摘要
Due to the high costs and relative instability of natural enzymes, highly efficient enzyme mimics have attracted much research interest in constructing nanozymes of biosensors. This study fabricated Co 9 S 8 nanozymes with diverse morphologies by adjusting the sulfur content in a facile and efficient solvothermal strategy using the Co-glycerate microsphere as the sacrificial template. Our findings revealed that sulfur-mediated surface reconstruction, especially at an optimal sulfur concentration, enables the fabrication of the M−Co 9 S 8 nanozyme with a hollow nanosphere structure. The nanozyme exhibits exceptional peroxidase-like activity. In the presence of H 2 O 2 , M−Co 9 S 8 nanozyme significantly enhanced the oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB), resulting in a pronounced color change, thereby enabling the colorimetric sensing of glutathione (GSH). The systematic studies, including radical scavengers and electron spin resonance experiments, confirm that superoxide free radicals (·O 2 − ) play a key role in catalytic reactions and exhibit a synergistic effect with holes ( h + ). Based on these active radicals and the optimized electron transfer efficiency of the hollow porous spherical shell structure, the M−Co 9 S 8 nanozyme showed a catalytic efficiency of 5.44 times higher than that of L-Co 9 S 8 solid nanospheres with low sulfur content. The strategy demonstrated high sensitivity, excellent specificity, and robust stability. It featured a 5-order linear range and a detection limit as low as 3.16 nM for the detection of GSH, rendering it highly promising for clinical sample detection. A deeper understanding of Co 9 S 8 ′s surface reconstruction could offer crucial insights for developing high-performance nanomaterials and biosensors, broadening their potential applications in biosensing and biomedicine.
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