<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ru C</submitter><funding>111 Project</funding><funding>National Natural Science Foundation of China</funding><funding>Research Funds for the Key Laboratory of Petroleum Resources Research</funding><funding>Higher Education Discipline Innovation Project</funding><funding>Special Fund Project of Guiding Scientific Technological Innovation Development of Gansu Province</funding><pagination>e2204055</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9762295</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(35)</volume><pubmed_abstract>High concentrations of active carriers on the surface of a semiconductor through energy/electron transfer are the core process in the photocatalytic hydrogen production from water. However, it remains a challenge to significantly improve photocatalytic performance by modifying simple molecular modulation. Herein, a new strategy is proposed to enhance the photocatalytic hydrogen evolution performance using boron and nitrogen elements to construct B←N coordination bonds. Experimental results show that polynaphthopyridine borane (PNBN) possessing B←N coordination bonds shows a hydrogen evolution rate of 217.4 µmol h&lt;sup>-1&lt;/sup> , which is significantly higher than that of the comparison materials 0 µmol h&lt;sup>-1&lt;/sup> for polyphenylnaphthalene (PNCC) and 0.66 µmol h&lt;sup>-1&lt;/sup> for polypyridylnaphthalene (PNNC), mainly attributed to the formation of a strong built-in electric field that promotes the separation of photo-generated electrons/holes. This work opens up new prospects for the design of highly efficient polymeric photocatalysts at the molecular level.</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Enhanced Built-in Electric Field Promotes Photocatalytic Hydrogen Performance of Polymers Derived from the Introduction of B←N Coordination Bond.</pubmed_title><pmcid>PMC9762295</pmcid><funding_grant_id>SZDKFJJ20201202</funding_grant_id><funding_grant_id>B20027</funding_grant_id><funding_grant_id>21901082</funding_grant_id><funding_grant_id>2019ZX-04</funding_grant_id><funding_grant_id>22071093</funding_grant_id><funding_grant_id>22171111</funding_grant_id><pubmed_authors>Pan X</pubmed_authors><pubmed_authors>Ru C</pubmed_authors><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Chen P</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Chen C</pubmed_authors><pubmed_authors>Wu X</pubmed_authors><pubmed_authors>Zhao H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Enhanced Built-in Electric Field Promotes Photocatalytic Hydrogen Performance of Polymers Derived from the Introduction of B←N Coordination Bond.</name><description>High concentrations of active carriers on the surface of a semiconductor through energy/electron transfer are the core process in the photocatalytic hydrogen production from water. However, it remains a challenge to significantly improve photocatalytic performance by modifying simple molecular modulation. Herein, a new strategy is proposed to enhance the photocatalytic hydrogen evolution performance using boron and nitrogen elements to construct B←N coordination bonds. Experimental results show that polynaphthopyridine borane (PNBN) possessing B←N coordination bonds shows a hydrogen evolution rate of 217.4 µmol h&lt;sup>-1&lt;/sup> , which is significantly higher than that of the comparison materials 0 µmol h&lt;sup>-1&lt;/sup> for polyphenylnaphthalene (PNCC) and 0.66 µmol h&lt;sup>-1&lt;/sup> for polypyridylnaphthalene (PNNC), mainly attributed to the formation of a strong built-in electric field that promotes the separation of photo-generated electrons/holes. This work opens up new prospects for the design of highly efficient polymeric photocatalysts at the molecular level.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2024-11-19T15:22:18.781Z</modification><creation>2024-11-19T15:22:18.781Z</creation></dates><accession>S-EPMC9762295</accession><cross_references><pubmed>36285682</pubmed><doi>10.1002/advs.202204055</doi></cross_references></HashMap>