Publication | Open Access
Three‐Channel Electron Engineered Fe‐88A@CeO <sub>2</sub> /CDs Nanozyme with Enhanced Oxidase‐Like Activity for Efficient Biomimetic Catalysis
12
Citations
45
References
2025
Year
Iron-based metal-organic framework (MOF) nanozymes have garnered considerable attention owing to a large specific surface area, adjustable porosity, large Fe-O clusters, and unsaturated Fe sites. However, the sluggish charge-transfer rate and restricted active sites of the nanozymes lead to poor enzyme-like activity and further impede their biomimetic catalysis. Herein, a three-channel electron-engineered Fe-88A@CeO<sub>2</sub>/carbon dots (Fe-88A@CeO<sub>2</sub>/CDs) nanozyme is proposed for efficient biomimetic catalysis. Fe-88A@CeO<sub>2</sub>/CDs nanozyme is prepared by incorporation of CeO<sub>2</sub> and CDs into the porosity of Fe-88A. Specifically, the original Fe (II)/Fe (III) and the introduced Ce (III)/Ce (IV) redox couples of the nanozyme constitute a dual electron transfer channel. Furthermore, the presence of CDs produces another electron transfer channel. The three-channel electron engineering strategy for nanozymes can accelerate the electron transfer process accompanied with more active sites, thereby greatly enhancing the oxidase-like activity of Fe-88A@CeO<sub>2</sub>/CDs for biomimetic catalysis. The nanozyme can efficiently convert oxygen to · <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:semantics><mml:msubsup><mml:mi>O</mml:mi> <mml:mn>2</mml:mn> <mml:mo>-</mml:mo></mml:msubsup> <mml:annotation>${\mathrm{O}}_2^ - $</mml:annotation></mml:semantics> </mml:math> , oxidizing colorless 3,3',5,5'-tetramethylbenzidine (TMB) to blue ox-TMB, and meanwhile the ox-TMB effectively quenches the fluorescence of CDs. As proof of concept, the nanozyme is utilized to construct a colorimetric-fluorescence bimodal immunosensor for monitoring Staphylococcal enterotoxin B with excellent performance. This work provides promising insight into designing excellent nanozymes for effective biomimetic catalysis in various fields.
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