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Area‐selective deposition (ASD) shows great promise for sub‐10 nm manufacturing in nanoelectronics, but significant challenges remain in scaling to ultrasmall dimensions and understanding feature‐dependent nonuniformity and selectivity loss. This work addresses these problems by simultaneously quantifying uniformity and selectivity for passivation/deposition/etch supercycles in 45 nm half‐pitch TiN/SiO2 line/space patterns. This work employs three selective processes that are uniquely suited for supercycle processing: dimethylamino‐trimethylsilane (DMA‐TMS) inhibition, TiO2 atomic layer deposition (ALD), and HBr/BCl3 plasma etch. The DMA‐TMS inhibition selectively passivates the SiO2 nongrowth surface without affecting deposition on the TiN and TiO2 growth surfaces. The plasma etch removes TiO2 defect particles at a faster rate than the conformal TiO2 film or SiO2 lines. Using three supercycles of this process, this work demonstrates 8 nm of TiO2 with 88% uniformity and ≈100% selectivity according to transmission electron microscopy (TEM), a 2×improvement in film thickness from previous reports in similar nanoscale patterns. Integrated consideration of uniformity and selectivity at specific feature scales will facilitate the effective design of selective deposition processes for nanoscale electronic devices. [ABSTRACT FROM AUTHOR]

Small-molecule inhibitors have recently been introduced for passivation during area-selective deposition (ASD). Small silanes like (N,N-dimethylamino)trimethylsilane (DMATMS) selectively react with −OH sites on SiO2 to form a less reactive –OSi(CH3)3 terminated surface. The –OSi(CH3)3 surface termination can inhibit many atomic layer deposition (ALD) processes, including TiCl4/H2O ALD. However, the mechanisms by which ALD is inhibited and by which selectivity is eventually lost are not well understood. This study uses in situ Fourier-transform infrared spectroscopy to probe the adsorption of DMATMS on SiO2 and the subsequent reactions when the passivated surface is exposed to TiCl4/H2O ALD. The chemisorption of DMATMS on isolated –OH groups on SiO2 is shown to inhibit the reaction with TiCl4. Further, we find that starting with an inherently inhibiting H-terminated Si surface, DMATMS can also react with residual –OH groups and reduce the extent of nucleation. Finally, using Rutherford backscattering spectrometry, the effectiveness of DMATMS passivation on SiO2 and H-terminated Si is quantified during extended ALD cycle numbers. The insight into the mechanisms of passivation by DMATMS and passivation loss can enable the rational design of highly selective ASD processes by carefully matching compatible surfaces, passivating agents, and ALD precursors. [ABSTRACT FROM AUTHOR]

Nanoelectronics holds significant promise for two-dimensional (2D) semiconducting transition metal dichalcogenide (TMD) applications. On a polycrystalline WS2 monolayer created by metal-organic chemical vapor deposition (MOCVD) at 950 °C, we studied the nucleation, growth, and development of Al2O3 atomic layer deposition (ALD) on a SiO2/Si substrate. In this investigation, we used various complementary characterization methods, such as Raman spectroscopy, elastic recoil detection, atomic force microscopy, and time-of-flight secondary ion mass spectrometry, to understand thoroughly the intrinsic reactivity of WS2. Strong peak intensity changes at the interfaces in the Raman line scans of the SiO2/Si patterns suggest extremely crystalline WS2. After multiple ALD cycles, triangular WS2 crystals were decorated to provide a two-dimensional growth mode with a great selectivity for grain boundaries and step edges. The results of this work can be used for further exploration of the TMD monolayer structure and properties, which is essential for tailoring 2D materials for a specific application in devices. [ABSTRACT FROM AUTHOR]

The impact of chlorine residue concentration in thin Hf[O.sub.2] films on the MOSFET device time-dependent dielectric breakdown (TDDB) is discussed. The results have shown that the presence of chlorine residue has no important impact on the trap generation and reliability of atomic layer deposition (ALD) Hf[O.sub.2] layers.

An effective technique and methodology for the estimation of fixed charge components in high-kappa stacks was demonstrated by varying both the SiO[sub 2] and high-kappa dielectric thicknesses. Layers with different thickness of both the nitrided and non-nitrided hafnium-silicate layers were grown on wafers to estimate the entire interfacial and bulk charge components. This method was used to compare the fixed charge levels in Hf-silicates (HfSiO) and nitrided-Hf-silicate (HfSiON) layers.

Low equivalent oxide thickness (EOT) and high-performing n-channel transistors with a Hf[O.sub.2]/TaN gate stack and a low thermal-budget process is demonstrated using solid-phase epitaxial regrowth of the source and drain junctions. The thinnest devices have an EOT of 8 Angstrom, a leakage current of 1.5/a[cm.sup.2] at [V.sub.G] = 1 V, a peak mobility of 190 [cm.sup.2]/V .s and a drive current of 815 [mu]A/[mu]m at an OFF-state current of 0.1 [mu]A/mum for [V.sub.DD]= 1.2V.

