Flexible SERS substrates for hazardous materials detection: recent advances

This article reviews the most recent advances in the development of flexible substrates used as surface-enhanced Raman scattering (SERS) platforms for detecting several hazardous materials (e.g., explosives, pesticides, drugs, and dyes). Different flexible platforms such as papers/filter papers, fabrics, polymer nanofibers, and cellulose fibers have been investigated over the last few years and their SERS efficacies have been evaluated. We start with an introduction of the importance of hazardous materials trace detection followed by a summary of different SERS methodologies with particular attention on flexible substrates and their advantages over the nanostructures and nanoparticle-based solid/hybrid substrates. The potential of flexible SERS substrates, in conjunction with a simple portable Raman spectrometer, is the power to enable practical/on-field/point of interest applications primarily because of their low-cost and easy sampling.


Introduction
In the present-day scenario, human health, and environmental safety are the foremost concerns worldwide. Hazardous materials are referred to as those which have been determined to be capable of presenting an unreasonable risk to human health, safety, and property. The main characteristics of these materials are ignitability, corrosivity, reactivity, or toxicity. The specific categories among these materials are explosives, flammable liquids, gases, oxidizers, corrosives, flammable solids, radioactive materials, poisonous/infectious substances, and dangerous substances. We start with a short overview of various hazardous materials followed by the introduction of Raman spectroscopy and surface enhanced Rama spectroscopy/scattering (SERS) techniques. This review aims to report on the detection of hazardous materials such as explosives, pesticides, and simulants of chemical warfare agents using flexible SERS substrates.

Hazardous materials
Explosives/high energy materials (HEMs) are those materials that contain nitro groups (which are energetic) and release an enormous amount of energy in the form of light and heat when they are subjected to an external stimulus such as (a) spark (b) shock or even (c) friction. Explosives are commonly categorized as primary and secondary depending on their detonation (velocity, pressure etc.) and sensitivity parameters. Primary explosives are extremely sensitive and release enormous energy even with a small perturbation such as shock/collision. Therefore, the difficulty is generally high while handling the primary explosives. They act as boosters or initiators for detonating secondary explosives. Lead azide and mercury fulminate are a few examples of primary explosives, while 1,3,5,7-Tetranitro-1,3,5,7-tetrazocane (HMX), 1,3,5-Trinitroperhydro-1,3,5-triazine (RDX), trinitrotoluene (TNT), etc. are representative of secondary explosives secondary explosives secondary explosives seconda. Interestingly, there are few home-prepared explosives utilized in the preparation of improvised explosive devices (IEDs). These are now easily synthesized at the laboratory level from simple molecules such as ammonium nitrate (AN), dinitrotoluene (DNT), picric acid (PA), etc.. Pesticides are the chemicals used by farmers/transporters to protect the crops/vegetables/ fruits from insects/pests/rodents. The overused pesticides will remain as residues in the food, which may cause risk to human health (cancer/allergies/intoxications) and the ecosystem (surface water/soil) 2 . Malathion, Carbofuran, methyl parathion, Carbaryl, etc., are a few examples of various pesticides available in the market. For example, thiram is the most used pesticide, which averts fungal diseases, but it causes damage to the skin and is very harmful to the health. Chemical warfare agents (CWAs) 3,4 are the chemical weapons used in a terrorist attacks, which are an intensified threat to the environment and civilian population. The principal compounds are mustard, lewisite, G-series nerve agents [Tabun (GA); Sarin (GB); Soman (GD)], and V-series nerve agents [O-ethyl S-(2-diisopropylaminoethyl) methylphosphonothioate (VX)]. Sarin was used as a chemical weapon by terrorists in the 1995 exposure incident in the Tokyo subway system wherein more than 1000 people were affected. At room temperature, these are volatile liquids that cause a serious risk (paralysis, loss of consciousness, depression of the