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Passivation of InSb surface for manufacturing infrared devices

机译:用于制造红外设备的InSb表面钝化

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We studied the reduction of active surface states at the InSb/insulator interface by the reduction of hysteresis in C-V plots and by the performance of InSb diodes operated in photovoltaic mode. The InSb wafers were cleaned with CP4A etchant (HNO3:CH3-COOH:HF:H2O at 2:1:1:10). Then layers of 0.4 mu m SiO2, 0.4 mu m Si3N4 and 0.5 mu m Si3N4/SiO2 were deposited on the cleaned surfaced by plasma enhanced chemical vapor deposition (PECVD). After measuring the surface morphology by atomic force microscopy (AFM) the atomic percentage of each element in each compound (e.g. Si and O-2 in SiO2 layer) was studied by energy-dispersive X-ray spectroscopy (EDX). By using photoemisiion spectroscopy (XPS), we showed that the SiO2, Si3N4 and Si3N4/SiO2 layers include Sb and/or SbOx and the Sb-1n antisite during deposition occurred and for this reason their etch rates differ from pure SiO2, Si3N4 and Si3N4/SiO2 layers. Then the gold metal:. was deposited on the samples and capacitance voltage measurement was made on the MIS samples. The results showed hysteresis free curves if the surface has been cleaned correctly. Finally by depositing the 0.4 mu m SiO2, 0.4 mu m Si3N4 and 0.5 mu m Si3N4/SiO2 on diode structure of InSb, the performance of diode in this case was compared with the anodic oxidation method. The results showed the performance of device is better than for the anodic oxidation method. (c) 2007 Elsevier B.V. All rights reserved.
机译:我们研究了通过降低C-V图中的磁滞以及通过以光伏模式工作的InSb二极管的性能来降低InSb /绝缘体界面处的有效表面态。用CP4A蚀刻剂(HNO3:CH3-COOH:HF:H2O的2:1:1:10)清洗InSb晶片。然后,通过等离子增强化学气相沉积(PECVD)在清洁过的表面上沉积0.4μmSiO2、0.4μmSi3N4和0.5μmSi3N4 / SiO2的层。在通过原子力显微镜(AFM)测量表面形态后,通过能量色散X射线光谱(EDX)研究了每种化合物(例如SiO2层中的Si和O-2)中每种元素的原子百分比。通过使用光电子能谱(XPS),我们发现SiO2,Si3N4和Si3N4 / SiO2层包含Sb和/或SbOx,并且在沉积过程中发生了Sb-1n反位,因此其蚀刻速率不同于纯SiO2,Si3N4和Si3N4 / SiO2层。然后是金金属:。沉积在样品上,并在MIS样品上进行电容电压测量。如果正确清洁了表面,结果将显示无滞后曲线。最后,通过在InSb的二极管结构上沉积0.4μm的SiO2、0.4μm的Si3N4和0.5μm的Si3N4 / SiO2,将这种情况下的二极管性能与阳极氧化法进行比较。结果表明,该装置的性能优于阳极氧化法。 (c)2007 Elsevier B.V.保留所有权利。

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