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Colloidal solutions of perovskite nanocrystals with good optical and emissive properties are synthesized in ambient conditions, without ligands and in green solvents.

Optically detected magnetophoresis, using Boundary Element Method calculations, is exploited for characterizing the magnetic properties of low amounts of nanoparticles.

Surface-enhanced Raman scattering (SERS) has become a promising method for the detection of contaminants or biomolecules in aqueous media. The low interference of water, the unique spectral fingerprint, and the development of portable and handheld equipment for in situ measurements underpin its predominance among other spectroscopic techniques. Among the SERS nanoparticle substrates, those composed of plasmonic and magnetic components are prominent examples of versatility and efficiency. These substrates harness the ability to capture the target analyte, concentrate it, and generate unique hotspots for superior enhancement. Here, we have evaluated the use of gold-coated magnetite nanorods as a novel multifunctional magnetic-plasmonic SERS substrate. The nanostructures were synthesized starting from core-satellite structures. A series of variants with different degrees of Au coatings were then prepared by seed-mediated growth of gold, from core-satellite structures to core-shell with partial and complete shells. All of them were tested, using a portable Raman instrument, with the model molecule 4-mercaptobenzoic acid in colloidal suspension and after magnetic separation. Experimental results were compared with the boundary element method to establish the mechanism of Raman enhancement. The results show a quick magnetic separation of the nanoparticles and excellent Raman enhancement for all the nanoparticles both in dispersion and magnetically concentrated with limits of detection up to the nM range (∼50 nM) and a quantitative calibration curve. The nanostructures were then tested for the sensing of the antibiotic ciprofloxacin, highly relevant in preventing antibiotic contaminants in water reservoirs and drug monitoring, showing that ciprofloxacin can be detected using a portable Raman instrument at a concentration as low as 100 nM in a few minutes, which makes it highly relevant in practical point-of-care devices and in situ use.

Surface-enhanced Raman scattering (SERS) is a powerful and sensitive technique for the detection of fingerprint sig-nals of molecules and for the investigation of a series of surface chemical reactions. Many studies introduced quantita-tive applications of SERS in various fields and several SERS methods have been implemented for each specific applica- tion, ranging in performance characteristics, analytes used, instruments, and analytical matrices. In general, very few methods have been validated according to international guidelines. As a consequence, the application of SERS in high-ly- regulated environments is still considered risky and the perception of a poorly reproducible and insufficiently robust analytical technique has persistently retarded its routine implementation. Collaborative trials are a type of interlabora-tory study (ILS) frequently performed to ascertain the quality of a single analytical method. The idea of an ILS of quan- tification with SERS arose within the framework of Working Group 1 (WG1) of the COST Action BM1401 Ra-man4Clinics32 in an effort to overcome the problematic perception of quantitative SERS methods. Here we report the first interlaboratory SERS study ever conducted, involving 15 laboratories and 41 researchers. In this study we tried to define a methodology to assess the reproducibility and trueness of a quantitative SERS method, and to compare differ- ent methods. In our opinion, this is a first important step toward a “standardization” process of SERS protocols, not proposed by a single laboratory but by a larger community.

Anisotropic gold nanostructures are attracting attention due to the strong correlation between their shape and the localized surface plasmon resonances, which allows tuning their optical responses ...

Direct absorption solar collectors operating with nanofluids represent a promising technology in the field of solar thermal systems. However, the stability and the reliability of such fluids in real time operation is still an open issue, since their absorption performance has been mainly evaluated at lab-scale under stagnant conditions and their optical properties can be subject to degradation due to multiple reasons. A novel technique based on the combined use of pyranometers is here presented for measuring the absorption rate of nanofluids circulating in a volumetric solar receiver. In the present work, the absorption capability of a Single-Wall-Carbon-NanoHorns (SWCNHs) based nanofluid is experimentally investigated when varying temperature (between 25 °C and 45 °C) and mass flow rate (between 5 kg h−1 and 315 kg h−1). The optical efficiency of the nanofluid is found to be slightly affected by the temperature of the circulating fluid. The optical efficiency is checked for more than 80 hours of operation.

