Changes in the optical constants of a layer of ZnO nanoparticles (5 nm diameter) induced by UV illumination in O 2 -free atmosphere are determined by using spectroscopic ellipsometry. The onset of optical absorption of ZnO shifts to higher photon energy after illumination. This is interpreted in terms of a Moss-Burstein shift. From the magnitude of the shift, the charge carrier density in the conduction band after UV illumination was determined to be 2 × 10 19 cm -3 , about one carrier per particle. Kelvin probe measurements give a lower limit for the density of 10 18 cm -3 . The free carrier density after illumination is high enough to explain the formation of quasi-ohmic contacts between ZnO and the polymeric p-type conductor poly(3,4-ethylenedioxythiophene) (PEDOT).
Remote plasma atomic layer deposition ͑ALD͒ of SrTiO 3 films with different ͓Sr͔/͓Ti͔ ratios is reported, employing Star-Ti ͓͑pentamethylcyclopentadienyl͒trimethoxy-titanium, ͑CpMe 5 ͒Ti͑OMe͒ 3 ͔ and Hyper-Sr ͓bis͑trisisopropylcyclopentadienyl͒-strontium with 1,2-dimethoxyethane adduct, Sr͑ i Pr 3 Cp͒ 2 DME͔ precursors and O 2 plasma. The as-deposited films were amorphous, but crystallized after post-deposition anneal above 500°C. For annealed SrTiO 3 films with ͓Sr͔/͓Ti͔ = 1.3 and a thickness of 50 nm, a high dielectric constant k Ͼ 80 and low leakage current of ϳ10 −7 A/cm 2 at 1 V were obtained. It is demonstrated that changes in the composition and microstructure are apparent in the optical dielectric function of the SrTiO 3 films, as obtained by spectroscopic ellipsometry.Next-generation dynamic random access memories with an equivalent oxide thickness ͑EOT͒ ഛ 0.35 nm ͑Refs. 1 and 2͒, and high-density metal-insulator-metal ͑MIM͒ capacitors with specific capacitance Ͼ500 nF/mm 2 for automotive and decoupling applications, require ultrahigh permittivity dielectric films ͑preferentially, k Ͼ 100͒ that are conformally deposited in high-aspect ratio structures. Among the perovskite oxide materials with their high dielectric constant for the crystalline films, 3,4 strontium titanate ͓SrTiO 3 ͑STO͒, bulk k ϳ 300, Ref. 3͔ is of particular interest because of its relatively low crystallization temperature between 500 and 600°C ͑Ref. 5͒ which is compatible with the process integration schemes limited to a maximum temperature of 600°C. 4 Due to the stringent requirements on the conformality of Ͼ95% step coverage for aspect ratios Ͼ20-30, targeted thickness of 5-50 nm, and low process temperature, atomic layer deposition ͑ALD͒ is considered as the method of choice for the synthesis of these SrTiO 3 films for such MIM capacitors ͓requirements formulated by MaxCaps Consortium ͑2009͔͒.Various ALD processes for SrTiO 3 using different Ti and Sr precursors have already been reported. They share the approach of alternating the ALD processes of TiO 2 and SrO in a certain ratio to allow for the control of the film properties of the ternary oxide, such as composition, crystallization temperature, and dielectric constant. 5-12 The challenge for the STO ALD processes is to optimally tune the material properties within the ALD process windows of TiO 2 and SrO. For example, the process temperature is commonly chosen as high as possible to yield the material with lowest impurities levels and best electrical performance. The maximum deposition temperature allowed is, however, limited by the thermal stability of the Ti and Sr precursors employed.A new class of ALD Sr precursors with cyclopentadienyl ͑Cp͒ ligands were introduced by Vehkamäki et al. 6,7 These Cp-based precursors allowed for the thermal ALD with H 2 O at reasonably high temperatures ͑ Ͻ 300°C͒ while providing an adequate vapor pressure. Recently, also Cp-compounds of titanium with improved thermal stability have become available. However, these precursors are not suitable...
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2025 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.