A protein-based three terminal electronic device.

: Because of their natural functional characteristics, involving inter- and intramolecular electron transfer, metalloproteins are good candidates for biomolecular nanoelectronics. In particular, blue copper proteins, such as azurin, can bind gold via a disulfide site present on its surface and they have a natural electron transfer activity that can be exploited for the realization of molecular switches whose conduction state can be controlled by tuning their redox state through an external voltage source. We report on the implementation of a prototype of protein transistor operating in air and in the solid state, based on this class of proteins. The three terminal devices exhibit various functions depending on the relative source-drain and gate-drain voltages bias, opening a way to the implementation of a new generation of logic architectures

SFM study of the surface of halogen-bonded hybrid co-crystals containing long-chain perfluorocarbons

Different scanning force microscopy (SFM) techniques were employed to investigate the structure and composition of the fundamental crystal faces of prototype halogen-bonded co-crystals of long-chain perfluorocarbons. These crystals were found to show surfaces with well-defined ledges formed by intersecting crystal planes having different chemical compositions with the perfluorocarbons (PFCs) covering the largest area of the crystal as a reminiscence of the strong segregation observed in the bulk crystal structure

Influence of laser wavelength and pulse duration on the degradation of polymeric films embedding photochromic molecules

Abstract An extensive investigation of the photodegradation of the photochromic molecule 1′,3′-dihydro-1′,3′,3′-trimethyl-6-nitrospiro[2 H -1-benzopyran-2,2′-(2 H )-indole] in a polymer matrix is studied under irradiation with ultraviolet (UV) laser pulses of 248 and 308 nm wavelength. Apart from the effect of the wavelength, the effect of the pulse duration is also presented using pulses of 30 ns and 500 fs for the 248 nm wavelength. To tackle the problem of oxidative degradation upon irradiation of the photochromic molecules which is known to play a principal role in the photodegradation process, we incorporate Iron(II) phthalocyanine molecules in the examined matrices. These molecules upon UV irradiation are dissociated into photoproducts that can interact efficiently with electron acceptor groups in the polymer, partly responsible for the photochromic degradation. The phthalocyanine molecules seem to protect efficiently the photochromic molecules only at low laser fluences. Moreover, in the case of ultrashort pulses the degradation of the photochromic molecules is found to be more intense that in the case of ns pulses, indicating multiphoton absorption mechanisms, unless low laser fluences are used

A microfluidic method for passive trapping of sperms in microstructures

Sperm motility is a prerequisite for male fertility. Enhancing the concentration of motile sperms in assisted reproductive technologies - for human and animal reproduction - is typically achieved through aggressive methods such as centrifugation. Here we propose a passive technique for the amplification of motile sperm concentration, with no externally imposed forces or flows. The technique is based upon the disparity between probability rates, for motile cells, of entering in and escaping from complex structures. The effectiveness of the technique is demonstrated in microfluidic experiments with microstructured devices, comparing the trapping power in different geometries. In these micro-traps we observe an enhancement of cells concentration close to 10, with a contrast between motile and non-motile increased by a similar factor. Simulations of suitable interacting model sperms in realistic geometries reproduce quantitatively the experimental results, extend the range of observations and highlight the ingredients that are key to optimal trap design

Self-assembled monolayers of cobalt(II)- (4-tert-butylphenyl)-porphyrins: the influence of the electronic dipole on scanning tunneling microscopy images.

Self-assembled monolayers (SAMs) of cobalt(II) 5,10,15,20-tetrakis(4-teit-butylphenyl)-porphyrin, a promising material for optical, photoelectrochemical, and chemical sensor applications, were prepared on Au(111) via axial ligation to 4-aminothiophenol, and studied by several surface science techniques. Scanning tunneling microscopy (STM) and spectroscopy (STS) measurements showed the apparent topology of the Au(111) herringbone structure reconstruction. but with bias-dependent contrast images and asymmetric W characteristics. Photoelectron spectroscopy confirmed the presence of metalloporphyrins on the surface, whereas near-edge X-ray absorption (NEXAFS) measurements revealed that the porphyrin ring was tilted by about 70degrees with respect to the surface plane. The above effects are ascribed to the presence of oriented molecular dipole layers between the metal and the organic material as confirmed by a comparison with first-principles density-functional theory calculations. The measured bias-dependent STM profiles have been reproduced by a simple monodimensional tunneling model

A nanobiosensor to detect single hybridization events

An economical nanoarray method to electrically detect hybridization events is demonstrated. As a proof of concept, we fabricated a sensor for DNA sequencing, in which targets are oligonucleotides conjugated to gold nanoparticles. As a consequence of target–probe binding events, a conductive bridge forms between two electrodes, resulting in a quantized change in conductivity. This enables a robust detection of a few (down to single) hybridization events and can be potentially applied also to other binding events (like specific interactions between proteins, antibodies, ligands and receptors). Moreover, target amplification techniques (such as PCR) are no longer necessary

Field Effect Transistor Based on a Modified DNA Base

In this work, a field effect transistor based on a deoxyguanosine derivative (a DNA base) is demonstrated. Our experiments on transport through the source and drain electrodes interconnected by self-assembled guanine ribbons (Gottarelli et al. Helv. Chim. Acta 1998, 81, 2078; Gottarelli et al. Chem. Eur. J. 2000, 6, 3242; Giorgi et al. Chem Eur. J. 2002, 8, 2143) suggest that these devices behave like p-channel MOSFETs, The devices exhibit a maximum voltage gain of 0.76. This prototype transistor represents a starting point toward the development of biomolecular electronic devices

Hybrid molecular electronic (HME) transistor based on deoxyguanosine derivatives

In this work, a field effect transistor based on deoxyguanosine derivatives (a DNA basis) is demonstrated by means of systematic transport experiments. Our nanodevices were fabricated starting from a deoxyguanosine derivative (dG(C-10)(2)) layer interconnecting planar nano-electrodes, with separation in the 20-40nm range. The three terminal devices exhibit a maximum voltage gain of 0.76. Though the quick aging and the reproducibility of the devices have to be improved, the realization of a transistor-like device represents a starting point towards the development of planar solid-state bio-molecular electronic devices

Azurin for Biomolecular Electronics: a Reliability Study

The metalloprotein azurin, used in biomolecular electronics, is investigated with respect to its resilience to high electric fields and ambient conditions, which are crucial reliability issues. Concerning the effect of electric fields, two models of different complexity agree indicating an unexpectedly high robustness. Experiments in device-like conditions confirm that no structural modifications occur, according to fluorescence spectra, even after a 40-min exposure to tens of MV/m. Ageing is then investigated experimentally, at ambient conditions and without field, over several days. Only a small conformational rearrangement is observed in the first tens of hours, followed by an equilibrium state

Nano-scaled Biomolecular Field-Effect Transistors: Prototypes and Evaluations

As modern electronics rapidly approach the ultimate level of integration (typically thought to be at the nanoscale level), the fascinating world of biomolecules provides new opportunities and directions for further miniaturization. In this work we review our results in the field of biomolecular electronics, starting from the fabrication of nanojunctions up to the implementation of hybrid devices