The active targeting strategy has emerged as a promising approach to achieve selectivity in nanobiotechnology applications. Peptides are particularly suited as targeting moieties because the multiv...

10 Figuras, 2 Tablas, Graphene oxide nanoribbons (GONRs), obtained from the oxidative unzipping of carbon nanotubes, have been investigated as building blocks towards reaching active platforms in surface‐enhanced Raman scattering (SERS). The complete development of carbon nanomaterials is strongly related to the exploitation of their chemical versatility, so this work is focused on the positive effect that a specific chemical functionalization provides to the SERS effect when gold nanoparticles are used. The covalent derivatization of GONRs with terminal thiol groups boosts their interaction with different types of gold nanoparticles (namely, ‘naked’ or citrate‐stabilized), and the resulting two‐dimensional aggregates show an intense enhancement of the Raman scattering from the carbon nanostructures because of their two‐dimensional extended aggregation pattern. The SERS effect has been corroborated by theoretical calculations and a conceptual proof of SERS‐based sensing., AC, LL and MM would like to thank the University of Padova for funding (P‐DiSC #04BIRD2016‐UNIPD and the strategic program NAMECA). This project has received funding from the European Union's Horizon 2020 Research and Innovation Programme under the Marie Skłodowska‐Curie Grant Agreement n° 734834 (INFUSION) and from the PEOPLE Programme (Marie Curie Actions) of the European Union's Seventh Framework Programme FP7 Grant Agreement n°290023 (RADDEL).

Competitive reactions, on the surface of plasmonic nanostructures, allow exploiting SERS signals for quantitative Therapeutic Drug Monitoring. As an example, the concentration of Erlotinib, an anti-EGFR small molecule, used for the treatment of non-small cell lung and pancreatic cancer, is determined. The numerous side effects and the variability of patient responses make Erlotinib a good candidate for monitoring. The new SERS based sensor can estimate Erlotinib down to nanomolar concentration and is based on the chemical reaction of the drug and of a competitor SERS reporter on the surface of gold nanostructures. Colloid solutions of naked gold nanoparticles obtained by laser ablation in solution were used for obtaining nanostructures with very efficient hot spots for SERS and with a clean surface for chemistry. Detection of the drug in the nanomolar concentration range is shown to be possible also in spiked plasma samples.

We studied the hysteresis and electric field effects on planar CH3NH3PbI3 perovskite devices, synthetized from laser-ablated precursors, by means of electrical characterizations at different scan rates and optical measurements. The aim of our investigation is to characterize the phenomena behind perovskite degradation under prolonged applied electric field. Using a perovskite more resistant to electric field induced degradation, we run long time characterizations that were not accomplishable before. Thus, we distinguished all the degradation-involved phenomena. The results point to the presence of ions migrating in the perovskite when the device is biased. Our data showed that ion migration degrades the interfaces with the consequent creation of degradation layers that limit the current injected in the device and the extracted photocurrent. These layers where detected also by means of optical Raman characterization. In order to explain the details of the mechanisms concurring to the observed behaviors, we presented a qualitative model. The observed phenomena exacerbated by the planar structure are even more destructive on standard solution processed perovskites to which the results of this work can be extended. Since, the same degradation dynamics occur on vertical devices, typical on perovskite solar cells, this work provides a useful in-depth analysis of the ionic migration effects.

Cell targeting has been considered an important strategy in diagnostic and therapeutic applications. Among different targeting units, peptides have emerged for their ability to bind to many different cellular targets, their scarce immunogenicity and the possibility of introducing multiple copies on nanosystems, providing high avidity for the target. However, their sensitivity to proteases strongly limits their applications in vivo. Here, we show that when presented on the surface of nanostructures, peptide stability to proteolysis is strongly improved without reducing the targeting activity. We prepared plasmonic nanostructures functionalized with a dodecapeptide (GE11) which targets EGFR, a protein overexpressed on different types of tumors. Two types of nanosystems were prepared in which the targeting unit was either directly linked to gold nanoparticles or through a PEG chain, resulting in a different peptide density on the surface of nanostructures. The peptide was rapidly degraded in 20% human serum or in the presence of isolated serine proteases, whereas no significant proteolytic fragments were detected during incubation of the nanosystems and after 24 h digestion, the nanostructures maintained their targeting activity and selectivity on colon cancer cells. Molecular dynamic calculations of the interaction of the nanostructure with chymotrypsin suggest that the formation of the enzyme-peptide complex, the first step in the mechanism of peptide hydrolysis, is highly unlikely because of the constraint imposed by the link of the peptide to the nanoparticle. These results support the utilization of peptides as active targeting units in nanomedicine.

