<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xuan R</submitter><funding>Wuhan Polytechnic University</funding><funding>National Natural Science Foundation of China</funding><pagination>25247-25255</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11320058</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(35)</volume><pubmed_abstract>Photocatalytic CO&lt;sub>2&lt;/sub> reduction into value-added chemical fuels using sunlight as the energy input has been a thorny, challenging and long-term project in the environment/energy fields because of to its low efficiency. Herein, a series of CdS/Co-BDC composite photocatalysts were constructed by incorporating CdS nanoparticles into Co-BDC using a dual-solvent &lt;i>in situ&lt;/i> growth strategy for improving photocatalytic CO&lt;sub>2&lt;/sub> reduction efficiency. The composites were characterized through XRD, SEM, TEM, XPS, DRS and EPR techniques in detail. 18% CdS/Co-BDC composites showed superior performance for the photocatalytic CO&lt;sub>2&lt;/sub> reduction to CO, which was 8.9 and 19.6 times higher than that showed by the pure CdS and Co-BDC, respectively. The mechanism of enhanced photocatalytic CO&lt;sub>2&lt;/sub> reduction performance was analyzed. The CdS/Co-BDC composites showed better adsorption for CO&lt;sub>2&lt;/sub>. Detailed analysis of XPS, transient photocurrent responses, and electrochemical impedance spectroscopy (EIS) shows the existence of strong charge interaction between CdS and Co-BDC and the photo-electrons of CdS can be transferred to Co-BDC. Additionally, Co-oxo of Co-BDC plays the role of a redox-active site and promotes the reduction performance &lt;i>via&lt;/i> the method of valence transition of Co(ii)/Co(iii) redox.</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Enhanced photocatalytic CO&lt;sub>2&lt;/sub> conversion of a CdS/Co-BDC nanocomposite &lt;i>via&lt;/i> Co(ii)/Co(iii) redox cycling.</pubmed_title><pmcid>PMC11320058</pmcid><funding_grant_id>202410496023</funding_grant_id><funding_grant_id>2024J03</funding_grant_id><funding_grant_id>52102111</funding_grant_id><funding_grant_id>XQ2024004</funding_grant_id><pubmed_authors>Dou Y</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Jiang Z</pubmed_authors><pubmed_authors>Yan J</pubmed_authors><pubmed_authors>Xuan R</pubmed_authors><pubmed_authors>Chai B</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Ding D</pubmed_authors><pubmed_authors>Mo J</pubmed_authors><pubmed_authors>Wang X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Enhanced photocatalytic CO&lt;sub>2&lt;/sub> conversion of a CdS/Co-BDC nanocomposite &lt;i>via&lt;/i> Co(ii)/Co(iii) redox cycling.</name><description>Photocatalytic CO&lt;sub>2&lt;/sub> reduction into value-added chemical fuels using sunlight as the energy input has been a thorny, challenging and long-term project in the environment/energy fields because of to its low efficiency. Herein, a series of CdS/Co-BDC composite photocatalysts were constructed by incorporating CdS nanoparticles into Co-BDC using a dual-solvent &lt;i>in situ&lt;/i> growth strategy for improving photocatalytic CO&lt;sub>2&lt;/sub> reduction efficiency. The composites were characterized through XRD, SEM, TEM, XPS, DRS and EPR techniques in detail. 18% CdS/Co-BDC composites showed superior performance for the photocatalytic CO&lt;sub>2&lt;/sub> reduction to CO, which was 8.9 and 19.6 times higher than that showed by the pure CdS and Co-BDC, respectively. The mechanism of enhanced photocatalytic CO&lt;sub>2&lt;/sub> reduction performance was analyzed. The CdS/Co-BDC composites showed better adsorption for CO&lt;sub>2&lt;/sub>. Detailed analysis of XPS, transient photocurrent responses, and electrochemical impedance spectroscopy (EIS) shows the existence of strong charge interaction between CdS and Co-BDC and the photo-electrons of CdS can be transferred to Co-BDC. Additionally, Co-oxo of Co-BDC plays the role of a redox-active site and promotes the reduction performance &lt;i>via&lt;/i> the method of valence transition of Co(ii)/Co(iii) redox.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2024-11-05T16:08:40.052Z</modification><creation>2024-11-05T16:08:40.052Z</creation></dates><accession>S-EPMC11320058</accession><cross_references><pubmed>39139241</pubmed><doi>10.1039/d4ra04842c</doi></cross_references></HashMap>