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缺陷与S-C键的协同作用增强了空心球状FeS/SC的过氧化物酶样活性。

Peroxidase-like activity of hollow sphere-like FeS/SC boosted by synergistic action of defects and S-C bonding.

作者信息

Tan Hao, Nan Zhaodong

机构信息

School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, China.

出版信息

Dalton Trans. 2023 Mar 21;52(12):3821-3834. doi: 10.1039/d3dt00044c.

Abstract

Pyrite FeS has been applied as a peroxidase due to its easy preparation and low cost. However, the low peroxidase-like (POD) activity limited its wide application. A hollow sphere-like composite (FeS/SC-5.3%) composed of pyrite FeS and sulfur-doped hollow sphere-shaped carbon was synthesized by a facile solvothermal method, where the S-doped carbon was formed during FeS formation. The synergistic action such as the defects at the carbon surface and the formation of S-C bonding improved the nanozyme activity. The S-C bonding was a bridge between the carbon and the Fe atom in FeS, which enhanced the electron transfer between the Fe atom and the carbon and accelerated the conversion from Fe to Fe. The optimum experimental conditions were obtained by the response surface methodology (RSM). The POD-like activity of FeS/SC-5.3% was significantly improved compared to that of FeS. The Michaelis-Menten constant () of FeS/SC-5.3% is 80 times lower than that of horseradish peroxidase (HRP, natural enzyme). FeS/SC-5.3% can be used to detect cysteine (Cys) with a limit of detection (LOD) as small as 0.061 μM at room temperature in only 1 min.

摘要

黄铁矿FeS因其制备简便且成本低廉而被用作过氧化物酶。然而,其类过氧化物酶(POD)活性较低限制了它的广泛应用。通过一种简便的溶剂热法合成了一种由黄铁矿FeS和硫掺杂空心球形碳组成的空心球状复合材料(FeS/SC-5.3%),其中硫掺杂碳是在FeS形成过程中生成的。碳表面的缺陷和S-C键的形成等协同作用提高了纳米酶活性。S-C键是碳与FeS中Fe原子之间的桥梁,增强了Fe原子与碳之间的电子转移,加速了Fe向Fe的转化。通过响应面法(RSM)获得了最佳实验条件。与FeS相比,FeS/SC-5.3%的类POD活性显著提高。FeS/SC-5.3%的米氏常数()比辣根过氧化物酶(HRP,天然酶)低80倍。FeS/SC-5.3%可用于在室温下仅1分钟内检测半胱氨酸(Cys),检测限低至0.061μM。

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