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首页> 外文期刊>Electrochimica Acta >Formation and characterization of low resistivity sub-100nm copper films deposited by electroless on SAM
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Formation and characterization of low resistivity sub-100nm copper films deposited by electroless on SAM

机译:在SAM上化学沉积低电阻率低于100nm的铜膜的形成和表征

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摘要

Thin Cu films of microelectronic quality and low electrical resistivity were created by electro-less deposition (ELD) onto SiO_2 surface modified first with self-assembled monolayer (SAM) of 3-aminopropyltrimethoxysilane (APTMS) and activated then by 5nm gold nano-particles (AuNPs). The presence of highly oriented amino-terminated SAM was revealed by XPS and ToF-SIMS analyses. The Cu films were deposited in boron- and phosphorous-free tartrate/formaldehyde electrolyte. Controlling the deposition rate via the solution pH permitted a minimum value in resistivity p. XPS depth profile revealed that diffusion of Cu into SiO_2 modified by APTMS did not take place after annealing at 220℃, 4 h. Moreover, annealing resulted in the drop of electrical resistivity to ρ = 4 ± 0.4 μΩ cm for the films with the thickness of 35-100 nm. This value of p is several times smaller than those reported in literature for sub-100nm Cu films deposited by electroless on different SAMs. It is speculated that nano-scale porosity and corrugated structure observed by HRTEM and AFM in the ELD Cu films contribute to the resistivity. The obtained results demonstrate a viable route for formation of low resistivity, sub-100nm Cu films on dielectrics for microelectronic application.
机译:通过先在3-氨基丙基三甲氧基硅烷(APTMS)的自组装单分子膜(SAM)上改性的SiO_2表面上进行无电沉积(ELD)来创建微电子质量和低电阻率的Cu薄膜,然后用5nm的金纳米颗粒活化( AuNPs)。 XPS和ToF-SIMS分析揭示了高度取向的氨基末端SAM。将铜膜沉积在无硼和无磷的酒石酸盐/甲醛电解液中。通过溶液pH值控制沉积速率允许电阻率p为最小值。 XPS深度剖面表明,在220℃,4 h退火后,铜没有扩散到APTMS改性的SiO_2中。此外,退火导致厚度为35-100 nm的薄膜的电阻率下降至ρ= 4±0.4μΩcm。 p的这个值比文献报道的通过化学沉积在不同SAM上的100nm以下的Cu膜小几倍。据推测,通过HRTEM和AFM观察到的ELD Cu膜中的纳米级孔隙率和波纹结构有助于电阻率。获得的结果证明了在微电子应用的电介质上形成低电阻率,低于100nm的Cu膜的可行途径。

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