Single-wall carbon nanohorn (SWCNHs)-based nanofluids have been proven to be promising media for the direct absorption of solar radiation due to their favorable optical properties and potential low cost. Still their stability in real working conditions is an open issue because they have been studied mainly under stagnant conditions, while limited information is available on the performance of these nanofluids during circulation in real systems. In the present work, the optical behavior of SWCNH-based nanofluids has been investigated with the aim of detecting possible effects of circulation and exposure to radiation, avoiding other effects such as thermal instability. An ad hoc experimental apparatus has been realized to check the stability of the circulating fluids in situ using a novel approach based on the use of pyranometers. Three suspensions are tested, two are surfactant stabilized and one is based on preoxidized and functionalized SWCNHs. Efficiency values higher than 90% were measured for more than 65 h of circulation. The effects of fluid circulation and exposure to solar radiation have been addressed, finding that the absorption efficiency decreases during tests due to the degradation of the optical properties and the nanofluid circulation is the main responsible for such degradation.

The presence of non-hexagonal rings in the honeycomb carbon arrangement of graphene produces rippled graphene layers with valuable chemical and physical properties. In principle, a bottom-up approach to introducing distortion from planarity of a graphene sheet can be achieved by careful insertion of curved polyaromatic hydrocarbons during the growth of the lattice. Corannulene, the archetype of such non-planar polyaromatic hydrocarbons, can act as an ideal wrinkling motif in 2D carbon nanostructures. Herein we report an electrochemical bottom-up method to obtain egg-box shaped nanographene structures through a polycondensation of corannulene that produces a new conducting layered material. Characterization of this new polymeric material by electrochemistry, spectroscopy, electron microscopy (SEM and TEM), scanning probe microscopy, and laser desorption-ionization time of flight mass spectrometry provides strong evidence that the anodic polymerization of corannulene, combined with electrochemically induced oxidative cyclodehydrogenations (Scholl reactions), leads to polycorannulene with a wavy graphene-like structure., A bottom-up synthesis of wavy graphene structures obtained through an anodic polymerization process, combined with an electrochemically triggered oxidative cyclodehydrogenation, of the bowl-shaped polyaromatic hydrocarbon corannulene.

Liquid biopsy represents a new frontier of cancer diagnosis and prognosis, which allows the isolation of tumor cells released in the blood stream. The extremely low abundance of these cells needs appropriate methodologies for their identification and enumeration. Herein we present a new protocol based on surface enhanced resonance Raman scattering (SERRS) gold multivalent nanostructures to identify and enumerate tumor cells with epithelial and mesenchimal markers. The validation of the protocol is obtained with spiked samples of peripheral blood mononuclear cells (PBMC). Gold nanostructures are functionalized with SERRS labels and with antibodies to link the tumor cells. Three types of such nanosystems were simultaneously used and the protocol allows obtaining the identification of all individual tumor cells with the help of a Random Forest ensemble learning method.

The ability of carbon nanohorns (CNHs) to cross biological barriers makes them potential carriers for delivery purposes. In this work, we report the design of a new selective antibody-drug nanosystem based on CNHs for the treatment of prostate cancer (PCa). In particular, cisplatin in a prodrug form and the monoclonal antibody (Ab) D2B, selective for PSMA+ cancer cells, have been attached to CNHs due to the current application of this antigen in PCa therapy. The hybrids Ab-CNHs, cisplatin-CNHs and functionalised- CNHs have been also synthesized to be used as control systems. The efficacy and specificity of the D2B-cisplatin-CNHs conjugate to selectively target and kill PSMA+ prostate cancer cells have been demonstrated in comparison with the other derivatives. The developed strategy to functionalise CNHs is fascinating because it can allow a fine tuning of both drug and Ab molecules attached to the nanostructure in order to modulate the activity of the nanosystem. Finally, the herein described methodology can be used for the incorporation of almost any drugs or Abs in the platforms in order to create new targeted drugs for the treatment of different diseases.

