The chemical mechanical planarization (CMP) process is critical in fabricating ultra large scale integrated (ULSI) circuit devices in semiconductor industry. In a typical aluminum damascene interconnect scheme, Al is usually blanket deposited over a liner layer to fill contact holes and vias. After deposition, the excess of Al is removed by CMP, leaving Al only in the holes and vias to form interconnects. Since the slurries used for aluminum CMP typically contain an oxidant and other chemical additives, the electrochemical behavior of Al and the liner may be expected to affect the polishing rates. In addition, when the excess of Al is removed, a surface transition from Al to liner occurs. Since Al and the liner may exhibit different electrochemical behaviors in the slurry, galvanic coupling between Al and the underlayer is a possibility. Such a coupling may lead to localized corrosion or rate control problems. The objective of this research was to characterize the fundamental electrochemical behavior of thin aluminum-0.5%copper, titanium and aluminum/titanium stack films before, during and after abrasion in a commercially available alumina based slurry containing iodate as an oxidant. A special apparatus in which electrochemical tests can be carried out during polishing was fabricated and used for this research. It was found that the electrochemical corrosion rates during abrasion were much smaller than the actual polishing rates obtained with the simulated CMP apparatus, indicating that the mechanism of Al removal by the iodate based slurry may not be dominated by electrochemical factors. A sharp rise in corrosion potential (Ecorr) during the transition from Al to Ti film was measured during polishing of the Al/Ti film stack. This potential change during transition was of the order of 1V on the Al film deposited at room temperature. The transition was much sharper with the low-temperature (25°C) Al film than the high-temperature (475°C) Al thin film. The slower transition in OCP in high-temperature films is most likely due to a Ti-Al intermetallic compound formed at the Al/Ti interface. The galvanic corrosion between Al and Ti during polishing and Al post-polishing corrosion issues were also investigated. It was found that the galvanic corrosion rate between Al and Ti is 6*10⁻⁴ A/cm² and the corrosion potential is -0.24 V. Also, the corrosion current density for Al after abrasion and immersion in de-ionized water is lower than that in the slurry. In addition, the post polishing corrosion of Al in after abrasion in the iodate based alumina slurry was also investigated. It was found that the corrosion of Al in DI water after abrasion was insignificant.
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机译:化学机械平面化(CMP)工艺对于制造半导体行业中的超大规模集成(ULSI)电路器件至关重要。在典型的铝镶嵌互连方案中,通常将Al毯式沉积在衬层上,以填充接触孔和通孔。沉积后,通过CMP去除多余的Al,仅将Al留在孔和通孔中以形成互连。因为用于铝CMP的浆料通常包含氧化剂和其他化学添加剂,所以可以预期Al和衬里的电化学行为会影响抛光速率。另外,当去除过量的Al时,发生从Al到衬里的表面过渡。由于铝和衬里在浆料中可能表现出不同的电化学行为,因此铝和底层之间的电流耦合是可能的。这种耦合可能导致局部腐蚀或速率控制问题。这项研究的目的是表征在含碘酸盐作为氧化剂的市售氧化铝基浆料中磨蚀之前,之中和之后的0.5%铜铝薄膜,钛和铝/钛堆叠薄膜的基本电化学行为。制造了一种可以在抛光过程中进行电化学测试的特殊设备,并将其用于该研究。已经发现,磨损期间的电化学腐蚀速率远小于用模拟CMP设备获得的实际抛光速率,这表明基于碘酸盐的浆料去除Al的机理可能不受电化学因素的控制。在抛光Al / Ti膜叠层期间,测量了从Al膜转变为Ti膜时腐蚀电位(Ecorr)的急剧上升。在转变过程中,在室温下沉积的Al膜上的电位变化约为1V。低温(25°C)的Al薄膜比高温(475°C)的Al薄膜的转变要明显得多。由于在Al / Ti界面处形成了Ti-Al金属间化合物,因此高温薄膜中OCP的过渡较慢。还研究了抛光过程中铝和钛之间的电偶腐蚀和铝后抛光腐蚀问题。发现Al和Ti之间的电化腐蚀速率为6×10 -4 A / cm 2,腐蚀电位为-0.24V。而且,在去离子水中磨蚀和浸没后,Al的腐蚀电流密度低于在泥浆中。另外,还研究了在基于碘酸盐的氧化铝浆料中磨蚀后Al对抛光后的腐蚀。结果发现,磨损后去离子水中的铝腐蚀不明显。
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