Showing papers on "Nanoparticle published in 2016"
TL;DR: This review summarizes the major progress in the field, including the principles that permit atomically precise synthesis, new types of atomic structures, and unique physical and chemical properties ofatomically precise nanoparticles, as well as exciting opportunities for nanochemists to understand very fundamental science of colloidal nanoparticles.
Abstract: Colloidal nanoparticles are being intensely pursued in current nanoscience research. Nanochemists are often frustrated by the well-known fact that no two nanoparticles are the same, which precludes the deep understanding of many fundamental properties of colloidal nanoparticles in which the total structures (core plus surface) must be known. Therefore, controlling nanoparticles with atomic precision and solving their total structures have long been major dreams for nanochemists. Recently, these goals are partially fulfilled in the case of gold nanoparticles, at least in the ultrasmall size regime (1–3 nm in diameter, often called nanoclusters). This review summarizes the major progress in the field, including the principles that permit atomically precise synthesis, new types of atomic structures, and unique physical and chemical properties of atomically precise nanoparticles, as well as exciting opportunities for nanochemists to understand very fundamental science of colloidal nanoparticles (such as the s...
2,144 citations
TL;DR: In this paper, the synthesis of multi-wall carbon nanotubes and silica nanocomposite (CNT/SiO2) was demonstrated by scanning electron microscopy, energy dispersive X-ray spectroscopy, Fourier transform infrared and high-resolution transmission electron microscope studies.
Abstract: This paper demonstrates the synthesis of multi-wall carbon nanotubes and silica nanocomposite (CNT/SiO2). Successful realization of MWCNT/SiO2 nanostructure was observed by scanning electron microscopy, energy dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy and high-resolution transmission electron microscopy studies. The as-prepared nanocomposite was evaluated as an adsorbent to remove lead, Pb(II), from aqueous solutions. The resulting MWCNT/SiO2 manifests propitious adsorption performance (~95%) over silica nanoparticles (~50%) and CNTs (~45%). Lagergren’s pseudo-first order, pseudo-second order and intraparticle diffusion models were used to analyse the kinetic data obtained at different initial Pb(II) concentrations. The adsorption kinetic data were described well by the pseudo-second order model with R2 of 0.99. The activation energy (Ea) of the adsorption process was calculated as 15.8 kJ mol−1. Adsorption data were described well by the Langmuir and Temkin models. Th...
504 citations
TL;DR: Results demonstrate the size-dependent activities of nanoparticles as a general means to design synergetic functionality in binary nanoparticle systems and reveal a strong interdependency of the methanol synthesis activity and the Zn coverage.
Abstract: Promoter elements enhance the activity and selectivity of heterogeneous catalysts. Here, we show how methanol synthesis from synthesis gas over copper (Cu) nanoparticles is boosted by zinc oxide (ZnO) nanoparticles. By combining surface area titration, electron microscopy, activity measurement, density functional theory calculations, and modeling, we show that the promotion is related to Zn atoms migrating in the Cu surface. The Zn coverage is quantitatively described as a function of the methanol synthesis conditions and of the size-dependent thermodynamic activities of the Cu and ZnO nanoparticles. Moreover, experimental data reveal a strong interdependency of the methanol synthesis activity and the Zn coverage. These results demonstrate the size-dependent activities of nanoparticles as a general means to design synergetic functionality in binary nanoparticle systems.
503 citations
TL;DR: In this paper, a mini-review presented photocatalytic reduction of Cr(VI) into Cr(III) in some MOFs or their derivatives/composites.
Abstract: This mini-review presented photocatalytic reduction of Cr(VI) into Cr(III) in some MOFs or their derivatives/composites. The reported examples are collected and analyzed; and the reaction mechanism, the influence of various factors on the photocatalytic performance, the involved challenges, and the outlooks of MOFs as photocatalyst to carry out Cr(VI) reduction are discussed. It can be found that the optical properties of MOFs can be flexible modulated via incorporation into NH 2 group, conductor photocatalysts like ZnO and metal sulfides nanoparticles, noble metal nanoparticles and graphene oxide (GO). It is clear that MOFs have a bright prospective in the fields of photocatalytic reduction of Cr(VI), or even dual functional photcatalysts to carry out Cr(VI) reduction and organic pollutants degradation under visible light irradiation.
