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Corrosion Behavior of Copper Thin Films in Organic HF-Containing Cleaning Solution for Semiconductor Applications

机译:铜薄膜在半导体应用有机HF清洗液中的腐蚀行为

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摘要

The corrosion behavior of electrochemically deposited copper thin films in deaerated and non-deaerated commercial cleaning solutions containing HF was investigated. Potentiodynamic polarization experiments were carried out to determine active, active–passive, passive, and transpassive regions. Corrosion rates were calculated from Tafel slopes. The addition of hydrogen peroxide to the solution and its influence on corrosion was also investigated by employing inductively coupled plasma-mass spectroscopy (ICP-MS) and X-ray photoelectron spectroscopy (XPS). The ICP-MS and potentiodynamic methods yielded comparable Cu dissolution rates. Surface analysis using atomic force microscopy and scanning electron microscopy, performed before and after the cleaning solution treatment, did not reveal any indication of pitting corrosion. The presence of hydrogen peroxide in the cleaning solution led to more than an order of magnitude suppression of copper dissolution rate. We ascribe this phenomenon to the formation of interfacial CuO detected by XPS on the wafer surface that dissolves at a slower rate in dilute HF.
机译:研究了在含HF的脱气和非脱气商业清洁溶液中电化学沉积的铜薄膜的腐蚀行为。进行了电位动力极化实验,以确定主动,主动-被动,被动和跨被动区域。腐蚀速率由塔菲尔斜率计算得出。还通过采用电感耦合等离子体质谱(ICP-MS)和X射线光电子能谱(XPS)研究了溶液中过氧化氢的添加及其对腐蚀的影响。 ICP-MS和电位动力学方法得出的铜溶解速率相当。在清洗液处理之前和之后使用原子力显微镜和扫描电子显微镜进行的表面分析未发现任何点蚀的迹象。清洁溶液中过氧化氢的存在导致铜溶解速率的抑制超过一个数量级。我们将此现象归因于XPS在晶圆表面上形成的界面CuO形成,该界面以较慢的速度溶解于稀HF中。

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