<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hai Z</submitter><funding>NIMHD NIH HHS</funding><pagination>10829-10835</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4892124</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>1(36)</volume><pubmed_abstract>Au, Cu and bimetallic Au-Cu nanoparticles were synthesized on the surface of commercial TiO&lt;sub>2&lt;/sub> compounds (P25) by reduction of the metal precursors with tetrakis (hydroxymethyl) phosphonium chloride (THPC) (0.5 % in weight). The alloyed structure of Au-Cu NPs was confirmed by HAADF-STEM, EDS, HRTEM and XPS techniques. The photocatalytic properties of the modified TiO&lt;sub>2&lt;/sub> have been studied for phenol photodegradation in aqueous suspensions under UV-visible irradiation. The modification by the metal nanoparticles induces an increase in the photocatalytic activity. The highest photocatalytic activity is obtained with Au-Cu/TiO&lt;sub>2&lt;/sub> (Au/Cu 1:3). Their electronic properties have been studied by time resolved microwave conductivity (TRMC) to follow the charge-carrier dynamics. TRMC measurements show that the TiO&lt;sub>2&lt;/sub> modification with Au, Cu and Au-Cu nanoparticles plays a role in charge-carrier separations increasing the activity under UV-light. Indeed, the metal nanoparticles act as a sink for electron, decreasing the charge carrier recombination. The TRMC measurements show also that the bimetallic Au-Cu nanoparticles are more efficient in electron scavenging than the monometallic Au and Cu ones.</pubmed_abstract><journal>Journal of materials chemistry. A</journal><pubmed_title>Modification of TiO&lt;sub>2&lt;/sub> by Bimetallic Au-Cu Nanoparticles for Wastewater Treatment.</pubmed_title><pmcid>PMC4892124</pmcid><funding_grant_id>G12 MD007591</funding_grant_id><pubmed_authors>Etcheberry A</pubmed_authors><pubmed_authors>Uribe DB</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Remita H</pubmed_authors><pubmed_authors>Vigneron J</pubmed_authors><pubmed_authors>Beaunier P</pubmed_authors><pubmed_authors>Sorgues S</pubmed_authors><pubmed_authors>Kolli NE</pubmed_authors><pubmed_authors>Colbeau-Justin C</pubmed_authors><pubmed_authors>Jose-Yacaman M</pubmed_authors><pubmed_authors>Hai Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Modification of TiO&lt;sub>2&lt;/sub> by Bimetallic Au-Cu Nanoparticles for Wastewater Treatment.</name><description>Au, Cu and bimetallic Au-Cu nanoparticles were synthesized on the surface of commercial TiO&lt;sub>2&lt;/sub> compounds (P25) by reduction of the metal precursors with tetrakis (hydroxymethyl) phosphonium chloride (THPC) (0.5 % in weight). The alloyed structure of Au-Cu NPs was confirmed by HAADF-STEM, EDS, HRTEM and XPS techniques. The photocatalytic properties of the modified TiO&lt;sub>2&lt;/sub> have been studied for phenol photodegradation in aqueous suspensions under UV-visible irradiation. The modification by the metal nanoparticles induces an increase in the photocatalytic activity. The highest photocatalytic activity is obtained with Au-Cu/TiO&lt;sub>2&lt;/sub> (Au/Cu 1:3). Their electronic properties have been studied by time resolved microwave conductivity (TRMC) to follow the charge-carrier dynamics. TRMC measurements show that the TiO&lt;sub>2&lt;/sub> modification with Au, Cu and Au-Cu nanoparticles plays a role in charge-carrier separations increasing the activity under UV-light. Indeed, the metal nanoparticles act as a sink for electron, decreasing the charge carrier recombination. The TRMC measurements show also that the bimetallic Au-Cu nanoparticles are more efficient in electron scavenging than the monometallic Au and Cu ones.</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Sep</publication><modification>2025-04-04T02:42:56.679Z</modification><creation>2019-03-27T02:15:15Z</creation></dates><accession>S-EPMC4892124</accession><cross_references><pubmed>27274844</pubmed><doi>10.1039/C3TA11684K</doi><doi>10.1039/c3ta11684k</doi></cross_references></HashMap>