Demonstrates improved performance in top-gated FETs with H2O2-based dielectrics, suggesting enhanced device suitability.
Two-dimensional (2D) transition-metal dichalcogenides are promising channel materials, but integrating ultrathin high-k gate dielectrics remains challenging because their surfaces lack dangling bonds. Atomic layer deposition (ALD) enables conformal dielectric growth on these 2D materials, with oxidant selection introducing a trade-off between water (H 2 O), which yields poor nucleation, and ozone (O 3 ), which affords uniform coverage at the expense of interface/channel degradation via oxygen substitution. Here, we demonstrate that hydrogen peroxide (H 2 O 2 )-driven ALD of high-k oxides yields uniform dielectric coverage while minimizing performance degradation by controlling Mo-sulfate formation at the interface on molybdenum disulfide (MoS 2 ). This chemistry offers nucleation sites while preserving the 2D channel integrity through S–O interfacial bonding. Top-gated MoS 2 field-effect transistors (FETs) with H 2 O 2 -based ALD hafnium oxide (HfO 2 ) gate dielectrics achieve steep subthreshold slopes (∼70 mV/dec), low hysteresis (∼42 mV), and an equivalent oxide thickness (EOT) of ∼0.9 nm. Benchmarking shows that these devices exhibit improved performance compared with previously reported single-dielectric top-gated MoS 2 FETs. These findings establish H 2 O 2 -driven ALD of a high-k dielectric as a promising approach for complementary metal-oxide-semiconductor (CMOS)-compatible 2D gate stacks and suggest that robust S–O interfacial bonding can enable 3D-integrated, low-power device operation.
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Lee et al. (2026) studied this question.
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