My research interests are in the fundamental studies of atomically thin two-dimensional transition metal dichalcogenides (TMDs). In particular, we study the electronic and electrochemical properties of 2D TMDs. This involves synthesis by chemical exfoliation or chemical vapor deposition, characterization using advanced analytical techniques and fabrication of nanoscale devices. We also study phase transformations in monolayered materials and utilization of phases with disparate properties for catalysis and energy storage.
In state of the art short-channel FETs, leakage current leads to power dissipation in the OFF state due poor gate electrostatics. In FETs with 2D semiconductors, charge carriers are confined within atomically thin channels and hence are uniformly influenced by the gate voltage – giving rise to excellent gate electrostatics so that OFF state current is reduced. Contact resistance, however, is a major concern for FETs with 2D semiconductors. The aim of this research is to understand how ultra-clean electrical contacts on 2D semiconductors can be realized and how the work function can be engineered to facilitate both electron and hole injection.
We have pioneered microelectrochemical cells that allow precise identification of catalytically active sites. We can accurately quantify the catalytic activity from edge sites or the basal plane for the hydrogen & oxygen evolution reactions as well as oxygen, CO2 and N2 reduction reactions. We can lithographically pattern devices so that only specific regions of the catalyst material (e.g. edge or basal plane) with well-defined number of atoms are exposed to the electrolyte. Thus, we can accurately quantify the activity of edge sites or the basal plane and because we know the exact area of the patterned electrocatalytically active region, it is possible to precisely extract fundamental parameters such as the exchange current density, the turnover frequency, and Tafel slopes for atomic active sites. We can only use this technique to make micro-batteries on a chip to study electro-chemo-mechanical changes that occur on the electrodes during charging and discharging.
Metallic 2D materials have recently emerged as a class of potentially inexpensive catalysts with enhanced activity and increased stability. However, their overall activity relative to state-of-the art noble metal catalysts is limited by slower reaction kinetics and high charge transfer resistance. Our group’s seminal work several years ago revealed that these factors can be mitigated by metallic 2D materials. In subsequent works, we have shown that increasing the metallic phase concentration and lowering the electrical resistance between the support and catalyst nanoparticles can lead to substantial improvement in catalytic performance. An example of this is metallic NbS2 where it is possible to achieve very high current densities (several Amps-cm-2) in proof of concept electrolyzer devices for electrocatalytically generating hydrogen. We expect metallic nanosheets to be exceptionally good catalysts for the HER or CO2RR and N2RR. We are therefore investigating the properties of 2D materials towards CO2 reduction and the hydrogen evolution reactions to identify the best candidates for both reactions.