494 citations
TL;DR: It was noticed that the smallest-sized spherical AgNPs demonstrated a better antibacterial activity against both bacterial strains as compared to the triangular and larger spherical shaped AgnPs.
Abstract: Silver nanoparticles (AgNPs) of different shapes and sizes were prepared by solution-based chemical reduction routes. Silver nitrate was used as a precursor, tri-sodium citrate (TSC) and sodium borohydride as reducing agents, while polyvinylpyrrolidone (PVP) was used as a stabilizing agent. The morphology, size, and structural properties of obtained nanoparticles were characterized by scanning electron microscopy (SEM), UV-visible spectroscopy (UV-VIS), and X-ray diffraction (XRD) techniques. Spherical AgNPs, as depicted by SEM, were found to have diameters in the range of 15 to 90 nm while lengths of the edges of the triangular particles were about 150 nm. The characteristic surface plasmon resonance (SPR) peaks of different spherical silver colloids occurring in the wavelength range of 397 to 504 nm, whereas triangular particles showed two peaks, first at 392 nm and second at 789 nm as measured by UV-VIS. The XRD spectra of the prepared samples indicated the face-centered cubic crystalline structure of metallic AgNPs. The in vitro antibacterial properties of all synthesized AgNPs against two types of Gram-negative bacteria, Pseudomonas aeruginosa and Escherichia coli were examined by Kirby–Bauer disk diffusion susceptibility method. It was noticed that the smallest-sized spherical AgNPs demonstrated a better antibacterial activity against both bacterial strains as compared to the triangular and larger spherical shaped AgNPs.
486 citations
TL;DR: In this article, a green approach for the synthesis of zinc oxide nanoparticles employing aqueous flower extract of Nyctanthes arbor-tristis was presented, and the resulting nanopowder was stored in dried form and was found to be stable after 4 months.
483 citations
TL;DR: These CoMnP nanoparticles are capable of catalyzing water oxidation at an overpotential of 0.33 V with a 96% Faradaic efficiency when deposited as an ink with carbon black and Nafion and a slight decrease in activity is observed after 500 cycles.
Abstract: The development of efficient water oxidation catalysts based on inexpensive and Earth-abundant materials is a prerequisite to enabling water splitting as a feasible source of alternative energy. In this work, we report the synthesis of ternary cobalt manganese phosphide nanoparticles from the solution-phase reaction of manganese and cobalt carbonyl complexes with trioctylphosphine. The CoMnP nanoparticles (ca. 5 nm in diameter) are nearly monodisperse and homogeneous in nature. These CoMnP nanoparticles are capable of catalyzing water oxidation at an overpotential of 0.33 V with a 96% Faradaic efficiency when deposited as an ink with carbon black and Nafion. A slight decrease in activity is observed after 500 cycles, which is ascribed to the etching of P into solution, as well as the oxidation of the surface of the nanoparticles. Manganese-based ternary phosphides represent a promising new system to explore for water oxidation catalysis.
450 citations
TL;DR: An intraparticle molecular orbital engineering approach to simultaneously enhance photoacoustic brightness and photothermal therapy efficacy of semiconducting polymer nanoparticles (SPNs) for in vivo imaging and treatment of cancer is reported.
