Multifunctional Nanocrystalline Thin Films of Er2O3: Interplay between Nucleation Kinetics and Film Characteristics

In this study, thin films of Er2O3 are deposited by low‐pressure metal–organic chemical vapor deposition (MOCVD) using a tris(isopropylcyclopentadienyl)erbium precursor and O2 on various substrates, including p‐type Si(100), Si(111), Corning glass, and c‐axis‐oriented α‐Al2O3(0001). The resulting fi...

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Published in:Advanced functional materials Vol. 17; no. 17; pp. 3607 - 3612
Main Authors: Losurdo, M., Giangregorio, M. M., Capezzuto, P., Bruno, G., Toro, R. G., Malandrino, G., Fragalà, I. L., Armelao, L., Barreca, D., Tondello, E., Suvorova, A. A., Yang, D., Irene, E. A.
Format: Journal Article
Language:English
Published: Weinheim WILEY-VCH Verlag 23-11-2007
WILEY‐VCH Verlag
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Summary:In this study, thin films of Er2O3 are deposited by low‐pressure metal–organic chemical vapor deposition (MOCVD) using a tris(isopropylcyclopentadienyl)erbium precursor and O2 on various substrates, including p‐type Si(100), Si(111), Corning glass, and c‐axis‐oriented α‐Al2O3(0001). The resulting films are extensively characterized in order to demonstrate their applicability as antireflective and protective coatings and as high‐k gate dielectrics. The interplay existing among the substrate, the nucleation kinetics, and the resulting structural, morphological, optical, and electrical properties of Er2O3 thin films is explored. Fast nucleation governed by surface energy minimization characterizes the growth of (111)‐oriented Er2O3 on Si(100), glass, and α‐Al2O3. Conversely, nonhomogeneous nucleation leads to polycrystalline Er2O3 on Si(111) substrates. Er2O3 films grown on Si(100) possess superior characteristics. A high refractive index of 2.1 at 589.3 nm, comparable to the value for bulk single crystalline Er2O3, a high transparency in the near UV‐vis range, and an optical bandgap of 6.5 eV make Er2O3 interesting as an antireflective and protective coating. A static dielectric constant of 12–13 and a density of interface traps as low as 4.2 × 1010 cm2 eV–1 for 5–10 nm thick Er2O3 layers grown on Si(100) render the present Er2O3 films interesting also as high‐k dielectrics in complementary metal oxide semiconductor (CMOS) devices. Thin films of Er2O3 are deposited by low‐pressure metal–organic chemical vapor deposition (MOCVD) on various substrates, including p‐type Si(100), Si(111), Corning glass, and α‐Al2O3(0001). The high dielectric values determined (see figure) confirm the high quality of the prepared films. The applicability of the prepared films as antireflective and protective coatings and as a high‐k gate dielectrics in CMOS devices is demonstrated.
Bibliography:ark:/67375/WNG-S11SXQN2-H
FIRB-MIUR RBNE033KMA
This work was supported by INSTM (Consorzio Interuniversitario Nazionale per la Scienza e Tecnologia dei Materiali) through the PRISMA project "Oxide films with high dielectric constants from liquid and vapor phase routes". L.A. is also indebted to the research programs CNR-INSTM PROMO and FIRB-MIUR RBNE033KMA "Molecular compounds and hybrid nanostructured materials with resonant and nonresonant optical properties for photonic devices" for financial support. The authors thank Mr. Alberto Sacchetti and Mr Antonio Mazzone at IMIP-CNR for assistance in performing deposition experiments.
CNR-INSTM PROMO
INSTM (Consorzio Interuniversitario Nazionale per la Scienza e Tecnologia dei Materiali)
istex:524DE7925F6903E8691993E1C17450274111F7B6
ArticleID:ADFM200700524
This work was supported by INSTM (Consorzio Interuniversitario Nazionale per la Scienza e Tecnologia dei Materiali) through the PRISMA project “Oxide films with high dielectric constants from liquid and vapor phase routes”. L.A. is also indebted to the research programs CNR‐INSTM PROMO and FIRB‐MIUR RBNE033KMA “Molecular compounds and hybrid nanostructured materials with resonant and nonresonant optical properties for photonic devices” for financial support. The authors thank Mr. Alberto Sacchetti and Mr Antonio Mazzone at IMIP‐CNR for assistance in performing deposition experiments.
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ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.200700524