central respiratory drive) from exposure (dermal contact with a liquid nerve agent). Inhalation of the low vapor nerve agent even for a few minutes (for e.g., ~10 min) causes the contraction of the pupils of the eye, tightness of the chest, headache, rhinorrhea, etc 3 . These are extremely toxic, and their usage is restricted in non-surety laboratories because of the risk in exposure assessments. Chemical warfare agent simulants are recently developed, and they mimic the actual CWAs carrying all the relevant chemical and physical properties without accompanying their toxicological properties. Vinod Kumar et al 5 . reported the development of CWAs, their toxicity, and first usage as weapons worldwide. He discussed the different principles and chemical sensing methods of CWAs and developments in chromo-fluorogenic sensing techniques. Most of the CWA simulants are odorless, colorless, and tasteless. Distilled mustard (HD-C 4 H 8 Cl 2 S), methyl salicylate (MS-C 8  Therefore, rapid and reliable detection of these hazardous molecules is the primary concern of both governmental agencies and research community to reduce the risk to society. Razdan and co-workers 6 have recently provided a comprehensive review on the laser based standoff detection of CWA. In this review, they clearly tabulated the classification, toxicity (lethal dose), and other important properties of the CWA. The significant global research progress in the laser-based sensors such as Raman sensors and DIAL [Differential Absorption LIDAR (Light Detection and Ranging)] sensors in the detection of CWA. There exists a variety of analytical methods (reported in the literature) for the detection of such hazardous materials either in residue/bulk form or in concealed places. Some of the tested and mature techniques include ion-mobility spectroscopy (IMS), terahertz (THz) spectroscopy, laser-induced breakdown spectroscopy (LIBS), Raman spectroscopy and variants, photo-acoustic, and gas chromatography, etc 7−14 . Some of these techniques either cause partial sample destruction or require isolation of sample, which is very difficult in the case of traces. Additionally, a few of these techniques do not favor the usage of low quantity samples and require a skilled person for instrument calibration and measurements. Furthermore, high water absorption, poor specificity, and difficulty in instrumentation limit the usage of these techniques for on-field explosive detection 15,16 .

Raman spectroscopy and variants
Raman spectroscopy is a simple, rapid, and a non-destructive spectroscopic technique based on molecular vibrations as signatures in the spectra. The Raman spectrum of any analyte molecule provides specific information and conveys chemical/structural information. This is important in the case of explosives (in pure form or even in the mixture form) irrespective of solid, liquid, powder, or gas state 17−22 . However, Raman scattering is a very weak process and, consequently, requires either large quantities of the analyte or high input laser powers to obtain the molecular signatures. Surface-enhanced Raman scattering is one of the advanced and developed Raman techniques for overcoming these limitations (intrinsically low Raman signal intensity for low concentration of the analyte molecules) 1 . This is based on the huge electric field enhancements in the vicinity of nanostructured metals resulting in a strong Raman signal.
In the present times, flexible SERS substrates have received great interest due to them possessing the advantages of (a) easy sampling by swabbing/wrapping directly on any curved/rough surfaces (b) large scalability by printing/roll to roll manufacturing/electrospinning etc. and (c) low overall cost of the sensing system. The development of handy flexible substrates with compact Raman devices/smart-phones can possibly provide portable sensors in real-world sensing/safety applications and serve as a powerful analytical tool for on-field analysis. For example, the possibility of detection of ultralow concentrations [picomolar (10 −12 M or pM) to femtomolar (10 −15 M or fM)] of two nerve gases, VX and Tabun was reported recently by Hakonen et al 23 . using flexible Au covered Si nanopillars (SERS substrates) and, significantly, using a handheld Raman spectrometer. Furthermore, the time involved in a typical detection can be reduced to practically acceptable levels (<5 sec) using these portable and low-cost disposable SERS substrates.