In this work we study the surface enhanced Raman scattering (SERS) produced by hierarchical nanostructures obtained by coupling different anisotropic nanomaterial of two SERS active metals, namely Ag nanostars (AgNSs) and Au nanowires (AuNWs). Ag nanostars (AgNSs) are prepared, by a two-step one-pot synthesis by reduction of AgNO3 with hydroxylamine, trisodium citrate and NaOH. AuNWs are obtained by electroless templated synthesis in track-etched polycarbonate membranes with following etching of the template. The two precursors are bound together by bridging with the bifunctional cysteamine molecule, obtaining AgNS@AuNW hierarchical structures. Benzenethiol (BT) is adsorbed on the nanostructured material and used as SERS probe to study the amplification of Raman signals. Experimental results indicate significantly larger Raman enhancement when BT is adsorbed onto the AgNS@AuNW in comparison to AuNWs alone or decorated with quasi-spherical silver nanoparticles obtaining AgNP@AuNW. Digital simulations performed by the boundary element method agree with the experimental findings, showing higher number of hot spots and significantly higher SERS enhancements for AgNS@AuNW versus AuNWs or AgNSs or AgNP@AuNW.

We demonstrate that the protonation chemistry of molecules adsorbed at nanometer distances from the surface of anisotropic gold nanoparticles can be manipulated through the effect of surface morphology on the local proton density of an organic coating. Direct evidence of this remarkable effect was obtained by monitoring surface-enhanced Raman scattering (SERS) from mercaptobenzoic acid and 4-aminobenzenethiol molecules adsorbed on gold nanostars. By smoothing the initially sharp nanostar tips through a mild thermal treatment, changes were induced on protonation of the molecules, which can be observed through changes in the measured SERS spectra. These results shed light on the local chemical environment near anisotropic colloidal nanoparticles and open an alternative avenue to actively control chemistry through surface morphology. LL and LML-M acknowledge funding from European Commission Grant (EUSMI 731019). Funding is also acknowledged from the Spanish MINECO (MAT2017-86659-R and MDM-2017-0720 to LML-M; MAT2017-88492-R and SEV2015-0522 to JGA) and the European Research Council (Advanced Grant 787510 4DBIOSERS to LML-M; Advanced Grant 789104-eNANO to JGA).

Surface enhanced Raman spectroscopy (SERS) is a highly sensitive technique for the non- or minimally invasive identification of molecules at very low concentrations. In this work, SERS is exploited using naked laser-ablated gold nanoparticles (AuNPs) for the detection of dyes on artificially aged paper inked with a ballpoint pen. Although several studies on inks with SERS are present in the literature, most of them report on the investigations on freshly prepared products, and less information is present on the detection of aged dyes and inks using SERS. Ballpoint inks are commonly used in daily activities, but have also been employed by several contemporary artists. These inks are very sensitive to light, and they discolor rapidly, making their detection demanding. In the present work, the SERS spectra of a ballpoint pen ink on two types of paper were analyzed after light-induced ageing, and the importance of the dye–AuNP interaction is discussed. The results show that the interpretation of the SERS spectra of the aged samples, such as those of interest in the Cultural Heritage field, is a tricky and delicate operation and that the diffusion of the dyes to the hot spot regions of the plasmonic nanoparticles plays a pivotal role in the detection of degraded ink components. Therefore, appropriate evaluation of the factors affecting the molecule–plasmonic nanoparticle interactions and of the history of the artwork to be analyzed is fundamental to avoiding the misinterpretation of the spectra and, consequently, of the original composition of the analyzed artwork.

In the field of nanomaterials, multifunctional nanosystems play a prominent role in many applications as new magnetically recoverable catalysts, information processing, fuel cells, efficient bio/na...