Abstract: Optical theranostic nanoagents that seamlessly and synergistically integrate light-generated signals with photothermal or photodynamic therapy can provide opportunities for cost-effective precision medicine, while the potential for clinical translation requires them to have good biocompatibility and high imaging/therapy performance. We herein report an intraparticle molecular orbital engineering approach to simultaneously enhance photoacoustic brightness and photothermal therapy efficacy of semiconducting polymer nanoparticles (SPNs) for in vivo imaging and treatment of cancer. The theranostic SPNs have a binary optical component nanostructure, wherein a near-infrared absorbing semiconducting polymer and an ultrasmall carbon dot (fullerene) interact with each other to induce photoinduced electron transfer upon light irradiation. Such an intraparticle optoelectronic interaction augments heat generation and consequently enhances the photoacoustic signal and maximum photothermal temperature of SPNs by 2.6- a...
423 citations
TL;DR: It is shown that the charge transfer per Pt atom is largest for Pt particles of around 50 atoms, and mechanistic and quantitative insights into charge transfer will help to make better use of particle size effects and electronic metal-support interactions in metal/oxide nanomaterials.
Abstract: Electronic interactions between metal nanoparticles and oxide supports control the functionality of nanomaterials, for example, the stability, the activity and the selectivity of catalysts. Such interactions involve electron transfer across the metal/support interface. In this work we quantify this charge transfer on a well-defined platinum/ceria catalyst at particle sizes relevant for heterogeneous catalysis. Combining synchrotron-radiation photoelectron spectroscopy, scanning tunnelling microscopy and density functional calculations we show that the charge transfer per Pt atom is largest for Pt particles of around 50 atoms. Here, approximately one electron is transferred per ten Pt atoms from the nanoparticle to the support. For larger particles, the charge transfer reaches its intrinsic limit set by the support. For smaller particles, charge transfer is partially suppressed by nucleation at defects. These mechanistic and quantitative insights into charge transfer will help to make better use of particle size effects and electronic metal-support interactions in metal/oxide nanomaterials.
422 citations
TL;DR: The design and synthesis of triphenylphosphonium-conjugated ceria nanoparticles that localize to mitochondria and suppress neuronal death in a 5XFAD transgenic Alzheimer's disease mouse model are reported.
Abstract: Mitochondrial oxidative stress is a key pathologic factor in neurodegenerative diseases, including Alzheimer's disease. Abnormal generation of reactive oxygen species (ROS), resulting from mitochondrial dysfunction, can lead to neuronal cell death. Ceria (CeO2) nanoparticles are known to function as strong and recyclable ROS scavengers by shuttling between Ce(3+) and Ce(4+) oxidation states. Consequently, targeting ceria nanoparticles selectively to mitochondria might be a promising therapeutic approach for neurodegenerative diseases. Here, we report the design and synthesis of triphenylphosphonium-conjugated ceria nanoparticles that localize to mitochondria and suppress neuronal death in a 5XFAD transgenic Alzheimer's disease mouse model. The triphenylphosphonium-conjugated ceria nanoparticles mitigate reactive gliosis and morphological mitochondria damage observed in these mice. Altogether, our data indicate that the triphenylphosphonium-conjugated ceria nanoparticles are a potential therapeutic candidate for mitochondrial oxidative stress in Alzheimer's disease.
414 citations
TL;DR: The excellent absorbing performance together with lightweight and ultrathin thickness endows the CNTs/Co composite with the potential for application in the electromagnetic wave absorbing field.
Abstract: Porous carbon nanotubes/cobalt nanoparticles (CNTs/Co) composite with dodecahedron morphology was synthesized by in situ pyrolysis of the Co-based zeolitic imidazolate framework in a reducing atmosphere. The morphology and microstructure of the composite can be well tuned by controlling the pyrolysis conditions. At lower pyrolysis temperature, the CNTs/Co composite is composed of well-dispersed Co nanoparticles and short CNT clusters with low graphitic degree. The increase of pyrolysis temperature/time promotes the growth and graphitization of CNTs and leads to the aggregation of Co nanoparticles. The optimized CNTs/Co composite exhibits strong dielectric and magnetic losses as well as a good impedance matching property. Interestingly, the CNTs/Co composite displays extremely strong electromagnetic wave absorption with a maximum reflection loss of −60.4 dB. More importantly, the matching thickness of the absorber is as thin as 1.81 mm, and the filler loading of composite in the matrix is only 20 wt %. The...
