A novel and better approach for detecting non-uniformities in the optical properties of two-dimensional (2D) materials could potentially open the door to new uses for these materials, such as for drug detection, according to a team of researchers.

“The Two-Dimensional Crystal Consortium (2DCC) is a world leader in 2D materials research, and my lab often works with the 2DCC doing materials characterization for novel 2D materials,” said Slava Rotkin, professor of engineering science and mechanics with an appointment in the Materials Research Institute at Penn State. “There is a big challenge in these studies: frequently, optical properties of 2D materials are not uniform in space. Furthermore, they may vary at a very small spatial scale, down to a single atom.”

Rotkin and other researchers have now taken a step toward a possible solution to this challenge, as they report in a paper in ACS Nano. While Rotkin stresses that they only gave a demonstration of the principle in the study, the solution they propose was used for van der Waals heterostructures that could form the basis for sensors made with 2D materials.

Identifying and understanding the variability of properties in materials could be extremely important for using 2D materials as sensors. This is because the sensor material can typically only interact with an analyte at its surface. Thus, the material’s surface is an active area, while the material’s volume is not. The larger the ratio of surface to volume, the lower the fraction of material which cannot be used.

Atomically thin 2D materials have the ultimate surface-to-volume ratio for sensor use and may possess surface non-uniformities at the nanometer scale. These include atomic impurities, adsorbates, defects, wrinkles, ruptures, etc. Such features can modulate the optical properties.

"Despite this being critical for effectiveness in certain application of 2D materials, there is currently no truly effective approach to detect these variabilities,” Rotkin said. “Due to their being so tiny, they are undetectable by optical tools and non-optical tools cannot resolve optical contrast.”

The researchers conducted experiments using a heterostructure material made of graphene and the inorganic compound molybdenum disulfide (MoS2). Molybdenum disulfide gives off a photoluminescence signal that reflects the amount of charge transfer between the graphene and molybdenum disulfide layers. This means the heterostructure can detect changes in this charge transfer caused by the presence of an analyte, which in this case was the cancer treatment drug doxorubicin.

These changes are also detectable in graphene via analysis by Raman spectroscopy, which monitors unique vibrations in molecules. A Raman microscope picks up shifts in the frequency of the photons in a laser beam caused by these vibrations.

“The two channels together allow a better calibration of the two signals against analyte concentration and the type of analyte,” Rotkin said. “And additionally, graphene enhances the Raman signal of the analyte itself to the extent one can ‘see’ a signal from just a few molecules.”

The researchers used doxorubicin as their analyte because it is a common cancer drug used in chemotherapy, and there is an acute need for biosensors to detect it to help regulate dosage and reduce side effects. There are two types of biosensors that work for this purpose: label-free biosensors, which can be used to detect a variety of drugs; and label-based biosensors, which can detect only a specific drug. The researchers used label-free biosensing in this study.

“The label-based biosensor is like a lock that can be opened with only one key, but the label-free biosensor is like a lock with many different keys,” Rotkin said. “We did not invent label-free multimodal biosensing, this approach has been in other studies. But an actual demonstration with a specific material is new and still important by itself.”

This advance could help solve various healthcare challenges. “Keeping in mind that there is a gap between fundamental research and its applications, I would say we contributed a brick to building a large set of nanotechnology/nanomaterials for biosensing and other applications,” Rotkin said. “Label-free detection lays the groundwork for smart and integrated sensors, new bio-threat safety techniques and more individualized medicine and treatments, among other benefits.”

The advance is also significant because creating a label-free biosensor is more challenging than developing a label-based biosensor.

"We make it work by merging several sensors in one device, think about the lock and key analogy as three locks on one chain,” Rotkin said “Specifically, we apply the doxorubicin to our 2D material, which produces three different optical signals, constituting a multimodal sensing. By measuring three signals at once instead of just one like in a normal sensor, this allows us to detect doxorubicin using label-free biosensing.”

Along with the biosensing possibilities, there are also more immediate benefits to this research. "This work gives us deeper knowledge of overall optical properties of 2D materials,” Rotkin said. “We uncovered some of the mechanisms for one specific structure, graphene and MoS2. But our nanoimaging method is applicable to many others, if not to all. Also, we hope to attract additional attention to the physics of 2D material heterostructures such as our composite material, which combined the properties of graphene and MoS2 single-layer materials.”

The next steps for this research will include applying the materials component of their work to other projects at the 2DCC and at Penn State’s National Science Foundation Materials Research Science and Engineering Center, the Center for Nanoscale Science. This includes projects involving quantum plasmonics and 2D non-linear optics. In addition, the research team will be looking for partners to explore practical applications.

“Since label-free detection is universal, we are not limited by a type of analyte, application nor problem,” Rotkin said. “Still, there needs to be someone with a real problem to apply the approach. We are looking for collaborators from the world of medicine for some exciting new joint research.”

This story is adapted from material from Penn State, with editorial changes made by Materials Today. The views expressed in this article do not necessarily represent those of Elsevier. Link to original source.

A molecule of the cancer drug doxorubicin (foreground) can be detected using the van der Waals vertical heterostructure biosensor (background). The background shows a nanoscale scattering scanning near-field optical microscopy image of the heterostructure. The large triangle is a single-layer molybdenum disulfide island, the smaller triangle is a partially oxidized MoOS island, and the whole sample is covered with a monolayer of graphene, with several wrinkles clearly seen in the image. The darker graphene area corresponds to a region of extra charge doping. Image: Elizabeth Flores-Gomez Murray/Jennifer McCann/Slava Rotkin, Penn state.
A molecule of the cancer drug doxorubicin (foreground) can be detected using the van der Waals vertical heterostructure biosensor (background). The background shows a nanoscale scattering scanning near-field optical microscopy image of the heterostructure. The large triangle is a single-layer molybdenum disulfide island, the smaller triangle is a partially oxidized MoOS island, and the whole sample is covered with a monolayer of graphene, with several wrinkles clearly seen in the image. The darker graphene area corresponds to a region of extra charge doping. Image: Elizabeth Flores-Gomez Murray/Jennifer McCann/Slava Rotkin, Penn state.