Spiro-OMeTAD is the mostly employed molecular hole transporting material (HTM) in n-i-p perovskite solar cells (PSCs). Ease of processing from solution and good filmability on top of the perovskite photo-active layer are characteristics that make this HTM outstanding and incomparable for the role. However, both chemical doping with tert-butylpyridine (tBP) and lithium bis(trifluoromethylsulfonyl)-imide (LiTFSI), coupled to further oxidation steps, are required in order to achieve high hole mobility and conductivity. Previous investigations revealed that tBP is fundamental for addressing the best morphology in the hole-transporting layer during processing. We provide here for the first time a spectroscopic evidence of the detrimental impact on long-term conservation of Spiro-OMeTAD structural and electrical properties when tBP is used as additive. These aspects are crucial for the future design and understanding of new molecular HTMs for PSCs.

Nanostructures can strongly interact with cells or other biological structures; furthermore when they are functionalized with targeting units, they are of great interest for a variety of applications in the biotechnology field like those for efficient imaging, diagnosis and therapy and in particular for cancer theranostics. Obtaining targeting with good specificity and sensitivity is a key necessity, which, however, is affected by the complexity of the interactions between the nanostructures and the biological components. In this work we report the study of specificity and sensitivity of gold nanoparticles functionalized with the peptide GE11 for the targeting of the epidermal growth factor receptor, expressed on many cells and, in particular, on many types of cancer cells. We show how a combination of spectroscopic measurements and molecular dynamics simulations allows the comprehension of the targeting activity of peptides linked to the surface of gold nanostructures and how the targeting is tuned by the presence of polyethylene glycol chains.

Early detection is the most effective mean of improving prognosis for many fatal diseases such as cancer. In this context, the Surface Enhanced Resonance Raman Scattering (SERRS) technique is being proposed as alternative to fluorescent methods in detection of biomarkers, because SERRS nanostructures are bright as fluorescent tags but more stable and clearly detectable using the narrow Raman “fingerprints” of a suitable reporter. Here we show that biocompatible SERRS active gold nanostructures, functionalized with an engineered PreS1 peptide (AuNP@PEG-PreS1), detect the presence of the SerpinB3 antigen overexpressed on liver tumor cells, a biomarker of the onset of liver cell carcinomatous transformation. A proper engineering of the targeting unit, linked to the nanostructure by a polymer chain, affords a sensitivity and specificity larger than 80%, at subnanomolar concentrations. Taking into account the high sensitivity of SERRS and that SB3 overexpression is an early event in liver cell carcinomatous transformation, AuNP@PEG-PreS1 nanostructures could be used in routine diagnostic activities, to improve the accuracy of HCC detection in particular in patients with chronic liver diseases.

Summary Spiro-OMeTAD is the most-employed molecular hole-transporting material (HTM) in n-i-p perovskite solar cells (PSCs). Ease of processing from solution and good filmability on top of the perovskite photo-active layer are characteristics that make this HTM outstanding and incomparable for the role. However, chemical doping with both tert-butylpyridine (tBP) and lithium bis(trifluoromethylsulfonyl)-imide (LiTFSI), coupled with further oxidation steps, is required in order to achieve high hole mobility and conductivity. Previous investigations have revealed that tBP is fundamental for addressing the best morphology in the hole-transporting layer during processing. Here, we provide spectroscopic evidence of the detrimental impact on long-term conservation of Spiro-OMeTAD structural and electrical properties when tBP is used as an additive. These aspects are crucial for the future design and understanding of new molecular HTMs for PSCs.

Colloidal gold nanostructures are nowadays widely involved in sensor applications. One of the most interesting techniques that takes advantage of them is certainly the Surface Enhanced Raman Scattering (SERS) effect, even if it is often considered a tricky technique due to structural constraints required by the nanostructured substrates to obtain high enhancement factors (EFs), i.e. the presence of hot spots. Because of the easy preparation and high number of hot spots, aggregated gold nanospheres seem to be the most efficient through the SERS colloids, but their characteristic high disorder makes them unpredictable and difficult to compare between different batches. For this reason, less SERS effective, but more regular and organized substrates are usually preferred. In this study, a method based on Boundary Element Method (BEM) simulation is used to accurately predict the colloidal SERS EFs of gold nanoparticle (AuNP) aggregates, starting from their experimental extinction spectra. Surprisingly, it was found that larger aggregates do not exhibit stronger hot spots, but rather higher amounts of them, influencing the overall predicted EFs, which well reflect the results obtained experimentally.

