Search for: All records

Abstract Tomonaga-Luttinger liquid (TLL) behavior in one-dimensional systems has been predicted and shown to occur at semiconductor-to-metal transitions within two-dimensional materials. Reports of one-dimensional defects hosting a Fermi liquid or a TLL have suggested a dependence on the underlying substrate, however, unveiling the physical details of electronic contributions from the substrate require cross-correlative investigation. Here, we study TLL formation within defectively engineered WS₂atop graphene, where band structure and the atomic environment is visualized with nano angle-resolved photoelectron spectroscopy, scanning tunneling microscopy and spectroscopy, and non-contact atomic force microscopy. Correlations between the local density of states and electronic band dispersion elucidated the electron transfer from graphene into a TLL hosted by one-dimensional metal (1DM) defects. It appears that the vertical heterostructure with graphene and the induced charge transfer from graphene into the 1DM is critical for the formation of a TLL. 

W e present a scalable solution-processing method for fabricating high-quality graphene and graphene/1T-MoS 2 heterostructure films. The process begins with the synthesis of potassium-intercalated graphite (KC 8 ), which is exfoliated in tetrahydrofuran (THF) to produce stable dispersions of negatively charged (electron rich) graphene sheets. The graphene is subsequently transferred to water, forming a surfactant-free aqueous dispersion suitable for creating homogenous graphene films via vacuum filtration and stamping. Additionally, graphene is combined with 1T-MoS 2 nanosheets to fabricate graphene/1T-MoS 2 bulk heterostructure films. Comprehensive characterization, including X-ray diffraction (XRD), absorption spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy ( TEM), Raman spectroscopy, and X-ray photon emission spectroscopy (XPS), reveals that the heterostructure films exhibit enhanced optical and electronic properties, including improved light absorption, which could lead to novel photo-responsive devices. Raman spectroscopy shows significant changes in the graphene’s structural a nd electronic properties upon interaction with MoS 2 , indicating strong interlayer coupling and potential charge transfer between the layered components. The g raphene films demonstrate highly sensitive detection of dopamine (DA), while the graphene/1T-MoS 2 b ulk heterostructure films exhibit capacitance values up to 3 8.3 Fg − 1 at 5 mV/s in non-aqueous electrolytes. These results highlight the potential of these films for advanced applications in molecular sensing and energy storage. 

Thin conducting films are distinct from bulk materials and have become prevalent over the past decades as they possess unique physical, electrical, optical, and mechanical characteristics. Comprehending these essential properties for developing novel materials with tailored features for various applications is very important. Research on these conductive thin films provides us insights into the fundamental principles, behavior at different dimensions, interface phenomena, etc. This study comprehensively analyzes the intricacies of numerous commonly used thin conducting films, covering from the fundamentals to their advanced preparation methods. Moreover, the article discusses the impact of different parameters on those thin conducting films’ electronic and optical properties. Finally, the recent future trends along with challenges are also highlighted to address the direction the field is heading towards. It is imperative to review the study to gain insight into the future development and advancing materials science, thus extending innovation and addressing vital challenges in diverse technological domains. 

Early virus identification is a key component of both patient treatment and epidemiological monitoring. In the case of influenza A virus infections, where the detection of subtypes associated with bird flu in humans could lead to a pandemic, rapid subtype-level identification is important. Surface-enhanced Raman spectroscopy coupled with machine learning can be used to rapidly detect and identify viruses in a label-free manner. As there is a range of available excitation wavelengths for performing Raman spectroscopy, we must choose the best one to permit discrimination between highly similar subtypes of a virus. We show that the spectra produced by influenza A subtypes H1N1 and H3N2 exhibit a higher degree of dissimilarity when using 785 nm excitation wavelength in comparison with 532 nm excitation wavelength. Furthermore, the cross-validated area under the curve (AUC) for identification was higher for the 785 nm excitation, reaching 0.95 as compared to 0.86 for 532 nm. Ultimately, this study suggests that exciting with a 785 nm wavelength is better able to differentiate two closely related influenza viruses and likely can extend to other closely related pathogens. 

C–H bond activation enables the facile synthesis of new chemicals. While C–H activation in short-chain alkanes has been widely investigated, it remains largely unexplored for long-chain organic molecules. Here, we report light-driven C–H activation in complex organic materials mediated by 2D transition metal dichalcogenides (TMDCs) and the resultant solid-state synthesis of luminescent carbon dots in a spatially-resolved fashion. We unravel the efficient H adsorption and a lowered energy barrier of C–C coupling mediated by 2D TMDCs to promote C–H activation and carbon dots synthesis. Our results shed light on 2D materials for C–H activation in organic compounds for applications in organic chemistry, environmental remediation, and photonic materials. 

C–H bond activation enables the facile synthesis of new chemicals. While C–H activation in short-chain alkanes has been widely investigated, it remains largely unexplored for long-chain organic molecules. Here, we report light-driven C–H activation in complex organic materials mediated by 2D transition metal dichalcogenides (TMDCs) and the resultant solid-state synthesis of luminescent carbon dots in a spatially-resolved fashion. We unravel the efficient H adsorption and a lowered energy barrier of C–C coupling mediated by 2D TMDCs to promote C–H activation and carbon dots synthesis. Our results shed light on 2D materials for C–H activation in organic compounds for applications in organic chemistry, environmental remediation, and photonic materials.