Hemi Qu

Detection of Volatile Organic Compounds Using Microfabricated Resonator Array Functionalized with Supramolecular Monolayers

This paper describes the detection of volatile organic compounds (VOCs) using an e-nose type integrated microfabricated sensor array, in which each resonator is coated with different supramolecular monolayers: p-tert-butyl calix[8]arene (Calix[8]arene), 2,3,7,8,12,13,17,18-octaethyl-21H,23H-porphine (Porphyrin), β-cyclodextrin (β-CD), and cucurbit[8]uril (CB[8]). Supramolecular monolayers fabricated by Langmuir-Blodgett techniques work as specific sensing interface for different VOCs recognition which increase the sensor selectivity. Microfabricated ultrahigh working frequency film bulk acoustic resonator (FBAR) transducers (4.4 GHz) enable their high sensitivity toward monolayer gas sensing which facilitate the analyses of VOCs adsorption isotherms and kinetics. Two affinity constants (K1, K2) are obtained for each VOC, which indicate the gas molecule adsorption happen inside and outside of the supramolecular cavities. Additional kinetic information on adsorption and desorption rate constants (ka, kd) are obtained as well from exponential fitting results. The five parameters, one from the conventional frequency shift signals of mass transducers and the other four from the indirect analyses of monolayer adsorption behaviors, thus enrich the sensing matrix (Δf, K1, K2, ka, kd) which can be used as multiparameter fingerprint patterns for highly selective detection and discrimination of VOCs.

Detection of Volatile Organic Compounds by Self-assembled Monolayer Coated Sensor Array with Concentration-independent Fingerprints.

In this paper, we have modeled and analyzed affinities and kinetics of volatile organic compounds (VOCs) adsorption (and desorption) on various surface chemical groups using multiple self-assembled monolayers (SAMs) functionalized film bulk acoustic resonator (FBAR) array. The high-frequency and micro-scale resonator provides improved sensitivity in the detections of VOCs at trace levels. With the study of affinities and kinetics, three concentration-independent intrinsic parameters (monolayer adsorption capacity, adsorption energy constant and desorption rate) of gas-surface interactions are obtained to contribute to a multi-parameter fingerprint library of VOC analytes. Effects of functional group’s properties on gas-surface interactions are also discussed. The proposed sensor array with concentration-independent fingerprint library shows potential as a portable electronic nose (e-nose) system for VOCs discrimination and gas-sensitive materials selections.

Tuning the Resonant Frequency of Resonators Using Molecular Surface Self-assembly Approach

In this work, a new method to tune the resonant frequency of microfabricated resonator using molecular layer-by-layer (LbL) self-assembly approach is demonstrated. By simply controlling the polymer concentration and the number of layers deposited, precisely tuning the frequency of microfabricated resonators is realized. Due to its selective deposition through specific molecular recognitions, such technique avoids the high-cost and complex steps of conventional semiconductor fabrications and is able to tune individual diced device. Briefly, film bulk acoustic resonator (FBAR) is used to demonstrate the tuning process and two types of LbL deposition methods are compared. The film thickness and morphology have been characterized by UV-vis reflection spectra, ellipsometer and AFM. As a result, the maximum resonant frequency shift of FBAR reaches more than 20 MHz, meaning 1.4% tunability at least. The minimum frequency shift is nearly 10 kHZ per bilayer, indicating 7 ppm tuning resolution. Pressure cooker test (PCT) is performed to evaluate the reliability of LbL coated FBAR. Furthermore, applications for wireless broadband communication and chemical sensors of LbL coated FBAR have been demonstrated.

Localized ultrahigh frequency acoustic fields induced micro-vortices for submilliseconds microfluidic mixing

We present an acoustic microfluidic mixing approach via acousto-mechanically induced micro-vortices sustained by localized ultrahigh frequency (UHF) acoustic fields. A micro-fabricated solid-mounted thin-film piezoelectric resonator (SMR) with a frequency of 1.54 GHz has been integrated into microfluidic systems. Experimental and simulation results show that UHF-SMR triggers strong acoustic field gradients to produce efficient and highly localized acoustic streaming vortices, providing a powerful source for microfluidic mixing. Homogeneous mixing with 87% mixing efficiency at a Peclet number of 35520 within 1 ms has been achieved. The proposed strategy shows a great potential for microfluidic mixing and enhanced molecule transportation in minimized analytical systems.

Smartphone-Enabled Colorimetric Trinitrotoluene Detection Using Amine-Trapped Polydimethylsiloxane Membranes

A smartphone-enabled platform for easy and portably colorimetric analysis of 2,4,6-trinitrotoluene (TNT) using amine-trapped PDMS is designed and implemented. The amine-trapped polydimethylsiloxane (PDMS) is simply prepared by immersing the cured PDMS in aminosilane solutions forming an amine-containing polymer. After contacting with TNT-containing solutions, the colorless PDMS showed a rapid colorimetric change which can be easily identified by the naked eye. The amine-trapped PDMS was carefully optimized to achieve visible detection of TNT at concentrations as low as 1 μM. Using an integrated camera in the smartphone, pictures of colored PDMS membranes can be analyzed by a home-developed mobile application. Thus, the TNT amount can be precisely quantified. Direct TNT detection in real samples (e.g., drinking, tap, and lake waters) is demonstrated as well. The smartphone-enabled colorimetric method using amine-trapped PDMS membranes realizes a convenient and efficient approach toward a portable system for field TNT detections.