Laser synthesis emerges as a suitable technique to produce ligand-free nanoparticles, alloys and functionalized nanomaterials for catalysis, imaging, biomedicine, energy and environmental applications. In the last decade, laser ablation and nanoparticle generation in liquids has proven to be a unique and efficient technique to generate, excite, fragment and conjugate a large variety of nanostructures in a scalable and clean way. In this work, we give an overview on the fundamentals of pulsed laser synthesis of nanocolloids and new information about its scalability towards selected applications. Biomedicine, catalysis and sensing are the application areas mainly discussed in this review, highlighting advantages of laser-synthesized nanoparticles for these types of applications and, once partially resolved, the limitations to the technique for large-scale applications.

Biodegradation of carbon-based nanomaterials has been pursued intensively in the last few years, as one of the most crucial issues for the design of safe, clinically relevant conjugates for biomedical applications. In this paper it is demonstrated that specific functional molecules can enhance the catalytic activity of horseradish peroxidase (HRP) and xanthine oxidase (XO) for the degradation of carbon nanotubes. Two different azido coumarins and one cathecol derivative are linked to multi-walled carbon nanotubes (MWCNTs). These molecules are good reducing substrates and strong redox mediators to enhance the catalytic activity of HRP. XO, known to metabolize various molecules mainly in the mammalian liver, including human, was instead used to test the biodegradability of MWCNTs modified with an azido purine. The products of the biodegradation process are characterized by transmission electron microscopy and Raman spectroscopy. The results indicate that coumarin and catechol moieties have enhanced the biodegradation of MWCNTs compared to oxidized nanotubes, likely due to the capacity of these substrates to better interact with and activate HRP. Although azido purine-MWCNTs are degraded less effectively by XO than oxidized nanotubes, the data uncover the importance of XO in the biodegradation of carbon-nanomaterials leading to their better surface engineering for biomedical applications. journal article research support, non-u.s. gov't 2015 Dec 2015 08 28 imported

Multimodal contrast agents offer new interesting diagnostic possibilities, summing the benefits of multiple imaging techniques. Magnetic resonance and optical imaging are complementary techniques. The first allows total body screening, even though it suffers from low spatial resolution and needs high loadings, whereas the second shows lower penetration, but bright signals, and a higher spatial resolution and needs lower loadings. We present a plasmonic nanosystem as a MRI (magnetic resonance imaging) and SERRS (surface enhanced resonance Raman scattering) multimodal contrast agent. Naked gold nanoparticles, obtained by laser ablation synthesis in solution, are organized as a highly efficient SERRS substrate with a naphthalocyanine reporter and functionalized with a MRI contrast agent with a newly synthesized 3DOTA-PEG polymer, with a high GdIII loading. As a proof of concept, in vivo and ex vivo MRI and SERRS experiments are also performed. The plasmonic property of the nanosystem is then exploited to show its usefulness for localized hyperthermia.

Magneto-plasmonic nanostructures functionalized with cell targeting units are of great interest for nanobiotechnology applications. Photothermal treatment of cells targeted with antibody functionalized nanostructures and followed by magnetic isolation, allows killing selected cells and hence is one of the applications of great interest. The magneto-plasmonic nanostructures reported herein were synthesized using naked gold and magnetite nanoparticles obtained through a green approach based on laser ablation of bulk materials in water. These particles do not need purifications steps for biocompatibility and are functionalized with a SERRS (surface enhanced resonance Raman scattering) active molecule for detection and with an antibody for targeting prostate tumor cells. Quantitative results for the cell targeting and selection efficiency show an overall accuracy of 94% at picomolar concentrations. The photothermal treatment efficiently kills targeted and magneto-selected cells producing a viability below 5% after 3 min of irradiation, compared with almost 100% viability of incubated and irradiated, but non targeted cells.

