Charge Transfer Modulation in Vanadium-Doped WS2 /Bi2 O2 Se Heterostructures.

The field of photovoltaics is revolutionized in recent years by the development of two-dimensional (2D) type-II heterostructures. These heterostructures are made up of two different materials with different electronic properties, which allows for the capture of a broader spectrum of solar energy than traditional photovoltaic devices. In this study, the potential of vanadium (V)-doped WS2 is investigated, hereafter labeled V-WS2 , in combination with air-stable Bi2 O2 Se for use in high-performance photovoltaic devices. Various techniques are used to confirm the charge transfer of these heterostructures, including photoluminescence (PL) and Raman spectroscopy, along with Kelvin probe force microscopy (KPFM). The results show that the PL is quenched by 40%, 95%, and 97% for WS2 /Bi2 O2 Se, 0.4 at.% V-WS2 /Bi2 O2 Se, and 2 at.% V-WS2 /Bi2 O2 Se, respectively, indicating a superior charge transfer in V-WS2 /Bi2 O2 Se compared to pristine WS2 /Bi2 O2 Se. The exciton binding energies for WS2 /Bi2 O2 Se, 0.4 at.% V-WS2 /Bi2 O2 Se and 2 at.% V-WS2 /Bi2 O2 Se heterostructures are estimated to be ≈130, 100, and 80 meV, respectively, which is much lower than that for monolayer WS2 . These findings confirm that by incorporating V-doped WS2 , charge transfer in WS2 /Bi2 O2 Se heterostructures can be tuned, providing a novel light-harvesting technique for the development of the next generation of photovoltaic devices based on V-doped transition metal dichalcogenides (TMDCs)/Bi2 O2 Se.

Toward understanding the phase-selective growth mechanism of films and geometrically-shaped flakes of 2D MoTe2.

Two-dimensional (2D) molybdenum ditelluride (MoTe2) is an interesting material for fundamental study and applications, due to its ability to exist in different polymorphs of 2H, 1T, and 1T', their phase change behavior, and unique electronic properties. Although much progress has been made in the growth of high-quality flakes and films of 2H and 1T'-MoTe2 phases, phase-selective growth of all three phases remains a huge challenge, due to the lack of enough information on their growth mechanism. Herein, we present a novel approach to growing films and geometrical-shaped few-layer flakes of 2D 2H-, 1T-, and 1T'-MoTe2 by atmospheric-pressure chemical vapor deposition (APCVD) and present a thorough understanding of the phase-selective growth mechanism by employing the concept of thermodynamics and chemical kinetics involved in the growth processes. Our approach involves optimization of growth parameters and understanding using thermodynamical software, HSC Chemistry. A lattice strain-mediated mechanism has been proposed to explain the phase selective growth of 2D MoTe2, and different chemical kinetics-guided strategies have been developed to grow MoTe2 flakes and films.

Ultrathin Bi2O2S nanosheet near-infrared photodetectors.

Recently, a zipper two-dimensional (2D) material Bi2O2Se belonging to the layered bismuth oxychalcogenide (Bi2O2X: X = S, Se, Te) family, has emerged as an alternate candidate to van der Waals 2D materials for high-performance electronic and optoelectronic applications. This hints towards exploring the other members of the Bi2O2X family for their true potential and bismuth oxysulfide (Bi2O2S) could be the next member for such applications. Here, we demonstrate for the first time, the scalable room-temperature chemical synthesis and near-infrared (NIR) photodetection of ultrathin Bi2O2S nanosheets. The thickness of the freestanding nanosheets was around 2-3 nm with a lateral dimension of ∼80-100 nm. A solution-processed NIR photodetector was fabricated from ultrathin Bi2O2S nanosheets. The photodetector showed high performance, under 785 nm laser illumination, with a photoresponsivity of 4 A W-1, an external quantum efficiency of 630%, and a normalized photocurrent-to-dark-current ratio of 1.3 × 1010 per watt with a fast response time of 100 ms. Taken together, the findings suggest that Bi2O2S nanosheets could be a promising alternative 2D material for next-generation large-area flexible electronic and optoelectronic devices.

Elastic properties and breaking strengths of GaS, GaSe and GaTe nanosheets.

