{"title":"Porous nanostructured cationic conjugated polyelectrolyte/titanium dioxide nanosheet heterojunction for enhanced cocatalyst-free photocatalytic hydrogen evolution.","authors":"Mingsong Dou, Yongzheng Hu, Xue Yue, Taiping Lu, Li Yang, Yu He, Yingying Du, Anning Zhu, Haokai Yang, YuMing Zhu, Jiahao Wang, Dongyue Yu, Wei Zhou, Shaolin Lu, Xudong Chen","doi":"10.1016/j.jcis.2025.138644","DOIUrl":null,"url":null,"abstract":"<p><p>Modified TiO<sub>2</sub> photocatalysts face challenges dependence on cocatalysts, weak interfacial interactions, and poor wettability. This work presents an effective strategy by coupling donor-donor (D-D) type cationic conjugated polyelectrolyte poly[(9,9-bis(3'-((N,N-dimethyl)-N-ethylammonium)-propyl)-2,7-fluorene)-alt-2,7-(9,9-dioctylfluorene)]dibromide (PFN-Br) with two-dimensional TiO<sub>2</sub> (2D-TiO₂) nanosheets to construct type-II heterojunctions rich in active sites. Under optimal conditions, the 2D-TiO<sub>2</sub>/50 wt% PFN-Br (2D-Ti/PBr-50) heterojunction achieved a hydrogen evolution reaction of 2621.01 μmol g<sup>-1</sup> h<sup>-1</sup> without any cocatalyst-representing 21.86 times higher than that of pristine 2D-TiO₂ nanosheets. This significant enhancement is mainly attributed to the strong visible-light absorption capability of PFN-Br, well-matched band alignment with 2D-TiO₂ nanosheets, reinforced interfacial interactions via hydrogen bonding and electrostatic forces, the porous nanostructure of the 2D-Ti/PBr heterojunction, and good interfacial wettability due to the ionic side chains of PFN-Br. This study offers new insights into polyelectrolyte-assisted TiO<sub>2</sub> photocatalysts for cocatalyst-free applications.</p>","PeriodicalId":351,"journal":{"name":"Journal of Colloid and Interface Science","volume":"701 ","pages":"138644"},"PeriodicalIF":9.7000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Colloid and Interface Science","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.jcis.2025.138644","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/7 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Modified TiO2 photocatalysts face challenges dependence on cocatalysts, weak interfacial interactions, and poor wettability. This work presents an effective strategy by coupling donor-donor (D-D) type cationic conjugated polyelectrolyte poly[(9,9-bis(3'-((N,N-dimethyl)-N-ethylammonium)-propyl)-2,7-fluorene)-alt-2,7-(9,9-dioctylfluorene)]dibromide (PFN-Br) with two-dimensional TiO2 (2D-TiO₂) nanosheets to construct type-II heterojunctions rich in active sites. Under optimal conditions, the 2D-TiO2/50 wt% PFN-Br (2D-Ti/PBr-50) heterojunction achieved a hydrogen evolution reaction of 2621.01 μmol g-1 h-1 without any cocatalyst-representing 21.86 times higher than that of pristine 2D-TiO₂ nanosheets. This significant enhancement is mainly attributed to the strong visible-light absorption capability of PFN-Br, well-matched band alignment with 2D-TiO₂ nanosheets, reinforced interfacial interactions via hydrogen bonding and electrostatic forces, the porous nanostructure of the 2D-Ti/PBr heterojunction, and good interfacial wettability due to the ionic side chains of PFN-Br. This study offers new insights into polyelectrolyte-assisted TiO2 photocatalysts for cocatalyst-free applications.
期刊介绍:
The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality.
Emphasis:
The journal emphasizes fundamental scientific innovation within the following categories:
A.Colloidal Materials and Nanomaterials
B.Soft Colloidal and Self-Assembly Systems
C.Adsorption, Catalysis, and Electrochemistry
D.Interfacial Processes, Capillarity, and Wetting
E.Biomaterials and Nanomedicine
F.Energy Conversion and Storage, and Environmental Technologies