The reactions of (super 1)S and (super 3)D Cu(super +) ions with N2O are studied using the help of ab initio methods. The calculations showed that bare (super 1)S Cu(super +) ions are relatively inert with respect to N2O.

The reaction of 3d transition metal atoms with N2O is studied to examine charge transfer process in the reaction mechanism by combination of density functional theory and the coupled cluster method CCSD(T). Results showed no charge transfer from the transition metal toward N2O for Sc, Ti and V transition state, whereas charge transfer between the metal 4s orbital and the in-plane N2O LUMO is an important process, when moving from Cr to Cu in the 3d transition series.

The structure, crystallinity and properties of as-deposited two-dimensional (2D) transition metal dichalcogenides are determined by nucleation mechanisms in the deposition process. 2D materials grown by atomic layer deposition (ALD) in the absence of a template are polycrystalline or amorphous. Little is known about their nucleation mechanisms. Therefore, the nucleation behavior of WS2 during plasma enhanced ALD from WF6, H2 plasma and H2S at 300 °C is investigated on amorphous ALD Al2O3 starting surface and on monocrystalline, bulk sapphire. Preferential interaction of the precursors with the Al2O3 starting surface promotes fast closure of the WS2 layer. The WS2 layers are fully continuous at WS2 content corresponding to only 1.2 WS2 monolayers. On amorphous Al2O3, (0002) textured and polycrystalline WS2 layers form with grain size of 5 to 20 nm due to high nucleation density (∼1014 nuclei/cm2). The WS2 growth mode changes from 2D (layer-by-layer) growth on the initial Al2O3 surface to three-dimensional (Volmer-Weber) growth after WS2 layer closure. Further growth proceeds from both WS2 basal planes in register with the underlying WS2 grain and from or over grain boundaries of the underlying WS2 layer with different in-plane orientation. In contrast, on monocrystalline sapphire, WS2 crystal grains can locally align along a preferred in-plane orientation. Epitaxial seeding occurs locally albeit a large portion of crystals remain randomly oriented, presumably due to the low deposition temperature. The WS2 sheet resistance is 168 MΩμm, suggesting that charge transport in the WS2 layers is limited by grain boundaries. [ABSTRACT FROM AUTHOR]

Atomic layer deposition (ALD) with HfCl4 as a precursor is widely used for HfO2 fabrication. Due to the nature of the precursor under study, i.e., HfCl4 and H2O, the presence of chlorine residues in the film due to insufficient hydrolysis is eminent. Obviously, the chlorine residue in the HfO2 film is suspected to affect the quality of the HfO2 film. In this paper, we reduced the concentration of chlorine residues by increasing the H2O oxidant pulse time in between the deposition cycles from 0.3 to 10 and 90s. Time-of-flight secondary ion mass spectrometry analysis shows that this decreases the chlorine concentration in the HfO2 film by more than one order of magnitude. However, time-dependent dielectric breakdown analysis shows that the lifetime remains quasi unaffected (within identical error bars) for the different injection cycles. Charge pumping analysis was done by varying both pulse frequency and amplitude to investigate the creation of defects, but negligible differences were observed. Therefore, we conclude that the presence of chlorine residues has no significant impact on the trap generation and reliability of ALD HfO2 layers, and this result corresponded with the mobility result. The experimental picture is confirmed with first-principle calculations that show that the presence of chlorine residues does not induce defect levels in the bandgap of HfO2. [ABSTRACT FROM AUTHOR]

The authors demonstrate high-performing n-channel transistors with a HfO2/TaN gate stack and a low thermal-budget process using solid-phase epitaxial regrowth of the source and drain junctions. The thinnest devices have an equivalent oxide thickness (EOT) of 8 Å, a leakage current of 1.5 A/cm² at VG = 1 V, a peak mobility of 190 cm²/V · s, and a drive-current of 815 μA/μm at an OFF-state current of 0.1 μA/μm for VDD = 1.2 V. Identical gate stacks processed with a 1000-°C spike anneal have a higher peak mobility at 275 cm²/V · s, but a 5-Å higher EOT and a reduced drive current at 610 μA/μm. The observed performance improvement for the low thermal-budget devices is shown to be mostly related to the lower EOT. The time-to-breakdown measurements indicate a maximum operating voltage of 1.6 V (1.2 V at 125 °C) for a ten-year lifetime, whereas positive-bias temperature-instability :measurements indicate a sufficient lifetime for operating voltages below 0.75 V. [ABSTRACT FROM AUTHOR]