Conductive polymer nanowire gas sensor fabricated by nanoscale soft lithography

Resistive devices composed of one-dimensional nanostructures are promising candidates for the next generation of gas sensors. However, the large-scale fabrication of nanowires is still challenging, which restricts the commercialization of such devices. Here, we report a highly efficient and facile approach to fabricating poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) nanowire chemiresistive gas sensors by nanoscale soft lithography. Well-defined sub-100 nm nanowires are fabricated on silicon substrate, which facilitates device integration. The nanowire chemiresistive gas sensor is demonstrated for NH3 and NO2 detection at room temperature and shows a limit of detection at ppb level, which is compatible with nanoscale PEDOT:PSS gas sensors fabricated with the conventional lithography technique. In comparison with PEDOT:PSS thin-film gas sensors, the nanowire gas sensor exhibits higher sensitivity and a much faster response to gas molecules.

Detection of volatile organic compunds by high-Q piezotransduced single-crystal silicon bulk acoustic resonator arrays

This paper demonstrates a novel electronic nose (e-nose) system for volatile organic compounds (VOCs) detections which is composed of three high-Q piezotransduced single-crystal silicon bulk acoustic resonators (PSBARs) and functionalized with different self-assembled monolayers (SAMs). The different sensitivities of the PSBARs to VOCs are utilized to constitute unique identification codes for IPA, ethanol, hexane and heptane detections, and successfully realizing discriminations of different VOCs. Besides, ethanol vapor with concentration as low as 50 ppm has been successfully measured by SAM modified PSBAR.

VOC detection using multimode E-nose composed of bulk acoustic wave resonator and silicon nanowire field effect transistor array

Electronic nose (e-nose) is a useful tool for gas detection in environment monitoring, food industry and medical diagnosing. It utilizes sensor arrays to generate recognition pattern in identifying odor or specific analyte. Here a novel multimode e-nose is demonstrated for the detection of volatile organic compounds (VOCs) by integrating both gravimetric-sensitive sensor and electric-sensitive sensor. In this system, film bulk acoustic resonator (FBAR) is used to gain mass related information and silicon nanowire field effect transistor (Si-NW FET) to collect electrical related information for the analytes. The electronic nose is applied to discriminate the ethanol-hexane mixture and the concentration of each gas can be successfully calculated by simple math without using complex mathematic model. The hybrid e-nose system shows potential for the analysis of VOC mixture in the future.

Dual-Mode Gas Sensor Composed of a Silicon Nanoribbon Field Effect Transistor and a Bulk Acoustic Wave Resonator: A Case Study in Freons

In this paper, we develop a novel dual-mode gas sensor system which comprises a silicon nanoribbon field effect transistor (Si-NR FET) and a film bulk acoustic resonator (FBAR). We investigate their sensing characteristics using polar and nonpolar organic compounds, and demonstrate that polarity has a significant effect on the response of the Si-NR FET sensor, and only a minor effect on the FBAR sensor. In this dual-mode system, qualitative discrimination can be achieved by analyzing polarity with the Si-NR FET and quantitative concentration information can be obtained using a polymer-coated FBAR with a detection limit at the ppm level. The complementary performance of the sensing elements provides higher analytical efficiency. Additionally, a dual mixture of two types of freons (CFC-113 and HCFC-141b) is further analyzed with the dual-mode gas sensor. Owing to the small size and complementary metal-oxide semiconductor (CMOS)-compatibility of the system, the dual-mode gas sensor shows potential as a portable integrated sensing system for the analysis of gas mixtures in the future.

A chemiresistive sensor array from conductive polymer nanowires fabricated by nanoscale soft lithography

One-dimensional organic nanostructures are essential building blocks for high performance gas sensors. Constructing an e-nose type sensor array is the current golden standard in developing portable systems for the detection of gas mixtures. However, facile fabrication of nanoscale sensor arrays is still challenging due to the high cost of the conventional nanofabrication techniques. In this work, we fabricate a chemiresistive gas sensor array composed of well-ordered sub-100 nm wide conducting polymer nanowires using cost-effective nanoscale soft lithography. Poly(3,4-ethylene-dioxythiophene)-poly(styrene sulfonate) (PEDOT:PSS) nanowires functionalized with different self-assembled monolayers (SAMs) are capable of identifying volatile organic compounds (VOCs) at a low concentration range. The side chains and functional groups of the SAMs introduce different sensitivities and selectivities to the targeted analytes. The distinct response pattern of each chemical is subjected to pattern recognition protocols, which leads to a clear separation towards ten VOCs, including ketones, alcohols, alkanes, aromatics and amines. These results of the chemiresistive gas sensor array demonstrate that nanoscale soft lithography is a reliable approach for fabricating nanoscale devices and has the potential of mass producibility.