Highly active pt nanoparticles supported on SrTiO3 for photocatalytic hydrogen production

被引:0
|
作者
Souri, A. P. [1 ,2 ]
Skliri, E. [1 ]
Vamvasakis, I. [2 ]
Armatas, G. S. [2 ]
Binas, V. [1 ,3 ]
机构
[1] FORTH, Inst Elect Struct & Laser IESL, POB 1527, GR-71110 Iraklion, Greece
[2] Univ Crete, Dept Mat Sci & Technol, Iraklion 71003, Crete, Greece
[3] Aristotle Univ Thessaloniki, Dept Chem, Thessaloniki 54124, Greece
来源
关键词
SrTiO3; Pt photodeposition; H-2; production; Photocatalytic mechanism; MECHANISM; EVOLUTION; DRIVEN; CDS;
D O I
10.1007/s00339-024-07967-w
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Loading of cocatalysts, and especially noble metal nanoparticles, on the surface of photocatalysts has been proven to be an effective strategy to enhance H-2 production, by facilitating charge separation and migration and acting as catalytically active sites. In this work, highly active Pt nanoparticles were loaded with an easy and quick photochemical way on SrTiO3 (STO) and the photocatalytic H-2 production was tested under solar and visible irradiation. Characterization techniques such as X-ray diffraction (XRD), scanning electron microscopy, energy dispersive X-ray spectroscopy (SEM/EDX) and transmission electron microscopy (TEM) were used to determine the physical properties of the samples. Additionally, a combination of UV-vis spectroscopy, photoluminescence spectroscopy (PL) and electrochemical impedance spectroscopy (EIS) was used to gain insights into the photocatalytic mechanism and the variation in photocatalytic activity among the samples. Notably, the photocatalyst with the optimum Pt loading (i.e., sample STO-0.4Pt with 0.4 wt% Pt) reached a hydrogen evolution rate of 15,805 mu mol g(-1) h(-1), which was found to be similar to 8 times higher than the pristine STO sample under solar irradiation.
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页数:11
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