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Synergy-Compensation Effect of Ferroelectric Polarization and Cationic Vacancy Collaboratively Promoting CO 2 Photoreduction
Photocatalytic CO reduction is severely limited by the rapid recombination of photo-generated charges and insufficient reactive sites. Creating electric field and defects are effective strategies to inhibit charge recombination and enrich catalytic sites, respectively. Herein, a coupled strategy of...
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Published in: | Small (Weinheim an der Bergstrasse, Germany) Germany), 2023-02, Vol.19 (5), p.e2203559 |
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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: | Photocatalytic CO
reduction is severely limited by the rapid recombination of photo-generated charges and insufficient reactive sites. Creating electric field and defects are effective strategies to inhibit charge recombination and enrich catalytic sites, respectively. Herein, a coupled strategy of ferroelectric poling and cationic vacancy is developed to achieve high-performance CO
photoreduction on ferroelectric Bi
MoO
, and their interesting synergy-compensation relationship is first disclosed. Corona poling increases the remnant polarization of Bi
MoO
to enhance the intrinsic electric field for promoting charge separation, while it decreases the CO
adsorption. The introduced Mo vacancy (V
) facilitates the adsorption and activation of CO
, and surface charge separation by creating local electric field. Unfortunately, V
largely reduces the remnant polarization intensity. Coupling poling and V
not only integrate their advantages, resulting in an approximately sevenfold increased surface charge transfer efficiency, but also compensate for their shortcomings, for example, V
largely alleviates the negative effects of ferroelectric poling on CO
adsorption. In the absence of co-catalyst or sacrificial agent, the poled Bi
MoO
with V
exhibits a superior CO
-to-CO evolution rate of 19.75 µmol g
h
, ≈8.4 times higher than the Bi
MoO
nanosheets. This work provides new ideas for exploring the role of polarization and defects in photocatalysis. |
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ISSN: | 1613-6810 1613-6829 |
DOI: | 10.1002/smll.202203559 |