<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Sheng Q</submitter><funding>National Natural Science Foundation of China</funding><pubmed_abstract>Conjugated microporous polymers (CMPs), as a kind of two-dimensional material, have attracted extensive attention due to their advantages in visible light-driven photocatalytic splitting of water for hydrogen evolution. However, improving the microstructure and electronic structure of the material to enhance their photocatalytic performance for hydrogen evolution remains a challenge. We designed and reported two analogous CMPs including CMP-1 and CMP-2 that contain triazine and dibenzothiophene-&lt;i>S&lt;/i>,&lt;i>S&lt;/i>-dioxide units, which were prepared by Pd-catalyzed Suzuki-Miyaura coupling reaction. The main difference of two CMPs is that the triazine units are connected to benzene unit (CMP-1) or thiophene unit (CMP-2). Both of the CMPs exhibit excellent light capture capability, and compared with CMP-2, CMP-1 has faster separation rates and lower recombination rates for the charge carriers (electron/hole), and then, a higher hydrogen evolution rate was obtained from water decomposition reaction. We find the H&lt;sub>2&lt;/sub> production rate of CMP-1 can be up to 9,698.53 μmol g&lt;sup>-1&lt;/sup>h &lt;sup>-1&lt;/sup>, which is about twice of that of CMP-2. This work suggests that molecular design is a potent method to optimize the photocatalytic performance toward hydrogen evolution of the CMPs.</pubmed_abstract><journal>Frontiers in chemistry</journal><pagination>854018</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8990882</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Triazine-Based Conjugated Microporous Polymers With Different Linkage Units for Visible Light-Driven Hydrogen Evolution.</pubmed_title><pmcid>PMC8990882</pmcid><pubmed_authors>Shang Q</pubmed_authors><pubmed_authors>Dong Y</pubmed_authors><pubmed_authors>Xie Y</pubmed_authors><pubmed_authors>Sheng Q</pubmed_authors><pubmed_authors>Zhong X</pubmed_authors><pubmed_authors>Du Y</pubmed_authors><pubmed_authors>Zhao J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Triazine-Based Conjugated Microporous Polymers With Different Linkage Units for Visible Light-Driven Hydrogen Evolution.</name><description>Conjugated microporous polymers (CMPs), as a kind of two-dimensional material, have attracted extensive attention due to their advantages in visible light-driven photocatalytic splitting of water for hydrogen evolution. However, improving the microstructure and electronic structure of the material to enhance their photocatalytic performance for hydrogen evolution remains a challenge. We designed and reported two analogous CMPs including CMP-1 and CMP-2 that contain triazine and dibenzothiophene-&lt;i>S&lt;/i>,&lt;i>S&lt;/i>-dioxide units, which were prepared by Pd-catalyzed Suzuki-Miyaura coupling reaction. The main difference of two CMPs is that the triazine units are connected to benzene unit (CMP-1) or thiophene unit (CMP-2). Both of the CMPs exhibit excellent light capture capability, and compared with CMP-2, CMP-1 has faster separation rates and lower recombination rates for the charge carriers (electron/hole), and then, a higher hydrogen evolution rate was obtained from water decomposition reaction. We find the H&lt;sub>2&lt;/sub> production rate of CMP-1 can be up to 9,698.53 μmol g&lt;sup>-1&lt;/sup>h &lt;sup>-1&lt;/sup>, which is about twice of that of CMP-2. This work suggests that molecular design is a potent method to optimize the photocatalytic performance toward hydrogen evolution of the CMPs.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-19T00:43:38.796Z</modification><creation>2025-04-07T11:48:50.937Z</creation></dates><accession>S-EPMC8990882</accession><cross_references><pubmed>35402380</pubmed><doi>10.3389/fchem.2022.854018</doi></cross_references></HashMap>