多孔性
材料科学
检出限
基质(水族馆)
介孔材料
纳米技术
选择性
多孔介质
分析物
拉曼光谱
光谱学
光电子学
电磁场
化学工程
钼
工作(物理)
纳米颗粒
领域(数学)
氧化物
停留时间(流体动力学)
极限(数学)
有限元法
等离子体子
近场和远场
表面增强拉曼光谱
氢
作者
Xiaoyu Zhang,Zhi Yang,Mingyue Li,Min Li,Chengju Guo,Muhammad Saleem,Muhammad Zahid,Jianbao Liu,Shuai Qiu,Mei Liu
标识
DOI:10.1002/lpor.202503240
摘要
ABSTRACT The application of surface‐enhanced Raman spectroscopy (SERS) into gas sensing, particularly for breath‐based diagnostics, is hindered by the challenge of simultaneously achieving high sensitivity, selectivity, and stability. This work introduces a synergistic enhancementarchitecture based on porous molybdenum oxide (MoO x ) nanobowl arrays to overcome this trilemma. This architecture is designed to couple electromagnetic field enhancement, efficient gas adsorption/concentration, and specific molecular recognition within a single unit cell. Finite element simulations confirm that the concave geometry creates densely packed electromagnetic hotspots, while the mesoporous structure induces gas vortices that prolong analyte residence time precisely within these enhancement zones. Functionalized with 4‐aminothiophenol (4‐ATP), the substrate achieves a detection limit of 0.95 ppb for 4‐ethylbenzaldehyde (EBA), maintains high selectivity in complex simulated breath matrices, and exhibits remarkable long‐term stability. This study proposes a potential design principle for next‐generation, non‐metal SERS platforms, supporting their potential in non‐invasive early disease diagnosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI