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Polarization-Enhanced direct Z-scheme ZnO-WO3-x nanorod arrays for efficient piezoelectric-photoelectrochemical Water splitting
[Display omitted] •Direct Z-scheme ZnO-WO3-x was constructed by in-situ solvothermal treatment.•Suitable band structure and Fermi level drive the formation of Z-scheme structure.•Stirring leads to piezoelectric polarization of ZnO, and enhances Z-scheme effect.•Zn-W-5 shows very high piezoelectric-p...
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Published in: | Applied catalysis. B, Environmental Environmental, 2019-12, Vol.259, p.118079, Article 118079 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Direct Z-scheme ZnO-WO3-x was constructed by in-situ solvothermal treatment.•Suitable band structure and Fermi level drive the formation of Z-scheme structure.•Stirring leads to piezoelectric polarization of ZnO, and enhances Z-scheme effect.•Zn-W-5 shows very high piezoelectric-photoelectrochemical activities.
Photosynthesis with Z-scheme charge transfer has been recognized as an efficient pathway to achieve solar-energy conversion. Herein, the all-solid-state direct Z-scheme ZnO-WO3-x nanorod arrays were synthesized by in-situ solvothermal treatment for highly piezoelectric (PE)-photoelectrochemical (PEC) water splitting. The chemical bonding between WO3-x and ZnO via W-O-Zn and the inherent band structures/Fermi levels drive the formation of direct Z-scheme charge-transfer pathway. Importantly, the optimized structure (Zn-W-5) shows higher PEC activities with high photocurrent density of 2.39 mA/cm2 at 1.23 V vs. RHE, which is 2.13 times higher than pure ZnO. Surprisingly, the obvious PE polarization of ZnO increases its Fermi level toward conduction band and significantly enhances Z-scheme effect between ZnO and WO3-x. Especially, the best sample (Zn-W-5-1000 rpm) shows a photocurrent of 3.38 mA/cm2 at 1.23 V vs. RHE, which is 3.02 times higher than pure ZnO. This work provides a facile PE polarization approach for enhancement of Z-scheme charge-transfer process. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2019.118079 |