原子层沉积
材料科学
选择性
基质(水族馆)
纳米技术
沉积(地质)
薄膜
蚀刻(微加工)
图层(电子)
吸附
氮化物
纳米结构
化学工程
硅烷
化学
有机化学
复合材料
催化作用
古生物学
沉积物
工程类
生物
海洋学
地质学
作者
Jinseon Lee,Jeong‐Min Lee,Hongjun Oh,Chang-Han Kim,Jiseong Kim,Dae Hyun Kim,Bonggeun Shong,Tae Joo Park,Woo‐Hee Kim
标识
DOI:10.1002/adfm.202102556
摘要
Abstract Area‐selective atomic layer deposition (AS‐ALD) offers tremendous advantages in comparison with conventional top‐down patterning processes that atomic‐level selective deposition can achieve in a bottom‐up fashion on pre‐defined areas in multi‐dimensional structures. In this work, a method for exploiting substrate‐dependent selectivity of aminosilane precursors for oxides versus nitrides through chemo‐selective adsorption is reported. For this purpose, AS‐ALD of SiO 2 thin films on SiO 2 substrates rather than on SiN substrates are investigated. Theoretical screening using density functional theory (DFT) calculations are performed to identify Si precursors that maximize adsorption selectivity; results indicate that di(isopropylamino)silane (DIPAS) has the potential to function as a highly chemo‐selective precursor. Application of this precursor to SiN and SiO 2 substrates result in inherent deposition selectivity of ≈4 nm without the aid of surface inhibitors. Furthermore, deposition selectivity is enhanced using an ALD‐etch supercycle in which an etching step inserts periodically after a certain number of ALD SiO 2 cycles. Thereby, enlarged deposition selectivity greater than ≈10 nm is successfully achieved on both blanket‐ and SiO 2 /SiN‐patterned substrates. Finally, area‐selective SiO 2 thin films over 4–5 nm are demonstrated inside 3D nanostructure. This approach for performing inherent AS‐ALD expands the potential utility of bottom‐up nanofabrication techniques for next‐generation nanoelectronic applications.
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