材料科学
催化作用
胆碱
Atom(片上系统)
纳米技术
兴奋剂
肉眼
碳纤维
组合化学
检出限
光电子学
化学
计算机科学
有机化学
嵌入式系统
复合数
复合材料
生物化学
色谱法
作者
Qijun Sun,Xiaoyu Xu,Song Liu,Xinzhao Wu,Chenhui Yin,Meng Wu,Yuxue Chen,Na Niu,Ligang Chen,Fu‐Quan Bai
标识
DOI:10.1021/acsami.3c04761
摘要
Single-atom nanozymes (SANs) have attracted great attention in constructing devices for instant biosensing due to their excellent stability and atom utilization. Here, Mo atoms were immobilized in 2D nitrogen-doped carbon films by cascade-anchored one-pot pyrolysis to obtain Mo single-atom nanozyme (Mo-SAN) with high atomic loading (4.79 wt %) and peroxidase-like activity. The coordination environment and enzyme-like activity mechanism of Mo-SAN were studied by combining synchrotron radiation and density functional theory. The strong oxophilicity of single-atom Mo makes the catalytic center more capable of transferring electrons to free radicals to selectively generate •OH in the presence of H2O2. Choline oxidase and Mo-SAN were used as signal opening unit and signal amplification unit, respectively. Combining the portability and visualization functions of smartphone and test strips, a paper-based visual sensing platform was constructed, which can accurately identify choline at a concentration of 0.5-35 μM with a limit of detection as low as 0.12 μM. The recovery of human serum samples was 96.4-102.2%, with an error of less than 5%. Furthermore, the potential of Mo-SAN to efficiently generate toxic •OH in tumor cells was intuitively confirmed. This work provides a technical and theoretical basis for designing highly active SANs and detecting neurological markers.
科研通智能强力驱动
Strongly Powered by AbleSci AI