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Tantalum- and ruthenium-based diffusion barriers/adhesion promoters for copper/silicon dioxide and copper/low kappa integration.

机译:用于铜/二氧化硅和铜/低kappa集成的基于钽和钌的扩散阻挡层/粘附促进剂。

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摘要

The TaSiO6 films, ∼8A thick, were formed by sputter deposition of Ta onto ultrathin SiO2 substrates at 300 K, followed by annealing to 600 K in 2 torr O2. X-ray photoelectron spectroscopy (XPS) measurements of the films yielded a Si(2p) binding energy at 102.1 eV and Ta(4f7/2) binding energy at 26.2 eV, indicative of Ta silicate formation. O(1s) spectra indicate that the film is substantially hydroxylated. Annealing the film to >900 K in UHV resulted in silicate decomposition to SiO2 and Ta2O5. The Ta silicate film is stable in air at 300K. XPS data show that sputter-deposited Cu (300 K) displays conformal growth on Ta silicate surface (TaSiO6) but 3-D growth on the annealed and decomposed silicate surface. Initial Cu/silicate interaction involves Cu charge donation to Ta surface sites, with Cu(I) formation and Ta reduction. The results are similar to those previously reported for air-exposed TaSiN, and indicate that Si-modified Ta barriers should maintain Cu wettability under oxidizing conditions for Cu interconnect applications.; XPS has been used to study the reaction of tert-butylimino tris(diethylamino) tantalum (TBTDET) with atomic hydrogen on SiO2 and organosilicate glass (OSG) substrates. The results on both substrates indicate that at 300K, TBTDET partially dissociates, forming Ta-O bonds with some precursor still attached. Subsequent bombardment with atomic hydrogen at 500K results in stoichiometric TaN formation, with a Ta(4f7/2) feature at binding energy 23.2 eV and N(1s) at 396.6 eV, leading to a TaN phase bonded to the substrate by Ta-O interactions. Subsequent depositions of the precursor on the reacted layer on SiO2 and OSG, followed by atomic hydrogen bombardment, result in increased TaN formation. These results indicate that TBTDET and atomic hydrogen may form the basis for a low temperature atomic layer deposition (ALD) process for the formation of ultraconformal TaN x or Ru/TaNx barriers.; The interactions of sputter-deposited ruthenium with OSG at 300 K have been studied by XPS for Ru coverages from ∼0.1 monolayer to several monolayers, using in-situ sample transfer between the deposition and analysis chambers. The results indicate Stranski-Krastanov (SK) type growth, with the completion of the first layer of Ru at an average thickness corresponding to 1 monolayer average coverage. Ru(0) is the only electronic state present. XPS core level spectra indicate weak chemical interactions between Ru and the substrate. A less pronounced tendency towards SK growth was observed for Ru deposition on parylene. Deposition of Ru on OSG followed by electroless deposition of Cu resulted in the formation of a shiny copper film that failed the ScotchRTM tape test. Results indicate failure mainly at the Ru/OSG interface.
机译:通过在300 K下将Ta溅射沉积到超薄SiO2衬底上,然后在2 torr O2中退火至600 K,形成约8A厚的TaSiO6膜。薄膜的X射线光电子能谱(XPS)测量得出在102.1 eV的Si(2p)结合能和在26.2 eV的Ta(4f7 / 2)结合能,表明形成了Ta硅酸盐。 O(1s)光谱表明该膜已基本羟基化。在UHV中将膜退火至> 900 K,导致硅酸盐分解为SiO2和Ta2O5。硅酸钽薄膜在300K的空气中稳定。 XPS数据显示,溅射沉积的Cu(300 K)在Ta硅酸盐表面(TaSiO6)上显示共形生长,而在退火和分解的硅酸盐表面上显示3-D生长。最初的铜/硅酸盐相互作用涉及将铜电荷捐赠给Ta表面部位,并形成Cu(I)和Ta还原。结果与先前报道的暴露于空气中的TaSiN的结果相似,表明Si修饰的Ta势垒应在氧化条件下保持Cu润湿性以用于Cu互连应用。 XPS已用于研究叔丁基亚氨基三(二乙氨基)钽(TBTDET)与氢原子在SiO2和有机硅玻璃(OSG)基材上的反应。两种底物上的结果均表明,在300K时,TBTDET部分解离,形成Ta-O键,且某些前驱物仍附着。随后以500K原子氢轰击会形成化学计量的TaN,在结合能23.2 eV处具有Ta(4f7 / 2)特征,在396.6 eV时具有N(1s),导致TaN相通过Ta-O相互作用键合到基底上。随后将前体沉积在SiO2和OSG上的反应层上,随后进行原子氢轰击,导致TaN形成增加。这些结果表明,TBTDET和原子氢可构成低温原子层沉积(ALD)工艺的基础,以形成超共形TaN x或Ru / TaNx势垒。 XPS已使用沉积和分析室之间的原位样品转移,通过XPS研究了Ru覆盖范围从〜0.1单层到数个单层的溅射沉积钌与OSG的相互作用。结果表明Stranski-Krastanov(SK)型生长,第一层Ru的平均厚度对应于1个单层平均覆盖率。 Ru(0)是唯一存在的电子状态。 XPS核心能级谱表明Ru与底物之间的化学相互作用较弱。对于Ru在聚对二甲苯上的沉积,观察到SK生长的趋势不太明显。在OSG上沉积Ru,然后化学沉积Cu导致形成了发亮的铜膜,该膜未能通过ScotchRTM胶带测试。结果表明故障主要在Ru / OSG接口上。

著录项

  • 作者

    Zhao, Xiaopeng.;

  • 作者单位

    University of North Texas.;

  • 授予单位 University of North Texas.;
  • 学科 Chemistry Analytical.
  • 学位 Ph.D.
  • 年度 2004
  • 页码 97 p.
  • 总页数 97
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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