Author
Listed:
- Shuo Wang
(Nankai University)
- Chenyang Li
(Nankai University)
- Yu Qi
(Chinese Academy of Sciences)
- Jiaming Zhang
(ShanghaiTech University)
- Ningning Wang
(Nankai University)
- Meng Liu
(ShanghaiTech University)
- Boyang Zhang
(ShanghaiTech University)
- Xuefen Cai
(Shenzhen University)
- Hongbo Zhang
(Nankai University)
- Su-huai Wei
(Eastern Institute of Technology)
- Guijun Ma
(ShanghaiTech University)
- Jingxiu Yang
(Jilin Jianzhu University)
- Shanshan Chen
(Nankai University)
- Fuxiang Zhang
(Chinese Academy of Sciences)
Abstract
Charge separation of particulate photocatalysts has been considered as the rate-determining step in artificial photocatalysis since the finding of Honda-Fujishima effect, whose efficiency is generally much lower than that of natural photosynthesis. To approach its upper limit, it requires the photoexcited electrons and holes be efficiently transferred to the spatially separated redox reaction sites over a single photocatalyst particle. Herein, it is demonstrated the spatial charge separation among facets of BiVO4:Mo can be notably promoted by creating an electron transfer layer. It not only favors electrons to transfer to its surface, but also promotes the built-in electric field intensity of the inter-facet junction by over 10 times. Consequently, the charge separation efficiency of the modified BiVO4:Mo with loading of CoFeOx oxidation cocatalyst exceeds 90% at 420 nm, comparable to that of the natural photosynthesis system, over which notably enhanced photocatalytic activities are achieved. Our findings demonstrate the effectiveness of electron transfer layer in intensifying charge separation of particulate photocatalysts.
Suggested Citation
Shuo Wang & Chenyang Li & Yu Qi & Jiaming Zhang & Ningning Wang & Meng Liu & Boyang Zhang & Xuefen Cai & Hongbo Zhang & Su-huai Wei & Guijun Ma & Jingxiu Yang & Shanshan Chen & Fuxiang Zhang, 2025.
"Etched BiVO4 photocatalyst with charge separation efficiency exceeding 90%,"
Nature Communications, Nature, vol. 16(1), pages 1-9, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-59076-8
DOI: 10.1038/s41467-025-59076-8
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-59076-8. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.