AnS‑Scheme MOF-on-MXene Heterostructure forEnhanced Photocatalytic Periodate Activation

Fully understanding the periodate (PI) activation system is still a great challenge, which calls for efficient heterogeneous catalysts with a sophisticated structure. Herein, we developed “MOF-on-MXene” heterostructures. By constructing S-scheme heterostructures MXene/Z67<sub>450</sub>, the internal electric field is generated via the Ti–O–Co bonds at the interface, favoring the excitation of the photogenerated electrons, providing a driving force for accelerating the charge transfer, and enhancing redox performances. Further contributed by the synergy of Ti–O–Co and Co–N<sub>4</sub> bonds, the MXene/Z67<sub>450</sub> composites exhibit enhanced ability for activating the periodate system to degrade organic pollutants via building a donor–catalyst–acceptor system. In the presence of periodate and light, MXene/Z67<sub>450</sub> degraded ∼100% of tetracycline hydrochloride (TCH) in only 10 min. The active sites of the heterostructures can react with the periodate and give the intermediate MXene/Z67<sub>450</sub>-PI (*PI). As a result, it efficiently reduced the PI adsorption energy and promoted the decomposition of PI and the formation of holes/electrons, singlet oxygen (<sup>1</sup>O<sub>2</sub>) as well as hydroxyl radical (•OH). In addition, the MXene/Z67<sub>450</sub> composites exhibit high stability, reusability, selectivity, and environmental robustness. Our study provides a research direction for rationally designing MXene-based heterojunctions and applying them in the periodate activation system.

Publication Details

Journal
Figshare
Published
2025-02-05
DOI
https://doi.org/10.1021/acsnano.4c18864.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
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article
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article

AnS‑Scheme MOF-on-MXene Heterostructure forEnhanced Photocatalytic Periodate Activation

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Mycorrhizal Fungi and Plant Interactions
article

AnS‑Scheme MOF-on-MXene Heterostructure forEnhanced Photocatalytic Periodate Activation

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Abstract

Fully understanding the periodate (PI) activation system is still a great challenge, which calls for efficient heterogeneous catalysts with a sophisticated structure. Herein, we developed “MOF-on-MXene” heterostructures. By constructing S-scheme heterostructures MXene/Z67<sub>450</sub>, the internal electric field is generated via the Ti–O–Co bonds at the interface, favoring the excitation of the photogenerated electrons, providing a driving force for accelerating the charge transfer, and enhancing redox performances. Further contributed by the synergy of Ti–O–Co and Co–N<sub>4</sub> bonds, the MXene/Z67<sub>450</sub> composites exhibit enhanced ability for activating the periodate system to degrade organic pollutants via building a donor–catalyst–acceptor system. In the presence of periodate and light, MXene/Z67<sub>450</sub> degraded ∼100% of tetracycline hydrochloride (TCH) in only 10 min. The active sites of the heterostructures can react with the periodate and give the intermediate MXene/Z67<sub>450</sub>-PI (*PI). As a result, it efficiently reduced the PI adsorption energy and promoted the decomposition of PI and the formation of holes/electrons, singlet oxygen (<sup>1</sup>O<sub>2</sub>) as well as hydroxyl radical (•OH). In addition, the MXene/Z67<sub>450</sub> composites exhibit high stability, reusability, selectivity, and environmental robustness. Our study provides a research direction for rationally designing MXene-based heterojunctions and applying them in the periodate activation system.

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