Molecularly Imprinted Polymer (MIP)-Coated Microbeam MEMS Sensor for Chemical Detection

This sensor enables rapid detection and identification of chemical warfare agents and energetic materials.

Monitoring trace gases is of great importance in a wide range of applications. Detecting a diverse range of chemical agents requires an adaptable sensor platform capable of identifying threats before they cause harm. Research and development in hazardous-materials detection technology focuses on increasing speed, sensitivity, and selectivity while reducing size and cost. Although the current state-of-the-art vapor detector (Joint Chemical Agent Detector) is lightweight, handheld, and easily attaches to a belt, it still provides added bulk to a soldier on foot. Recently, microcantilever-based technology has emerged as a viable platform due to its many advantages such as small size, high sensitivity, and low cost. However, microcantilevers lack the inherent ability to selectively identify chemicals of interest. The key to overcoming this challenge is to functionalize the top surface of the microcantilever with a sorbent layer (i.e., polymer) that allows for selective binding between the microbeam and analyte(s) of interest.

A simplified schematic of molecularly imprinted polymer fabrication.

Molecular imprinting involves arranging polymerizable functional monomers around a template, followed by polymerization and template removal (see figure). Arrangement is generally achieved by noncovalent or reversible covalent interactions. In both types of molecular imprinting, once the template is removed, three-dimensional cavities are generated within the final materials that are complementary to the template molecule in size, shape, and functionality. Essentially, one creates a molecular “memory” within the imprinted polymer matrix. This allows preparation of polymers that are selective for the adsorption of the target molecule of interest. Other advantages of this technique include robustness and stability under a wide range of chemical and physical conditions, and an ability to easily design recognition sites for a plethora of target chemicals (e.g., pesticides, energetic materials, pharmaceuticals, and proteins).

The polymer materials of interest are sol-gel-derived xerogels, which have been used as a platform for MIP-based sensor development. These materials are attractive because their physicochemical properties can be adjusted by choice of precursor( s) and the processing protocol. Precursors were chosen based on potential interactions with the explosive 2,4,6-trinitrotoluene (TNT). These specific interactions allow for increased target recognition.

A MIP alone does not meet the requirements for a sensor without some form of a transducer to convert the analyte interaction into a measureable signal. There is evidence of a variety of gravimetrical detection techniques applied to convert a MIP into a “sensor.” Low-mass, highfrequency, and low-cost micro/nano sensors utilizing mass loading of microcantilevers have drawn increasing attention in the area of gravimetric sensing, and MIPs have become an attractive thin film coating for many microelectromechanical systems (MEMS)-based sensors. In this work, molecularly imprinted xerogel thin films have demonstrated selectivity and stability in combination with a fixed-fixed beam MEMS cantilever.

The sensors are fixed-fixed beams of varied lengths and widths. The beam thickness was 2 μm. The values were chosen so that the natural frequencies of the beams were less than half the natural frequency of the shear piezo actuator (330 kHz) used to drive the device. The microbeams were fabricated using a standard silicon on insulator (SOI) process. The SOI wafer used was 2 μm silicon (Si) device layer with 1 μm buried oxide and 520 μm Si handle. First, oxide was grown on both sides of the wafer. Silicon nitride (Si3N4) was deposited on the backside on top of silicon oxide; together they serve as masks to protect the backside for potassium hydroxide (KOH) etch in a later step. After front side oxide removal, it was then spun with photoresist and pattern was transferred. Then a deep reactive-ion etching was used to define the device features. Back side mask features were defined using photolithography and inductively coupled plasma. The front side was spun with a ProTEK® coating to protect features during back side release etch. The back side was opened by anisotropic KOH etch and stopped at the buried oxide. The device was then finished with removal of ProTEK and buried oxide layer.

The work reported here validates the MIP-coated microcantilever sensing concept and demonstrates the feasibility of this MEMS sensor for the detection of explosive compounds and CWAs. To date, this is one of the only demonstrations of a MIP-coated microbeam MEMS sensing platform for these targets. Although preliminary, the data suggests that this combination is an effective and robust chemical nanosensing scheme. Further investigations will focus on refinement of the MIP (i.e., xerogel formulation) for improved selectivity. Finally, the MIPcoated microcantilever sensor platform evaluation should be expanded to include other explosives and chemical warfare agents of interest to the Army. A successful MIP-coated microbeam MEMS sensing format could reduce sensor cost and size, while maintaining the high sensitivity, selectivity, and portability needed for military applications.

This work was done by Ellen L. Holthoff of the Army Research Laboratory and Lily Li, Tobias Hiller, and Kimberly L. Turner of the University of California Santa Barbara. ARL-0191



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Aerospace & Defense Technology Magazine

This article first appeared in the April, 2016 issue of Aerospace & Defense Technology Magazine (Vol. 1 No. 2).

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Overview

The document titled "A Molecularly Imprinted Polymer (MIP)-Coated Microbeam MEMS Sensor for Chemical Detection," authored by Ellen L. Holthoff and collaborators from the US Army Research Laboratory and the University of California Santa Barbara, presents a novel approach to chemical detection using advanced sensor technology. Published in September 2015, this report details the development and experimental validation of a micro-electromechanical systems (MEMS) sensor coated with molecularly imprinted polymers (MIPs).

MIPs are synthetic materials designed to have specific recognition sites for target molecules, allowing for selective binding and detection. The integration of MIPs with MEMS technology enhances the sensitivity and specificity of chemical sensors, making them suitable for various applications, including environmental monitoring, security, and defense.

The report outlines the experimental setup used for gas sensing, providing a simplified diagram to illustrate the methodology. The authors discuss the advantages of using MIP coatings, such as improved selectivity and the ability to detect low concentrations of target analytes. The sensor's design leverages the mechanical properties of microbeams, which can respond to changes in mass or mechanical stress caused by the binding of target molecules.

The findings indicate that the MIP-coated MEMS sensor demonstrates promising performance in detecting specific chemicals, showcasing its potential for real-world applications. The report emphasizes the importance of this technology in enhancing chemical detection capabilities, which is critical for various sectors, including military and civilian safety.

Additionally, the document includes standard disclaimers and notices regarding the findings, ensuring that they are not construed as an official position of the Department of the Army unless specified. The report is approved for public release, allowing for broader dissemination of the research outcomes.

In summary, this document presents a significant advancement in chemical detection technology through the development of a MIP-coated MEMS sensor. The innovative approach combines the specificity of molecular imprinting with the sensitivity of MEMS technology, paving the way for enhanced detection methods in various applications. The research contributes valuable insights into the field of chemical sensing, highlighting the potential for future developments and applications.