Surface-enhanced Raman scattering (SERS)
Martin Fleischmann and co-workers had reported a fortunate discovery way back in 1974, in which they observed enhanced Raman signals of a pyridine molecule adsorbed on an electrochemically roughened silver surface 24 . They reported the enhancement in the Raman cross-section of pyridine vibrations by a factor of ~106. This enhancement of the Raman signal in the vicinity of the metal nanostructure was named "surface-enhanced Raman scattering. " In the year 1977, Van Duyne 25 and Albrecht 26 groups separately explained the mechanism of enhanced Raman signals from the metal surface. In 1985, Moskovits et al 27 . reported all the primary explanations for the enhancement mechanisms such as (a) electromagnetic (EM) enhancement and (b) chemical (CM) enhancement. The long-range EM enhancement is attributed to the so-called localized surface plasmon resonance (LSPR) in the near-field metallic surface. The interaction of the incident EM field with metal NPs possess-ing negative real and small positive imaginary (absorption) dielectric constant induces a collective and coherent electron oscillations, called plasmons, in the vicinity of the NP or nanostructure (NS). The interaction of electromagnetic (EM) fields with the NPs affect their optical properties which are prevailed by the material's dielectric constant at the excitation wavelength and also the surrounding media. The plasmonic noble-metal materials (mainly Au and Ag) exhibits high SERS activity because of their LSPR in the visible region, and the materials such as aluminum (Al), gallium (Ga), platinum (Pt) palladium (Pd), titanium (Ti), bismuth (Bi), indium (In), rhodium (Rh), and ruthenium (Ru), etc. exhibit the plasmonic resonance in the deep ultraviolet (UV) region 28 . Several review articles presented throughout this review discussed the significance of various optical materials used in SERS studies. The short-range CM enhancement is due to the charge transfer mechanism between the analyte molecule and the substrate 29 . Noble-metal-free SERS materials, for example semiconductors (Si, GaAs and etc.) and two-dimensional (2D) layered materials 30,31 (MoS 2 , graphene, HBN and etc.) exhibit the CM enhancement. Usually, Raman signals of the molecules can be enhanced by 10 4 to 10 10 times because of the large EM enhancements supported and provided by the plasmonic nanostructures in close proximity (~1 nm). The CM enhancement is at least 2-3 orders of magnitude less than that of EM enhancement. During the last two decades, several scientists have extensively studied the effective parameters influencing the enhancement of the SERS signal 32,33 . Enhancements in the Raman signal is a result of several contributions and it is virtually difficult to separate them into distinct components. Several factors including the platform, SERS active material, analyte properties, excitation laser mainly affect the enhancement of the Raman signals and are illustrated and explained as a schematic in Fig. 1.

Reviews on different SERS studies
A variety of review reports on SERS have been published over the last decades addressing the issues concerned with fabrication techniques, applications, and their developments. For example, Fan et al 34 . reviewed the various fabrication studies of SERS substrates such as electron-beam lithography, focused ion beam (FIB) milling, and also template-based techniques. The advantage of these nanostructured substrates is the fine control over the nanostructured geometries, which provide high reproducibility in the intensity of SERS signals. They discussed the application of those solid SERS substrates in biosensing, environmental, and optical fiber sensing. Mahadeva et al. 35 , in the year 2015, reviewed the applications of paper as sensors in different fields like electronic devices, biosensors, strain sensors, gas sensors, and piezoelectric devices. Further, their limitations in the commercialization of these devices were also discussed.  19 . reviewed the on-site application of SERS by the combined portable Raman spectrometer and SERS substrates (the year 2020). The choice of an appropriate substrate is extremely essential in the SERS measurements. The requirements of an ideal SERS substrate for practical applications are a) sensitivity (able to detect very low concentrations of analyte molecules), b) uniformity (similar SERS signal strength over the entire substrate), c) reproducibility (similar data should be obtained from measurements spanning different batches, time periods etc.), d) recyclability (should be able to detect different analyte molecules with a single substrates by simple cleaning and to reduce the cost of SERS substrates), e) stability (SERS signal should not fall drastically over a period of few weeks, at least), f) flexibility (should be able to collect samples from uneven surfaces), as well as g) low fabrication cost (ideally SERS substrates should cost less since the Raman spectrometer cost is very high). A schematic of key points of SERS substrates requirements is illustrated clearly in the Fig. 2. Each of these factors and their significance are discussed in detail in the next section.
