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Atomic layer deposition of Y(2)O(3) films using a novel liquid homoleptic yttrium precursor tris(sec-butylcyclopentadienyl)yttrium [Y((s)BuCp)(3)] and water

Atomic layer deposition (ALD) of Y(2)O(3) thin films was studied using a novel homoleptic yttrium ALD precursor: tris(sec-butylcyclopentadienyl)yttrium [Y((s)BuCp)(3)]. Y((s)BuCp)(3) is a liquid at room temperature. The thermogravimetry curve for Y((s)BuCp)(3) is clean, with no indication of decompo...

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Autores principales: Nishida, Akihiro, Katayama, Tsukasa, Matsuo, Yasutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10496032/
https://www.ncbi.nlm.nih.gov/pubmed/37705987
http://dx.doi.org/10.1039/d3ra05217f
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author Nishida, Akihiro
Katayama, Tsukasa
Matsuo, Yasutaka
author_facet Nishida, Akihiro
Katayama, Tsukasa
Matsuo, Yasutaka
author_sort Nishida, Akihiro
collection PubMed
description Atomic layer deposition (ALD) of Y(2)O(3) thin films was studied using a novel homoleptic yttrium ALD precursor: tris(sec-butylcyclopentadienyl)yttrium [Y((s)BuCp)(3)]. Y((s)BuCp)(3) is a liquid at room temperature. The thermogravimetry curve for Y((s)BuCp)(3) is clean, with no indication of decomposition or residue formation. Thermogravimetry–differential thermal analysis measurements showed that Y((s)BuCp)(3) is stable for 18 weeks at 190 °C. Y((s)BuCp)(3) has a homoleptic structure. Thus, a reduction in manufacturing costs is expected compared to those associated with heteroleptic precursors because additional chemical synthesis steps are usually necessary to produce heteroleptic compounds. In addition, ALD of Y(2)O(3) was demonstrated using Y((s)BuCp)(3) and water as a co-reactant. The deposition temperature was varied from 200 to 350 °C. The growth rate was 1.7 Å per cycle. In addition, neither carbon nor nitrogen contamination was detected in the Y(2)O(3) films by X-ray photoelectron spectroscopy. Furthermore, smooth films were confirmed by X-ray secondary-electron microscopy. The root-mean-square roughness was measured to be 0.660 nm by atomic force microscopy. Metal–insulator–semiconductor (MIS) Pt/Y(2)O(3)/p-Si devices were fabricated to evaluate the electrical properties of the Y(2)O(3) films. An electric breakdown field of −6.5 MV cm(−1) and a leakage current density of ∼3.2 × 10(−3) A cm(−2) at 1 MV cm(−1) were determined. The permittivity of Y(2)O(3) was estimated to be 11.5 at 100 kHz. Therefore, compared with conventional solid precursors, Y((s)BuCp)(3) is suitable for use in ALD manufacturing processes.
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spelling pubmed-104960322023-09-13 Atomic layer deposition of Y(2)O(3) films using a novel liquid homoleptic yttrium precursor tris(sec-butylcyclopentadienyl)yttrium [Y((s)BuCp)(3)] and water Nishida, Akihiro Katayama, Tsukasa Matsuo, Yasutaka RSC Adv Chemistry Atomic layer deposition (ALD) of Y(2)O(3) thin films was studied using a novel homoleptic yttrium ALD precursor: tris(sec-butylcyclopentadienyl)yttrium [Y((s)BuCp)(3)]. Y((s)BuCp)(3) is a liquid at room temperature. The thermogravimetry curve for Y((s)BuCp)(3) is clean, with no indication of decomposition or residue formation. Thermogravimetry–differential thermal analysis measurements showed that Y((s)BuCp)(3) is stable for 18 weeks at 190 °C. Y((s)BuCp)(3) has a homoleptic structure. Thus, a reduction in manufacturing costs is expected compared to those associated with heteroleptic precursors because additional chemical synthesis steps are usually necessary to produce heteroleptic compounds. In addition, ALD of Y(2)O(3) was demonstrated using Y((s)BuCp)(3) and water as a co-reactant. The deposition temperature was varied from 200 to 350 °C. The growth rate was 1.7 Å per cycle. In addition, neither carbon nor nitrogen contamination was detected in the Y(2)O(3) films by X-ray photoelectron spectroscopy. Furthermore, smooth films were confirmed by X-ray secondary-electron microscopy. The root-mean-square roughness was measured to be 0.660 nm by atomic force microscopy. Metal–insulator–semiconductor (MIS) Pt/Y(2)O(3)/p-Si devices were fabricated to evaluate the electrical properties of the Y(2)O(3) films. An electric breakdown field of −6.5 MV cm(−1) and a leakage current density of ∼3.2 × 10(−3) A cm(−2) at 1 MV cm(−1) were determined. The permittivity of Y(2)O(3) was estimated to be 11.5 at 100 kHz. Therefore, compared with conventional solid precursors, Y((s)BuCp)(3) is suitable for use in ALD manufacturing processes. The Royal Society of Chemistry 2023-09-12 /pmc/articles/PMC10496032/ /pubmed/37705987 http://dx.doi.org/10.1039/d3ra05217f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Nishida, Akihiro
Katayama, Tsukasa
Matsuo, Yasutaka
Atomic layer deposition of Y(2)O(3) films using a novel liquid homoleptic yttrium precursor tris(sec-butylcyclopentadienyl)yttrium [Y((s)BuCp)(3)] and water
title Atomic layer deposition of Y(2)O(3) films using a novel liquid homoleptic yttrium precursor tris(sec-butylcyclopentadienyl)yttrium [Y((s)BuCp)(3)] and water
title_full Atomic layer deposition of Y(2)O(3) films using a novel liquid homoleptic yttrium precursor tris(sec-butylcyclopentadienyl)yttrium [Y((s)BuCp)(3)] and water
title_fullStr Atomic layer deposition of Y(2)O(3) films using a novel liquid homoleptic yttrium precursor tris(sec-butylcyclopentadienyl)yttrium [Y((s)BuCp)(3)] and water
title_full_unstemmed Atomic layer deposition of Y(2)O(3) films using a novel liquid homoleptic yttrium precursor tris(sec-butylcyclopentadienyl)yttrium [Y((s)BuCp)(3)] and water
title_short Atomic layer deposition of Y(2)O(3) films using a novel liquid homoleptic yttrium precursor tris(sec-butylcyclopentadienyl)yttrium [Y((s)BuCp)(3)] and water
title_sort atomic layer deposition of y(2)o(3) films using a novel liquid homoleptic yttrium precursor tris(sec-butylcyclopentadienyl)yttrium [y((s)bucp)(3)] and water
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10496032/
https://www.ncbi.nlm.nih.gov/pubmed/37705987
http://dx.doi.org/10.1039/d3ra05217f
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