Nickolay V. Lavrik

Cantilever transducers as a platform for chemical and biological sensors

Since the late 1980s there have been spectacular developments in micromechanical or microelectro-mechanical (MEMS) systems which have enabled the exploration of transduction modes that involve mechanical energy and are based primarily on mechanical phenomena. As a result an innovative family of chemical and biological sensors has emerged. In this article, we discuss sensors with transducers in a form of cantilevers. While MEMS represents a diverse family of designs, devices with simple cantilever configurations are especially attractive as transducers for chemical and biological sensors. The review deals with four important aspects of cantilever transducers: (i) operation principles and models; (ii) microfabrication; (iii) figures of merit; and (iv) applications of cantilever sensors. We also provide a brief analysis of historical predecessors of the modern cantilever sensors.

Femtogram mass detection using photothermally actuated nanomechanical resonators

Nanomechanical devices with very small mass and size have the potential for mass sensing at the level of individual molecules. In the present study, we designed nanomechanical mass sensors, demonstrated their operation under ambient pressure and temperature, and achieved femtogram-level mass sensitivity. Our nanomechanical resonators were gold-coated silicon cantilevers with resonance frequencies in the range of 1 to 10 MHz, characteristic thicknesses of 50–100 nm, and force constants of about 0.1 N/m. Using a cantilever with a resonant frequency of 2.2 MHz that was excited photothermally, we measured a mass change of 5.5 fg upon chemisorption of 11-mercaptoundecanoic acid. Our analysis indicates that, by decreasing the mass of the cantilever and increasing the excitation amplitude, even higher mass sensitivity can be realized in an easily accessible frequency range (<100 MHz).

Performance of uncooled microcantilever thermal detectors

It has recently been shown that bimaterial microcantilevers can be used as uncooled infrared detectors. Bimaterial microcantilevers deform as their temperature changes due to the absorption of infrared photons. Infrared imaging using uncooled cantilever arrays has already been achieved by a number of groups. In this paper, we examined the performance of microcantilevers as uncooled infrared detectors with optical readout. As in the case of other kinds of uncooled thermal infrared detectors, temperature fluctuation noise and background fluctuation noise are fundamental limits to the performance of microcantilever thermal detectors. Since microcantilevers are mechanical devices, thermo-mechanical noise will also influence their performance. We fabricated a SiNx microcantilever thermal detector with an Al layer in the bimaterial region. For the microcantilever geometry and materials used, the background fluctuation noise equivalent temperature difference, NETDBF, calculated for f/1 optics and a 30 Hz frame r...

High-Performance Field-Effect Transistors Based on Polystyrene-b-Poly(3-hexylthiophene) Diblock Copolymers

Polystyrene-b-poly(3-hexylthiophene) (PS-b-P3HT) block copolymers with fixed PS block length have been synthesized by combined atom transfer radical polymerization (ATRP) and Grignard metathesis (GRIM) polymerization. The self-assembled structures of these diblock copolymer thin films based on PS-b-P3HT have been studied by TEM, SAED, GIXD, AFM, and additionally by first principles modeling and simulation. These block copolymers undergo microphase separation and form nanostructured spheres, lamellae, nanofibers, or nanoribbons in the films dictated by the molecular weight of the P3HT block. Within the diblock copolymer thin film, PS blocks segregate to form amorphous domains, and the covalently bonded conjugated P3HT blocks exist as highly ordered crystalline domains through intermolecular packing with their alkyl side chains aligned normal to the substrate while the thiophene rings align parallel to the substrate through π-π stacking. The conjugated PS-b-P3HT block copolymers exhibited significant improvements in organic field-effect transistor (OFET) performance and environmental stability as compared to P3HT homopolymers, with up to a factor of 2 increase in measured mobility (0.08 cm(2)/(V·s)) for the P4 (85 wt % P3HT). Overall, this work demonstrates that the high degree of molecular order induced by block copolymer phase separation can improve the transport properties and stability of conjugating polymers, which are critical for high-performance OFETs and other organic electronics.

Electrical and thermal conductivity of low temperature CVD graphene: the effect of disorder

In this paper we present a study of graphene produced by chemical vapor deposition (CVD) under different conditions with the main emphasis on correlating the thermal and electrical properties with the degree of disorder. Graphene grown by CVD on Cu and Ni catalysts demonstrates the increasing extent of disorder at low deposition temperatures as revealed by the Raman peak ratio, IG/ID. We relate this ratio to the characteristic domain size, La, and investigate the electrical and thermal conductivity of graphene as a function of La. The electrical resistivity, ρ, measured on graphene samples transferred onto SiO2/Si substrates shows linear correlation with La(-1). The thermal conductivity, K, measured on the same graphene samples suspended on silicon pillars, on the other hand, appears to have a much weaker dependence on La, close to K∼La1/3. It results in an apparent ρ∼K3 correlation between them. Despite the progressively increasing structural disorder in graphene grown at lower temperatures, it shows remarkably high thermal conductivity (10(2)-10(3) W K(-1) m(-1)) and low electrical (10(3)-3×10(5) Ω) resistivities suitable for various applications.