Sensitivity is the biggest virtue of a good SERS substrate is the detection of molecules at very low concentrations [traces meaning parts per billion (ppb) or parts per trillion (ppt) or parts per quadrillion (ppq)]. The sensitivity is generally expressed in terms of the lowest quantity of probe molecule detection possible with a given SERS substrate. The Raman signal disappears when the molecule concentrations reach a limit value. The sensitivity of the SERS substrate varies from molecule to molecule. The sensitivity of the SERS substrate is typically represented by the enhancement factor (limit of detection for a particular vibration mode of the probe molecule). Therefore, one should be judicious with the SERS substrate and select one with a higher enhancement factor or a lower limit of detection (LOD) over a wide range of analytes. Reproducibility is related to the variation of SERS intensity of the probe molecule over the NS surface. The smaller the variation in the signal, the higher the reproducibility and it is generally reported in terms of RSD (relative standard deviation) of the SERS signal. This depends mainly on the distribution of hotspots on the substrate. Low reproducibility of any SERS substrate affects the potential usage in practical applications. It is highly challenging to produce a highly reproducible SERS platform along with a homogeneous distribution of hotspots. This aging effect for the SERS substrates is also another important factor for storage in air/vacuum for days/months/year and their performance afterwards. Finally, the fabrication cost of the substrates is very important for the bulk production and commercialization of substrates for regular usage. Despite the long history of SERS, flexibility garnered much interest only recently because of easy sample collection from any uneven surface by simple swabbing/swiping etc. Producing uniform, stable, and highly sensitive SERS substrates has been a major obstacle for real-field applications. Therefore, the main task for the SERS community has been to develop the substrates with high sensitivity/reproducibility, long stability, low cost, and easy to handle, as well as flexible for sample collection. The important results from the literature survey over the last 5−10 years concerning the usage of flexible SERS substrate for various hazardous materials detection is also summarized in this article. A large number of  papers have been published in this area. To demonstrate the magnitude of research, a simple search for papers published in the journals and conferences, including the title/keywords/abstract "flexible Surface Enhanced Raman Spectroscopy " OR "flexible Surface Enhanced Raman Scattering " OR "flexible SERS " as indexed by the Scopus search engine, resulted in typically >100 papers in 2019, >100 papers in 2020 and >40 in the year 2021 alone. The corresponding data obtained is plotted as a bar graph and is shown in Fig. 3. The identification of all the developments and practical applications of flexible SERS studies in various fields will be difficult to be presented in this review. Therefore, we have acknowledged the most important recent review articles and those are listed in the  Year of publishing  • Easy-to-use nature for on-site detection of a wide range of probe molecules.
• Flexibility in sample collection, i.e., possible to collect the probe molecules/sample directly from any rough surface (e.g., suitcase, bag, table surface, fruit, etc.) with the substrate by simple swabbing/swiping.
The merits of the SERS technique with the portable Raman spectrometer now widely used in national security, food safety, and environmental monitoring.
Recently explosives detection was approached by fabricating various flexible SERS substrates. Liyanage et al 58 . synthesized flexible SERS sensors with an adhesive film (Scotch magic-tape) loaded with Au triangular nanoprisms by simple self-assembly method as shown in Fig.  4. The estimated LOD of TNT, RDX, and PETN was 900, ~50, and ~50 ppq (parts per quadrillion), respectively. Furthermore, they have also demonstrated direct sampling detection of TNT which was collected from fingerprints by simple swabbing of samples which were TNT RDX PETN 400 800 1600 1200  prepared by placing the thumb onto a series of 10 glass slides. And they successfully proved these flexible SERS substrates have the stability with a "shelf life" of at least 5 months. Gao et al 70 . synthesized light trapping wrinkled nanocones (50−60 nm) flexible SERS substrates using colloidal (polystyrene microspheres-1 μm) lithography and oxygen plasma etching (5 minutes) on polyethylene terephthalate (PET) film followed by 30 nm gold film by electron beam deposition. The optimized wrinkled nanocone 4-ATP labelled flexible substrate was used to detect four explosive molecules RDX, HMX, PETN, and TNT. The TNT residue collection and SERS spectra of TNT residues from the cloth bag by bended to brush collection is followed by 5 min immersion in 4-ATP-labelled AgNPs.

