[en] Nanoscale materials have been gaining increasing interest in the area of environmental remediation because of their unique physical, chemical and biological properties. One emerging area of research has been the development of novel materials with increased affinity, capacity, and selectivity for heavy metals because conventional technologies are often inadequate to reduce concentrations in wastewater to acceptable regulatory standards. Genetic and protein engineering have emerged as the latest tools for the construction of nanoscale materials that can be controlled precisely at the molecular level. With the advent of recombinant DNA techniques, it is now possible to create 'artificial' protein polymers with fundamentally new molecular organization. The most significant feature of these nanoscale biopolymers is that they are specifically pre-programmed within a synthetic gene template and can be controlled precisely in terms of sizes, compositions and functions at the molecular level. In this review, the use of specifically designed protein-based nano-biomaterials with both metal-binding and tunable properties for heavy metal removal is summarized. Several different strategies for the selective removal of heavy metals such as cadmium and mercury are highlighted

[en] A facile technique was demonstrated for the controlled assembly and alignment of multi-segment nanowires using bioengineered polypeptides. An elastin-like-polypeptide (ELP)-based biopolymer consisting of a hexahistine cluster at each end (His₆-ELP-His₆) was generated and purified by taking advantage of the reversible phase transition property of ELP. The affinity between the His₆ domain of biopolymers and the nickel segment of multi-segment nickel/gold/nickel nanowires was exploited for the directed assembly of nanowires onto peptide-functionalized electrode surfaces. The presence of the ferromagnetic nickel segments on the nanowires allowed the control of directionality by an external magnetic field. Using this method, the directed assembly and positioning of multi-segment nanowires across two microfabricated nickel electrodes in a controlled manner was accomplished with the expected ohmic contact

[en] This report summarizes the development of sensor particles for remote detection of trace chemical analytes over broad areas, e.g residual trinitrotoluene from buried landmines or other unexploded ordnance (UXO). We also describe the potential of the sensor particle approach for the detection of chemical warfare (CW) agents. The primary goal of this work has been the development of sensor particles that incorporate sample preconcentration, analyte molecular recognition, chemical signal amplification, and fluorescence signal transduction within a ''grain of sand''. Two approaches for particle-based chemical-to-fluorescence signal transduction are described: (1) enzyme-amplified immunoassays using biocompatible inorganic encapsulants, and (2) oxidative quenching of a unique fluorescent polymer by TNT

[en] A low-cost heterostructure of a wide-bandgap nanostructured semiconductor on top of a transparent conductor (TC) fabricated from abundant sustainable materials is of great interest for optoelectronic devices, such as heterojunction photovoltaic cells. Due to its high optical transparency and electron mobility, graphene is an attractive carbon-based material to replace the costly traditional TCs (i.e. ITO), which pose health hazards and destructive environmental impact thorough their life cycle. However, for the industrial application of graphene as TC it is necessary to interface it with other materials, like oxides, while maintaining the sp² network that provides its excellent electronic properties. We report the optimized electrodeposition of ZnO on graphene to obtain a textured layer of vertically aligned crystalline semiconducting nanorods (ZVNRs) evenly coating the graphene surface. Lattice distortions and mosaicity in the crystals indicate that the ZVNRs grow under out-of-plane compressive strain. The stability of the sp² network of graphene during in situ growth of ZnO is demonstrated using Raman spectroscopy from the front and backside of the heterostructure, in a novel approach to investigate junctions of 2D–3D nanomaterials. Despite the structural stability of graphene, its R _□ is found to increase by ∼100% with ZVNRs electrodeposition, which is attributed to reduction of mobility due to charge carrier scattering, reduction of carrier concentration due to doping, and/or interfacial strain. The cathodic electrodeposition is demonstrated to be an effective and versatile method to grow crystalline nanostructures in the surface of single layer-graphene while protecting its sp² hybridization, and it provides relative fast deposition rates, affordability, and low processing temperatures that would allow using polymeric flexible substrates and. These findings on interfacial properties are important to advance the functionality of graphene as TC material and develop nano-heterostructures for myriad technological applications. (paper)

[en] A microbial biosensor is an analytical device that couples microorganisms with a transducer to enable rapid, accurate and sensitive detection of target analytes in fields as diverse as medicine, environmental monitoring, defense, food processing and safety. The earlier microbial biosensors used the respiratory and metabolic functions of the microorganisms to detect a substance that is either a substrate or an inhibitor of these processes. Recently, genetically engineered microorganisms based on fusing of the lux, gfp or lacZ gene reporters to an inducible gene promoter have been widely applied to assay toxicity and bioavailability. This paper reviews the recent trends in the development and application of microbial biosensors. Current advances and prospective future direction in developing microbial biosensor have also been discussed

