Acar, Eminegul GencInce, TuncayYuzer, A. CelilYanalak, GizemGecgel, CihanAslan, EmreInce, Mine2025-03-172025-03-1720231088-42461099-1409https://doi.org/10.1142/S1088424622500882https://hdl.handle.net/20.500.13099/1753Two zinc phthalocyanine derivatives (ZnPc 1 and 2) carrying bulky 2,6-diisopropylthiophenoxy peripheral substituents have been synthesized and their performances as photosensitizers in photochemical hydrogen production evaluated. To examine the influence of the spacer on the performance of ZnPc 1 and 2, the carboxyl group has been linked to the macrocycle ring either directly or via the phenyl ring, respectively. The photocatalytic activities of ZnPcs (ZnPc 1 and ZnPc 2) as sensitizers of TiO(2 )for hydrogen production were investigated in the presence of Pt. ZnPc 1 and ZnPc 2 sensitized TiO(2 )produced 0.687 mmolg(-1)h(-1) and 0.436 mmol g(-1)h(-1) hydrogens, which also reached 3.986 and 2.091 mmolg(-1) after 8h illumination, respectively, under visible light (>= 420 nm) irradiation. In addition, STH efficiencies of ZnPc 1/TiO2 and ZnPc 2/TiO2 were determined as 1.77% and 1.12%, respectively. ZnPc 1/TiO2 exhibited 1.9-fold more photocatalytic hydrogen amount than ZnPc 2/TiO2, and the hydrogen evolution performance of the photocatalyst in the presence of Pt enhanced to 3.021 mmol g(-1)h(-1) and 0.911mmol g(-1)h(-1) for ZnPc 1 and ZnPc 2, respectively.eninfo:eu-repo/semantics/closedAccessartificial photosynthesisphthalocyaninephotoelectrochemical hydrogen evolutiondye-sensitized photocatalystphotocatalytic hydrogen evolutionArticle10.1142/S1088424622500882271260267Q4WOS:0009001629000012-s2.0-85145459784Q3