Area-selective deposition (ASD) based on self-aligned technology has emerged as a promising solution for resolving misalignment issues during ultrafine patterning processes. Despite its potential, the problems of area-selectivity losing beyond a certain thickness remain critical in ASD applications. This study reports a novel approach to sustain the area-selectivity of Ir films as the thickness increases. Ir films are deposited on AlO as the growth area and SiO as the non-growth area using atomic-layer-deposition with tricarbonyl-(1,2,3-η)-1,2,3-tri(tert-butyl)-cyclopropenyl-iridium and O. O exhibits a dual effect, facilitating both deposition and etching. In the steady-state growth regime, O solely contributes to deposition, whereas in the initial growth stages, longer exposure to O etches the initially formed isolated Ir nuclei through the formation of volatile IrO. Importantly, longer O exposure is required for the initial etching on the growth area(AlO) compared to the non-growth area(SiO). By controlling the O injection time, the area selectivity is sustained even above a thickness of 25 nm by suppressing nucleation on the non-growth area. These findings shed light on the fundamental mechanisms of ASD using O and offer a promising avenue for advancing thin-film technologies. Furthermore, this approach holds promise for extending ASD to other metals susceptible to forming volatile species.
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http://dx.doi.org/10.1002/smll.202402543 | DOI Listing |
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