<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rahimi MG</submitter><funding>National Basic Research Program of China</funding><funding>Chinese Academy of Sciences</funding><pagination>40916-40922</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9057785</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(67)</volume><pubmed_abstract>Nowadays, it is necessary and challenging to prepare monolithic catalysts, which are ready for use, preventing the tedious and complicated integration procedure of the powder materials onto a porous substrate. Herein, Cu&lt;sub>2&lt;/sub>O nanoparticles are successfully synthesized onto a porous Cu foam in one pot &lt;i>via&lt;/i> the surface oxidation, coordination and precipitation reactions in a NH&lt;sub>4&lt;/sub>OH and HCl solution, and the optimum synthesis conditions are a NH&lt;sub>3&lt;/sub> : HCl ratio of 1 : 0.9, oxidation temperature of 80 °C and time of 18 h. The obtained Cu&lt;sub>2&lt;/sub>O/Cu catalyst (mostly &lt;100 nm) shows a highly active O&lt;sub>3&lt;/sub> decomposition performance with >98% and >80% conversion efficiency in dry and 90% relative humidity air for >10 h at an O&lt;sub>3&lt;/sub> concentration of 20 ppm and a gas hourly space velocity of 12 500 h&lt;sup>-1&lt;/sup>. The high efficiency can be attributed to the porous Cu foam providing a large contact area, abundant crystal defects in the nanometer-sized Cu&lt;sub>2&lt;/sub>O materials serving as the active sites, and also to the Schottky barrier formed in the Cu&lt;sub>2&lt;/sub>O/Cu interface facilitating the electron transfer for O&lt;sub>3&lt;/sub> degradation. All these results show the potency of the easily fabricated monolithic Cu&lt;sub>2&lt;/sub>O/Cu catalyst for the highly efficient O&lt;sub>3&lt;/sub> contaminant removal.</pubmed_abstract><journal>RSC advances</journal><pubmed_title>A one-pot synthesis of a monolithic Cu&lt;sub>2&lt;/sub>O/Cu catalyst for efficient ozone decomposition.</pubmed_title><pmcid>PMC9057785</pmcid><funding_grant_id>XDB05050400</funding_grant_id><funding_grant_id>2016YFC0207100</funding_grant_id><pubmed_authors>Wang A</pubmed_authors><pubmed_authors>Han N</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Rahimi MG</pubmed_authors><pubmed_authors>Ma G</pubmed_authors></additional><is_claimable>false</is_claimable><name>A one-pot synthesis of a monolithic Cu&lt;sub>2&lt;/sub>O/Cu catalyst for efficient ozone decomposition.</name><description>Nowadays, it is necessary and challenging to prepare monolithic catalysts, which are ready for use, preventing the tedious and complicated integration procedure of the powder materials onto a porous substrate. Herein, Cu&lt;sub>2&lt;/sub>O nanoparticles are successfully synthesized onto a porous Cu foam in one pot &lt;i>via&lt;/i> the surface oxidation, coordination and precipitation reactions in a NH&lt;sub>4&lt;/sub>OH and HCl solution, and the optimum synthesis conditions are a NH&lt;sub>3&lt;/sub> : HCl ratio of 1 : 0.9, oxidation temperature of 80 °C and time of 18 h. The obtained Cu&lt;sub>2&lt;/sub>O/Cu catalyst (mostly &lt;100 nm) shows a highly active O&lt;sub>3&lt;/sub> decomposition performance with >98% and >80% conversion efficiency in dry and 90% relative humidity air for >10 h at an O&lt;sub>3&lt;/sub> concentration of 20 ppm and a gas hourly space velocity of 12 500 h&lt;sup>-1&lt;/sup>. The high efficiency can be attributed to the porous Cu foam providing a large contact area, abundant crystal defects in the nanometer-sized Cu&lt;sub>2&lt;/sub>O materials serving as the active sites, and also to the Schottky barrier formed in the Cu&lt;sub>2&lt;/sub>O/Cu interface facilitating the electron transfer for O&lt;sub>3&lt;/sub> degradation. All these results show the potency of the easily fabricated monolithic Cu&lt;sub>2&lt;/sub>O/Cu catalyst for the highly efficient O&lt;sub>3&lt;/sub> contaminant removal.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Nov</publication><modification>2025-04-04T20:21:57.597Z</modification><creation>2025-04-04T20:21:57.597Z</creation></dates><accession>S-EPMC9057785</accession><cross_references><pubmed>35519179</pubmed><doi>10.1039/d0ra05157h</doi></cross_references></HashMap>