The isolation of thermodynamically stable, free standing materials with single to few atom thicknesses has brought about a revolution in materials science, condensed matter physics and device engineering for opto-electronic applications. These two dimensional (2D) materials cover a broad range of electronic properties ranging from zero-band gap, semi-metallic graphene to wide band gap semiconductors in sulfides and selenides of Mo and W to metallic behavior in Ti, Nb and Ta sulfides and selenides. This permits their potential application in opto-electronic devices from terahertz frequencies up to the ultraviolet portion of the spectrum. However, their atomically thin nature poses fundamental challenges in driving efficient light-matter interactions. A range of strategies have been explored from the area of photonics and resonant optics that enhance the coupling and interaction of light with atomically thin layers to overcome this challenge. By comparing and contrasting critical advantages of integrating nanophotonic elements with 2D materials, this review highlights the challenges and advantages of such opto-electronic devices.
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http://dx.doi.org/10.1039/c8cs00206a | DOI Listing |
Angew Chem Int Ed Engl
January 2025
University of Regensburg, Faculty of Chemistry and Pharmacy, Institute of Inorganic Chemistry, Universitätsstraße 31, D-93053, Regensburg, GERMANY.
Aminophosphates are the focus of research on prebiotic phosphorylation chemistry. Their bifunctional nature also makes them a powerful class of organocatalysts. However, the structural chemistry and dynamics of proton-binding in phosphorylation and organocatalytic mechanisms are still not fully understood.
View Article and Find Full Text PDFInorg Chem
January 2025
Testing and Analysis Center, Hebei Normal University, Shijiazhuang 050024, China.
The bipyridyl tantalum complex (2,6-PrCHO)Ta(bipy) () is synthesized by the reaction of (2,6-PrCHO)TaCl () and 2,2'-bipyridine in the presence of excess potassium graphite (KC). Complex coordinates readily with pyridine and 4-(dimethylamino)pyridine (dmap) to form Lewis base adducts (2,6-PrCHO)Ta(bipy)(L) (L = py (), dmap ()), and it exhibits rich redox reactivity toward small molecules: (a) single electron transfer (SET) occurs upon exposure of to phenyl sulfide or selenide dimer, giving the open-shell, bipy-centered radical complexes (2,6-PrCHO)Ta(bipy)(PhE) (E = S (), Se ()). (b) Regioselective C-C σ-bond formation via radical coupling is observed in the SET reaction of and aldehydes, ketones, or imines to furnish insertion products -, namely, sterically more crowded benzophenone, acetophenone, 2,6-dichlorobenzaldehyde, and benzophenone imine couple with C6 or C6' of bipy in , respectively, whereas sterically less hindered benzaldehyde, cyclohexanone, and benzylideneaniline couple with C2 or C2' of bipy, respectively.
View Article and Find Full Text PDFJ Org Chem
January 2025
Institute of Materia Medica, School of Pharmaceutical Sciences, Nanjing Tech University, Nanjing 211816, P. R. China.
In this study, we present a novel catalyst-free energy transfer mediated radical rearrangement strategy for the aryl-heterofunctionalization of unactivated alkynes, leading to the synthesis of polyfunctional olefins with exceptional stereoselectivity. This innovative approach, driven by visible light, exemplifies green chemistry principles by eliminating the reliance on transition metals, external oxidants, and photocatalysts. The broad applicability of our method is demonstrated through the successful synthesis of a diverse array of compounds, including vinyl sulfones, vinyl selenides, and vinyl sulfides.
View Article and Find Full Text PDFJ Colloid Interface Sci
April 2025
Key Lab of Eco-Environments Related Polymer Materials of MOE, Key Lab of Bioelectrochemistry and Environmental Analysis of Gansu Province, College of Chemistry and Chemical Engineering, Northwest Normal University, Gansu International Scientific and Technological Cooperation Base of Water-Retention Chemical Functional Materials, Lanzhou 730070, PR China. Electronic address:
Transition metal sulfides (TMSs) have significant potential in energy storage applications due to their high theoretical capacity and diverse reaction mechanisms. However, performance limitations in supercapacitors arise from various intrinsic defects, including low active material utilization and poor cycling stability caused by unstable electrical conductivity. To address these issues, this paper incorporates selenium atoms into sulfides, aiming to leverage selenium's high conductivity to enhance the electroactivity of transition metal sulfides.
View Article and Find Full Text PDFSmall
December 2024
Institute of Photoelectronic Thin Film Devices and Technology, Renewable Energy Conversion and Storage Center, State Key Laboratory of Photovoltaic Materials and Cells, Nankai University, Tianjin, 300350, P. R. China.
Photovoltaic-driven electrochemical (PV-EC) carbon dioxide reduction (COR) coupled with sulfide oxidation (SOR) can efficiently convert the solar energy into chemical energy, expanding its applications. However, developing low-cost electrocatalysts that exhibit high selectivity and efficiency for both COR and SOR remains a challenge. Herein, a bifunctional copper selenide catalyst is developed with copper vacancies (v-CuSe) for the COR-SOR.
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