Low-adhesive superhydrophobic surface-enhanced Raman spectroscopy substrate fabricated by femtosecond laser ablation for ultratrace molecular detection

Andong Wang, Lan Jiang, Xiaowei Li*, Qian Xie, Bohong Li, Zhi Wang, Kun Du, Yongfeng Lu

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

74 Citations (Scopus)

Abstract

Ultratrace molecular detections from a limited amount of highly diluted solutions can offer unprecedented benefits in the biomedical/analytical fields, such as in precancer diagnosis, forensic analysis, and food safety. However, huge difficulties exist in completely concentrating the target molecules within a sensitive area and thereby enhancing the detection sensitivity. Herein, we report the ultratrace molecular detection using a low-adhesive superhydrophobic surface-enhanced Raman spectroscopy (LAS-SERS) substrate fabricated by femtosecond laser ablation. The LAS-SERS substrate has good characteristics, including a contact angle as high as 154°, a contact angle hysteresis below 5°, and a simulated Raman signal enhancement factor of up to 6 × 106. Compared to the previously developed superhydrophobic SERS (S-SERS) methods, the low-adhesive nature of the LAS-SERS method can greatly reduce the final contact area, thus significantly enhancing the detection limit. In our experiments, the final contact area of the LAS-SERS substrate was reduced by 19.5 times, corresponding to an 88.1 times increase in the concentration effect, as compared to the highly adhesive S-SERS substrates fabricated using the same technique. The enhanced condensation effect led to a detection limit as low as 10−14 M, which shows an obvious improvement compared to that of the other non-photolithography methods. The method reported herein offers a facile and efficient approach to the cost-effective fabrication of a high-performance LAS-SERS substrate for ultratrace molecular detection.

Original languageEnglish
Pages (from-to)777-784
Number of pages8
JournalJournal of Materials Chemistry B
Volume5
Issue number4
DOIs
Publication statusPublished - 2017

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