With an integrated resonance exciting heater and a self-sensing piezoresistor, resonant micro-cantilever bio/chemical sensors are optimally designed and fabricated by micromachining techniques. This study is emphasized on the optimization of the integrated heating resistor. Previous research has put the heater at either the cantilever clamp end, the midpoint or the free end. Aiming at sufficiently high and stable resonant amplitude, our research indicates that the optimized location of the thermal-electric exciting resistor is the clamp end instead of other positions. By both theoretical analysis and resonance experiments where three heating resistors are placed at the three locations of the fabricated cantilever, it is clarified that the clamp end heating provides the most efficient resonance excitation in terms of resonant amplitude, Q-factor and resonance stability. Besides, the optimized combination of dc bias and ac voltage is determined by both analysis and experimental verification. With the optimized heating excitation, the resonant cantilever is used for biotin–avidin-specific detection, resulting in a ±0.1 Hz ultra-low noise floor of the frequency signal and a 130 fg mass resolution. In addition to resonance excitation, the heater is used to heat up the cantilever for speed-up desorption after detection that helps rapid and repeated sensing to chemical vapor. The clamp end is determined (by simulation) as the optimal heating location for uniform temperature distribution on the cantilever. Using the resonant cantilever, a rapid and repeated sensing experiment on dimethyl methylphosphonate (DMMP) vapor shows that a short-period heating at the detection interval significantly quickens the signal recovery and enhances the sensing repeatability.

Featuring a huge surface-to-volume ratio, synthesized SBA-15 mesoporous silica is functionalized by inner-channel-wall modification of sensing groups for highly specific chemical-vapor detection at trace level. With the developed sensing material loaded on resonant microcantilevers, the specifically adsorbed chemical-vapor molecules act as an added mass to shift the cantilever resonant frequency for gravimetric sensing signal readout. Two kinds of sensing materials for trinitrotoluene (TNT) and ammonia/amine are respectively prepared by inner-wall layer-by-layer grafting functionalization. By using hexafluoro-2-propanol-functionalized mesoporous silica (HFMS), experimental results show highly specific and rapid detection of TNT vapor, with a ppt-level detection limit; functionalized with a carboxyl (COOH) group, the mesoporous silica is loaded onto the cantilever resonating sensor that experimentally exhibits an ultrafine detection limit of tens of ppb to ammonia/amine gases.

According to the demand for an ultrasensitive mass sensor for bio/chemical molecular detection, resonant cantilever sensors are developed for detection in an air environment. Both a piezoresistive bridge and a metal coil are integrated in the cantilever for signal sensing and Lorentz-force resonance excitation, respectively. Compared with conventional first flexure mode resonance, measurement results for the second mode resonance show an improved mass-sensing resolution from 0.17 pg to 0.06 pg due to the higher quality factor. For further improving the resolution, an optimized electromagnetic excitation method specifically for the second resonant mode is proposed and developed. The optimized method provides a two-point excitation that matches the second mode shape function of the cantilever deflection and excites the second mode more efficiently. Compared to a cantilever with a conventional excitation method, the optimally excited cantilever improves the quality factor from 307 to 857. Based on the experimental results for the optimally excited second mode resonant sensor, 29 × 10−15 g resolution for in-air mass sensing is achieved. The developed second mode resonant cantilever sensor with piezoresistive sensing element integrated on-chip is promising for use in high-performance portable biological/chemical sensing applications.

Composite materials of porous pyrolyzed polyacrylonitrile-sulfur@graphene nanosheet (pPAN-S@GNS) are fabricated through a bottom-up strategy. Microspherical particles are formed by spray drying of a mixed aqueous colloid of PAN nanoparticles and graphene nanosheets, followed by a simple heat treatment with elemental sulfur. The pPAN-S primary nanoparticles are wrapped homogeneously and loosely within a three-dimensional network of graphene nanosheets (GNS). The hierarchical pPAN-S@GNS composite shows a high reversible capacity of 1449.3 mAh g(-1) sulfur or 681.2 mAh g(-1) composite in the second cycle; after 300 cycles at a 0.2 C charge/discharge rate the capacity retention is 88.8 % of its initial reversible value. Additionally, the coulombic efficiency (CE) during cycling is near 100 %, apart from in the first cycle, in which CE is 81.1 %. A remarkable capacity of near 700 mAh g(-1) sulfur is obtained, even at a high discharge rate of 10 C. The superior performance of pPAN-S@GNS is ascribed to the spherical secondary GNS structure that creates an electronically conductive 3D framework and also reinforces structural stability.

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On the basis of microgravimetric sensing data, an analytical modeling method is proposed for comprehensive evaluation and optimization of gas sensing or adsorbing related functional materials. Resonant microcantilever is loaded with the material to be evaluated for a gravimetric sensing experiment. With sensing isotherm curves obtained at different temperatures, key thermodynamic and kinetic parameters of the material, such as enthalpy ΔH°, Gibbs free energy, adsorption rate constant Ka, and coverage θ, etc., can be quantitatively extracted for optimal selection and design. On the basis of the gravimetric experiment, the modeling method is used on three sorts of trimethylamine sensing nanomaterials of mesoporous silica nanoparticles (MSNs). The COOH-functionalized material is clearly identified as the best sensing material among the three similar ones, thereby validating high accuracy of the proposed model. Broad applicability of the modeling method to other sensing materials and/or target gases is also experimentally confirmed, where sensing properties of a functionalized hyper-branched polymer to organophorous simulant of dimethyl methylphosphonate (DMMP) are still evaluated well. In addition to sensing materials, the gravimetric experiment-based modeling method can be expanded to other functional materials like moisture absorbents or detoxification agents. Water adsorbing experiment on KIT-5 mesoporous-silica is modeled, with the low -ΔH° value (i.e., low adsorption heat) result, indicating that the KIT-5 is a good adsorbent to humidity. Alternatively, the modeled high -ΔH° value (i.e., high reaction heat) shows promising usage of SBA-15 mesoporous-silica as detoxification material to hazardous organophorous chemicals. Therefore, the analytical modeling technology can be used for developing and evaluating new adsorbing materials for gas sensing, fixing, and detoxification applications.

We explore the temporal relationship between microwave/HXR emission and Doppler velocity during the impulsive phase of a solar flare on 2014 October 27 (SOL2014-10-27), which displays a pulse on the light curves in microwave (34 GHz) and hard X-ray (HXR, 25−50 keV) bands before the flare maximum. Imaging observation shows that this pulse mainly comes from one footpoint of a solar flare loop. The slit of Interface Region Imaging Spectrograph (IRIS) stays at this footpoint during this solar flare. The Doppler velocities of Fe XXI 1354.09Å and Si IV 1402.77Å are extracted from the Gaussian fitting method. We find that the hot line of Fe XXI 1354.09Å (logT ∼7.05) in corona exhibits blue shift, while the cool line of Si IV 1402.77Å (logT ∼4.8) in transition region exhibits red shift, indicating explosive chromospheric evaporation. The evaporative upflows along the flare loop are also observed in the AIA 131Å image. To our knowledge, this is the first report of chromospheric evaporation evidence from both spectral and imaging observations in the same flare. Both microwave and HXR pulses are well correlated with the Doppler velocities, suggesting that the chromospheric evaporation is driven by nonthermal electrons around this footpoint of a solar flare loop.