4.7 Article

Thienoacene-Based Conjugated Porous Polymer/TiO2 Hybrids as Photocatalysts in Artificial Photosynthesis

Journal

ADVANCED SUSTAINABLE SYSTEMS
Volume -, Issue -, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsu.202300330

Keywords

artificial photosynthesis; charge transfers; conjugated porous polymers; thienoacenes

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This study describes the design and synthesis of CPPs based on thienoacene units and their electronic alignment and photo(thermal) stability with TiO2. The simultaneous UV-vis irradiation of these materials leads to higher H2 production compared to solely irradiating the CPPs with visible light, due to charge-transfer mechanisms. Additionally, in gas phase CO2 photoreduction tests, the IEP-15@T-10 hybrid shows a significant increase in CH4 evolution and selectivity compared to TiO2.
Herein, the design and synthesis of a couple of CPPs based on thienoacene units (named as IEP-14 and IEP-15, stand for IMDEA Energy Polymer numbers 14 and 15) are described, which show high BET surface areas, good photo(thermal) stabilities, and appropriate electronic alignment with TiO2 to prepare hybrids (named as IEP-x@T-10, X = 14 and 15, being 10 wt% of polymer loading). It is shown that the simultaneous UV-vis irradiation of both materials leads to better H-2 production (ca. 925 and 827 mu mol g(-1) h(-1) by IEP-15@T-10 and IEP-14@T-10, 12 and 11-fold higher production than bare TiO2) than the solely irradiation at visible of the CPPs (ca. 124 and 90 mu mol g(-1) h(-1) by IEP-15@T-10 and IEP-14@T-10 when TiO2 is photocatalytically inactive). The reason is attributed to the charge-transfer mechanisms that occur between the counterparts of the hybrid material: in the first case it consists in a Z-scheme charge transfer mechanism, while in the second one is a sensitization charge transfer mechanism. Both mechanisms are elucidated by advanced techniques. Furthermore, in a gas phase CO2 photoreduction test, IEP-15@T-10 shows sixfold higher CH4 evolution than TiO2, which result in a selectivity shift from CO to CH4 (i.e., >26% greater selectivity than bare TiO2)(.)

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