A major challenge in cancer treatment is the quantification of biomarkers associated with a specific cancer type. Important biomarkers are the circulating tumor cells (CTCs) detached from the main cancer and circulating in the blood. CTCs are very rare and their identification is still an issue. Although CTCs quantification can be estimated by using fluorescent markers, all the fluorescence techniques are strongly limited by the number of emissions (therefore markers) that can be discriminated with one exciting line, by their bleaching characteristics, and by the intrinsic autofluorescence of biological samples. An emerging technique that can overcome these limitations is Surface Enhanced Raman Scattering (SERS). Signals of vibrational origin with intensity similar to those of fluorescence, but narrower bandwidths, can be easily discriminated even by exciting with a single laser line. We recently showed the benefit of this method with cells fixed on a surface. However, this approach is too demanding to be applied in clinical routine. To effectively increase the throughput of the SERS analysis, microfluidics represents a promising tool. We report two different hydrodynamic strategies, based on device geometry and liquids viscosity, to successfully combine a microfluidic design with SERS.

Micro and nanomechanical resonators represent a promising platform for proteins label-free detection because of their extreme sensitivity, fast response and low cost. Micro-pillars are columnar resonators that can be easily arranged in dense arrays of several thousand sensors in a squared mm. To exploit such a large density, however, a method for tracking independently micropillars resonance frequency is required. Here we present a detection method based on CCD imaging and software image analysis, which can measure the resonance frequency of tens of pillars in parallel. Acquiring simultaneously the frequency shift of up to 40 sensors and applying a proper statistical analysis, we were able to overcome the variability of the single measures improving the device sensitivity at low analyte concentration range. As a proof of concept, this method has been tested for the detection of a tumor marker, the Prostate Specific Membrane Antigen (PSMA). Pillars have been functionalized with an antibody against PSMA. The tumor marker (PSMA) has been detected in a range of concentrations between 300 pM and 100 nM, in buffer and in diluted bovine serum. The sensitivity of our method was limited only by the affinity constant of the antigen–antibody recognition. Moreover, this detection technique demonstrated to be effective in the 1–6 nM range, which is the window of PSMA concentration of clinical interest.

Plasmonic nanostructures show important properties for biotechnological applications, but they have to be guided on the target for exploiting their potentialities. Antibodies are the natural molecules for targeting. However, their possible adverse immunogenic activity and their cost have suggested finding other valid substitutes. Small molecules like peptides can be an alternative source of targeting agents, even if, as single molecules, their binding affinity is usually not very good. GE11 is a small dodecapeptide with specific binding to the epidermal growth factor receptor (EGFR) and low immunogenicity. The present work shows that thousands of polyethylene glycol (PEG) chains modified with lysines and functionalized with GE11 on clusters of naked gold nanoparticles, obtained by laser ablation in water, achieves a better targeting activity than that recorded with nanoparticles decorated with the specific anti-EGFR antibody Cetuximab (C225). The insertion of the cationic spacer between the polymeric part of the ligand and the targeting peptide allows for a proper presentation of GE11 on the surface of the nanosystems. Surface enhanced resonance Raman scattering signals of the plasmonic gold nanoparticles are used for quantifying the targeting activity. Molecular dynamic calculations suggest that subtle differences in the exposition of the peptide on the PEG sea are important for the targeting activity.

The present research is focused on the setting up of an advanced analytical system for the detection of synthetic dyes. The system is based on the combination of an innovative thin layer chromatography (TLC) plate coupled with enhanced infrared (MU-ATR, metal underlayer attenuated total reflection) and Surface Enhanced Raman (SERS) spectroscopy. In particular, a TLC plate made of silver iodide (AgI) applied onto a gold coated glass slide (AgI@Au) is proposed as an efficient stationary phase for the separation of dyes mixtures. The separated dyes are then identified by means of both enhanced FTIR and SERS, performed directly on the same eluted spots. The use of a mid-IR transparent inorganic salt as stationary phase coupled with the underneath gold layer avoids spectral interferences, enhancing the signal obtained from ATR analyses. At the same time, SERS spectra can be recorded as the TLC plate may act as a SERS active substrate due to the photoreduction of AgI to metallic Ag caused by the exposure to the laser during the Raman analysis. Different mixtures of synthetic dyes of known composition, widely used in dyeing processes, have been tested and the method resulted to be effective in identifying trace amounts in the order of tens nanograms. Moreover, the method has been further evaluated on a real case study represented by dyes extracted from dyed wool.

