<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5(10)</volume><submitter>Hsiao SN</submitter><pubmed_abstract>Hafnium(IV) oxide (HfO&lt;sub>2&lt;/sub>)-based materials have attracted substantial interest owing to their outstanding performance in advanced ultrathin semiconductor devices. However, achieving atomic-level precision and smoothness in HfO&lt;sub>2&lt;/sub> etching remains a major challenge, primarily due to the nonvolatility of reaction products formed with halogen-based chemicals at room temperature. Herein, a facile cyclic atomic-layer etching (ALE) process capable of etching HfO&lt;sub>2&lt;/sub> films at room temperature without the use of halogen-based chemicals is reported. The ALE process consists of a surface nitrogenation step via N&lt;sup>+&lt;/sup>-ion bombardment during N&lt;sub>2&lt;/sub> plasma exposure, followed by O&lt;sub>2&lt;/sub> plasma treatment to remove the surface-modified layer through the formation of volatile etching byproducts-most likely hafnium nitrates. This process enables precise, subatomic-level etching of HfO&lt;sub>2&lt;/sub>, achieving an etch depth per cycle ranging from 0.23 to 1.07 Å/cycle, depending on the N&lt;sup>+&lt;/sup> ion energy. Additionally, this cyclic ALE method effectively smooths the HfO&lt;sub>2&lt;/sub> surface, yielding a 60% reduction in surface roughness after 20 cycles. Based on the proposed mechanism, this facile ALE process can be extended to other transition metal oxides and offers a sustainable route for fabricating advanced functional oxide-based devices, without generating corrosive or toxic wastes.</pubmed_abstract><journal>Small science</journal><pagination>2500251</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12499433</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Halogen-Free Anisotropic Atomic-Layer Etching of HfO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; at Room Temperature.</pubmed_title><pmcid>PMC12499433</pmcid><pubmed_authors>Yiu PM</pubmed_authors><pubmed_authors>Hori M</pubmed_authors><pubmed_authors>Hsiao SN</pubmed_authors><pubmed_authors>Chang LC</pubmed_authors><pubmed_authors>Sekine M</pubmed_authors><pubmed_authors>Lee JW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Halogen-Free Anisotropic Atomic-Layer Etching of HfO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; at Room Temperature.</name><description>Hafnium(IV) oxide (HfO&lt;sub>2&lt;/sub>)-based materials have attracted substantial interest owing to their outstanding performance in advanced ultrathin semiconductor devices. However, achieving atomic-level precision and smoothness in HfO&lt;sub>2&lt;/sub> etching remains a major challenge, primarily due to the nonvolatility of reaction products formed with halogen-based chemicals at room temperature. Herein, a facile cyclic atomic-layer etching (ALE) process capable of etching HfO&lt;sub>2&lt;/sub> films at room temperature without the use of halogen-based chemicals is reported. The ALE process consists of a surface nitrogenation step via N&lt;sup>+&lt;/sup>-ion bombardment during N&lt;sub>2&lt;/sub> plasma exposure, followed by O&lt;sub>2&lt;/sub> plasma treatment to remove the surface-modified layer through the formation of volatile etching byproducts-most likely hafnium nitrates. This process enables precise, subatomic-level etching of HfO&lt;sub>2&lt;/sub>, achieving an etch depth per cycle ranging from 0.23 to 1.07 Å/cycle, depending on the N&lt;sup>+&lt;/sup> ion energy. Additionally, this cyclic ALE method effectively smooths the HfO&lt;sub>2&lt;/sub> surface, yielding a 60% reduction in surface roughness after 20 cycles. Based on the proposed mechanism, this facile ALE process can be extended to other transition metal oxides and offers a sustainable route for fabricating advanced functional oxide-based devices, without generating corrosive or toxic wastes.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-06-04T06:58:30.413Z</modification><creation>2026-05-06T03:12:54.442Z</creation></dates><accession>S-EPMC12499433</accession><cross_references><pubmed>41058728</pubmed><doi>10.1002/smsc.202500251</doi></cross_references></HashMap>