Abstract

In this work, Sr1−1.5xTbxWO4 (0 ≤ x ≤ 0.2) solid solutions were synthesized via a traditional high-temperature solid state method. Le Bail fitting on the powder X-ray diffraction (XRD) pattern showed that these solid solutions are pure phase. Scanning electron microscopy showed that the SrWO4 and Sr0.82Tb0.12WO4 samples are composed of micrometer particles and submicron crystallites, respectively. Ultraviolet–visible diffuse reflectance spectra suggested that the bandgaps of Sr1−1.5xTbxWO4 are narrower than the undoped sample. The Sr0.82Tb0.12WO4 sample, with the assistance of 1.5 wt % Ru-cocatalyst, exhibits the best performance for H2 evolution in 5 vol % aqueous triethanolamine (TEOA), which results in about 6.1 and 2.8 times efficiency improvement compared with the intrinsic SrWO4 in methanol and aqueous TEOA, respectively. All the photocatalysts recycled after the photocatalytic reactions showed no degradation when checked by powder XRD.

Highlights

  • Photocatalytic technology is a green way to obtain clean energy hydrogen via semiconductor from water under sunlight irradiation [1]

  • Le Bail fitting on powder X-ray diffraction (XRD) verified high purity and crystallinity of the as-prepared samples, and the fitting on powder XRD verified high purity and crystallinity of the as-prepared samples, and the Scanning electron microscopy (SEM) images showed that the SrWO4 and Sr0.82 La0.12 WO4 were composed of micron and submicron

  • 2p orbitals, and the conduction band minimum was composed of both band maximum was composed of O 2p orbitals, and the conduction band minimum was composed

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Summary

Introduction

Photocatalytic technology is a green way to obtain clean energy hydrogen via semiconductor from water under sunlight irradiation [1]. The sulfide and oxynitride materials generally have excellent photocatalytic activities, both of them are not stable enough in aqueous solution under light irradiation. Suitable SrWO4 crystal structures are able to degrade various dyes and organic materials under ultraviolet light [15,16,17,18,19,20,21]. Materials 2019, 12, 1487 single report of H2 evolution by SrWO4 micro/nanostructures in aqueous methanol under ultraviolet light irradiation [22]. The photocatalytic H2 evolution of scheelite structure SrWO4 was improved by doping rare earth ions and cocatalysts. The Sr1−1.5x Tbx WO4 solid solutions were studied for the first time in aqueous TEOA under ultraviolet light irradiation, and their photocatalytic activity was improved by loading various cocatalysts, such as Cu, Ag, Au, Pt, Ni, and Ru

Preparations of the Catalysts
Theoretical Calculations
Photocatalytic Performance Evaluation
Preparation
Discussion
H evolution ratesrates of Srof
Conclusions
1.References

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