[en] Electrical and gas sensing properties of single-walled carbon nanotube networks functionalized with polyaniline (PANI-SWNTs) were systematically investigated to understand the gas sensing mechanisms and optimize sensing performance. The temperature-dependent electrical resistance and field-effect transistor (FET) transfer characteristics indicated that the electrical properties of PANI-SWNTs are dominated by the PANI coating. The FET transfer characteristics of PANI-SWNTs exposed to different NH₃ concentrations indicated that the dominant sensing mechanism is the deprotonation of PANI by NH₃. Sensing experiments with different gas analytes revealed that PANI-SWNTs responded positively to NH₃, and negatively to NO₂ and H₂S with sensitivities of 5.8% per ppm_v of NH₃, 1.9% per ppm_v of NO₂, and 3.6% per ppm_v of H₂S. The lower detection limits were 50, 500, and 500 ppb for NH₃, NO₂, and H₂S, respectively.

[en] Biological synthesis of gold nanostructures could potentially offer an environmentally friendly alternative to traditional chemical synthetic methods. During the last decades, various biomolecules, including amino acids, have been successfully used as reducing and capping agents to synthesize multi-shaped gold nanostructures. A grand challenge in this field is to increase our ability to control the size and shape of gold nanostructures formed precisely by systematic synthetic approaches based on the understanding of the mechanism for structural determination. In this study, using glycine as the model amino acid and chloroaurate (AuCl₄ ^-) ions as the precursor solution, we report the finding that the shape of the gold nanostructures synthesized showed a strong correlation with the speciation of gold complexes determined by the pH, precursor concentration and chloride concentration of the solvent system. The gold chloro-hydroxy speciation [AuCl_x(OH)_4-x]^- (with x = 0–4) influenced the shape of the gold nanostructures formed, with gold nanoplatelets, nanotriangles, nanokites and nanoribbons observed at x = 4, 3, 2 and 1, respectively, and spherical nanoparticles observed at x = 0. Glycine was found to play a role as a reducing agent, but no significant effect on the morphology was observed, indicating the dominance of gold chloro-hydroxy speciation in the structural formation. These results collectively provide synthetic considerations to systematically synthesize non-spherical to spherical biosynthesized gold nanostructures by controlling the speciation of [AuCl_x(OH)_4-x]^-. (paper)

[en] SnO₂ nanotubes with controlled diameter and length were synthesized using an electrochemical method at room temperature. The length and wall thickness of the nanotubes increased monotonically with the deposition time and the diameter of the nanotubes was altered by varying the pore size of the scaffolds. Post-annealing at 400 deg. C in dry air significantly improved the crystallinity while maintaining the nanotube structure. The temperature-dependent photoluminescence spectra indicated an activation energy of 58 meV for emission centered at 410 nm. The temperature-dependent electrical resistance revealed that the dominant electrical conduction mechanism alters from the ionization of the main donor centers to impurity scattering as the temperature decreases. The electrical conductance of 200 nm diameter nanotubes increased to 33 times the original value upon UV illumination at 254 nm.

[en] Highlights: • The evolution of metals during wastewater treatment train was investigated. • The majority of lead was in particulate fraction (>0.45 μm) in real wastewater. • The majority of cadmium was in dissolved fraction (• Arsenic(III) was highly mobile during the whole wastewater treatment train. Understanding the behavior of heavy metals in wastewater is critical for the development of metal removal and detection techniques. In this study, we characterize the dynamic and evolving size and partitioning behavior of lead (Pb), cadmium (Cd), and arsenite (As(III)) throughout the wastewater treatment train (WWTT). Metal concentrations were determined in three size fractions (>0.45 μm, 0.45 μm – 5 kDa, and 3 was used as a flocculation agent, which led to the formation of arsenic/iron complexes. However, Pb was found primarily in complex forms or adsorbed onto inorganic particulates. The WWTT had little impact on the size and partitioning of Pb, except that the formation of the Pb/iron complex occurred after flocculation with FeCl₃. An increase of water hardness slightly increased the metals in the dissolved fraction. Overall, this study provides insight into the evolution of metals throughout the WWTT, offering guidance to users and researchers regarding their treatment and detection.

[en] We report the fabrication and characterization of poly(N-methylpyrrole) nanowires electrode junction based back-gated field-effect transistors under varying dopant atmosphere. Influences of the anionic radius of dopants on electrochemical, morphological, spectroscopic and electrical characteristics of synthesized nanowires have been investigated. The FET measurements have revealed highly efficient gate induced modulation of the channel conduction behaviour for all dopant cases and characteristic FET parameters have been estimated. The best observed device in terms of charge carrier mobility (μ) = 4.54 × 10⁻⁴ cm² V⁻¹ s⁻¹ and on-off ratio (I_on/I_off) = 8.5 × 10³ could be characterized with NaOH as dopant. Observed behaviour of the FET devices has been rationally related to the anionic radius of dopants. Plausible interpretation reflects that dopant dimension can be a significant and facile tool for optimized designing of polymeric FETs. (paper)