在ALD过程中,预计由于沉积反应产生的DMA以及含有红外活性C-H伸缩模式的物种在窗口上的沉积会产生潜在干扰。发现DMA的产生和物种在窗口上的沉积的干扰效应最多仅相当于观察到的总TDMAT密度的≈6%。然而,与典型的化学气相沉积过程相比,这种干扰水平可能相对较低,在典型的化学气相沉积过程中,共反应物会同时引入到反应室中。