Fullerenes have been extensively used for more than two decades for the development of organic photovoltaics (OPV). While OPV seems to be a technology almost ready for the market, in the last few years fullerenes are attracting a big interest for the improvement they afford on the already well-performing perovskite solar cells (PSCs). Thanks to PSC integration, interest in fullerenes is rising again, opening up new exciting perspectives for photovoltaics. This review article aims at analyzing the landmark contributions that gave birth to the novel application of fullerenes in PSCs and to the technological solutions that are emerging with them.

Nanoclusters with plasmonic and magnetic properties are obtained with naked gold (AuNP) and iron oxide nanoparticles (FeOxNP) separately synthesized by laser ablation in water and simply assembled by using their opposite surface charges. Controlling the amount of AuNP and FeOxNP, we obtained nanoclusters with both good surface-enhanced resonance Raman scattering (SERRS) signals and superparamagnetic properties. Nanoclusters are incubated with murine macrophage cells which, after mixing with other macrophages, can be magnetically guided in solution by sorting them in less than 10 min. SERRS signals, observed at the single cell level, were recorded for the sorted macrophages, showing that the nanoclusters are active also in a biological environment and allow the identification of the incubated macrophage cells.

Single layer boron-doped graphene layers have been grown on polycrystalline copper foils by chemical vapor deposition using methane and diborane as carbon and boron sources, respectively. Any attempt to deposit doped layers in one-step has been fruitless, the reason being the formation of very reactive boron species as a consequence of diborane decomposition on the Cu surface, which leads to disordered nonstoichiometric carbides. However, a two-step procedure has been optimized: as a first step, the surface is seeded with pure graphene islands, while the boron source is activated only in a second stage. In this case, the nonstochiometric boron carbides formed on the bare copper areas between preseeded graphene patches can be exploited to easily release boron, which diffuses from the peripheral areas inward of graphene islands. The effective substitutional doping (of the order of about 1%) has been demonstrated by Raman and photoemission experiments. The electronic properties of doped layers have been char...

Laser ablation synthesis in liquid solution (LASiS) is a "green" technique that gives access to the preparation of a library of nanomaterials. Bare noble metal spherical particles, multiphase core-shell oxides, metal-semiconductor heterostructures, layered organometallic compounds and other complex nanostructures can be obtained with the same experimental set up, just by varying a few synthetic parameters. How to govern such versatility is one of the current challenges of LASiS and requires a thorough understanding of the physical and chemical processes involved in the synthesis. In this perspective, the fundamental mechanisms of laser ablation in liquids are summarized, organized according to their temporal sequence and correlated with relevant examples taken from the library of nanomaterials disclosed by LASiS, in order to show how synthesis parameters influence the composition and the structure of products. The resulting framework suggests that, to date, much attention has been devoted to the physical aspects of laser-matter interaction and to the characterization of the final products of the synthesis. Conversely, the clarification of chemical processes active during LASiS deserves more research efforts and requires the synergy among multiple investigation techniques.

Photochromic molecules are part of a large class of materials in which light stimulus not only induces a color variation but also affects other physicochemical properties. However, the change of bulk electrical properties (e.g., electrical conductivity) via light excitation remains difficult to control because the intrinsically switchable molecules may lose their functionality when wired with conductive electrodes. In contrast with previous work based on single molecules, here we demonstrate a facile and accessible “wet-chemical” method to produce light-induced electrical switching. The electrical conductivity of a photochromic blend composed of diarylethene polymer and single-walled carbon nanotubes (SWNTs) is reversibly tuned according with UV–vis excitation. The devices present good thermal stability and remarkable fatigue resistance under ambient conditions. Supported by electrical and spectroscopic evidence, we show that the intertube electrical coupling, mediated by the light-induced electrocyclizat...