Gallium sulphide (GaS), gallium selenide (GaSe), and gallium telluride (GaTe), belonging to the group-III monochalcogenide family, have shown promising optoelectronic performance over graphene and monolayer molybdenum disulphide (MoS2). However, to date, the mechanical properties of these materials have not been investigated, which hinders their utilisation in flexible electronics and optomechanics. Here, we characterize the elastic properties and breaking strengths of suspended two-dimensional (2D) nanosheets of GaS, GaSe, and GaTe, using atomic force microscopy. The 2D Young's modulus values of ∼10 nm thick GaS, GaSe, and GaTe were found to be 1732 ± 154 N m-1, 819 ± 127 N m-1, and 246 ± 160 N m-1, respectively, corresponding to the three-dimensional (3D) Young's modulus values of 173 ± 15 GPa, 81.9 ± 12.7 GPa, and 24.6 ± 16 GPa, respectively. The pre-tension values of these nanosheets were estimated to be 0.34 ± 0.12 N m-1, 0.14 ± 0.04 N m-1, and 0.15 ± 0.03 N m-1 for GaS, GaSe, and GaTe, respectively. GaS nanosheets exhibited the highest Young's modulus (173 GPa) among these nanosheets, which is comparable to that of WS2 and WSe2. A failure characteristic study over these group-III monochalcogenides revealed that these materials can withstand stresses of up to 8 GPa and a maximal strain of 7% before breaking. Altogether, our findings indicate that GaS, GaSe, and GaTe are attractive candidates for use in stretchable electronic applications and in future optomechanical devices.

High-frequency electromechanical resonators based on thin GaTe.

Gallium telluride (GaTe) is a layered material, which exhibits a direct bandgap (∼1.65 eV) regardless of its thickness and therefore holds great potential for integration as a core element in stretchable optomechanical and optoelectronic devices. Here, we characterize and demonstrate the elastic properties and electromechanical resonators of suspended thin GaTe nanodrums. We used atomic force microscopy to extract the Young's modulus of GaTe (average value ∼39 GPa) and to predict the resonance frequencies of suspended GaTe nanodrums of various geometries. Electromechanical resonators fabricated from suspended GaTe revealed fundamental resonance frequencies in the range of 10-25 MHz, which closely match predicted values. Therefore, this study paves the way for creating a new generation of GaTe based nanoelectromechanical devices with a direct bandgap vibrating element, which can serve as optomechanical sensors and actuators.

Solution-Cast Photoconductive Photodetectors Based on CuInSe2 Nanoparticles.

We, herein, report an eco-friendly low temperature route for the gram-scale synthesis of copper indium selenide nanoparticles. We have also shown the possibility of using CuInSe2 nanoparticles in infrared photodetection by maneuvering the photoconductive property. We rationalize the long-lived trap states to be the cause for the observed photoconductive gain. It is worth noting that the photoresponse time of the device was found to be faster than 0.1 s.

Water activated doping and transport in multilayered germanane crystals.

The synthesis of germanane (GeH) has opened the door for covalently functionalizable 2D materials in electronics. Herein, we demonstrate that GeH can be electronically doped by incorporating stoichiometric equivalents of phosphorus dopant atoms into the CaGe2 precursor. The electronic properties of these doped materials show significant atmospheric sensitivity, and we observe a reduction in resistance by up to three orders of magnitude when doped samples are measured in water-containing atmospheres. This variation in resistance is a result of water activation of the phosphorus dopants. Transport measurements in different contact geometries show a significant anisotropy between in-plane and out-of-plane resistances, with a much larger out-of-plane resistance. These measurements along with finite element modeling results predict that the current distribution in top-contacted crystals is restricted to only the topmost, water activated crystal layers. Taken together, these results pave the way for future electronic and optoelectronic applications utilizing group IV graphane analogues.

Li intercalation into 1D TiS2(en) chains.

The intercalation of metal cations in 2D layered materials allows for the discovery of unique electronic, magnetic and correlated properties. We demonstrate that reversible Li intercalation is also achievable in the hybrid organic/inorganic dimensionally reduced 1D van der Waals solid TiS2(ethylenediamine). Upon intercalation, electrons are injected into the lattice as Ti(4+) is reduced to Ti(3+) leading to an order of magnitude decrease in electrical resistivity. This reversible intercalation process opens up new opportunities to fine-tune the physical properties in this emerging family of dimensionally reduced materials.

Infrared photodetectors based on reduced graphene oxide and graphene nanoribbons.

The use of reduced graphene oxide (RGO) and graphene nanoribbons (GNRs) as infrared photodetectors is explored, based on recent results dealing with solar cells, light-emitting devices, photodetectors, and ultrafast lasers. IR detection is demonstrated by both RGO and GNRs in terms of the time-resolved photocurrent and photoresponse. The responsivity of the detectors and their functioning are presented.

Negative differential resistance in GaN nanocrystals above room temperature.

Negative differential resistance (NDR) has been observed for the first time above room temperature in gallium nitride nanocrystals synthesized by a simple chemical route. Current-voltage characteristics have been used to investigate this effect through a metal-semiconductor-metal (M-S-M) configuration on SiO2. The NDR effect is reversible and reproducible through many cycles. The threshold voltage is approximately 7 V above room temperature.