TL;DR: In this review, some important applications of gold nanoparticles are explained, including those as sensing, image enhancement, and delivery agents in medicine.
Abstract: Nanoparticles are the simplest form of structures with sizes in the nanometer (nm) range. In principle any collection of atoms bonded together with a structural radius of 100 nm can be considered nano particles. Nanotechnology off ers unique approaches to probe and control a variety of biological and medical processes that occur at nanometer scales, and is expected to have a revolutionary impact on biology and medicine. Among the approaches for exploiting nanotechnology in medicine, nanoparticles off er some unique advantages as sensing, image enhancement, and delivery agents. Several varieties of nanoparticles with biomedical relevance are available including, polymeric nanoparticles, metal nanoparticles, liposomes, micelles, quantum dots, dendrimers, and nanoassemblies. To further the application of nanoparticles in disease diagnosis and therapy, it is important that the systems are biocompatible and capable of being functionalized for recognition of specifi c target sites in the body after systemic administration. In this review, we have explained some important applications of gold nanoparticles.
TL;DR: In this article, a kinetically controlled seeded-growth strategy was used to synthesize high monodisperse, biocompatible and functionalizable sub-10-nm citrate-stabilized gold nanoparticles (Au NPs).
Abstract: Highly monodisperse, biocompatible and functionalizable sub-10-nm citrate-stabilized gold nanoparticles (Au NPs) have been synthesized following a kinetically controlled seeded-growth strategy. The use of traces of tannic acid together with an excess of sodium citrate during nucleation is fundamental in the formation of a high number (7 × 1013 NPs/mL) of small ∼3.5 nm Au seeds with a very narrow distribution. A homogeneous nanometric growth of these seeds is then achieved by adjusting the reaction parameters: pH, temperature, sodium citrate concentration and gold precursor to seed ratio. We use this method to produce Au NPs with a precise control over their sizes between 3.5 and 10 nm and a versatile surface chemistry allowing studying the size-dependent optical properties in this transition size regime lying between clusters and nanoparticles. Interestingly, an inflection point is observed for Au NPs smaller than 8 nm in which the sensitivity of the localized surface plasmon resonance (LSPR) peak positio...
TL;DR: In this review, selected properties, such as structure, optical, catalytic and photocatalytic of noble metals-based bimetallic nanoparticles, are discussed together with preparation routes.
TL;DR: In this paper, the authors present a facile synthesis of nanocomposites comprising Nb2O5@Carbon core-shell nanoparticles and reduced graphene oxide (rGO).
Abstract: Sodium-ion hybrid supercapacitors (Na-HSCs) have potential for mid- to large-scale energy storage applications because of their high energy/power densities, long cycle life, and the low cost of sodium. However, one of the obstacles to developing Na-HSCs is the imbalance of kinetics from different charge storage mechanisms between the sluggish faradaic anode and the rapid non-faradaic capacitive cathode. Thus, to develop high-power Na-HSC anode materials, this paper presents the facile synthesis of nanocomposites comprising Nb2O5@Carbon core–shell nanoparticles (Nb2O5@C NPs) and reduced graphene oxide (rGO), and an analysis of their electrochemical performance with respect to various weight ratios of Nb2O5@C NPs to rGO (e.g., Nb2O5@C, Nb2O5@C/rGO-70, -50, and -30). In a Na half-cell configuration, the Nb2O5@C/rGO-50 shows highly reversible capacity of ≈285 mA h g−1 at 0.025 A g−1 in the potential range of 0.01–3.0 V (vs Na/Na+). In addition, the Na-HSC using the Nb2O5@C/rGO-50 anode and activated carbon (MSP-20) cathode delivers high energy/power densities (≈76 W h kg−1 and ≈20 800 W kg−1) with a stable cycle life in the potential range of 1.0–4.3 V. The energy and power densities of the Na-HSC developed in this study are higher than those of similar Li- and Na-HSCs previously reported.
