ABSTRACT
Ultratrace molecular detections are vital for precancer diagnosis, forensic analysis, and food safety. Superhydrophobic (SH) surface-enhanced Raman scattering (SERS) sensors are regarded as an ideal approach to improve detection performance by concentrating analyte molecules within a small volume. However, due to the low adhesion of SH surfaces, the analyte droplet is prone to rolling, making it hard to deposit molecules on a predetermined position. Furthermore, the sediment with a very small area on the SH-SERS surface is difficult to be captured even with a Raman microscope. In this study, femtosecond laser fabricated hybrid SH/hydrophobic (SH/HB) surfaces are successfully applied to realize a rapid and highly sensitive SERS detection. By modulating dual surface structures and wetting behaviors, the analyte molecules can be enriched at the edge of HB pattern. This improves the convenience and speed of Raman test. On a hybrid SH/HB SERS substrate with a circular HB pattern at 300-µm-diameter, a femtomolar level (10-14 M) of rhodamine 6G can be detected by using analyte volumes of just 5 µL. The SERS enhancement factor can reach 5.7×108 and a good uniformity with a relative standard deviation of 6.98% is achieved. Our results indicate that the laser fabrication of hybrid SERS sensor offers an efficient and cost-effective approach for ultratrace molecular detection.
