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Anisotropically Shaped Plasmonic WO3-x Nanostructure-Driven Ultrasensitive SERS Detection and Machine Learning-Based Differentiation of Nitro-Explosives

NCJ Number
310203
Journal
ACS Applied Materials & Interfaces Volume: 17 Issue: 7 Dated: Feb 2025 Pages: 11309–11324
Author(s)
M. Vitoria Simas; Gregory A. Davis Jr; Sumon Hati; Jingzhi Pu; John V. Goodpaster; Rajesh Sardar
Date Published
February 2025
Length
16 pages
Annotation

This article addresses a need for the development of analysis techniques regarding ultrasensitive detection and quantification of chemical and biological analytes; it reports on a research project, indicating that the structure of oxygen-deficient, LSPR-active, nonstoichiometric tungsten oxide NSs can control the SERS enhancement factor.

Abstract

Nanostructures (NSs) of noble metals such as Au, Ag, and Cu are the benchmarks for the preparation of highly efficient surface-enhanced Raman spectroscopy (SERS) substrates because of their unique localized surface plasmon resonance (LSPR) properties. Non-noble-metal SERS substrates, e.g., metal chalcogenide semiconductors and transition metal oxides, have been prepared to mitigate the cost; however, their low sensitivity restricts widespread applications. In this article, the authors report for the first time that the structure of oxygen-deficient, LSPR-active, nonstoichiometric tungsten oxide (i.e., WO3–x) NSs can control the SERS enhancement factor (EF). SERS substrates prepared with colloidally synthesized WO3–x nanowires, nanorods, and nanoplatelets display SERS EF of 2.5 × 106, 3.1 × 107, and 5.5 × 107, respectively, using rhodamine 6G (R6G) molecules as Raman probes. The authors’ experimentally acquired SERS data and spectroscopically determined electronic band structure of LSPR-active WO3–x NSs, and time-domain density functional theory (TDDFT)-based calculations support a dual enhancement scheme involving a strong plasmonic effect controlled electromagnetic field and their oxygen vacancy-induced chemical enhancement mechanisms, respectively. To demonstrate the practical utility of our WO3–x NCs, they are able to detect aromatic nitro-explosives (tetryl, TNT, and DNT) with a very low limit of detection (LOD, 10–9 M). Importantly, machine learning-driven chemometric analysis for SERS-based detection shows excellent classification between these three explosives. Finally, three nonaromatic, nitro-explosives, HMX, RDX, and PETN are also successfully detected utilizing our LSPR-active, WO3–x-based SERS substrates. To the best of the authors’ knowledge, this is the first example where LSPR-active, non-noble-metal NSs are used for the detection of both aromatic and aliphatic nitro-explosives. Taken together, this work represents the advancement of the fabrication of non-noble-metal-based SERS substrates, which can be widely employed for the low-cost detection of analytes across forensic science, chemistry, and biomedical fields. (Published Abstract Provided)

Sponsoring Agency
National Institute of Justice (NIJ)
Address

999 N. Capitol St. NE, Washington, DC 20531, United States

Corporate Author
Indiana University
Address

Bloomington, IN 47401, United States

Publication Format
Article
Publication Type
Research (Applied/Empirical)
Country
United States of America