TL;DR: A non-noble metal based 3D porous electrocatalyst is prepared by self-assembly of the liquid-exfoliated single-layer CoAl-layered double hydroxide nanosheets onto 3D graphene network, which exhibits higher catalytic activity and better stability for electrochemical oxygen evolution reaction.
Abstract: A non-noble metal based 3D porous electrocatalyst is prepared by self-assembly of the liquid-exfoliated single-layer CoAl-layered double hydroxide nanosheets (CoAl-NSs) onto 3D graphene network, which exhibits higher catalytic activity and better stability for electrochemical oxygen evolution reaction compared to the commercial IrO2 nanoparticle-based 3D porous electrocatalyst.
TL;DR: In this paper, the synthesis of Fe3O4decorated Co9S8 nanoparticles in situ grown on a reduced graphene oxide surface was reported and the use of it as a remarkably active and stable OER catalyst is first reported.
Abstract: Cobalt sulfide materials have attracted enormous interest as low-cost alternatives to noble-metal catalysts capable of catalyzing both oxygen reduction and oxygen evolution reactions. Although recent advances have been achieved in the development of various cobalt sulfide composites to expedite their oxygen reduction reaction properties, to improve their poor oxygen evolution reaction (OER) activity is still challenging, which significantly limits their utilization. Here, the synthesis of Fe3O4-decorated Co9S8 nanoparticles in situ grown on a reduced graphene oxide surface (Fe3O4@Co9S8/rGO) and the use of it as a remarkably active and stable OER catalyst are first reported. Loading of Fe3O4 on cobalt sulfide induces the formation of pure phase Co9S8 and highly improves the catalytic activity for OER. The composite exhibits superior OER performance with a small overpotential of 0.34 V at the current density of 10 mA cm−2 and high stability. It is believed that the electron transfer trend from Fe species to Co9S8 promotes the breaking of the Co–O bond in the stable configuration (Co–O–O superoxo group), attributing to the excellent catalytic activity. This development offers a new and effective cobalt sulfide-based oxygen evolution electrocatalysts to replace the expensive commercial catalysts such as RuO2 or IrO2.
TL;DR: A simple, fast, and robust protocol of cationic polymer-mediated gold nanocluster self-assembly into nanoparticles (NPs) of ca.
Abstract: Nanoparticles combining enhanced cellular drug delivery with efficient fluorescence detection are important tools for the development of theranostic agents. Here, we demonstrate this concept by a simple, fast, and robust protocol of cationic polymer-mediated gold nanocluster (Au NCs) self-assembly into nanoparticles (NPs) of ca. 120 nm diameter. An extensive characterization of the monodisperse and positively charged NPs revealed pH-dependent swelling properties, strong fluorescence enhancement, and excellent colloidal and photostability in water, buffer, and culture medium. The versatility of the preparation is demonstrated by using different Au NC surface ligands and cationic polymers. Steady-state and time-resolved fluorescence measurements give insight into the aggregation-induced emission phenomenon (AIE) by tuning the Au NC interactions in the self-assembled nanoparticles using the pH-dependent swelling. In vitro studies in human monocytic cells indicate strongly enhanced uptake of the NPs compared ...
TL;DR: The catalyst's outstanding performance may have resulted from the ultrahigh dispersion of Pt (several atomic layers coated on the nitride nanoparticles), and the excellent stability/durability may have been due to the good stability of nitride and synergetic effects between ultrathin Pt layer and the robust TiNiN support.
