Jasmine Sinha

Label-free brain injury biomarker detection based on highly sensitive large area organic thin film transistor with hybrid coupling layer

We describe a sensitive, large-area thin film transistor (TFT) sensor platform for real time detection of low-concentration protein analytes in solution. The sensing area is 7 mm by 7 mm. p-channel (pentacene) and n-channel (a naphthalenetetracarboxylic diimide, NTCDI) organic molecules were each used as semiconductors in conjunction with a newly designed receptor–antibody-functionalized top dielectric layer. This layer, incorporating both a fluorinated polymer and vapor-deposited hydrocarbon, provided maximum capacitive coupling and minimal interference from the aqueous analyte solution, and allowed convenient solvent processing of the antibody coupling layer. Additionally, a new antibody immobilization method was introduced, which led to high immobilization yield and surface coverage. Using glial fibrillary acidic protein (GFAP) as a model protein analyte, this sensor platform demonstrated significant selectivity and recognition of target protein even in much more concentrated non-target protein backgrounds. The dose–response relationship yielded a Langmuir isotherm from which a reasonable affinity constant was calculated for the protein and antibody. A zeta potential measurement provided further evidence of the surface potential change being detected by the TFTs. We explicitly verified for the first time that the response is in fact predominantly from perturbations of TFT channel current. To the best of our knowledge, this is the most sensitive organic TFT (OTFT) protein sensor yet reported, and also the first demonstration of the expected opposite current responses by p- and n-channel semiconductors to the same protein.

Design, synthesis, and static charge tuning of organic semiconductors for sensing applications

Organic and polymeric semiconductors are among the alternatives to silicon being considered for sensing devices and circuitry. Their synthesis is now well established, and some performance metrics such as charge carrier mobility and optoelectronic quantum yield exceed those of inorganic counterparts such as amorphous silicon. The best fit for organic semiconductors is in applications where inherent capabilities such as rational modification of carrier energy levels and covalent connection between charge channels and surface receptors are leveraged. This presentation will describe newly synthesized organic molecular solids and polymer films where these attributes are emphasized. For example, addition of a borane to a semiconductor enhances response to ammonia, and introduction of highly electron donating tetrathiafulvalenes into moderately electron-rich polymers enhances response to electron-poor analytes (for example, TNT), for the development of chemical sensors. Carrier energy levels are markedly and predictably altered by static charge embedded in polystyrene films adjacent to organic semiconductors, for multiple device activities to be obtained from a single device layout using one semiconductor, and also the avoidance of powering gate electrodes to set optimal sensor sensitivities during operation.

A Handheld Explosives Detector Based on Amplifying Fluorescent Polymer

Explosive detection has become more relevant today due to increased threats of terrorist activities and chemical warfare. In this context, amplifying fluorescent polymers, AFPs, provide an attractive platform as they are easy to synthesize and exhibit a high fluorescence quantum yield in solid state which is beneficial for a handheld detector. Furthermore, the easy functionalizing of AFPs allows one to introduce various receptors to broaden the scope of detection. The introduction of a “click”able pendant group in AFP enables one to design and develop various biomedical and chemical sensors based on the guest–host chemistry.