School of Chemistry and Chemical Engineering, Shandong University, Jinan, Shandong Province 250100, China.
School of Pharmaceutical Sciences, Shandong University, Jinan, Shandong Province 250012, China.
J Hazard Mater. 2022 Jun 5;431:128621. doi: 10.1016/j.jhazmat.2022.128621. Epub 2022 Mar 4.
Nanozymes have been widely utilized in colorimetric sensors and developing nanomaterials with multienzyme functions have more application prospects due to their cascaded catalytic efficiency. Here, a unique organic-inorganic nanocomposite CoFeO/HPPOP was synthesized by depositing CoFeO nanocubes on a fully conjugated porphyrin-based porous organic polymer (HPPOP) in situ. CoFeO/HPPOP revealed outstanding tetra-enzyme-like activities, namely oxidase-like, peroxidase-like, catalase-like and superoxide dismutase-like activities. Compared with pure CoFeO nanocubes, the catalytic activities of CoFeO/HPPOP were significantly boosted because of the large surface area and extended conjugated structure of HPPOP, abundant active substances (CoFeO) on the surface and the effective electronic transfer between CoFeO and HPPOP. Based on the oxidase-like activity of CoFeO/HPPOP, a colorimetric platform was constructed for Cr (VI) with a wide linear range (0.6-100 μM) and a low detection limit (26 nΜ). Further utilizing the double oxidase-like and peroxidase-like activities, a more sensitive colorimetric platform with a faster detection speed for Cr (VI) was realized with the LOD as low as 2 nΜ. This work opens up a new way to prepare multi-enzyme active nanozyme and excavates its potential for detecting environmental pollutants.
纳米酶已广泛应用于比色传感器中,而开发具有多种酶功能的纳米材料由于其级联催化效率,具有更多的应用前景。在这里,通过在完全共轭的卟啉基多孔有机聚合物(HPPOP)上原位沉积 CoFeO 纳米立方体,合成了一种独特的有机-无机纳米复合材料 CoFeO/HPPOP。CoFeO/HPPOP 表现出优异的四酶样活性,即氧化酶样、过氧化物酶样、过氧化氢酶样和超氧化物歧化酶样活性。与纯 CoFeO 纳米立方体相比,由于 HPPOP 的大表面积和扩展共轭结构、表面上丰富的活性物质(CoFeO)以及 CoFeO 和 HPPOP 之间的有效电子转移,CoFeO/HPPOP 的催化活性得到了显著提高。基于 CoFeO/HPPOP 的氧化酶样活性,构建了用于 Cr(VI)的比色平台,具有较宽的线性范围(0.6-100 μM)和较低的检测限(26 nM)。进一步利用双氧化酶样和过氧化物酶样活性,实现了一种更灵敏的比色平台,用于检测 Cr(VI)的检测速度更快,检测限低至 2 nM。这项工作为制备多种酶活性纳米酶开辟了新途径,并挖掘了其检测环境污染物的潜力。