Tollens Reagent-Directed Flower-like α-Ag <sub>3</sub> VO <sub>4</sub> Nanozyme for Signal-Amplified Colorimetric Detection of Epigallocatechin Gallate

Oxidase-like colorimetric sensors based on crystalline vanadates show great potential for polyphenol detection without H<sub>2</sub>O<sub>2</sub>. However, most inorganic nanozymes possess multienzyme activities and follow the "on-to-off" sensing mode, limiting sensitivity and accuracy in complex matrices. Herein, a flower-like α-Ag<sub>3</sub>VO<sub>4</sub> nanozyme was synthesized via a Tollens reagent-mediated method. Distinct from conventional vanadate-based materials, it activates O<sub>2</sub> molecules adsorbed on its oxygen-defective (010) surface through 0.86 eV energy transfer, thereby exerting exclusive oxidase-like activity with O<sub>2</sub><sup>•-</sup> and <sup>1</sup>O<sub>2</sub> as electron acceptors. EGCG accelerates charge transfer and boosts catalytic activity by over 6-fold within 1 min, allowing for an "off-to-on" colorimetric sensor. This unique phenomenon enables the construction of a rapid colorimetric sensor based on an "off-to-on" signal model, which differs fundamentally from reported nanozyme-based colorimetric systems for reducing targets. Compared with the widely used aluminum chloride method (detection limit, LOD = 3.54 μM), the proposed sensor exhibits excellent specificity, superior sensitivity (LOD = 0.16 μM) for EGCG, and comparable accuracy in real sample analysis. This work not only provides a synthetic chemistry approach to tailor the enzyme-like activity of inorganic materials but also offers a promising platform for the sensitive detection of reducing polyphenols.

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Publication Details

Journal
Inorganic Chemistry
Published
2026-03-09
DOI
https://doi.org/10.1021/acs.inorgchem.5c06098
Primary Topic
Advanced Nanomaterials in Catalysis
Type
article
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article

Tollens Reagent-Directed Flower-like α-Ag 3 VO 4 Nanozyme for Signal-Amplified Colorimetric Detection of Epigallocatechin Gallate

Haoyu Ma, Yun-Yun Wu, Xin Yang, Fan Lu et al.
Inorganic Chemistry
Advanced Nanomaterials in Catalysis
article

Tollens Reagent-Directed Flower-like α-Ag 3 VO 4 Nanozyme for Signal-Amplified Colorimetric Detection of Epigallocatechin Gallate

Haoyu Ma, Yun-Yun Wu, Xin Yang, Fan Lu, Shujie Feng, Dong-Dong Qin, Li Niu, Wei Wang, Wen-Sheng Zhang, Dong-Xue Han, Yong-Fei Ji
article en

Abstract

Oxidase-like colorimetric sensors based on crystalline vanadates show great potential for polyphenol detection without H<sub>2</sub>O<sub>2</sub>. However, most inorganic nanozymes possess multienzyme activities and follow the "on-to-off" sensing mode, limiting sensitivity and accuracy in complex matrices. Herein, a flower-like α-Ag<sub>3</sub>VO<sub>4</sub> nanozyme was synthesized via a Tollens reagent-mediated method. Distinct from conventional vanadate-based materials, it activates O<sub>2</sub> molecules adsorbed on its oxygen-defective (010) surface through 0.86 eV energy transfer, thereby exerting exclusive oxidase-like activity with O<sub>2</sub><sup>•-</sup> and <sup>1</sup>O<sub>2</sub> as electron acceptors. EGCG accelerates charge transfer and boosts catalytic activity by over 6-fold within 1 min, allowing for an "off-to-on" colorimetric sensor. This unique phenomenon enables the construction of a rapid colorimetric sensor based on an "off-to-on" signal model, which differs fundamentally from reported nanozyme-based colorimetric systems for reducing targets. Compared with the widely used aluminum chloride method (detection limit, LOD = 3.54 μM), the proposed sensor exhibits excellent specificity, superior sensitivity (LOD = 0.16 μM) for EGCG, and comparable accuracy in real sample analysis. This work not only provides a synthetic chemistry approach to tailor the enzyme-like activity of inorganic materials but also offers a promising platform for the sensitive detection of reducing polyphenols.

Inorganic ChemistryVol. 65(11)
Sun Yat-sen University (CN), Guangzhou University (CN)
Affordable and clean energy
Openalex Percentile: Top 30%
Advanced Nanomaterials in Catalysis
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