Gold Nano-Structures for Transduction of Biomolecular Interactions into Micrometer Scale Movements

Microfabricated cantilevers, similar to those commonly used in scanning probe microscopies, have recently become increasingly popular as transducers in chemical and biological sensors. Surface stress changes that accompany intermolecular interactions on the cantilever surfaces offer an attractive means to develop new generations of microfabricated sensors and actuators that respond directly to chemical stimuli. In the present study, we demonstrate that interfacial molecular recognition events can be converted into mechanical responses much more efficiently when quasi 3-dimensional interfaces with nano-size features are used. Some of the particularly useful approaches to creating such interfaces are surface immobilization of gold nano-spheres and dealloying of co-evaporated Au:Ag films. Preliminary evaluation of these nanostructured surfaces was performed by measuring mechanical stresses generated by receptor modified nano-structures and smooth gold surfaces in response to gas-phase hydrocarbon compounds. The most efficient chemi-mechanical transduction was achieved when the cantilevers were modified with 50 to 75 nm thick dealloyed gold nanostrutures. Cantilevers of this type were selected for liquid phase experiments. These cantilevers were found to undergo several micron deflections upon adsorption of protein A and biotin-labeled albumin on nanostructured gold surfaces. Additional micrometer scale movements of the cantilevers were observed upon interaction of the surface bound bioreceptors with, respectively, immunoglobulin G and avidin from the aqueous phase.

Nanofabrication of Densely Packed Metal–Polymer Arrays for Surface-Enhanced Raman Spectrometry

A key element to improve the analytical capabilities of surface-enhanced Raman spectroscopy (SERS) resides in the performance characteristics of the SERS-active substrate. Variables such as shape, size, and homogeneous distribution of the metal nanoparticles throughout the substrate surface are important in the design of more analytically sensitive and reliable substrates. Electron-beam lithography (EBL) has emerged as a powerful tool for the systematic fabrication of substrates with periodic nanoscale features. EBL also allows the rational design of nanoscale features that are optimized to the frequency of the Raman laser source. In this work, the efficiency of EBL fabricated substrates are studied by measuring the relative SERS signals of Rhodamine 6G and 1,10-phenanthroline adsorbed on a series of cubic, elliptical, and hexagonal nanopatterned pillars of ma-N 2403 directly coated by physical vapor deposition with 25 nm films of Ag or Au. The raw analyte SERS signals, and signals normalized to metal nanoparticle surface area or numbers of loci, are used to study the effects of nanoparticle morphology on the performance of a rapidly created, diverse collection of substrates. For the excitation wavelength used, the nanoparticle size, geometry, and orientation of the particle primary axis relative to the excitation polarization vector, and particularly the density of nanoparticles, are shown to strongly influence substrate performance. A correlation between the inverse of the magnitude of the laser backscatter passed by the spectrometer and SERS activities of the various substrate patterns is also noted and provides a simple means to evaluate possible efficient coupling of the excitation radiation to localized surface plasmons for Raman enhancement.

Uncooled infrared imaging using bimaterial microcantilever arrays

We report on fabrication and characterization of arrays of bimaterial microcantilevers and discuss their performance as uncooled infrared imagers. An optical readout was used to simultaneously measure deflections of all microcantilevers in the array. The fabricated arrays had an average noise equivalent temperature difference (NETD) and a response time of 1.5K and 6ms, respectively. Some microcantilevers in the array exhibited NETD values below 500mK, approaching our theoretical prediction of 151mK. A unique and valuable feature of the implemented approach is its straightforward scalability to higher resolution arrays, without progressively growing complexity and cost.

IR imaging using uncooled microcantilever detectors

Uncooled bimaterial microcantilever detectors were fabricated and used to obtain infrared (IR) images of objects at temperatures ranging from room temperature to a few hundred degrees C. Images were obtained using both single 50 micro m x 50 micro m microcantilever IR detectors and arrays of microcantilever detectors. Thermal radiation from the target object was imaged onto the detector and the resulting temperature change caused microcantilever bending due to the bimaterial effect. This micromechanical bending was measured using two different non-contact optical readout techniques and IR images were obtained. A smaller size (20 micro m x 20 micro m) microcantilever IR detector was also used to capture IR images of near room temperature objects.

Voltage-Gated Hydrophobic Nanopores

Hydrophobicity is a fundamental property that is responsible for numerous physical and biophysical aspects of molecular interactions in water. Peculiar behavior is expected for water in the vicinity of hydrophobic structures, such as nanopores. Indeed, hydrophobic nanopores can be found in two distinct states, dry and wet, even though the latter is thermodynamically unstable. Transitions between these two states are kinetically hindered in long pores but can be much faster in shorter pores. As it is demonstrated for the first time in this paper, these transitions can be induced by applying a voltage across a membrane with a single hydrophobic nanopore. Such voltage-induced gating in single nanopores can be realized in a reversible manner through electrowetting of inner walls of the nanopores. The resulting I-V curves of such artificial hydrophobic nanopores mimic biological voltage-gated channels.