Molybdenite Biosensor Outperforms Graphene

Monday, September 8, 2014

Molybdenite Biosensor Outperforms Graphene

 Biosensors
Researchers have demonstrated an atomically thin, ultrasensitive and scalable molybdenum disulfide field-effect transistor based biosensor and established their potential to detect single molecules.




An atomically thin, two-dimensional, ultrasensitive semiconductor material for biosensing developed by researchers at UC Santa Barbara promises to push the boundaries of biosensing technology in many fields, from health care to environmental protection to forensic industries.

Based on molybdenum disulfide or molybdenite (MoS2), the biosensor material — used commonly as a dry lubricant — surpasses graphene’s already high sensitivity, offers better scalability and lends itself to high-volume manufacturing. Results of the researchers’ study have been published in ACS Nano.

“This invention has established the foundation for a new generation of ultrasensitive and low-cost biosensors that can eventually allow single-molecule detection — the holy grail of diagnostics and bioengineering research,” said Samir Mitragotri, co-author and professor of chemical engineering and director of the Center for Bioengineering at UCSB. “Detection and diagnostics are a key area of bioengineering research at UCSB and this study represents an excellent example of UCSB’s multifaceted competencies in this exciting field.”

The MoS2 biosensors demonstrated by the UCSB team have already provided ultrasensitive and specific protein sensing with a sensitivity of 196 even at 100 femtomolar (a billionth of a millionth of a mole) concentrations.


The key, according to UCSB professor of electrical and computer engineering Kaustav Banerjee, who led this research, is MoS2’s band gap, the characteristic of a material that determines its electrical conductivity.

Semiconductor materials have a small but nonzero band gap and can be switched between conductive and insulated states controllably. The larger the band gap, the better its ability to switch states and to insulate leakage current in an insulated state. MoS2’s wide band gap allows current to travel but also prevents leakage and results in more sensitive and accurate readings.

While graphene has attracted wide interest as a biosensor due to its two-dimensional nature that allows excellent electrostatic control of the transistor channel by the gate, and high surface-to-volume ratio, the sensitivity of a graphene field-effect transistor (FET) biosensor is fundamentally restricted by the zero band gap of graphene that results in increased leakage current, leading to reduced sensitivity, explained Banerjee, who is also the director of the Nanoelectronics Research Lab at UCSB.

Graphene’s performance is limited by its zero band gap. Electrons travel freely across a graphene FET — hence, it cannot be “switched off” — which in this case results in current leakages and higher potential for inaccuracies.  Research in the graphene community has been devoted to compensating for this deficiency, either by patterning graphene to make nanoribbons or by introducing defects in the graphene layer — or using bilayer graphene stacked in a certain pattern that allows band gap opening upon application of a vertical electric field — for better control and detection of current.

Molybdenite overcomes these shortcomings.

Enter MoS2, a material already making waves in the semiconductor world for the similarities it shares with graphene, including its atomically thin hexagonal structure, and planar nature, as well as what it can do that graphene can’t: act like a semiconductor.

"This transformative technology enables highly specific, low-power, high-throughput physiological sensing that can be multiplexed to detect a number of significant, disease-specific factors in real time."


“Monolayer or few-layer MoS2 have a key advantage over graphene for designing an FET biosensor: They have a relatively large and uniform band gap (1.2-1.8 eV, depending on the number of layers) that significantly reduces the leakage current and increases the abruptness of the turn-on behavior of the FETs, thereby increasing the sensitivity of the biosensor,” said Banerjee.

Additionally, according to Deblina Sarkar, a PhD student in Banerjee’s lab and the lead author of the article, two-dimensional MoS2 is relatively simple to manufacture.

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“While one-dimensional materials such as carbon nanotubes and nanowires also allow excellent electrostatics and at the same time possess band gap, they are not suitable for low-cost mass production due to their process complexities,” she said. “Moreover, the channel length of MoS2 FET biosensor can be scaled down to the dimensions similar to those of small biomolecules such as DNA or small proteins, still maintaining good electrostatics, which can lead to high sensitivity even for detection of single quanta of these biomolecular species,” she added.

“In fact, atomically thin MoS2 provides the best of everything: great electrostatics due to their ultra-thin body, scalability (due to large band gap), as well as patternability due to their planar nature that is essential for high-volume manufacturing,” said Banerjee.

The MoS2 biosensors demonstrated by the UCSB team have already provided ultrasensitive and specific protein sensing with a sensitivity of 196 even at 100 femtomolar (a billionth of a millionth of a mole) concentrations. This protein concentration is similar to one drop of milk dissolved in a hundred tons of water. An MoS2-based pH sensor achieving sensitivity as high as 713 for a pH change by one unit along with efficient operation over a wide pH range (3-9) is also demonstrated in the same work.

“This transformative technology enables highly specific, low-power, high-throughput physiological sensing that can be multiplexed to detect a number of significant, disease-specific factors in real time,” commented Scott Hammond, executive director of UCSB’s Translational Medicine Research Laboratories.

Biosensors based on conventional FETs have been gaining momentum as a viable technology for the medical, forensic and security industries since they are cost-effective compared to optical detection procedures. Such biosensors allow for scalability and label-free detection of biomolecules — removing the step and expense of labeling target molecules with florescent dye. “In essence,” continued Hammond, “the promise of true evidence-based, personalized medicine is finally becoming reality.”



SOURCE  University of California Santa Barbara 

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