Paper-based SERS substrates
A detailed literature survey revealed that a variety of papers were used (as a base material) for preparing the SERS substrates such as filter paper 71 , chromatography paper 72 , A4 sized paper 73 , tissue papers 74 , and different GCM grade papers 75 . The porosity of the paper (which is typically a few μm) will affect the retention of NPs on its surface. There are numerous approaches for the fabrication of paper-based SERS substrates reported in recent literature including physical vapor deposition 76,77 , dipping method 67,71 , in-situ growth of metal NPs 78,79 , hydrophilic wells by wax printing followed by drop-casting of the NPs 80 , pen-on-paper technique 73 , inkjet printing 72,81 , etc.. Some of these techniques of the fabrication of paper substrates, collated from a few recent research reports, is illustrated in Fig. 5. The in-situ synthesis implies soaking of a cellulose paper in metal salts such as AgNO 3 /HAuCl 4 in conjunction with reducing agents (such as NaBH 4 /citric acid/Tollens agent). These methods later require additional processing such as heating/plasma treatment/rinsing/cleaning. Therefore, these synthesis procedures need multiple cycle processes 82−84 . Dip coating is a unpretentious method in which the NPs have to be first synthesized, then the NPs are deposited on to the paper. However, the NPs loading depends on the absorbance and soaking time of the paper (a comprehensive discussion on the above techniques is provided in ref. 1 ). Several recent studies have demonstrated the utility of different approaches for improving the loading [e.g., prior soaking of paper in NaCl, Glycidyl-trimethyl-ammonium chloride (GTAC)] 85,86 . The advantage of dip coating/immersion method is its ability to deposit NPs with different shapes, sizes, and compositions on the paper 87−89 . Another popular fabrication method is the inkjet/screen printing, which is a simple method of deposition of NPs on paper using a commercial desktop inkjet printer. The efficacy of the SERS substrate depends on the designing of substrate patterns, which is to preserve the viscosity and surface tension of the NPs ink, and printing cycles to upsurge the density of NPs. Inkjet printing offers easy-to-design complex geometries using a personal computer and it is feasible to print already prepared NPs (by laser-based or chemical methods) and in-situ synthesis is also possible by loading precursor agents in different color ink cartridges 90 . Furthermore, to improve the SERS substrate efficiency and to avoid unwanted spreading of NPs, hydrophobic modification of paper has been exploited before the printing of NPs 91 . Kim et al 92 . used a silicon rubber mask (3 mm diameter and 1 mm thickness) to construct SERS sensor arrays. Gold nanorods (AuNR, L/D: 44±2/10±1 nm) were dispersed on top of RC cellulose with vacuum-assisted filtration method on each well on RC hydrogel. The SERS activity and these AuNR array film was examined as a function of the AuNRs volume (8, 10, 12 and 14 μL) and different drying times (1,2, 3 and 24 hours), and better SERS activity is noticed for 12 μL with increasing drying time. These SERS arry demonstrated the simultaneous detection of multiple hazardous chemicals such as R6G (10 pM), RB, CV, 4-ATP, BPE, thiram (100 fM), tricyclazole, difenoconazole, and mancozeb. And the Multi-SERS spectra of thiram are recorded from each AuNR array on RC film. [i) 10 μM; ii) 1 μM; iii) 100 nM; iv) 10 nM; v) 1 nM]. And also, bending cycle tests were conducted for 500 times. These results show good sensitivity, stability and repeatability of low-cost flexible SERS substrates. Li Xian et al 93 . fabricated cellulose nanocrystal-Ag NPs embedded filter paper SERS substrate via in situ reduction. These CNC -Ag paper substrates were modified by soaking in dodecyl mercaptan at different concentrations ranging from 10 −4 to 10 −18 g/mL. The concentration was optimized as 10 −12 g/mL by performing contact angle and SERS measurements. Finally, the optimized SERS substrate was used to detect phenylethanolamine A and metronidazole with a LOD of 5 nM and 200 nM. Lan et al 74 . reported the inkjet-printed paper-based semiconducting (MoO 3−x ) SERS substrates to detect CV and MG on the fish surface by swabbing. Previously, our group presented a systematic study 94   through self-assembly technique. Finally, dual functional SERS platform was made via side of the paper with the NPs affixed onto PDMS using polymethyl methacrylate (PMMA) tape, as the schematic shows in Fig. 7(a). The SERS platform optimized by Au@Ag NRs with 1 to 6 layers were also assembled on the filter paper, and SERS measurements (CV) demonstrated that the Raman intensity of the probe molecule gradually decreases as the number of layers increases. The optimized monolayer SERS paper-based PDMS-assisted platform was used to detect thiram (0.75 ppm) on the surface of orange by just simple wiping and the presence of PDMS enables higher performance with better sensitivity of SERS. Further, various concentrations of thiram on orange surface (from 0.5 ppm to 50 ppm) and the concentration versus intensity Langmuir adsorption for the Raman spectra are shown in Fig. 7(b).

