Here, we present surface-enhanced Raman data for the calculation of signal uniformity and enhancement factor in SENSERS (surface-exposed nanoparticle sheet enhanced Raman spectroscopy). SEM was used to characterize the microstructure of the solid sample. The interaction between the solid sample and surface-exposed nanoparticle sheet was characterized using SERS and SEM. Based on these data a “skin” versus “sheet” type calculation method was used to calculate the magnitude of Raman signal enhancement within SENSERS. The data presented in this article is related to the research article entitled “Pressing Solids Directly Into Sheets of Plasmonic Nanojunctions Enables Solvent-Free Surface-Enhanced Raman Spectroscopy” (Xu et al., 2018).

The data presented in this article is related to the research article entitled "A One-Pot Method for Building Colloidal Nanoparticles into Bulk Dry Powders with Nanoscale Magnetic, Plasmonic and Catalytic Functionalities" (Ye et al., 2019) The data shows the hydrophobicity of the nanoparticle (NP) building blocks used for constructing NMPs obtained through contact angle measurements, along with the effect of NP hydrophobicity on the stability of the parent Pickering emulsions. SEM data of the morphology of NMPs is presented. Finally, a mathematical model is presented to predict the average diameter of NMPs produced via different experimental parameters.

Building easy-to-handle bulk materials with nanoproperties is crucial for many nanotechnology-based real-world applications. Here, we describe a simple one-pot method based on nanoparticle self-assembly of pickering emulsions and in situ polymer deposition for preparing particles consisting of a rigid micro-polymer core covered in exposed surface layers of nanoparticles, which we have named nano-micro-particles (NMPs). Unlike simple colloids, these NMPs can be filtered off from the aqueous suspensions in which they are prepared and dried to form free-flowing powders, which most importantly, retain the properties of the constituent nanoparticles in the surface layer. These NMPs can be stored for extended periods but then used either in the dry state or be re-suspended into liquid media as required. The preparation method is very general and can be readily extended to assemble various types of nanoparticles regardless of their material composition or morphology. In addition, functional components, such as magnetic particles or fluorescent tags, can be encapsulated within the polymer core. This method is a platform technology for building nanoparticles into bulk materials with nano-functionalities tailored toward real-life applications. This is illustrated with examples of the preparation of NMPs suitable for rapid and low-cost on-site water monitoring and remediation. (C) 2019 Published by Elsevier Ltd.

Rapid and accurate identification of pathogens in CF could ensure prompt treatment with the most appropriate antibiotic; potentially improving outcomes and shortening hospital stays. As traditional culture methods for detecting bacteria are time-consuming there is a growing interest in SERS as a novel culture-free technique that produces a whole-organism spectroscopic fingerprint at high speed. Bacterial isolates including Pseudomonas aeruginosa (n=32), Staphylococcus aureus (n=5), Streptococcus pneumoniae (n=5) were incubated for 6 h at 37 °C/180 r.p.m., with a starting optical density (OD) of 0.15. After adjustment of the OD to 0.3, bacterial cells were harvested by centrifugation at 9000 rcf for 3 min and washed three times with dH2O. Bacterial pellets were mixed with citrate reduced silver colloid (CRSC) and dried. Spectra were recorded (4×10 s at 785 nm) and analysed within GRAMS/Al using Principal Component Analysis (PCA). Spectra of P. aeruginosa isolates (n=32) were separated into two distinct groups; the spectra of one group (n=12) was dominated by the pigment pyocyanin with vibrational brands present at 1350, 1492, 1598 and 1615 cm-1. The other group (n=20) had characteristic vibrational bands at 661, 735 and 800 cm-1 which correspond to guanine, adenine and uracil, respectively. S. aureus has a main characteristic band at 735 cm-1 and S. pneumoniae has a characteristic band present at 480 cm-1. Bacterial species clustered separately when analysed by PCA. Reproducible and distinguishable SERS spectra of bacterial isolates were obtained, and it was possible to differentiate between different bacterial species using PCA. These results suggest SERS has the potential to rapidly detect bacteria.

In situ surface-enhanced Raman spectra of the headspace above cultures of six bacterial species showed strong characteristic bands from chemisorbed methyl sulfide. This marker compound is created by dissociation of dimethyl disulfide (DMDS), a fermentative metabolite of bacteria, on the surface of the enhancing Au or Ag nanoparticle films. Kinetic binding plots of media spiked with DMDS and of live cultures showed that the Au-based substrates were more suitable for the rapid detection of bacteria than Ag-based substrates. For E. coli DH5α, the sensitivity limit for headspace SERS detection was 1.5×107  CFU mL-1 , which corresponded to detection 15 min after inoculation of the growth medium. Since the metabolites are only produced by viable bacteria, antibiotic (gentamicin) treatment stopped the normal signal growth of the marker peak. This work is a promising step towards rapid bedside detection of bacterial infections and rapid screening of antibiotics against bacteria.

Often chemical analysis of solid materials begins with dissolving the sample in a solvent but this is undesirable, particularly if the physical form is important. In principle surface-enhanced Raman spectroscopy (SERS) should allow detection of solid analytes and offers attomolar sensitivity combined with molecular specificity. SERS requires the target molecules to sit in plasmonic hot-spots, which are normally nano junctions, just a few nm across. This means that solid samples normally need to be dissolved in a solvent so they can diffuse into the enhancing region. Here, we show that SERS spectra of picograms of solid analytes can be directly obtained by pressing them into a flexible SERS substrate with a dense field of exposed nanojunction hot-spots anchored on its surface. We demonstrate that this can be a powerful tool for straightforward and non-destructive forensic analysis of layered materials (crossing ink lines), solid explosives and illicit drugs as well as for studying previously intractable samples such as pharmaceutical co-crystals, whose important solid state structure is lost when they are dissolved. (C) 2018 Published by Elsevier Ltd.

Genetically engineered bacteria and reactive DNA networks detect edges of objects, as done in our retinas and as also found within computer vision. We now demonstrate that simple molecular logic systems (a combination of a pH sensor, a photo acid generator, and a pH buffer spread on paper) without any organization can achieve this relatively complex computational goal with good fidelity. This causes a jump in the complexity achievable by molecular logic-based computation and extends its applicability. The molecular species involved in light dose-driven "off-on-off" fluorescence is diverted in the "on" state by proton diffusion from irradiated to unirradiated regions where it escapes a strong quencher, thus visualizing the edge of a mask.

Molecular logic-based computation continues to throw up new applications in sensing and switching, the newest of which is the edge detection of objects. The scope of this phenomenon is mapped out by the use of structure-activity relationships, where several structures of the molecules and of the objects are examined. The different angles and curvatures of the objects are followed with good fidelity in the visualized edges, even when the objects are in reverse video.

The recently-discovered ability of small logical molecules to recognize edges is exploited to achieve outline drawing from binary templates. Outlines of arbitrary curvature, several colours and thicknesses down to 1 mm are drawn in around 30 min or less by employing a common laboratory two-colour ultraviolet lamp. The outlines and the light dose-driven XOR logic with fluorescence output or 'off-on-off' action which is observed in the irradiated regions are modelled by combining foundational principles of photochemistry, acid-base neutralization and diffusion.