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Local laser‐induced oxidation is an extremely valuable technique to perform high‐throughput optimization across multidimensional parameter sets. In this work, a versatile method is presented for the synthesis of titanium dioxide (TiO₂) thin‐films with varying crystalline structures through the use of localized, visible, continuous‐wave laser‐processing. By controlling the laser intensity and the exposure time, the conversion of amorphous titanium disulfide (a‐TiS₂) precursor films into distinct phases of TiO₂is achieved and a laser‐induced oxidation phase diagram is constructed with the resulting material phases, including anatase, rutile, and black TiO₂. By utilizing the dependence of phase formation on the rate and duration of laser energy input, mixtures of anatase and rutile phases are fabricated with controlled spatial arrangements. Photocatalytic properties of the synthesized films are evaluated using the degradation of nitrogen oxide (NO_x) gas under UV illumination and an organic dye under white‐light illumination, revealing that mixtures of anatase and rutile phases demonstrate superior photocatalytic activity. The laser‐induced oxidation method highlighted showcases a strategy for precisely tailored phase composition for directly tunable properties, paving the way for in‐depth studies into structure‐property relationships in photocatalysis and other applications of metal oxide films.

 

Developing characterization strategies to better understand nanoscale features in two-dimensional nanomaterials is of crucial importance, as the properties of these materials are many times driven by nanoscale and microscale chemical and structural modifications within the material. For the case of large area monolayer MoSe₂flakes, kelvin probe force microscopy coupled with tip-enhanced photoluminescence was utilized to evaluate such features including internal grain boundaries, edge effects, bilayer contributions, and effects of oxidation/aging, many of which are invisible to topographical mapping. A reduction in surface potential due ton-type behavior was observed at the edge of the flakes as well as near grain boundaries. Potential phase mapping, which corresponds to the local dielectric constant, depicted local biexciton and trion states in optically-active regions of interest such as grain boundaries. Finally, nanoscale surface potential and photoluminescence mapping was performed at several stages of oxidation, revealing that various oxidative states can be evaluated during the aging process. Importantly, all of the characterization performed in this study was non-destructive and rapid, crucial for quality evaluation of an exciting class of two-dimensional nanomaterials.

 

Low temperature synthesis of high quality two-dimensional (2D) materials directly on flexible substrates remains a fundamental limitation towards scalable realization of robust flexible electronics possessing the unique physical properties of atomically thin structures. Herein, we describe room temperature sputtering of uniform, stoichiometric amorphous MoS 2 and subsequent large area (>6.25 cm 2 ) photonic crystallization of 5 nm 2H-MoS 2 films in air to enable direct, scalable fabrication of ultrathin 2D photodetectors on stretchable polydimethylsiloxane (PDMS) substrates. The lateral photodetector devices demonstrate an average responsivity of 2.52 μW A −1 and a minimum response time of 120 ms under 515.6 nm illumination. Additionally, the surface wrinkled, or buckled, PDMS substrate with conformal MoS 2 retained the photoconductive behavior at tensile strains as high as 5.72% and over 1000 stretching cycles. The results indicate that the photonic crystallization method provides a significant advancement in incorporating high quality semiconducting 2D materials applied directly on polymer substrates for wearable and flexible electronic systems. 

Metamaterials and metasurfaces operating in the visible and near‐infrared (NIR) offer a promising route towards next‐generation photodetectors and devices for solar energy harvesting. While numerous metamaterials and metasurfaces using metals and semiconductors have been demonstrated, semimetals‐based metasurfaces in the vis‐NIR range are notably missing. This work experimentally demonstrates a broadband metasurface superabsorber based on large area, semimetallic, van der Waals platinum diselenide (PtSe₂) thin films in agreement with electromagnetic simulations. The results show that PtSe₂is an ultrathin and scalable semimetal that concurrently possesses high index and high extinction across the vis‐NIR range. Consequently, the thin‐film PtSe₂on a reflector separated by a dielectric spacer can absorb >85% for the unpatterned case and ≈97% for the optimized 2D metasurface in the 400–900 nm range making it one of the strongest and thinnest broadband perfect absorbers to date. The results present a scalable approach to photodetection and solar energy harvesting, demonstrating the practical utility of high index, high extinction semimetals for nanoscale optics.

 

Chemical sensors based on solution‐processed 2D nanomaterials represent an extremely attractive approach toward scalable and low‐cost devices. Through the implementation of real‐time impedance spectroscopy and development of a three‐element circuit model, redox exfoliated MoS₂nanoflakes demonstrate an ultrasensitive empirical detection limit of NO₂gas at 1 ppb, with an extrapolated ultimate detection limit approaching 63 ppt. This sensor construct reveals a more than three orders of magnitude improvement from conventional direct current sensing approaches as the traditionally dominant interflake interactions are bypassed in favor of selectively extracting intraflake doping effects. This same approach allows for an all solution‐processed, flexible 2D sensor to be fabricated on a polyimide substrate using a combination of graphene contacts and drop‐casted MoS₂nanoflakes, exhibiting similar sensitivity limits. Finally, a thermal annealing strategy is used to explore the tunability of the nanoflake interactions and subsequent circuit model fit, with a demonstrated sensitivity improvement of 2× with thermal annealing at 200 °C.