Polymer-based SERS substrates Nanofiber mats
Electrospinning is a method of translation of polymeric solution/melt (with or without additives) into solid nanofibers by applying the electric field 1 . The electrospun nanofiber films are identical to paper substrates in many aspects. For example, they have similar flexibility, porosity, and a high surface area. Moreover, their morphology, thickness, porosity, etc. (of the nanofiber films) can be varied by judiciously choosing the experimental parameters (i.e., solution parameters, process parameters, and ambient parameters) 53,96−98 . The concentration of polymer solution being used demonstrates an essential role in the electrospun fiber fabrication. At very low concentrations of the polymer solution, electrospraying occurs instead of electrospinning. Therefore, micro/nanodroplets are deposited on the collector drum. With a slight increase in polymer solution concentration, a mixture of microbeads and fibers has been observed 1 .
Smooth nanofibers are observed at an appropriate concentration depending on the polymer molecular weight. If the concentration is too high, nanofibers will not be formed, and only micro-ribbons will be observed 1 . Therefore, with an increase in the concentration of the polymer solution, the obtained fiber diameter will increase. Usually, the viscosity and surface tension of the solution can be modified by altering the concentration of the used polymer. At a very low viscosity or surface tension, continuous and smooth fibers cannot be attained. If the viscosity of the polymer solution is very high, it results in the hard ejection of polymer jet from the syringe      needle. The polymer molecular weight also affects the fiber morphology as a decrease in the molecular weight tends to form more beads rather than smooth fibers. Husain et al 99 . analyzed the fiber morphology of PLGA [poly (lactic-co-glycolic acid)] in acetone with a varying concentration between 2 and 25 wt%. At low concentration (2−4 wt%), a mixture of particles and beads-on strings are observed, and at high concentration (20−25 wt%), only fibers are obtained. The fiber morphology can be tuned with the processing parameters such as the applied voltage for the electrostatic force, flow rate, nozzlecollector distance, fiber collector humidity, and temperature, etc. Recently, Wan et al. 100 reported SiO 2 electrospun nanofiber loaded with Ag/Au nanoparticles SERS substrate with high sensitivity -10 -11 mol/L, stability -60 days, repeatability for various molecules (S. aureus, thiram, 4-MPh, and 4-MPA), and the schematic is illustrated in Fig. 8. The SERS performance of nanofiber depends on the properties of • nanofibers (polymer nature, fiber diameter, the morphology of the nanofibers, and spinning time, etc.) and • nanoparticles 101 (material type, size, shape, composition, and density), etc.
• Decoration of NPs on the fiber 102,103 (within the fiber, the surface of the fiber, etc.) • The loading of NPs on the nanofiber mat leads to the NPs assembly with extremely small spacing providing scope for abundant hot spots. These play a crucial factor in SERS response.
