RESUMO
Semiconductor nanowires (NWs), due to their intriguing structural and physical properties, offer tremendous potential for future technological applications. The existence of strain in NWs can greatly affect, for instance, their mechanical, electrical and optical properties. Here, we report an extraordinary electrostatic response of semiconductor BiFeO3 NW loops, based on Kelvin probe force microscopy (KPFM) and electrostatic force microscopy (EFM). A substantial â¼300 mV surface potential difference, accompanied by an â¼29% higher surface charge density, was found on the NW loop. We also found that the electrostatic enhancement is strongly related to the strain present at the curvature of the NW loops. We propose that the electric polarization coupled with mechanical strain (piezoelectric effect) or strain gradient (flexoelectricity) as possible reasons to account for our observation. These findings provide new insights into multiferroic based semiconductor NWs under external stimuli as well as significant inspiration towards strain sensors and electromechanical devices with multifunctional sensing abilities.
RESUMO
Mid-infrared (IR) photothermal spectroscopy of adsorbed molecules is an ideal technique for molecular recognition in miniature sensors with very small thermal mass. Here, we report on combining the photothermal spectroscopy with electrical resonance of a semiconductor nanowire for enhanced sensitivity, selectivity, and simplified readout. Wide band gap semiconductor bismuth ferrite nanowire, by virtue of its very low thermal mass and abundance of surface states in the band gap, facilitates thermally induced charge carrier trapping in the surface states, which affects its electrical resonance response. Electrical resonance response of the nanowire varies significantly depending on the photothermal spectrum of the adsorbed molecules. We demonstrate highly selective detection of mid-IR photothermal spectral signatures of femtogram level molecules physisorbed on a nanowire by monitoring internal dissipation response at its electrical resonance.
RESUMO
Broad-spectrum biosensing technologies examine sensor signals using biomarkers, such as proteins, DNA, antibodies, specific cells, and macromolecules, based on direct- or indirect-conformational changes. Here, we have investigated the pH-dependent conformational isomerization of human serum albumin (HSA) using microcantilevers as a sensing platform. Native and denatured proteins were immobilized on cantilever surfaces to understand the effect of pH on conformational changes of the protein with respect to the coupling ligand. Our results show that protonation and deprotonation of amino acid residues on proteins play a significant role in generating charge-induced cantilever deflection. Surface plasmon resonance (SPR) was employed as a complementary technique to validate the results.
Assuntos
Técnicas Biossensoriais/métodos , Albumina Sérica/química , Humanos , Concentração de Íons de Hidrogênio , Conformação ProteicaRESUMO
A surface dominant sub-bandgap photo-carrier generation has been observed in multiferroic BiFeO3 (BFO) nanowires, which is mainly attributed to the depopulation of surface states that exist within the bandgap. Mapping of surface potential using Kelvin probe force microscopy (KPFM) further supports the depopulation of surface states in BFO nanowires under sub-bandgap illumination. The mechanism of photovoltage generation in BFO nanowires is investigated by measuring the photoresponse with local illumination of visible laser pulses at different positions of the BFO nanowires. Interestingly, large photovoltage signals were observed when the laser spot was focused close to contact electrodes, showing a position dependent effect of photoresponse in the BFO nanowires. The sub-bandgap excitation of surface states in multiferroic nanowires offers potential new strategies for application in photovoltaic devices.
RESUMO
Electrospinning is a simple, versatile technique for fabricating fibrous nanomaterials with the desirable features of extremely high porosities and large surface areas. Using emulsion electrospinning, polytetrafluoroethylene/polyethene oxide (PTFE/PEO) membranes were fabricated, followed by a sintering process to obtain pure PTFE fibrous membranes, which were further utilized against a polyamide 6 (PA6) membrane for vertical contact-mode triboelectric nanogenerators (TENGs). Electrostatic force microscopy (EFM) measurements of the sintered electrospun PTFE membranes revealed the presence of both positive and negative surface charges owing to the transfer of positive charge from PEO which was further corroborated by FTIR measurements. To enhance the ensuing triboelectric surface charge, a facile negative charge-injection process was carried out onto the electrospun (ES) PTFE subsequently. The fabricated TENG gave a stabilized peak-to-peak open-circuit voltage (Voc) of up to â¼900 V, a short-circuit current density (Jsc) of â¼20 mA m-2, and a corresponding charge density of â¼149 µC m-2, which are â¼12, 14, and 11 times higher than the corresponding values prior to the ion-injection treatment. This increase in the surface charge density is caused by the inversion of positive surface charges with the simultaneous increase in the negative surface charge on the PTFE surface, which was confirmed by using EFM measurements. The negative charge injection led to an enhanced power output density of â¼9 W m-2 with high stability as confirmed from the continuous operation of the ion-injected PTFE/PA6 TENG for 30â¯000 operation cycles, without any significant reduction in the output. The work thus introduces a relatively simple, cost-effective, and environmentally friendly technique for fabricating fibrous fluoropolymer polymer membranes with high thermal/chemical resistance in TENG field and a direct ion-injection method which is able to dramatically improve the surface negative charge density of the PTFE fibrous membranes.
RESUMO
Spontaneous self-assemblies of biomolecules can generate geometrical patterns. Our findings provide an insight into the mechanism of self-assembled ring pattern generation by human serum albumin (HSA). The self-assembly is a process guided by kinetic and thermodynamic parameters. The generated protein ring patterns display a behavior which is geometrically related to a n-simplex model and is explained through thermodynamics and chemical kinetics.
Assuntos
Albumina Sérica Humana/química , Algoritmos , Humanos , Cinética , Microscopia de Força Atômica , Albumina Sérica Humana/ultraestrutura , TermodinâmicaRESUMO
According to Stokes' law, a moving solid surface experiences viscous drag that is linearly related to its velocity and the viscosity of the medium. The viscous interactions result in dissipation that is known to scale as the square root of the kinematic viscosity times the density of the gas. We observed that when an oscillating surface is modified with nanostructures, the experimentally measured dissipation shows an exponential dependence on kinematic viscosity. The surface nanostructures alter solid-gas interplay greatly, amplifying the dissipation response exponentially for even minute variations in viscosity. Nanostructured resonator thus allows discrimination of otherwise narrow range of gaseous viscosity making dissipation an ideal parameter for analysis of a gaseous media. We attribute the observed exponential enhancement to the stochastic nature of interactions of many coupled nanostructures with the gas media.
RESUMO
Lanthanide-doped vanadate thin films offer (i) a promising platform for luminescence-based noncontact temperature sensing; (ii) ratiometric/self-referencing absolute measurements; (iii) exceptional repeatability and reversibility for multirun uses and a long life cycle; (iv) 2% K(-1) maximum temperature sensitivity (among the highest recorded for inorganic nanothermometers); (v) a temperature resolution greater than 0.5 K; and (vi) the potential for high-resolution 2D temperature mapping.
RESUMO
Unlike physical patterning of materials at nanometer scale, manipulating soft matter such as biomolecules into patterns is still in its infancy. Self-assembled monolayer (SAM) with surface density gradient has the capability to drive biomolecules in specific directions to create hierarchical and discrete structures. Here, we report on a two-step process of self-assembly of the human serum albumin (HSA) protein into discrete ring structures based on density gradient of SAM. The methodology involves first creating a 2-dimensional (2D) polyethylene glycol (PEG) islands with responsive carboxyl functionalities. Incubation of proteins on such pre-patterned surfaces results in direct self-assembly of protein molecules around PEG islands. Immobilization and adsorption of protein on such structures over time evolve into the self-assembled patterns.