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Cu 2 O nanoparticles sensitize TiO 2 /CdS nanowire arrays to prolong charge carrier lifetime and highly enhance unassisted photoelectrochemical hydrogen generation with 4.3% efficiency
Effective separation of charge carriers and substantial prolongation of charge carrier lifetime are two vital issues for a photoanode to achieve highly efficient photoelectrochemical (PEC) hydrogen generation. Herein, a Cu 2 O-nanoparticle-sensitized TiO 2 /CdS (TiO 2 /CdS/Cu 2 O) nanowire array pho...
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Published in: | Dalton transactions : an international journal of inorganic chemistry 2020-07, Vol.49 (27), p.9282-9293 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Effective separation of charge carriers and substantial prolongation of charge carrier lifetime are two vital issues for a photoanode to achieve highly efficient photoelectrochemical (PEC) hydrogen generation. Herein, a Cu
2
O-nanoparticle-sensitized TiO
2
/CdS (TiO
2
/CdS/Cu
2
O) nanowire array photoanode is fabricated
via
subtly combining successive ionic layer adsorption and reaction with a chemical bath deposition method. Both the type-II band alignment with a stair-like structure and a p–n junction are integrated into this ternary photoanode. The fabricated photoanode shows a significant enhancement in the PEC H
2
production with 4.3% efficiency. The measurements of light absorption, photoluminescence and electrochemical spectra undoubtedly demonstrate that the enhanced PEC H
2
generation is ascribed to the remarkable enhancement of visible-light absorbing ability, efficient space charge separation and substantial prolongation of charge carrier lifetime, which are achieved by the synergetic effects of the type-II band alignment with a stair-like structure and the p–n junction. The enhanced PEC H
2
generation demonstrates the potential of the TiO
2
/CdS/Cu
2
O nanowire arrays as a photoanode to efficiently convert solar energy into chemical fuels. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/D0DT01643H |