Electrospinning polymer fibers can be used as SERS substrates by loading plasmonic NPs; similar to paper substrates, several methods are reported for embedding metal NPs onto the electrospun polymer films like dispersion of metal precursor and pre-mixing of metal NPs into the polymer solution and surface medications after electrospinning. Chamuah et al 104   adhesive acrylic polymer tape and polyethene terephthalate (PET)] film using the self-assembly method. Here, PET film was used to protect the Au@Ag NPs array from environment for long-term stability (60 days). While performing the SERS measurements, the protection PET film was peeled off carefully, and the T/Au@Ag substrate was utilized for sensing CV-1 nM with a LOD of 9×10 −10 M. These flexible T/Au@Ag substrates were further investigated for realistic applications like thiram residues extracted from the peel of apple, tomato, and cucumber. Zhang et al 114 . reported low cost large area high-throughput nanostructured polymer flexible SERS substrate, the schematic shown in Fig. 10(a). These were prepared in three steps (1) preparation of anodic aluminum oxide (AAO) mold (2) formation of polymer nanostructure using roll-to-roll ultraviolet (365 nm,    100 and 200). In the SERS signal intensity and peak positions plot, there was also no obvious difference with the corresponding spectra shown in Fig. 10 patterned polymer micro-/nano-structures were obtained and were subsequently coated with Ag using thermal evaporation technique. These flexible SERS substrates were used to detect R6G at a concentration of 10 −7 M. The advantages of the fs laser processing were its simplicity, high-speed, and possibility of preparing large area substrates, which leads to bulk sample preparation for practical applications. Over the last few years, our research group at the University of Hyderabad, India has successfully fabricated a variety of SERS substrates using fs laser ablation of bulk targets such as Au 116−118 , Si 119,120 , and Ag 121 , and optimized them by varying the various laser parameters. In future, we aim to prepare low-cost flexible SERS substrates using fs laser pulses for easy sample collection and real-world applications. The nanocolloids and nanostructures obtained with fs laser ablation (in liquids) technique are ubiquitous and versatile. The recent developments in this area of research have proven that these can now be produced in large quantities.

Textile based SERS substrates
The textile fabrics have also been investigated as an attractive SERS substrate (akin to paper and electrospun fiber substrate) because the fabric is naturally strong, flexible, soft, and a lightweight material. In textiles, various materials are available such as cotton, wool, silk, etc.. Comparable to other flexible substrates, the loading of NPs can be done in two ways, i.e., in-situ synthesis [soaking in different metal salts] and direct deposition of NPs [anisotropic silver nano-prisms and nano-disks to wool fabric has been reported recently 122 ]. Liu et al 123 . synthesized silk fabrics SERS substrate by soaking in HAuCl 4 (0.1−0.6 mM, 50 mL) for 30 minutes, followed by heating and cleaning. These Au NPs loaded silk fabrics were used to detect CV, 4-MPy, and PATP. Chen et al 124 . fabricated Ag-based cotton fabric by soaking in AgNO 3 (50−250 mM) followed by reduce-drying (30 °C for 30 min) process. The fabric soaked in 200 mM demonstrated better sensitivity (10 −12 M) with 20% reproducibility and 57 days stability in the detection of p-Aminothiophenol. Furthermore, these fabric substrates are having other applications UV protection, antibacterial, and self-cleaning 125,126 . Gao et al 127 . reported wash free metallic textile utilization as flexible SERS substrate for the detection of fungicide. They fabricated Ag-coated cotton fabric using magneton sputtering and the SERS performance was optimized with Ag film thickness as 100 nm from the series of thickness such as 50, 100, 150 and 200 nm on cotton fabric using MB as a probe molecule. The optimized 100 nm Ag-cotton fabric substrate used to detect MB at a low concentration of 10 −12 M, for the real time usage they detected thiram on 10 ppb. Additionally, they have shown the reusability of these substrates by alternative usage of MB and MG, this dye droplet was removed by a simple stream of air. Lu et al 128 . synthesized carbon fiber cloth substrate loaded with 3D Ag nanodendrites by electrochemical deposition. SERS substrate preparation was optimized by studying the effect of deposition voltage (1.1, 1.2, and 1.3 V) and deposition time (80,120,160,200, 240 s), and the optimal SERS substrate was selected by observing nanodendrites morphology and SERS efficiency as under a voltage of 1.3 V and with deposition time of 160 s, shown in Fig. 11. They reported the detection of 1 pM CV and simultaneous detection of three other molecules (4-MBA -5 ppm, DDTC -5 ppm, and thiram -5 ppm). They presented the real time detection data (SERS spectra) of thiram (5 ppm) and MG (5 ppm), respectively, on superhydrophobic Ag-NDs/carbon fiber cloth substrate. Further, they also demonstrated the detection of thiram and MG simultaneously in real lake water using superhydrophobic Ag NDs/carbon fiber cloth substrate. Zhang et al 129 . recently reported the synthesis of non-woven (NW) fabric based SERS substrate and utilized for carbaryl pesticides trace detection on fruits surfaces. NW@polydopamine (PDA) @AgNPs fabrics SERS substrates were fabricated by insitu growth using mussel-inspired PDA molecules. The schematic of the fabrication of flexible NW@PDA@Ag NPs substrate and their utilization by simple swabbing method are illustrated in Fig. 11(a). The substrate was optimized by monitoring the immersion time of NW@PDA fabrics in the [Ag(NH 3 ) 2 ] + solution. With increasing the immersion time from 4 hours to 12 hours, the amount of Ag NPs on fabric was increased, and the superior SERS signal was noticed for 12 hours. The optimized flexible NW@PDA@Ag NPs substrates were subsequently utilized to detect the sprayed diluted carbaryl on the surfaces of apples, oranges, and bananas. The collected SERS spectra of carbyl with concentra-tions ranging from mM to pM are shown in Fig. 11(b). This is a rapidly growing area of research and has strong potential in the preparation and utilization of flexible SERS substrates for detection of hazardous materials. Different plasmonic nanoparticles (sizes, shapes, preparation methods, concentrations etc.) need to tested and methods optimized with these textiles before we can think of any practical application. Table 2 summarizes the most important details of recently reported flexible SERS substrates including their preparation methods, materials used in those studies, and the sensitivities achieved. Such data is extremely im-

Pesticides
Silver mirror reaction Ag-filter paper Thiram-10 −7 M ref. 139 Pen on paper

Conclusions and outlook
In recent years the development and applications of flexible SERS substrate has received incredible attention towards the detection of hazardous materials. In this review, we summarized the most recent research (focusing particularly on the last 3−4 years of research) on flexible based SERS substrates, including paper/cellulose, polymer nanofibers, 3D sponges, fabrics, etc., and their potential on-site detection of explosives, pesticides, chemical warfare agents, drugs for homeland security, food safety, and medical fields. There is a tremendous scope for the flexible SERS substrates in the above-mentioned fields and many others not listed here. Particularly in the field of explosive trace detection, these substrates will be highly beneficial. For example, explosives trace swiping/swabbing from luggage surfaces, clothing, vehicle surfaces, post-blast sites will be easier with such flexible substrates. These explosive molecules are sticky and leave behind small traces while handling and transporting them (on various surfaces). Such traces can be easily detected using efficient SERS substrates. Combined with a portable or handheld Raman spectrometers enriched with database/libraries of all explosive molecules, it presents a very attractive methodology for identification and prevention of terrorist activities. Similarly, testing food materials with these substrates enables prevention of easy adulteration (e.g., drinking water, milk, edible oils). Although there are several issues (e.g., further improvements in the sensitivity, long-term stability, reducing the costs) that need to be addressed for each of these methods. But there is also a huge scope for research in these areas, and we firmly believe the developments in these research areas will lead to practical devices. Additionally, the recent developments in the understanding of SERS substrates (both plasmonic and nonplasmonic) and their potential have increased by leaps and bounds, the proof of which is evident from the number of review articles published in this area 196−198 Different real-world applications that can be envisaged with these SERS substrates include (a) Biomedical applications, bioimaging and biosensing 54,199,200 (b) Inspection in food quality and safety 201 206,207 , it is imperative that a huge number of efforts are out to identify the niche application(s) for each one of them. For example, one may need to compromise on the cost if we need detection of femtomolar concentration of desired analyte molecule. Similarly, sensitivity is not an issue in some specific cases and cost needs to be considered. There are also tremendous advances in the preparation of nanofibrous mats 208,209 and combination of potential SERS NPs/NSs incorporation in these mats can lead to development of agile, lowcost, and versatile SERS substrates for various applications.