Nanoetching TiO nanorod photoanodes to induce high-energy facet exposure for enhanced photoelectrochemical performance
Crystal facet engineering is considered as an effective way to improve photoelectrochemical (PEC) performance. Here, we have developed a nanoetching technology (TiO 2 → TiO 2 /Bi 4 Ti 3 O 12 → TiO 2 /BiVO 4 → etching-TiO 2 ) to treat rutile TiO 2 nanorod films. Interestingly, the technology can indu...
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Published in | Nanoscale Vol. 14; no. 42; pp. 15918 - 15927 |
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Main Authors | , , , , , , |
Format | Journal Article |
Published |
03.11.2022
|
Online Access | Get full text |
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Summary: | Crystal facet engineering is considered as an effective way to improve photoelectrochemical (PEC) performance. Here, we have developed a nanoetching technology (TiO
2
→ TiO
2
/Bi
4
Ti
3
O
12
→ TiO
2
/BiVO
4
→ etching-TiO
2
) to treat rutile TiO
2
nanorod films. Interestingly, the technology can induce the exposure of a large number of high energy (101) faces, and the etching-TiO
2
film (E-TiO
2
) showed a significantly enhanced PEC performance. A dynamic study indicates that charge separation and transfer have been obviously improved by such a nanoetching technology. In particular, the charge transfer efficiency (
η
trans
) of E-TiO
2
reaches 93.4% at 1.23 V
vs.
RHE without any loaded cocatalyst. The mechanism of PEC performance enhanced by the strategy is experimentally and theoretically unraveled. The improvement of PEC performance is mainly attributed to the shorter distance between H and the neighboring O-b for the HO* intermediates of the rutile (101) facet, which can reduce the energy barrier for the OER. Besides, the driving force for spatial charge separation between the (110) and (101) facets can promote charge separation. This work offers a new and versatile nanotechnology to induce the exposure of the high energy crystal facets and improve the PEC performance.
A nanoetching technology is demonstrated to induce the exposure of (101) facets of TiO
2
nanorods, exhibiting a significantly enhanced photoelectrochemical activity. |
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Bibliography: | https://doi.org/10.1039/d2nr04031j Electronic supplementary information (ESI) available. See DOI |
ISSN: | 2040-3364 2040-3372 |
DOI: | 10.1039/d2nr04031j |