Abstract: The main challenges to the commercial viability of polymer electrolyte membrane fuel cells are (i) the high cost associated with using large amounts of Pt in fuel cell cathodes to compensate for the sluggish kinetics of the oxygen reduction reaction, (ii) catalyst degradation, and (iii) carbon-support corrosion. To address these obstacles, our group has focused on robust, carbon-free transition metal nitride materials with low Pt content that exhibit tunable physical and catalytic properties. Here, we report on the high performance of a novel catalyst with low Pt content, prepared by placing several layers of Pt atoms on nanoparticles of titanium nickel binary nitride. For the ORR, the catalyst exhibited a more than 400% and 200% increase in mass activity and specific activity, respectively, compared with the commercial Pt/C catalyst. It also showed excellent stability/durability, experiencing only a slight performance loss after 10,000 potential cycles, while TEM results showed its structure had remained intact. The catalyst's outstanding performance may have resulted from the ultrahigh dispersion of Pt (several atomic layers coated on the nitride nanoparticles), and the excellent stability/durability may have been due to the good stability of nitride and synergetic effects between ultrathin Pt layer and the robust TiNiN support.
TL;DR: It was found that the SMSI between Au and HAP is general and could be extended to other phosphate-supported Au systems such as Au/LaPO4 and may open a new way to design and develop highly stable supported Au catalysts with controllable activity and selectivity.
Abstract: The strong metal–support interaction (SMSI) is of great importance for supported catalysts in heterogeneous catalysis. We report the first example of SMSI between Au nanoparticles (NPs) and hydroxyapatite (HAP), a nonoxide. The reversible encapsulation of Au NPs by HAP support, electron transfer, and changes in CO adsorption are identical to the classic SMSI except that the SMSI of Au/HAP occurred under oxidative condition; the opposite condition for the classical SMSI. The SMSI of Au/HAP not only enhanced the sintering resistance of Au NPs upon calcination but also improved their selectivity and reusability in liquid-phase reaction. It was found that the SMSI between Au and HAP is general and could be extended to other phosphate-supported Au systems such as Au/LaPO4. This new discovery may open a new way to design and develop highly stable supported Au catalysts with controllable activity and selectivity.
TL;DR: In this article, the synthesis of copper (Cu) and copper(I) oxide on Cu (Cu/Cu 2 O) nanoparticles via thermal decomposition method using a combination of oleic acid and oleylamine, involves a single nucleation step and control in growth of nanoparticles produces high monodispersity in shape and protects copper nanoparticles against oxidation.
TL;DR: This work provides a platform for the rapid generation of superstructured assemblies across a wide range of length scales, from nanometres to centimetres, based on the polyphenol surface-functionalization of micro- and nanoparticles, nanowires, nanosheets, nanocubes and even cells.
Abstract: The organized assembly of particles into superstructures is typically governed by specific molecular interactions or external directing factors associated with the particle building blocks, both of which are particle-dependent. These superstructures are of interest to a variety of fields because of their distinct mechanical, electronic, magnetic and optical properties. Here, we establish a facile route to a diverse range of superstructures based on the polyphenol surface-functionalization of micro- and nanoparticles, nanowires, nanosheets, nanocubes and even cells. This strategy can be used to access a large number of modularly assembled superstructures, including core-satellite, hollow and hierarchically organized supraparticles. Colloidal-probe atomic force microscopy and molecular dynamics simulations provide detailed insights into the role of surface functionalization and how this facilitates superstructure construction. Our work provides a platform for the rapid generation of superstructured assemblies across a wide range of length scales, from nanometres to centimetres.
TL;DR: WPC/MNPs-80 has an excellent EM wave absorbency with a wide absorption band at a relatively low loading and thin absorber thickness, and the design strategy could be extended as a general method to synthesize other high-performance absorbers.
