Scalable manufacturing of mesoporous nanograting SERS sensors for ultrasensitive molecular detection
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Abstract
Here, we report an extreme manufacturing strategy for fabricating mesoporous nanograting gold films (MNGFs) with uniformly distributed mesoporous architectures, designed to generate abundant SERS hotspots for ultra-sensitive chemical detection. These MNGFs were prepared via the electrochemical deposition of a mesoporous gold film onto a nanograting template using polymer micelles as a sacrificial agent. Notably, the width between the gratings could be adjusted with precision by varying the electrodeposition time, optimizing the SERS hotspots and nanogap formation. The resulting SERS substrates achieved a limit of detection (LoD) of 1 pM for rhodamine 6 G (R6G), with an analytical enhancement factor (AEF) of 4.55 × 109. To evaluate their performance, the MNGFs were employed to detect thiophenol (TP), serving as a safe simulant for thiol-based analytes. Remarkably, the substrates exhibited exceptional sensitivity, achieving a limit of detection of 81 aM. Furthermore, the MNGFs facilitated gas-phase detection of TP at concentrations as low as 3.73 parts per billion (ppb), underscoring their practical applicability. Moreover, the MNGFs demonstrated excellent spatial uniformity, with a relative standard deviation (RSD) of 9.68%, and could be reused up to four times, maintaining consistent SERS signals and enhancement. Overall, the 3D mesoporous nanograting architecture offers a scalable, reproducible, and high-performance sensing platform, representing a promising advancement in precision manufacturing for real-time, on-site hazardous chemical monitoring.
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