4.7 Article

Water dispersible cobalt single-atom catalysts with efficient Chemiluminescence enhancement for sensitive bioassay

期刊

TALANTA
卷 250, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.talanta.2022.123732

关键词

Cobalt single-atom catalysts; Reactive oxygen species; Carbendazim; Chemiluminescence; Immunoassay

资金

  1. National Natural Science Foundation of China [22074123]

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In this study, cobalt single-atom catalysts (CSACs) were synthesized by solvothermal method using hybridized MOFs Fe2O3/MIL-100(Fe) as carriers. The CSACs show high loading capacity and superior dispersion, and they greatly enhance the chemiluminescent emission of the luminol-H2O2 system. Furthermore, the CSACs are applied as sensitive probes for detecting carbendazim in Chinese medicinal herbs.
Single-atom catalysts (SACs) have been applied in various fields as they display extremely high utilization efficiency of catalytic sites. A majority of SACs prepared by high-temperature calcination suffer from poor water dispersion and lose of labelling groups. Herein cobalt SACs (CSACs) were synthesized with a solvothermal method by adopting hybridized MOFs Fe2O3/MIL-100(Fe) as the carriers to load cobalt atoms. Compared with original MOFs MIL-100(Fe), the carriers possess superior loading capacity, and the loading amount of cobalt element is up to 4.69 wt%. The implantation of cobalt atoms in hybridized MOFs Fe2O3/MIL-100(Fe) vastly improved the specific surface of the carriers for 68 times. CSACs at 1.0 mu g mL(-1) can catalyze H2O2 to generate numerous reactive oxygen species and enormously boost the chemiluminescent emission of luminol-H2O2 system up to 2297 times. The CSACs also exhibit satisfactory dispersion in aqueous medium. Benefiting from these attracting features, the CSACs were applied as sensitive signal probes for detecting carbendazim in Chinese medicinal herbs with a chemiluminescent immunoassay method. The dynamic range is 10 pg mL(-1) - 50 ng mL(-1) and the limit of detection is 1.8 pg mL(-1). The proof-of-principle work paves a pathway to the exploitation of SACs as sensitive probes for tracing biological recognition events.

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