Abstract: A method combining liquid–liquid phase separation and the pyrolysis process has been developed to fabricate the wormhole-like porous carbon/magnetic nanoparticles composite with a pore size of about 80 nm (WPC/MNPs-80). In this work, the porous structure was designed to enhance interaction between the electromagnetic (EM) wave and the absorber, while the magnetic nanoparticles were used to bring about magnetic loss ability. The structure, morphology, porosity and magnetic properties of WPC/MNPs-80 were investigated in detail. To evaluate its EM wave attenuation performance, the EM parameters of the absorber and wax composite were measured at 2–18 GHz. WPC/MNPs-80 has an excellent EM wave absorbency with a wide absorption band at a relatively low loading and thin absorber thickness. At the absorber thickness of 1.5 and 2.0 mm, minimum RL values of −29.2 and −47.9 dB were achieved with the RL below −10 dB in 12.8–18 and 9.2–13.3 GHz, respectively. The Co and Fe nanoparticles derived from the chemical reduction of Co0.2Fe2.8O4 can enhance the graphitization process of carbon and thus improve dielectric loss ability. Polarizations in the nanocomposite absorber also play an important role in EM wave absorption. Thus, EM waves can be effectively attenuated by dielectric loss and magnetic loss through multiple reflections and absorption in the porous structure. WPC/MNPs-80 could be an excellent absorber for EM wave attenuation; and the design strategy could be extended as a general method to synthesize other high-performance absorbers.
TL;DR: The encapsulation of platinum species in highly siliceous chabazite (CHA) crystallized in the presence of N,N,N-trimethyl-1-adamantammonium and a thiol-stabilized Pt complex shows enhanced stability toward metal sintering in a variety of industrial conditions, including H2, O2, and H2O.
Abstract: We report the encapsulation of platinum species in highly siliceous chabazite (CHA) crystallized in the presence of N,N,N-trimethyl-1-adamantammonium and a thiol-stabilized Pt complex. When compared to Pt/SiO2 or Pt-containing Al-rich zeolites, the materials in this work show enhanced stability toward metal sintering in a variety of industrial conditions, including H2, O2, and H2O. Remarkably, temperatures in the range 650–750 °C can be reached without significant sintering of the noble metal. Detailed structural determinations by X-ray absorption spectroscopy and aberration-corrected high-angle annular dark-field scanning transmission electron microscopy demonstrate subtle control of the supported metal structures from ∼1 nm nanoparticles to site-isolated single Pt atoms via reversible interconversion of one species into another in reducing and oxidizing atmospheres. The combined used of microscopy and spectroscopy is critical to understand these surface-mediated transformations. When tested in hydrogena...
TL;DR: In this paper, a review of recent advances in the development of screen-printed electrode-based biosensors is presented, together with examples of paper-based electrochemical devices, of multiple detections using arrays of screen printed electrodes, and of the most recent developments in the field of wearable sensors.
Abstract: This review addresses recent advances in the development of screen-printed electrode based biosensors modified with different nanomaterials such as carbon nanotubes, graphene, metallic nanoparticles as gold, silver and magnetic nanoparticles, and mediator nanoparticles (Prussian Blue, Cobalt Phthalocyanine, etc.), coupled with biological recognition elements such as enzymes, antibodies, DNA and aptamers to obtain probes with improved analytical features. Examples of clinical applications are illustrated, together with examples of paper-based electrochemical devices, of multiple detections using arrays of screen printed electrodes, and of the most recent developments in the field of wearable biosensors. Also the use of smartphones as final detectors is briefly depicted.
TL;DR: Efficient encapsulation by N,P-doped graphene effectively prevent nanoparticle from corrosion, exhibiting nearly unfading catalytic performance after 30 h testing and opens a door for unprecedented design and fabrication of novel low-cost metal phosphide electrocatalysts encapsulated by graphene.
Abstract: We developed a method to engineer well-distributed dicobalt phosphide (Co2P) nanoparticles encapsulated in N,P-doped graphene (Co2P@NPG) as electrocatalysts for hydrogen evolution reaction (HER). We fabricated such nanostructure by the absorption of initiator and functional monomers, including acrylamide and phytic acid on graphene oxides, followed by UV-initiated polymerization, then by adsorption of cobalt ions and finally calcination to form N,P-doped graphene structures. Our experimental results show significantly enhanced performance for such engineered nanostructures due to the synergistic effect from nanoparticles encapsulation and nitrogen and phosphorus doping on graphene structures. The obtained Co2P@NPG modified cathode exhibits small overpotentials of only −45 mV at 1 mA cm–2, respectively, with a low Tafel slope of 58 mV dec–1 and high exchange current density of 0.21 mA cm–2 in 0.5 M H2SO4. In addition, encapsulation by N,P-doped graphene effectively prevent nanoparticle from corrosion, exhi...
