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Evidencing enhanced charge-transfer with superior Photocatalytic degradation and Photoelectrochemical water splitting in Mg modified few-layered SnS2
摘要： Recently there has been immense interest in the exploration of richly available two-dimensional non-toxic layered material such as tin disulfide (SnS2) for potential employment in energy and environmental needs. In this regard, we report on the synthesis of few-layered Sn1?xMgxS2 nanosheets through a facile one-step hydrothermal route to address all such functions concerning photocatalysis and photoelectrochemical conversion. The crystalline order and structure of processed layered Sn1?xMgxS2 were initially found to exhibit a strong influence on their physicochemical properties. Their optical properties attest the Mg doping in SnS2 to benefit us with enhanced visible-light absorption via red-shift in their absorption edge. In the photoluminescence spectrum the emissions observed along visible and red region signifies the association of Mg related trap states in Sn1?xMgxS2. Next, the photocurrent and electrochemical impedance spectroscopic results revealed the Mg doping to promote the effective charge transfer process (which was beneficial to enhance their photocatalytic activity). Consequently, the layered Sn0.98Mg0.02S2 made photoanodes displayed 1.7 fold higher photocurrent density under simulated solar radiation with respect to their undoped counterpart. Furthermore, the layered Sn0.98Mg0.02S2 nanosheets exhibits enhanced visible light decomposition of organic dye while compared with pristine SnS2 nanosheets. The value of rate constants obtained for the Sn0.98Mg0.02S2 nanosheets was found to be 1.4 times higher than that of pristine SnS2. Finally, the results obtained through the present study projects the huge potential of layered Sn0.98Mg0.02S2 nanosheets for future multifunctional applications.
关键词： SnS2,Magnesium,Nanosheets,Photocatalysis,Few-layered,Photoelectrochemical water splitting
更新于2025-09-23 15:22:29
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Preparation of Few-Layered Wide Bandgap MoS2 with Nanometer Lateral Dimensions by Applying Laser Irradiation
摘要： In this study, we report a new method for the quick, green, and one-step preparation of few-layered molybdenum disulfide (MoS2) nanosheets with wide bandgap. MoS2 nanosheets with small lateral dimension and uniform size distribution were synthesized for various applications. MoS2 powder was synthesized using the hydrothermal method; then, thinned by applying laser irradiation with different energies from 40 to 80 mJ. Transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), UV-Vis absorption spectra, and photoluminescence (PL) spectra were applied for the characterization of the MoS2 nanosheets in terms of morphology, crystal structures, and optical properties. The widest calculated bandgap 4.7 eV was for the sample under 80 mJ laser energy. The results confirmed the successful preparation of highly pure, uniform, and few-layered MoS2 nanosheets. Furthermore, it was possible to enhance the production rate of MoS2 nanosheets (including nanosheets and nanoparticles) through laser irradiation. Thus, the present paper introduces a simple and green alternative approach for preparing few-layered MoS2 nanosheets of transition metal dichalcogenides or other layered materials.
关键词： low lateral dimension,few-layered,laser,molybdenum disulfide
更新于2025-09-23 15:19:57
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Natural organic matter inhibits aggregation of few-layered black phosphorus in mono- and divalent electrolyte solutions
摘要： Extensive synthesis and applications of few-layered black phosphorus (BPs) are accompanied by increasing concern over its stability and potential risk. However, the colloidal stability of BPs under environmentally relevant conditions remains unclear. Hence, we investigated the influences of two representative electrolytes (i.e., NaCl and CaCl2) and natural organic matter (NOM) on the aggregation behavior of BPs. Ca2+ ions exhibited a stronger destabilization effect on BPs than Na+ due to their stronger surface charge screening as well as intersheet bridging by the complexes of Ca2+ ions and oxidized phosphorus (POx) species on the BPs surface. Apart from the Ca2+-induced enhanced aggregation in the presence of high concentration of Ca2+, the aggregation behavior of BPs in the two electrolytes at different concentrations and their ratios of critical coagulation concentrations (CCCs) generally followed classical colloidal theory such as the Schulze–Hardy rule. Moreover, in the presence of 10 mg C/L NOM the CCC values of BPs in NaCl and CaCl2 solutions were both three times higher than that obtained without NOM, and the aggregation kinetics of BPs in these electrolytes containing NOM were qualitatively consistent with extended DLVO theory. Specifically, NOM significantly improved the stabilization of BPs in CaCl2 solutions via steric repulsion and isolation of Ca2+ ions from interaction with POx species on the surface of BPs. This stabilization mechanism derived from “NOM corona” structures was elucidated by a wide spectrum of characterization and quantification techniques. These findings provide new insights into evaluating the stability and fate of this nanomaterial in natural aquatic environments.
关键词： few-layered black phosphorus,colloidal stability,NOM corona,aggregation,electrolytes,natural organic matter
更新于2025-09-19 17:15:36