TL;DR: The as-prepared noble metal nanoparticles on MXene show a highly sensitive SERS detection of methylene blue (MB) with calculated enhancement factors on the order of 105, opening a pathway for extending visible-range SERS applications of novel 2D hybrid materials in sensors, catalysis, and biomedical applications.
Abstract: We report on one-step hybridization of silver, gold and palladium nanoparticles from solution onto exfoliated two-dimensional (2D) Ti3C2 titanium carbide (MXene) nanosheets. The produced hybrid materials can be used as substrates for surface-enhanced Raman spectroscopy (SERS). An approximate analytical approach is also developed for the calculation of the surface plasmon resonance (SPR) frequency of nanoparticles immersed in a medium, near the interface of two dielectric media with different dielectric constants. We obtained a good match with the experimental data for SPR wavelengths, 440 nm and 558 nm, respectively for silver and gold nanoparticles. In the case of palladium, our calculated SPR wavelength for the planar geometry was 160 nm, demonstrating that non-spherical palladium nanoparticles coupled with 2D MXene yield a broad, significanlty red-shifted SPR band with a peak at 230 nm. We propose a possible mechanism of the plasmonic hybridization of nanoparticles with MXene. The as-prepared noble metal nanoparticles on MXene show a highly sensitive SERS detection of methylene blue (MB) with calculated enhancement factors on the order of 105. These findings open a pathway for extending visible-range SERS applications of novel 2D hybrid materials in sensors, catalysis, and biomedical applications.
TL;DR: In this article, a technique to enhance optical absorption by platinum nanoparticles is exploited for driving photocatalytic redox reactions, which can be used to enhance the performance of redox reaction.
Abstract: A technique to enhance optical absorption by platinum nanoparticles is exploited for driving photocatalytic redox reactions.
TL;DR: By carbon layer coating, the optimized catalyst exhibits enhanced selectivity and stability applied to the solar-driven reduction of CO2 into CO through the surface-plasmon effect of iron particles, and thereby facilitates the final reaction activity.
Abstract: Highly efficient utilization of solar light with an excellent reduction capacity is achieved for plasmonic Fe@C nanostructures. By carbon layer coating, the optimized catalyst exhibits enhanced selectivity and stability applied to the solar-driven reduction of CO2 into CO. The surface-plasmon effect of iron particles is proposed to excite CO2 molecules, and thereby facilitates the final reaction activity.
TL;DR: A facile bottom-up approach to carbon nanodots (CNDs) is reported, using a microwave-assisted procedure under controlled conditions, and as-prepared nitrogen-doped CNDs show narrow size-distribution, abundant surface traps and functional groups, resulting in tunable fluorescent emission and excellent solubility in water.
Abstract: A facile bottom-up approach to carbon nanodots (CNDs) is reported, using a microwave-assisted procedure under controlled conditions. The as-prepared nitrogen-doped CNDs (NCNDs) show narrow size-distribution, abundant surface traps and functional groups, resulting in tunable fluorescent emission and excellent solubility in water. Moreover, we present a general method for the separation of NCNDs by low-pressure size-exclusion chromatography, leading to an even narrower size distribution, different surface composition, and optical properties. They display among the smallest size and the highest FLQYs reported so far. (13)C-enriched starting materials produced N(13) CNDs suitable for thorough NMR studies, which gave useful information on their molecular structure. Moreover, they can be easily functionalized and can be used as water-soluble carriers. This work provides an avenue to size- and surface-controllable and structurally defined NCNDs for applications in areas such as optoelectronics, biomedicine, and bioimaging.